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Update on therapies for lymphoproliferative disorders

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Update on therapies for lymphoproliferative disorders
Diabetes mellitus as a late effect of the treatment of Hodgkin lymphoma.1

 

Two recent follow-up studies of childhood cancer patients who had been treated with abdominal radiation revealed an increased risk of diabetes mellitus (DM) in the survivors. In the past, many patients with a diagnosis of Hodgkin lymphoma (HL) were also treated with infradiaphragmatic radiation. The para-aortic and splenic fields used for this treatment encompasses most of the pancreas, including the tail. Since diabetes is a risk factor for cardiovascular disease, it is conceivable that an increase in diabetes in survivors of HL might contribute to their increased risk of cardiovascular disease. In this recent study of adults, the results of the treatment of 2,352 Dutch 5-year survivors of HL treatment who were younger than 51 years at the time of diagnosis were analyzed. Detailed records of their treatment and late effects of treatment were obtained, including information about DM, hypertension, hypercholesterolemia, smoking, and obesity. Radiation dose to the pancreas was estimated. 

 

Click on the PDF icon at the top of this introduction to read the full article.

 

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The Journal of Community and Supportive Oncology - 13(1)
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34-36
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Hodgkin lymphoma, RESORT trial, lymphoma, lymphocytic leukemia
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Diabetes mellitus as a late effect of the treatment of Hodgkin lymphoma.1

 

Two recent follow-up studies of childhood cancer patients who had been treated with abdominal radiation revealed an increased risk of diabetes mellitus (DM) in the survivors. In the past, many patients with a diagnosis of Hodgkin lymphoma (HL) were also treated with infradiaphragmatic radiation. The para-aortic and splenic fields used for this treatment encompasses most of the pancreas, including the tail. Since diabetes is a risk factor for cardiovascular disease, it is conceivable that an increase in diabetes in survivors of HL might contribute to their increased risk of cardiovascular disease. In this recent study of adults, the results of the treatment of 2,352 Dutch 5-year survivors of HL treatment who were younger than 51 years at the time of diagnosis were analyzed. Detailed records of their treatment and late effects of treatment were obtained, including information about DM, hypertension, hypercholesterolemia, smoking, and obesity. Radiation dose to the pancreas was estimated. 

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Diabetes mellitus as a late effect of the treatment of Hodgkin lymphoma.1

 

Two recent follow-up studies of childhood cancer patients who had been treated with abdominal radiation revealed an increased risk of diabetes mellitus (DM) in the survivors. In the past, many patients with a diagnosis of Hodgkin lymphoma (HL) were also treated with infradiaphragmatic radiation. The para-aortic and splenic fields used for this treatment encompasses most of the pancreas, including the tail. Since diabetes is a risk factor for cardiovascular disease, it is conceivable that an increase in diabetes in survivors of HL might contribute to their increased risk of cardiovascular disease. In this recent study of adults, the results of the treatment of 2,352 Dutch 5-year survivors of HL treatment who were younger than 51 years at the time of diagnosis were analyzed. Detailed records of their treatment and late effects of treatment were obtained, including information about DM, hypertension, hypercholesterolemia, smoking, and obesity. Radiation dose to the pancreas was estimated. 

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Issue
The Journal of Community and Supportive Oncology - 13(1)
Issue
The Journal of Community and Supportive Oncology - 13(1)
Page Number
34-36
Page Number
34-36
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Update on therapies for lymphoproliferative disorders
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Update on therapies for lymphoproliferative disorders
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Hodgkin lymphoma, RESORT trial, lymphoma, lymphocytic leukemia
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Hodgkin lymphoma, RESORT trial, lymphoma, lymphocytic leukemia
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Immunotherapy moves into the breast cancer landscape

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Immunotherapy moves into the breast cancer landscape
At this year’s San Antonio Breast Cancer Symposium, investigators presented some encouraging findings for difficult-to-treat patient populations, but issues such as therapy side effects and fertility concerns in younger patients also highlighted the importance of looking closely at the risk-benefit relationship in delivering quality, personalized care to patients with breast cancer.  

 

Click on the PDF icon at the top of this introduction to read the full article.

 

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The Journal of Community and Supportive Oncology - 13(1)
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30-33
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breast cancer, immunotherapy, pembrolizumab, SOFT trial, ovarian supression, tamoxifen, fulvestrant
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At this year’s San Antonio Breast Cancer Symposium, investigators presented some encouraging findings for difficult-to-treat patient populations, but issues such as therapy side effects and fertility concerns in younger patients also highlighted the importance of looking closely at the risk-benefit relationship in delivering quality, personalized care to patients with breast cancer.  

 

Click on the PDF icon at the top of this introduction to read the full article.

 

At this year’s San Antonio Breast Cancer Symposium, investigators presented some encouraging findings for difficult-to-treat patient populations, but issues such as therapy side effects and fertility concerns in younger patients also highlighted the importance of looking closely at the risk-benefit relationship in delivering quality, personalized care to patients with breast cancer.  

