Research and Reviews for the Practicing Oncologist

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The generalist’s dilemma: training and staying current in the face of increasing specialization

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The generalist’s dilemma: training and staying current in the face of increasing specialization
So, let me ask you a question: How do you stay up-to-date in oncology and hematology? In particular, are you at an academic institution or in community practice? Do you do only oncology, or is your focus oncology and hematology? If you are in an academic institution, you probably are highly specialized in one tumor type. If your practice is in a community setting, you probably treat a range of cancer types as well as hematology. Throw into this mix the fact that new therapies and new indications for existing drugs are being approved, and that guidelines are routinely updated, and you realize the tremendous pressure you’re under to stay current, whether you’re a specialist or a generalist.  

 

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(5)
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So, let me ask you a question: How do you stay up-to-date in oncology and hematology? In particular, are you at an academic institution or in community practice? Do you do only oncology, or is your focus oncology and hematology? If you are in an academic institution, you probably are highly specialized in one tumor type. If your practice is in a community setting, you probably treat a range of cancer types as well as hematology. Throw into this mix the fact that new therapies and new indications for existing drugs are being approved, and that guidelines are routinely updated, and you realize the tremendous pressure you’re under to stay current, whether you’re a specialist or a generalist.  

 

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

 

So, let me ask you a question: How do you stay up-to-date in oncology and hematology? In particular, are you at an academic institution or in community practice? Do you do only oncology, or is your focus oncology and hematology? If you are in an academic institution, you probably are highly specialized in one tumor type. If your practice is in a community setting, you probably treat a range of cancer types as well as hematology. Throw into this mix the fact that new therapies and new indications for existing drugs are being approved, and that guidelines are routinely updated, and you realize the tremendous pressure you’re under to stay current, whether you’re a specialist or a generalist.  

 

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(5)
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169
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The generalist’s dilemma: training and staying current in the face of increasing specialization
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The generalist’s dilemma: training and staying current in the face of increasing specialization
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generalist, ASCO, American Society of Clinical Oncology, ASH, American Society of Hematology
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David Henry's JCSO podcast, April 2015

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David Henry's JCSO podcast, April 2015

In this month’s podcast for The Journal of Community and Supportive Oncology, Dr David Henry highlights two Original Reports, one on the effectiveness and safety of ipilimumab therapy in advanced melanoma, and another on the feasibility of implementing a community-based randomized trial of yoga for women who are undergoing chemotherapy for breast cancer. Also in the line-up are a Review article on sleep disorders in patients with cancer; a Community Translations examination of palonosetron and netupitant for the prevention of chemotherapy-induced nausea and vomiting in cancer patients; and Case Reports on distant skin metastases as primary presentation of gastric cancer, and sarcoidosis, complete heart block, and warm autoimmune hemolytic anemia in a young woman. The bimonthly New Therapies feature focuses on hard-to-treat tumors, specifically, glioblastoma, bone sarcoma, and liver cancer.

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ipilimumab, melanoma, yoga, breast cancer, quality of life, sleep disorders, palonosetron, netupitant, NEPA, chemotherapy-induced nausea and vomiting, CINV, distant skin metastases, gastric cancer, sarcoidosis, complete heart block, warm autoimmune hemolytic anemia, glioblastoma, GBM, bevacizumab, bone sarcoma, liver cancer, nivolumab, pembrolizumab, everolimus
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In this month’s podcast for The Journal of Community and Supportive Oncology, Dr David Henry highlights two Original Reports, one on the effectiveness and safety of ipilimumab therapy in advanced melanoma, and another on the feasibility of implementing a community-based randomized trial of yoga for women who are undergoing chemotherapy for breast cancer. Also in the line-up are a Review article on sleep disorders in patients with cancer; a Community Translations examination of palonosetron and netupitant for the prevention of chemotherapy-induced nausea and vomiting in cancer patients; and Case Reports on distant skin metastases as primary presentation of gastric cancer, and sarcoidosis, complete heart block, and warm autoimmune hemolytic anemia in a young woman. The bimonthly New Therapies feature focuses on hard-to-treat tumors, specifically, glioblastoma, bone sarcoma, and liver cancer.

In this month’s podcast for The Journal of Community and Supportive Oncology, Dr David Henry highlights two Original Reports, one on the effectiveness and safety of ipilimumab therapy in advanced melanoma, and another on the feasibility of implementing a community-based randomized trial of yoga for women who are undergoing chemotherapy for breast cancer. Also in the line-up are a Review article on sleep disorders in patients with cancer; a Community Translations examination of palonosetron and netupitant for the prevention of chemotherapy-induced nausea and vomiting in cancer patients; and Case Reports on distant skin metastases as primary presentation of gastric cancer, and sarcoidosis, complete heart block, and warm autoimmune hemolytic anemia in a young woman. The bimonthly New Therapies feature focuses on hard-to-treat tumors, specifically, glioblastoma, bone sarcoma, and liver cancer.

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David Henry's JCSO podcast, April 2015
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David Henry's JCSO podcast, April 2015
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ipilimumab, melanoma, yoga, breast cancer, quality of life, sleep disorders, palonosetron, netupitant, NEPA, chemotherapy-induced nausea and vomiting, CINV, distant skin metastases, gastric cancer, sarcoidosis, complete heart block, warm autoimmune hemolytic anemia, glioblastoma, GBM, bevacizumab, bone sarcoma, liver cancer, nivolumab, pembrolizumab, everolimus
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ipilimumab, melanoma, yoga, breast cancer, quality of life, sleep disorders, palonosetron, netupitant, NEPA, chemotherapy-induced nausea and vomiting, CINV, distant skin metastases, gastric cancer, sarcoidosis, complete heart block, warm autoimmune hemolytic anemia, glioblastoma, GBM, bevacizumab, bone sarcoma, liver cancer, nivolumab, pembrolizumab, everolimus
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Glioblastoma, bone sarcoma, and liver cancer: tough battles rage on for some tumors

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Glioblastoma, bone sarcoma, and liver cancer: tough battles rage on for some tumors
Improvements in our understanding of the molecular mechanisms of cancer combined with advances in genome sequencing have provided revolutionary new therapeutic options for several hard-to-treat tumors in recent decades. For other challenging tumor types these advancements have served only to highlight their significant complexity and, despite the development of novel treatments, there has been limited improvement in prognosis.

 

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(4)
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162-166
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Glioblastoma, bone sarcoma, liver cancer, GBM, VEGF, VEGFR,
osteosarcoma, chondrosarcoma, CS, Ewing sarcoma, ES, hepatocellular carcinoma, HCC
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Improvements in our understanding of the molecular mechanisms of cancer combined with advances in genome sequencing have provided revolutionary new therapeutic options for several hard-to-treat tumors in recent decades. For other challenging tumor types these advancements have served only to highlight their significant complexity and, despite the development of novel treatments, there has been limited improvement in prognosis.

 

Click on the PDF icon at the top of this introduction to read the full article.
 
Improvements in our understanding of the molecular mechanisms of cancer combined with advances in genome sequencing have provided revolutionary new therapeutic options for several hard-to-treat tumors in recent decades. For other challenging tumor types these advancements have served only to highlight their significant complexity and, despite the development of novel treatments, there has been limited improvement in prognosis.

 

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(4)
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The Journal of Community and Supportive Oncology - 13(4)
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162-166
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162-166
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Glioblastoma, bone sarcoma, and liver cancer: tough battles rage on for some tumors
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Glioblastoma, bone sarcoma, and liver cancer: tough battles rage on for some tumors
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Glioblastoma, bone sarcoma, liver cancer, GBM, VEGF, VEGFR,
osteosarcoma, chondrosarcoma, CS, Ewing sarcoma, ES, hepatocellular carcinoma, HCC
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Glioblastoma, bone sarcoma, liver cancer, GBM, VEGF, VEGFR,
osteosarcoma, chondrosarcoma, CS, Ewing sarcoma, ES, hepatocellular carcinoma, HCC
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Sarcoidosis, complete heart block, and warm autoimmune hemolytic anemia in a young woman

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Sarcoidosis, complete heart block, and warm autoimmune hemolytic anemia in a young woman

Sarcoidosis is a multisystem granulomatous disease that affects 10-40 people per 100,000 in the United States and Europe, with an increased prevalence among blacks compared with whites.1 The clinical presentation of sarcoidosis is variable. Sarcoidosis frequently involves the lungs and can have numerous extrapulmonary manifestations including skin, joint, cardiac, and eye lesions. We present a rare case of sarcoidosis with concurrent third-degree heart block and warm autoimmune hemolytic anemia and discuss possible mechanisms behind this presentation.
 