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Issue
The Journal of Community and Supportive Oncology - 13(1)
Issue
The Journal of Community and Supportive Oncology - 13(1)
Page Number
30-33
Page Number
30-33
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Immunotherapy moves into the breast cancer landscape
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Immunotherapy moves into the breast cancer landscape
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breast cancer, immunotherapy, pembrolizumab, SOFT trial, ovarian supression, tamoxifen, fulvestrant
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breast cancer, immunotherapy, pembrolizumab, SOFT trial, ovarian supression, tamoxifen, fulvestrant
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Radiation exposure from diagnostic procedures in patients with newly diagnosed breast cancer

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Radiation exposure from diagnostic procedures in patients with newly diagnosed breast cancer

Radiation exposure is associated with an increased risk of secondary cancers. Knowing the approximate radiation exposure from diagnostic procedures in the first year after a breast cancer diagnosis could help educate patients and allow physicians to monitor them more closely for potential risks.

 

Click on the PDF icon at the top of this introduction to read the full article.

 

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The Journal of Community and Supportive Oncology - 13(1)
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27-29
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breast cancer, radiation exposure, secondary cancer, diagnostic procedures
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Radiation exposure is associated with an increased risk of secondary cancers. Knowing the approximate radiation exposure from diagnostic procedures in the first year after a breast cancer diagnosis could help educate patients and allow physicians to monitor them more closely for potential risks.

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Radiation exposure is associated with an increased risk of secondary cancers. Knowing the approximate radiation exposure from diagnostic procedures in the first year after a breast cancer diagnosis could help educate patients and allow physicians to monitor them more closely for potential risks.

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Issue
The Journal of Community and Supportive Oncology - 13(1)
Issue
The Journal of Community and Supportive Oncology - 13(1)
Page Number
27-29
Page Number
27-29
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Radiation exposure from diagnostic procedures in patients with newly diagnosed breast cancer
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Radiation exposure from diagnostic procedures in patients with newly diagnosed breast cancer
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breast cancer, radiation exposure, secondary cancer, diagnostic procedures
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breast cancer, radiation exposure, secondary cancer, diagnostic procedures
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Rectal cancer management in elderly patients: experience of a single Portuguese institution

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Rectal cancer management in elderly patients: experience of a single Portuguese institution
Background The incidence of rectal cancer increases with age, and older patients are more likely to have other chronic conditions that can affect outcome and tolerability of treatment.

 

Objective To evaluate retrospectively the influence of age and comorbidities in the management of rectal cancer.

 

Methods 59 patients aged 75 years and older with stage II-III rectal cancer who were treated during a 3-year period were included in the study. Comorbidities were assessed using the Charlson Comorbidity Index (CCI) and the patients were divided into 2 groups based on their CCI scores: Fit (score of 0-1 points) and Vulnerable (score of ≥ 2). Primary endpoint was survival at 1 and 3 years.

 

Results The sample included 43 patients (72.9%) in the Fit group and 16 patients (27.1%) in the Vulnerable group. The most common comorbidities were myocardial infarction, diabetes, and chronic lung disease. One-year survival the same between the groups (P = .330), but 3-year survival was lower in the Vulnerable group patients (83.7% vs 56.3%, respectively; P = .040). The rates of neoadjuvant chemo- and radiotherapy use and low anterior resection performance were the same between the groups. Colostomy closure was achieved more frequently in the Fit group compared with the Vulnerable group (83.3% vs 55.6%; P = .083). There was no difference in mean disease-free survival, grade 3-4 toxicity, and dose reduction between the groups.

 

Conclusions Comorbidity assessment should always be included in standard oncological management of elderly patients. Fit patients can be managed with standard treatment and may benefit from a conventional, more aggressive approach in their therapy. 

 

Click on the PDF icon at the top of this introduction to read the full article.

 

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Issue
The Journal of Community and Supportive Oncology - 13(1)
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Page Number
8-13
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rectal cancer, Charlson Comorbidity index, CCI
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Background The incidence of rectal cancer increases with age, and older patients are more likely to have other chronic conditions that can affect outcome and tolerability of treatment.

 

Objective To evaluate retrospectively the influence of age and comorbidities in the management of rectal cancer.

 

Methods 59 patients aged 75 years and older with stage II-III rectal cancer who were treated during a 3-year period were included in the study. Comorbidities were assessed using the Charlson Comorbidity Index (CCI) and the patients were divided into 2 groups based on their CCI scores: Fit (score of 0-1 points) and Vulnerable (score of ≥ 2). Primary endpoint was survival at 1 and 3 years.

 

Results The sample included 43 patients (72.9%) in the Fit group and 16 patients (27.1%) in the Vulnerable group. The most common comorbidities were myocardial infarction, diabetes, and chronic lung disease. One-year survival the same between the groups (P = .330), but 3-year survival was lower in the Vulnerable group patients (83.7% vs 56.3%, respectively; P = .040). The rates of neoadjuvant chemo- and radiotherapy use and low anterior resection performance were the same between the groups. Colostomy closure was achieved more frequently in the Fit group compared with the Vulnerable group (83.3% vs 55.6%; P = .083). There was no difference in mean disease-free survival, grade 3-4 toxicity, and dose reduction between the groups.

 

Conclusions Comorbidity assessment should always be included in standard oncological management of elderly patients. Fit patients can be managed with standard treatment and may benefit from a conventional, more aggressive approach in their therapy. 

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Background The incidence of rectal cancer increases with age, and older patients are more likely to have other chronic conditions that can affect outcome and tolerability of treatment.