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

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Kate Chernow, BA; Timothy Donegan MD; Tatyana Milman MD; and David Henry, MD 

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Sarcoidosis is a multisystem granulomatous disease that affects 10-40 people per 100,000 in the United States and Europe, with an increased prevalence among blacks compared with whites.1 The clinical presentation of sarcoidosis is variable. Sarcoidosis frequently involves the lungs and can have numerous extrapulmonary manifestations including skin, joint, cardiac, and eye lesions. We present a rare case of sarcoidosis with concurrent third-degree heart block and warm autoimmune hemolytic anemia and discuss possible mechanisms behind this presentation.
 

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

Sarcoidosis is a multisystem granulomatous disease that affects 10-40 people per 100,000 in the United States and Europe, with an increased prevalence among blacks compared with whites.1 The clinical presentation of sarcoidosis is variable. Sarcoidosis frequently involves the lungs and can have numerous extrapulmonary manifestations including skin, joint, cardiac, and eye lesions. We present a rare case of sarcoidosis with concurrent third-degree heart block and warm autoimmune hemolytic anemia and discuss possible mechanisms behind this presentation.
 

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(4)
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The Journal of Community and Supportive Oncology - 13(4)
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159-161
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Sarcoidosis, complete heart block, and warm autoimmune hemolytic anemia in a young woman
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Sarcoidosis, complete heart block, and warm autoimmune hemolytic anemia in a young woman
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Sarcoidosis, complete heart block, warm autoimmune hemolytic anemia, WAHA,
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Distant skin metastases as primary presentation of gastric cancer

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Distant skin metastases as primary presentation of gastric cancer

Distant gastric metastasis to the skin is uncommonly a presenting symptom, although nonspecific paraneoplastic syndromes with dermatologic manifestation including diffuse seborrheic keratoses (Leser-Trelat sign), tripe palms, and acanthosis nigricans have been described in the literature. We report here the case of a 49-year-old woman with gastric adenocarcinoma who presented with cutaneous metastasis as an initial symptom. In our case, metastatic skin lesions responded significantly to EOX chemotherapy (epirubicin+oxaliplatin+capecitabine) despite progression of systemic disease. In similar presentations, a high index of clinical suspicion and skin biopsy are important.

 

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(4)
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156-158
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gastric adenocarcinoma, cutaneous metastasis, OX chemotherapy, epirubicin, oxaliplatin, capecitabine
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Distant gastric metastasis to the skin is uncommonly a presenting symptom, although nonspecific paraneoplastic syndromes with dermatologic manifestation including diffuse seborrheic keratoses (Leser-Trelat sign), tripe palms, and acanthosis nigricans have been described in the literature. We report here the case of a 49-year-old woman with gastric adenocarcinoma who presented with cutaneous metastasis as an initial symptom. In our case, metastatic skin lesions responded significantly to EOX chemotherapy (epirubicin+oxaliplatin+capecitabine) despite progression of systemic disease. In similar presentations, a high index of clinical suspicion and skin biopsy are important.

 

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

 

Distant gastric metastasis to the skin is uncommonly a presenting symptom, although nonspecific paraneoplastic syndromes with dermatologic manifestation including diffuse seborrheic keratoses (Leser-Trelat sign), tripe palms, and acanthosis nigricans have been described in the literature. We report here the case of a 49-year-old woman with gastric adenocarcinoma who presented with cutaneous metastasis as an initial symptom. In our case, metastatic skin lesions responded significantly to EOX chemotherapy (epirubicin+oxaliplatin+capecitabine) despite progression of systemic disease. In similar presentations, a high index of clinical suspicion and skin biopsy are important.

 

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(4)
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The Journal of Community and Supportive Oncology - 13(4)
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156-158
Page Number
156-158
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Distant skin metastases as primary presentation of gastric cancer
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Distant skin metastases as primary presentation of gastric cancer
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gastric adenocarcinoma, cutaneous metastasis, OX chemotherapy, epirubicin, oxaliplatin, capecitabine
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gastric adenocarcinoma, cutaneous metastasis, OX chemotherapy, epirubicin, oxaliplatin, capecitabine
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Feasibility of implementing a community-based randomized trial of yoga for women undergoing chemotherapy for breast cancer

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Background Treatment-related symptoms and decreased health-related quality of life (HRQoL) frequently occur during chemotherapy for breast cancer. Although research findings suggest that yoga can reduce symptoms and improve HRQoL after treatment, potential benefits of yoga during chemotherapy have received minimal attention.

Objective To estimate accrual, adherence, study retention, and preliminary efficacy of a yoga intervention compared with an active control group for breast cancer patients during chemotherapy.

Methods Women with stage I-III breast cancer were recruited from 3 community cancer clinics and randomized to 10 weeks of gentle yoga or wellness education. Depressive symptoms, fatigue, sleep, and HRQoL were assessed at baseline, mid-intervention (Week 5), and after intervention (Week 10).

Results 40 women aged 29-83 years (median, 48 years; 88% white) were randomized to yoga (n = 22) or wellness education (n = 18). The groups did not differ significantly on baseline characteristics, adherence, or study retention. Participant feedback was positive and comparable between groups. Meaningful within-group differences were identified for sleep adequacy and quantity in yoga participants and for somnolence in wellness-education participants.

Limitations Small sample size and lack of a usual-care control group.

Conclusions This study established feasibility of a community-based randomized trial of yoga and an active comparison group for women undergoing chemotherapy for breast cancer. Preliminary efficacy estimates suggest that yoga improves sleep adequacy. Symptom severity and interference remained stable during chemotherapy for the yoga group and showed a trend toward increasing in the control group. The study highlighted obstacles to multisite yoga research during cancer treatment.

Funding/sponsorship National Cancer Institute (3U10 CA081851, PI: Shaw; R25 CA122061, PI: Avis); Translational Science Institute, Wake Forest School of Medicine

 

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(4)
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139-147
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breast cancer, yoga, health-related quality of life, HRQoL, chemotherapy, wellness education, depressive symptoms, fatigue, sleep
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Background Treatment-related symptoms and decreased health-related quality of life (HRQoL) frequently occur during chemotherapy for breast cancer. Although research findings suggest that yoga can reduce symptoms and improve HRQoL after treatment, potential benefits of yoga during chemotherapy have received minimal attention.

Objective To estimate accrual, adherence, study retention, and preliminary efficacy of a yoga intervention compared with an active control group for breast cancer patients during chemotherapy.

Methods Women with stage I-III breast cancer were recruited from 3 community cancer clinics and randomized to 10 weeks of gentle yoga or wellness education. Depressive symptoms, fatigue, sleep, and HRQoL were assessed at baseline, mid-intervention (Week 5), and after intervention (Week 10).

Results 40 women aged 29-83 years (median, 48 years; 88% white) were randomized to yoga (n = 22) or wellness education (n = 18). The groups did not differ significantly on baseline characteristics, adherence, or study retention. Participant feedback was positive and comparable between groups. Meaningful within-group differences were identified for sleep adequacy and quantity in yoga participants and for somnolence in wellness-education participants.

Limitations Small sample size and lack of a usual-care control group.

Conclusions This study established feasibility of a community-based randomized trial of yoga and an active comparison group for women undergoing chemotherapy for breast cancer. Preliminary efficacy estimates suggest that yoga improves sleep adequacy. Symptom severity and interference remained stable during chemotherapy for the yoga group and showed a trend toward increasing in the control group. The study highlighted obstacles to multisite yoga research during cancer treatment.

Funding/sponsorship National Cancer Institute (3U10 CA081851, PI: Shaw; R25 CA122061, PI: Avis); Translational Science Institute, Wake Forest School of Medicine

 

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

 

Background Treatment-related symptoms and decreased health-related quality of life (HRQoL) frequently occur during chemotherapy for breast cancer. Although research findings suggest that yoga can reduce symptoms and improve HRQoL after treatment, potential benefits of yoga during chemotherapy have received minimal attention.

Objective To estimate accrual, adherence, study retention, and preliminary efficacy of a yoga intervention compared with an active control group for breast cancer patients during chemotherapy.

Methods Women with stage I-III breast cancer were recruited from 3 community cancer clinics and randomized to 10 weeks of gentle yoga or wellness education. Depressive symptoms, fatigue, sleep, and HRQoL were assessed at baseline, mid-intervention (Week 5), and after intervention (Week 10).

Results 40 women aged 29-83 years (median, 48 years; 88% white) were randomized to yoga (n = 22) or wellness education (n = 18). The groups did not differ significantly on baseline characteristics, adherence, or study retention. Participant feedback was positive and comparable between groups. Meaningful within-group differences were identified for sleep adequacy and quantity in yoga participants and for somnolence in wellness-education participants.