 

Objective To evaluate retrospectively the influence of age and comorbidities in the management of rectal cancer.

 

Methods 59 patients aged 75 years and older with stage II-III rectal cancer who were treated during a 3-year period were included in the study. Comorbidities were assessed using the Charlson Comorbidity Index (CCI) and the patients were divided into 2 groups based on their CCI scores: Fit (score of 0-1 points) and Vulnerable (score of ≥ 2). Primary endpoint was survival at 1 and 3 years.

 

Results The sample included 43 patients (72.9%) in the Fit group and 16 patients (27.1%) in the Vulnerable group. The most common comorbidities were myocardial infarction, diabetes, and chronic lung disease. One-year survival the same between the groups (P = .330), but 3-year survival was lower in the Vulnerable group patients (83.7% vs 56.3%, respectively; P = .040). The rates of neoadjuvant chemo- and radiotherapy use and low anterior resection performance were the same between the groups. Colostomy closure was achieved more frequently in the Fit group compared with the Vulnerable group (83.3% vs 55.6%; P = .083). There was no difference in mean disease-free survival, grade 3-4 toxicity, and dose reduction between the groups.

 

Conclusions Comorbidity assessment should always be included in standard oncological management of elderly patients. Fit patients can be managed with standard treatment and may benefit from a conventional, more aggressive approach in their therapy. 

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Issue
The Journal of Community and Supportive Oncology - 13(1)
Issue
The Journal of Community and Supportive Oncology - 13(1)
Page Number
8-13
Page Number
8-13
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Publications
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Article Type
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Rectal cancer management in elderly patients: experience of a single Portuguese institution
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Rectal cancer management in elderly patients: experience of a single Portuguese institution
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rectal cancer, Charlson Comorbidity index, CCI
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rectal cancer, Charlson Comorbidity index, CCI
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Use of atropine-diphenoxylate compared with hyoscyamine to decrease rates of irinotecan-related cholinergic syndrome

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Use of atropine-diphenoxylate compared with hyoscyamine to decrease rates of irinotecan-related cholinergic syndrome
Background Cholinergic syndrome is a well established acute adverse reaction associated with irinotecan. Cholinergic side effects can be ameliorated or prevented with anticholinergic agents. To date, no formal studies have compared atropine-diphenoxylate and hyoscyamine as premedications for prophylaxis of the cholinergic syndrome with irinotecan infusion.

 

Objective To compare the incidence of cholinergic syndrome with irinotecan using atropine-diphenoxylate or hyoscyamine as premedication.

 

Methods We conducted a retrospective, single-center, nonrandomized, cohort study of adult patients treated with atropine-diphenoxylate or hyoscyamine as premedication before receiving irinotecan. For all irinotecan infusions, intravenous atropine was administered for patients experiencing any cholinergic reaction.

 

Results A total of 532 irinotecan cycles (354 cycles for atropine-diphenoxylate group; 178 cycles for hyoscyamine group) were analyzed in 80 patients. Overall incidence of cholinergic syndrome did not differ between atropine-diphenoxylate (8.2%) and hyoscyamine (9.0%) groups (P = .76). The incidence of cholinergic syndrome after the first cycle of irinotecan was similar between the 2 arms, atropine-diphenoxylate (14.6%) and hyoscyamine (10.7%), with P = .74. The most common cholinergic symptoms documented were abdominal pain or cramping, and diarrhea.

 

Limitations This study was subjected to vulnerabilities to bias and random error because of its observational retrospective design and small number of participants.

 

Conclusions Lack of difference in the incidence of cholinergic syndrome observed in irinotecan-treated patients suggests atropine-diphenoxylate and hyoscyamine may both be effective prophylactic options. The findings support the need for a larger, randomized study to assess and compare these agents with other potential premedications such as scopolamine and atropine in prevention of irinotecan-related cholinergic syndrome.

 

Click on the PDF icon at the top of this introduction to read the full article.

 

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Issue
The Journal of Community and Supportive Oncology - 13(1)
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Page Number
3-7
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atropine-diphenoxylate, hyoscyamine, irinotecan, cholinergic syndrome
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Background Cholinergic syndrome is a well established acute adverse reaction associated with irinotecan. Cholinergic side effects can be ameliorated or prevented with anticholinergic agents. To date, no formal studies have compared atropine-diphenoxylate and hyoscyamine as premedications for prophylaxis of the cholinergic syndrome with irinotecan infusion.

 

Objective To compare the incidence of cholinergic syndrome with irinotecan using atropine-diphenoxylate or hyoscyamine as premedication.

 

Methods We conducted a retrospective, single-center, nonrandomized, cohort study of adult patients treated with atropine-diphenoxylate or hyoscyamine as premedication before receiving irinotecan. For all irinotecan infusions, intravenous atropine was administered for patients experiencing any cholinergic reaction.

 

Results A total of 532 irinotecan cycles (354 cycles for atropine-diphenoxylate group; 178 cycles for hyoscyamine group) were analyzed in 80 patients. Overall incidence of cholinergic syndrome did not differ between atropine-diphenoxylate (8.2%) and hyoscyamine (9.0%) groups (P = .76). The incidence of cholinergic syndrome after the first cycle of irinotecan was similar between the 2 arms, atropine-diphenoxylate (14.6%) and hyoscyamine (10.7%), with P = .74. The most common cholinergic symptoms documented were abdominal pain or cramping, and diarrhea.

 

Limitations This study was subjected to vulnerabilities to bias and random error because of its observational retrospective design and small number of participants.

 

Conclusions Lack of difference in the incidence of cholinergic syndrome observed in irinotecan-treated patients suggests atropine-diphenoxylate and hyoscyamine may both be effective prophylactic options. The findings support the need for a larger, randomized study to assess and compare these agents with other potential premedications such as scopolamine and atropine in prevention of irinotecan-related cholinergic syndrome.

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Background Cholinergic syndrome is a well established acute adverse reaction associated with irinotecan. Cholinergic side effects can be ameliorated or prevented with anticholinergic agents. To date, no formal studies have compared atropine-diphenoxylate and hyoscyamine as premedications for prophylaxis of the cholinergic syndrome with irinotecan infusion.

 

Objective To compare the incidence of cholinergic syndrome with irinotecan using atropine-diphenoxylate or hyoscyamine as premedication.

 

Methods We conducted a retrospective, single-center, nonrandomized, cohort study of adult patients treated with atropine-diphenoxylate or hyoscyamine as premedication before receiving irinotecan. For all irinotecan infusions, intravenous atropine was administered for patients experiencing any cholinergic reaction.

 

Results A total of 532 irinotecan cycles (354 cycles for atropine-diphenoxylate group; 178 cycles for hyoscyamine group) were analyzed in 80 patients. Overall incidence of cholinergic syndrome did not differ between atropine-diphenoxylate (8.2%) and hyoscyamine (9.0%) groups (P = .76). The incidence of cholinergic syndrome after the first cycle of irinotecan was similar between the 2 arms, atropine-diphenoxylate (14.6%) and hyoscyamine (10.7%), with P = .74. The most common cholinergic symptoms documented were abdominal pain or cramping, and diarrhea.

 

Limitations This study was subjected to vulnerabilities to bias and random error because of its observational retrospective design and small number of participants.

 

Conclusions Lack of difference in the incidence of cholinergic syndrome observed in irinotecan-treated patients suggests atropine-diphenoxylate and hyoscyamine may both be effective prophylactic options. The findings support the need for a larger, randomized study to assess and compare these agents with other potential premedications such as scopolamine and atropine in prevention of irinotecan-related cholinergic syndrome.

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Issue
The Journal of Community and Supportive Oncology - 13(1)
Issue
The Journal of Community and Supportive Oncology - 13(1)
Page Number
3-7
Page Number
3-7
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Use of atropine-diphenoxylate compared with hyoscyamine to decrease rates of irinotecan-related cholinergic syndrome
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Use of atropine-diphenoxylate compared with hyoscyamine to decrease rates of irinotecan-related cholinergic syndrome
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atropine-diphenoxylate, hyoscyamine, irinotecan, cholinergic syndrome
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atropine-diphenoxylate, hyoscyamine, irinotecan, cholinergic syndrome
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Dying in America: implications for oncology of the recent IOM report

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Dying in America: implications for oncology of the recent IOM report
Those of us who work in clinical oncology are used to thinking about how to improve care for our dying patients. We may be less familiar with efforts to extend the benefits of palliative care to patients and families facing other kinds of advancing catastrophic illnesses, such as lung, cardiac, and neurologic diseases. In September last year, the Institute of Medicine of the National Academies released a report titled Dying in America: improving quality and honoring individual preferences near the end of life.1 This ambitious work encompasses the needs of all patients with potentially lethal illnesses, not just cancer.

 

Click on the PDF icon at the top of this introduction to read the full article.

 

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The Journal of Community and Supportive Oncology - 13(1)
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1-2
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palliative care, person-centered, end of life, hospice, Institute of Medicine, IOM
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Those of us who work in clinical oncology are used to thinking about how to improve care for our dying patients. We may be less familiar with efforts to extend the benefits of palliative care to patients and families facing other kinds of advancing catastrophic illnesses, such as lung, cardiac, and neurologic diseases. In September last year, the Institute of Medicine of the National Academies released a report titled Dying in America: improving quality and honoring individual preferences near the end of life.1 This ambitious work encompasses the needs of all patients with potentially lethal illnesses, not just cancer.

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Those of us who work in clinical oncology are used to thinking about how to improve care for our dying patients. We may be less familiar with efforts to extend the benefits of palliative care to patients and families facing other kinds of advancing catastrophic illnesses, such as lung, cardiac, and neurologic diseases. In September last year, the Institute of Medicine of the National Academies released a report titled Dying in America: improving quality and honoring individual preferences near the end of life.1 This ambitious work encompasses the needs of all patients with potentially lethal illnesses, not just cancer.

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Issue
The Journal of Community and Supportive Oncology - 13(1)
Issue
The Journal of Community and Supportive Oncology - 13(1)
Page Number
1-2
Page Number
1-2
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Dying in America: implications for oncology of the recent IOM report
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Dying in America: implications for oncology of the recent IOM report
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palliative care, person-centered, end of life, hospice, Institute of Medicine, IOM
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Impact of a telehealth intervention on quality of life and symptom distress in patients with head and neck cancer

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Impact of a telehealth intervention on quality of life and symptom distress in patients with head and neck cancer
Background Patients undergoing treatment for head and neck cancer commonly experience significant changes in quality of life (QoL) and levels of symptom distress. It is not known if a telehealth intervention would mitigate these changes.