Limitations Small sample size and lack of a usual-care control group.

Conclusions This study established feasibility of a community-based randomized trial of yoga and an active comparison group for women undergoing chemotherapy for breast cancer. Preliminary efficacy estimates suggest that yoga improves sleep adequacy. Symptom severity and interference remained stable during chemotherapy for the yoga group and showed a trend toward increasing in the control group. The study highlighted obstacles to multisite yoga research during cancer treatment.

Funding/sponsorship National Cancer Institute (3U10 CA081851, PI: Shaw; R25 CA122061, PI: Avis); Translational Science Institute, Wake Forest School of Medicine

 

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(4)
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The Journal of Community and Supportive Oncology - 13(4)
Page Number
139-147
Page Number
139-147
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breast cancer, yoga, health-related quality of life, HRQoL, chemotherapy, wellness education, depressive symptoms, fatigue, sleep
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Effectiveness and safety of ipilimumab therapy in advanced melanoma: evidence from clinical practice sites in the US

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Effectiveness and safety of ipilimumab therapy in advanced melanoma: evidence from clinical practice sites in the US
Background Ipilimumab was approved in 2011 by the US Food and Drug Administration in 2011 for the treatment of unresectable or metastatic (advanced) melanoma, although pivotal data using the approved 3 mg/kg monotherapy q3w × 4 were available only for patients with previously treated disease.

 

Objective To investigate patient and disease characteristics, survival outcomes, and safety in treatment-naïve patients receiving ipilimumab therapy.

 

Methods Adult patients with treatment-naïve advanced melanoma who received ≥1 dose of ipilimumab 3 mg/kg during April 2011-Sept 2012, with ≥12 months having elapsed since the start of treatment, were identified from 34 US sites. Personnel from each study site retrospectively abstracted existing data from individual patient medical records, which were collected and validated by an independent research organization.

 

Results In all, 273 patients were included in the study. The median age of the total study population was 64 years (range, 26-91), and 64.8% were men. At diagnosis, 56.0% were stage IV M1c, and 12.1% had brain metastases. 50 patients had a BRAF mutation, 181 were BRAF wild-type, and BRAF status was not known for 42. 78% of patients received all 4 planned doses of ipilimumab. Median survival from initiation of ipilimumab treatment was 14.5 months (95% confidence index [CI], 12.9-18.7). The overall one-year survival rate was 59.2% (95% CI, 53.0-64.8); and 71.0% and 54.9% for patients with BRAF-mutated and wild-type tumors, respectively. Adverse events of any grade, grade 3, and grade 4 occurred in 164 patients (60.1%), 45 (16.5%), and 8 (2.9%), respectively. The most common grade 3 or 4 adverse events were colitis (4.0%), fatigue (2.9%), and diarrhea (1.5%). Drug-related adverse events were primarily immune-related and occurred in 147 patients (53.8%), including grade 3/4 in 15.7% of patients (13.9% and 1.8%, respectively). No deaths were attributed to ipilimumab.

 

Conclusions This observational study provides real-world, clinical practice evidence supporting improved survival with the approved ipilimumab 3 mg/kg monotherapy in patients with treatment-naïve advanced melanoma, including prolonged survival in some patients. The safety profile was consistent with that reported in clinical trials.

 

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(4)
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131-138
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ipilimumab, melanoma, BRAF mutation, BRAF wild-type
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Background Ipilimumab was approved in 2011 by the US Food and Drug Administration in 2011 for the treatment of unresectable or metastatic (advanced) melanoma, although pivotal data using the approved 3 mg/kg monotherapy q3w × 4 were available only for patients with previously treated disease.

 

Objective To investigate patient and disease characteristics, survival outcomes, and safety in treatment-naïve patients receiving ipilimumab therapy.

 

Methods Adult patients with treatment-naïve advanced melanoma who received ≥1 dose of ipilimumab 3 mg/kg during April 2011-Sept 2012, with ≥12 months having elapsed since the start of treatment, were identified from 34 US sites. Personnel from each study site retrospectively abstracted existing data from individual patient medical records, which were collected and validated by an independent research organization.