 

Objective To evaluate the impact of a telehealth intervention on QoL and symptom burden in patients undergoing initial treatment for head and neck cancers.

 

Methods A randomized clinical trial comparing the impact on QoL and symptom distress of telehealth intervention and standard care was conducted with 80 patients (45 treatment, 35 control) who had been diagnosed with head or neck cancer and were receiving 1 or more treatment modalities. Treatment group participants responded daily to symptom management algorithms using a simple telehealth messaging device. QoL was evaluated by the Functional Assessment of Cancer Therapy-Head&Neck Scale (FACT-HN) and symptom burden by the Memorial Symptom Assessment Scale (MSAS). Control group participants completed assessments while they received routine care.

 

Results In the posttreatment phase, the telehealth participants had significantly better scores than the controls for physical well-being (20.6 vs 17.0, P = .02) and trial outcome index (59.9 vs. 50.2, P = .04) on the FACT-HN, and total scores on the MSAS (0.9 vs. 1.2, P = .04).

 

Limitations The moderate sample size of 80 patients limits the power to measure more subtle impacts of the intervention.

 

Conclusions Using telehealth to provide support to patients with head and neck cancer during the acute phase of treatment improved some aspects of posttreatment QoL and symptom burden.

 

Funding Supported in part by NIH R21CA115345 from the National Cancer Institute. 

 

Click on the PDF icon at the top of this introduction to read the full article.

 

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Issue
The Journal of Community and Supportive Oncology - 13(1)
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Page Number
14-21
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telehealth, quality of life, QoL, symptom distress, head and neck cancer, Functional Assessment of Cancer Therapy, FACT-HN
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Background Patients undergoing treatment for head and neck cancer commonly experience significant changes in quality of life (QoL) and levels of symptom distress. It is not known if a telehealth intervention would mitigate these changes.

 

Objective To evaluate the impact of a telehealth intervention on QoL and symptom burden in patients undergoing initial treatment for head and neck cancers.

 

Methods A randomized clinical trial comparing the impact on QoL and symptom distress of telehealth intervention and standard care was conducted with 80 patients (45 treatment, 35 control) who had been diagnosed with head or neck cancer and were receiving 1 or more treatment modalities. Treatment group participants responded daily to symptom management algorithms using a simple telehealth messaging device. QoL was evaluated by the Functional Assessment of Cancer Therapy-Head&Neck Scale (FACT-HN) and symptom burden by the Memorial Symptom Assessment Scale (MSAS). Control group participants completed assessments while they received routine care.

 

Results In the posttreatment phase, the telehealth participants had significantly better scores than the controls for physical well-being (20.6 vs 17.0, P = .02) and trial outcome index (59.9 vs. 50.2, P = .04) on the FACT-HN, and total scores on the MSAS (0.9 vs. 1.2, P = .04).

 

Limitations The moderate sample size of 80 patients limits the power to measure more subtle impacts of the intervention.

 

Conclusions Using telehealth to provide support to patients with head and neck cancer during the acute phase of treatment improved some aspects of posttreatment QoL and symptom burden.

 

Funding Supported in part by NIH R21CA115345 from the National Cancer Institute. 

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Background Patients undergoing treatment for head and neck cancer commonly experience significant changes in quality of life (QoL) and levels of symptom distress. It is not known if a telehealth intervention would mitigate these changes.

 

Objective To evaluate the impact of a telehealth intervention on QoL and symptom burden in patients undergoing initial treatment for head and neck cancers.

 

Methods A randomized clinical trial comparing the impact on QoL and symptom distress of telehealth intervention and standard care was conducted with 80 patients (45 treatment, 35 control) who had been diagnosed with head or neck cancer and were receiving 1 or more treatment modalities. Treatment group participants responded daily to symptom management algorithms using a simple telehealth messaging device. QoL was evaluated by the Functional Assessment of Cancer Therapy-Head&Neck Scale (FACT-HN) and symptom burden by the Memorial Symptom Assessment Scale (MSAS). Control group participants completed assessments while they received routine care.

 

Results In the posttreatment phase, the telehealth participants had significantly better scores than the controls for physical well-being (20.6 vs 17.0, P = .02) and trial outcome index (59.9 vs. 50.2, P = .04) on the FACT-HN, and total scores on the MSAS (0.9 vs. 1.2, P = .04).

 

Limitations The moderate sample size of 80 patients limits the power to measure more subtle impacts of the intervention.

 

Conclusions Using telehealth to provide support to patients with head and neck cancer during the acute phase of treatment improved some aspects of posttreatment QoL and symptom burden.

 

Funding Supported in part by NIH R21CA115345 from the National Cancer Institute. 

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Issue
The Journal of Community and Supportive Oncology - 13(1)
Issue
The Journal of Community and Supportive Oncology - 13(1)
Page Number
14-21
Page Number
14-21
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Impact of a telehealth intervention on quality of life and symptom distress in patients with head and neck cancer
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Impact of a telehealth intervention on quality of life and symptom distress in patients with head and neck cancer
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telehealth, quality of life, QoL, symptom distress, head and neck cancer, Functional Assessment of Cancer Therapy, FACT-HN
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telehealth, quality of life, QoL, symptom distress, head and neck cancer, Functional Assessment of Cancer Therapy, FACT-HN
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Beneficial effects of animal-assisted visits on quality of life during multimodal radiation-chemotherapy regimens

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Beneficial effects of animal-assisted visits on quality of life during multimodal radiation-chemotherapy regimens
Objective To test the efficacy of AAVs in improving the quality of life in patients with head and neck cancer receiving combined chemotherapy-radiation therapy.

 

Methods 42 patients consented to daily AAVs during the time they received therapy for head and neck cancer. The Functional Assessment of Cancer Therapy-General Scale (FACT-G) was administered at baseline, week 3, and week 7 (at the end of therapy), and the Satisfaction With The AAV Intervention instrument, an 18-item scale adapted from the Pet Attitude Scale.

 

Results 37 patients completed at least baseline and 1 follow-up assessment for a single group analysis of change over time. Means for FACT-G subscales showed significant declines in Physical Well-Being (PWB, P < .001) and Functional Well-Being (FWB, P = .003). In contrast, Social Well-Being increased (SWB, P = .03). Controlling for declines in PWB at each time point, increases in Emotional Well-Being (EWB) were also significant (P = .004).

 

Limitations Scheduling and patient preference prevented conducting a randomized trial.

 

Conclusion FACT-G analysis showed significant increase in SWB and EWB despite high symptom burden and clinically evident and expected declines in PWB and FWB. Mean scores for satisfaction related to psychological symptoms, liking animals/pets, and contact with animals were consistently higher than neutral score or Unsure (all P < .001). Satisfaction related to physical symptoms was not significantly different from neutral. Though self-selected for an affinity to pets, patients endorsed a high level of satisfaction, which supports the usefulness of the intervention.

 

Funding Grant from the Good Dog Foundation and Pfizer Animal Health (now Zoetis Animal Health) 

 

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Issue
The Journal of Community and Supportive Oncology - 13(1)
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22-26
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animal-assisted visit, AAV, Functional Assessment of Cancer Therapy, FACT-G, multimodal radiation-chemotherapy
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Objective To test the efficacy of AAVs in improving the quality of life in patients with head and neck cancer receiving combined chemotherapy-radiation therapy.

 

Methods 42 patients consented to daily AAVs during the time they received therapy for head and neck cancer. The Functional Assessment of Cancer Therapy-General Scale (FACT-G) was administered at baseline, week 3, and week 7 (at the end of therapy), and the Satisfaction With The AAV Intervention instrument, an 18-item scale adapted from the Pet Attitude Scale.

 

Results 37 patients completed at least baseline and 1 follow-up assessment for a single group analysis of change over time. Means for FACT-G subscales showed significant declines in Physical Well-Being (PWB, P < .001) and Functional Well-Being (FWB, P = .003). In contrast, Social Well-Being increased (SWB, P = .03). Controlling for declines in PWB at each time point, increases in Emotional Well-Being (EWB) were also significant (P = .004).

 

Limitations Scheduling and patient preference prevented conducting a randomized trial.

 

Conclusion FACT-G analysis showed significant increase in SWB and EWB despite high symptom burden and clinically evident and expected declines in PWB and FWB. Mean scores for satisfaction related to psychological symptoms, liking animals/pets, and contact with animals were consistently higher than neutral score or Unsure (all P < .001). Satisfaction related to physical symptoms was not significantly different from neutral. Though self-selected for an affinity to pets, patients endorsed a high level of satisfaction, which supports the usefulness of the intervention.

 

Funding Grant from the Good Dog Foundation and Pfizer Animal Health (now Zoetis Animal Health) 

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Objective To test the efficacy of AAVs in improving the quality of life in patients with head and neck cancer receiving combined chemotherapy-radiation therapy.

 

Methods 42 patients consented to daily AAVs during the time they received therapy for head and neck cancer. The Functional Assessment of Cancer Therapy-General Scale (FACT-G) was administered at baseline, week 3, and week 7 (at the end of therapy), and the Satisfaction With The AAV Intervention instrument, an 18-item scale adapted from the Pet Attitude Scale.

 

Results 37 patients completed at least baseline and 1 follow-up assessment for a single group analysis of change over time. Means for FACT-G subscales showed significant declines in Physical Well-Being (PWB, P < .001) and Functional Well-Being (FWB, P = .003). In contrast, Social Well-Being increased (SWB, P = .03). Controlling for declines in PWB at each time point, increases in Emotional Well-Being (EWB) were also significant (P = .004).

 

Limitations Scheduling and patient preference prevented conducting a randomized trial.

 

Conclusion FACT-G analysis showed significant increase in SWB and EWB despite high symptom burden and clinically evident and expected declines in PWB and FWB. Mean scores for satisfaction related to psychological symptoms, liking animals/pets, and contact with animals were consistently higher than neutral score or Unsure (all P < .001). Satisfaction related to physical symptoms was not significantly different from neutral. Though self-selected for an affinity to pets, patients endorsed a high level of satisfaction, which supports the usefulness of the intervention.