 

Results In all, 273 patients were included in the study. The median age of the total study population was 64 years (range, 26-91), and 64.8% were men. At diagnosis, 56.0% were stage IV M1c, and 12.1% had brain metastases. 50 patients had a BRAF mutation, 181 were BRAF wild-type, and BRAF status was not known for 42. 78% of patients received all 4 planned doses of ipilimumab. Median survival from initiation of ipilimumab treatment was 14.5 months (95% confidence index [CI], 12.9-18.7). The overall one-year survival rate was 59.2% (95% CI, 53.0-64.8); and 71.0% and 54.9% for patients with BRAF-mutated and wild-type tumors, respectively. Adverse events of any grade, grade 3, and grade 4 occurred in 164 patients (60.1%), 45 (16.5%), and 8 (2.9%), respectively. The most common grade 3 or 4 adverse events were colitis (4.0%), fatigue (2.9%), and diarrhea (1.5%). Drug-related adverse events were primarily immune-related and occurred in 147 patients (53.8%), including grade 3/4 in 15.7% of patients (13.9% and 1.8%, respectively). No deaths were attributed to ipilimumab.

 

Conclusions This observational study provides real-world, clinical practice evidence supporting improved survival with the approved ipilimumab 3 mg/kg monotherapy in patients with treatment-naïve advanced melanoma, including prolonged survival in some patients. The safety profile was consistent with that reported in clinical trials.

 

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

 

Background Ipilimumab was approved in 2011 by the US Food and Drug Administration in 2011 for the treatment of unresectable or metastatic (advanced) melanoma, although pivotal data using the approved 3 mg/kg monotherapy q3w × 4 were available only for patients with previously treated disease.

 

Objective To investigate patient and disease characteristics, survival outcomes, and safety in treatment-naïve patients receiving ipilimumab therapy.

 

Methods Adult patients with treatment-naïve advanced melanoma who received ≥1 dose of ipilimumab 3 mg/kg during April 2011-Sept 2012, with ≥12 months having elapsed since the start of treatment, were identified from 34 US sites. Personnel from each study site retrospectively abstracted existing data from individual patient medical records, which were collected and validated by an independent research organization.

 

Results In all, 273 patients were included in the study. The median age of the total study population was 64 years (range, 26-91), and 64.8% were men. At diagnosis, 56.0% were stage IV M1c, and 12.1% had brain metastases. 50 patients had a BRAF mutation, 181 were BRAF wild-type, and BRAF status was not known for 42. 78% of patients received all 4 planned doses of ipilimumab. Median survival from initiation of ipilimumab treatment was 14.5 months (95% confidence index [CI], 12.9-18.7). The overall one-year survival rate was 59.2% (95% CI, 53.0-64.8); and 71.0% and 54.9% for patients with BRAF-mutated and wild-type tumors, respectively. Adverse events of any grade, grade 3, and grade 4 occurred in 164 patients (60.1%), 45 (16.5%), and 8 (2.9%), respectively. The most common grade 3 or 4 adverse events were colitis (4.0%), fatigue (2.9%), and diarrhea (1.5%). Drug-related adverse events were primarily immune-related and occurred in 147 patients (53.8%), including grade 3/4 in 15.7% of patients (13.9% and 1.8%, respectively). No deaths were attributed to ipilimumab.

 

Conclusions This observational study provides real-world, clinical practice evidence supporting improved survival with the approved ipilimumab 3 mg/kg monotherapy in patients with treatment-naïve advanced melanoma, including prolonged survival in some patients. The safety profile was consistent with that reported in clinical trials.

 

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(4)
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The Journal of Community and Supportive Oncology - 13(4)
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131-138
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131-138
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Effectiveness and safety of ipilimumab therapy in advanced melanoma: evidence from clinical practice sites in the US
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Effectiveness and safety of ipilimumab therapy in advanced melanoma: evidence from clinical practice sites in the US
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Palonosetron and netupitant for prevention of chemotherapy-induced nausea and vomiting

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Palonosetron and netupitant for prevention of chemotherapy-induced nausea and vomiting

The US Food and Drug Administration (FDA) recently approved NEPA, an oral fixed-dose combination of netupitant and palonosetron for treatment of chemotherapy-induced nausea and vomiting (CINV). Palonosetron is a pharmacologically distinct, best-in-class serotonin (5-hydroxytryptamine) type 3 (5-HT3) receptor antagonist, which prevents CINV during the acute phase (0-24 h) after administration of chemotherapy, and netupitant is a potent and selective neurokinin-1 (NK-1) receptor antagonist, which prevents CINV during both the acute and delayed (25-120 h) phases. The 2 agents have also been shown potentially to act synergistically in inhibiting NK-1 receptor activity.