 

Funding Grant from the Good Dog Foundation and Pfizer Animal Health (now Zoetis Animal Health) 

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Issue
The Journal of Community and Supportive Oncology - 13(1)
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The Journal of Community and Supportive Oncology - 13(1)
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22-26
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22-26
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Beneficial effects of animal-assisted visits on quality of life during multimodal radiation-chemotherapy regimens
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Beneficial effects of animal-assisted visits on quality of life during multimodal radiation-chemotherapy regimens
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animal-assisted visit, AAV, Functional Assessment of Cancer Therapy, FACT-G, multimodal radiation-chemotherapy
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animal-assisted visit, AAV, Functional Assessment of Cancer Therapy, FACT-G, multimodal radiation-chemotherapy
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JCSO 2015;13:22-26
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David Henry's JCSO podcast, December 2014

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David Henry's JCSO podcast, December 2014

In his monthly podcast for The Journal of Community and Supportive Oncology, Dr David Henry discusses articles on the recent approval of ramucirumab for advanced gastric or GEJ adenocarcinoma in previously treated patients with disease progression and the “small victories” in honing new therapies for hard-to-treat cancers such as ovarian, melanoma, and pancreatic. Quality of care and patient quality of life are the basis for the 3 Original Reports that Dr Henry addresses: one study looks at the impact of patient navigation on diagnostic resolution in women with abnormal screenings for breast or cervical cancer; a second examines how the information and communication needs of Chinese American women with breast cancer can be channeled into improving quality of life after treatment for cancer; and a third reports on how dignity therapy as an intervention in patients with advanced colorectal cancer can positively affect the quality of end-of-life care, treatment choices, and cost efficiency.

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ramucirumab, gastric cancer, GEJ adenocarcinoma, gastroesophageal junction adenocarcinoma, Chinese American, breast cancer, survivorship care, patient information needs, patient-provider communication, dignity therapy, colorectal cancer, quality of life, quality of care, end-of-life care, diagnostic resolution, patient navigation, ovarian cancer, melanoma, pancreatic cancer, hard-to-treat cancers, PARP inhibitors, ipilimumab, pembrolizumab, FOLFIRINOX, nab-paclitaxel, erlotinib
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In his monthly podcast for The Journal of Community and Supportive Oncology, Dr David Henry discusses articles on the recent approval of ramucirumab for advanced gastric or GEJ adenocarcinoma in previously treated patients with disease progression and the “small victories” in honing new therapies for hard-to-treat cancers such as ovarian, melanoma, and pancreatic. Quality of care and patient quality of life are the basis for the 3 Original Reports that Dr Henry addresses: one study looks at the impact of patient navigation on diagnostic resolution in women with abnormal screenings for breast or cervical cancer; a second examines how the information and communication needs of Chinese American women with breast cancer can be channeled into improving quality of life after treatment for cancer; and a third reports on how dignity therapy as an intervention in patients with advanced colorectal cancer can positively affect the quality of end-of-life care, treatment choices, and cost efficiency.

In his monthly podcast for The Journal of Community and Supportive Oncology, Dr David Henry discusses articles on the recent approval of ramucirumab for advanced gastric or GEJ adenocarcinoma in previously treated patients with disease progression and the “small victories” in honing new therapies for hard-to-treat cancers such as ovarian, melanoma, and pancreatic. Quality of care and patient quality of life are the basis for the 3 Original Reports that Dr Henry addresses: one study looks at the impact of patient navigation on diagnostic resolution in women with abnormal screenings for breast or cervical cancer; a second examines how the information and communication needs of Chinese American women with breast cancer can be channeled into improving quality of life after treatment for cancer; and a third reports on how dignity therapy as an intervention in patients with advanced colorectal cancer can positively affect the quality of end-of-life care, treatment choices, and cost efficiency.

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David Henry's JCSO podcast, December 2014
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David Henry's JCSO podcast, December 2014
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ramucirumab, gastric cancer, GEJ adenocarcinoma, gastroesophageal junction adenocarcinoma, Chinese American, breast cancer, survivorship care, patient information needs, patient-provider communication, dignity therapy, colorectal cancer, quality of life, quality of care, end-of-life care, diagnostic resolution, patient navigation, ovarian cancer, melanoma, pancreatic cancer, hard-to-treat cancers, PARP inhibitors, ipilimumab, pembrolizumab, FOLFIRINOX, nab-paclitaxel, erlotinib
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ramucirumab, gastric cancer, GEJ adenocarcinoma, gastroesophageal junction adenocarcinoma, Chinese American, breast cancer, survivorship care, patient information needs, patient-provider communication, dignity therapy, colorectal cancer, quality of life, quality of care, end-of-life care, diagnostic resolution, patient navigation, ovarian cancer, melanoma, pancreatic cancer, hard-to-treat cancers, PARP inhibitors, ipilimumab, pembrolizumab, FOLFIRINOX, nab-paclitaxel, erlotinib
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Predictors of resolution in navigated patients with abnormal cancer screening tests

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Predictors of resolution in navigated patients with abnormal cancer screening tests
Background Patient navigation has been effective in improving cancer care, yet little is known about what predicts timely outcomes in navigated patients.

Objective To identify predictors of resolution of abnormal cancer screening tests in patients who received navigation.

Methods We examined data on patients with abnormal breast (n = 256) or cervical (n = 150) screening tests or symptoms who received navigation as part of the Ohio Patient Navigator Research Program during 2007-2010. We used multivariable Cox proportional hazards regression models to identify predictors of time to resolution (ie, when a patient’s clinical abnormality or abnormal screening test was determined to be a benign condition or a cancer diagnosis).

Results The median time to resolution was 183 days for navigated patients with breast abnormalities and 172 days for navigated patients with cervical abnormalities. In patients with breast abnormalities, those who reported at least 1 barrier to care during navigation (HR, 0.66; 95% CI, 0.51-0.86) or higher perceived stress (HR, 0.90; 95% CI, 0.82-0.98) had slower resolution. Among patients with cervical abnormalities, those who reported at least 1 barrier to care during navigation had slower resolution (HR, 0.62; 95% CI, 0.42-0.91). Patients with cervical abnormalities had faster resolution if they had private health insurance, but this effect was present only in younger women (interaction P = .003).

Limitations Unknown generalizability of results because patients were female and from clinics in central Ohio.

Conclusions Several variables predicted whether patient navigation led to faster resolution, and predictors differed somewhat by disease site. Results will be useful in improving current patient navigation programs and designing future programs.

Funding American Cancer Society and the National Institutes of Health 

 

Click on the PDF icon at the top of this introduction to read the full article.

 

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The Journal of Community and Supportive Oncology - 12(12)
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439-445
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breast cancer, cervical cancer, patient navigator
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Background Patient navigation has been effective in improving cancer care, yet little is known about what predicts timely outcomes in navigated patients.

Objective To identify predictors of resolution of abnormal cancer screening tests in patients who received navigation.

Methods We examined data on patients with abnormal breast (n = 256) or cervical (n = 150) screening tests or symptoms who received navigation as part of the Ohio Patient Navigator Research Program during 2007-2010. We used multivariable Cox proportional hazards regression models to identify predictors of time to resolution (ie, when a patient’s clinical abnormality or abnormal screening test was determined to be a benign condition or a cancer diagnosis).

Results The median time to resolution was 183 days for navigated patients with breast abnormalities and 172 days for navigated patients with cervical abnormalities. In patients with breast abnormalities, those who reported at least 1 barrier to care during navigation (HR, 0.66; 95% CI, 0.51-0.86) or higher perceived stress (HR, 0.90; 95% CI, 0.82-0.98) had slower resolution. Among patients with cervical abnormalities, those who reported at least 1 barrier to care during navigation had slower resolution (HR, 0.62; 95% CI, 0.42-0.91). Patients with cervical abnormalities had faster resolution if they had private health insurance, but this effect was present only in younger women (interaction P = .003).

Limitations Unknown generalizability of results because patients were female and from clinics in central Ohio.

Conclusions Several variables predicted whether patient navigation led to faster resolution, and predictors differed somewhat by disease site. Results will be useful in improving current patient navigation programs and designing future programs.

Funding American Cancer Society and the National Institutes of Health 

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Background Patient navigation has been effective in improving cancer care, yet little is known about what predicts timely outcomes in navigated patients.

Objective To identify predictors of resolution of abnormal cancer screening tests in patients who received navigation.

Methods We examined data on patients with abnormal breast (n = 256) or cervical (n = 150) screening tests or symptoms who received navigation as part of the Ohio Patient Navigator Research Program during 2007-2010. We used multivariable Cox proportional hazards regression models to identify predictors of time to resolution (ie, when a patient’s clinical abnormality or abnormal screening test was determined to be a benign condition or a cancer diagnosis).

Results The median time to resolution was 183 days for navigated patients with breast abnormalities and 172 days for navigated patients with cervical abnormalities. In patients with breast abnormalities, those who reported at least 1 barrier to care during navigation (HR, 0.66; 95% CI, 0.51-0.86) or higher perceived stress (HR, 0.90; 95% CI, 0.82-0.98) had slower resolution. Among patients with cervical abnormalities, those who reported at least 1 barrier to care during navigation had slower resolution (HR, 0.62; 95% CI, 0.42-0.91). Patients with cervical abnormalities had faster resolution if they had private health insurance, but this effect was present only in younger women (interaction P = .003).

Limitations Unknown generalizability of results because patients were female and from clinics in central Ohio.

Conclusions Several variables predicted whether patient navigation led to faster resolution, and predictors differed somewhat by disease site. Results will be useful in improving current patient navigation programs and designing future programs.

Funding American Cancer Society and the National Institutes of Health 

 

Click on the PDF icon at the top of this introduction to read the full article.

 

Issue
The Journal of Community and Supportive Oncology - 12(12)
Issue
The Journal of Community and Supportive Oncology - 12(12)
Page Number
439-445
Page Number
439-445
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Publications
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Article Type
Display Headline
Predictors of resolution in navigated patients with abnormal cancer screening tests
Display Headline
Predictors of resolution in navigated patients with abnormal cancer screening tests
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breast cancer, cervical cancer, patient navigator
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breast cancer, cervical cancer, patient navigator
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JCSO 2014;12:431-438
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