 

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The Journal of Community and Supportive Oncology - 13(4)
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128-130
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Palonosetron, netupitant, chemotherapy-induced nausea and vomiting, CINV
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The US Food and Drug Administration (FDA) recently approved NEPA, an oral fixed-dose combination of netupitant and palonosetron for treatment of chemotherapy-induced nausea and vomiting (CINV). Palonosetron is a pharmacologically distinct, best-in-class serotonin (5-hydroxytryptamine) type 3 (5-HT3) receptor antagonist, which prevents CINV during the acute phase (0-24 h) after administration of chemotherapy, and netupitant is a potent and selective neurokinin-1 (NK-1) receptor antagonist, which prevents CINV during both the acute and delayed (25-120 h) phases. The 2 agents have also been shown potentially to act synergistically in inhibiting NK-1 receptor activity.

 

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

 

The US Food and Drug Administration (FDA) recently approved NEPA, an oral fixed-dose combination of netupitant and palonosetron for treatment of chemotherapy-induced nausea and vomiting (CINV). Palonosetron is a pharmacologically distinct, best-in-class serotonin (5-hydroxytryptamine) type 3 (5-HT3) receptor antagonist, which prevents CINV during the acute phase (0-24 h) after administration of chemotherapy, and netupitant is a potent and selective neurokinin-1 (NK-1) receptor antagonist, which prevents CINV during both the acute and delayed (25-120 h) phases. The 2 agents have also been shown potentially to act synergistically in inhibiting NK-1 receptor activity.

 

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(4)
Issue
The Journal of Community and Supportive Oncology - 13(4)
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128-130
Page Number
128-130
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Palonosetron and netupitant for prevention of chemotherapy-induced nausea and vomiting
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Palonosetron and netupitant for prevention of chemotherapy-induced nausea and vomiting
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Palonosetron, netupitant, chemotherapy-induced nausea and vomiting, CINV
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Palonosetron, netupitant, chemotherapy-induced nausea and vomiting, CINV
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Managing change in oncology

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Managing change in oncology
As I write this, the permanent fix to the sustainable growth rate (SGR) has been passed overwhelmingly in the US House of Representatives. The Senate has adjourned for spring break so has yet to vote on the fix, but there is optimism that it will pass when the session resumes. Doctors have feared that the 21% payment reduction that would automatically be triggered if the SGR fix were not passed would result in them having to close their doors to Medicare patients. Congress has postponed the SGR cuts 17 times since 2003. The uncertainty around this legislation and the time that practicing oncologists have spent conjuring up temporary solutions since 2003 is maddening.

 

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The Journal of Community and Supportive Oncology - 13(4)
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125
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sustainable growth rate, SGR, Medicare, meaningful use, 340B
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As I write this, the permanent fix to the sustainable growth rate (SGR) has been passed overwhelmingly in the US House of Representatives. The Senate has adjourned for spring break so has yet to vote on the fix, but there is optimism that it will pass when the session resumes. Doctors have feared that the 21% payment reduction that would automatically be triggered if the SGR fix were not passed would result in them having to close their doors to Medicare patients. Congress has postponed the SGR cuts 17 times since 2003. The uncertainty around this legislation and the time that practicing oncologists have spent conjuring up temporary solutions since 2003 is maddening.

 

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

 

As I write this, the permanent fix to the sustainable growth rate (SGR) has been passed overwhelmingly in the US House of Representatives. The Senate has adjourned for spring break so has yet to vote on the fix, but there is optimism that it will pass when the session resumes. Doctors have feared that the 21% payment reduction that would automatically be triggered if the SGR fix were not passed would result in them having to close their doors to Medicare patients. Congress has postponed the SGR cuts 17 times since 2003. The uncertainty around this legislation and the time that practicing oncologists have spent conjuring up temporary solutions since 2003 is maddening.

 

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(4)
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The Journal of Community and Supportive Oncology - 13(4)
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125
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125
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Managing change in oncology
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Managing change in oncology
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sustainable growth rate, SGR, Medicare, meaningful use, 340B
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Sleep disorders in patients with cancer

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Sleep disorders in patients with cancer

Sleep disturbances are common among patients with cancer for many reasons. Sleep problems can be present at any stage during treatment for cancer and in some patients, sleep disturbance may be the presenting symptoms that lead to the diagnosis of some types of cancer. Poor sleep impairs quality of life In people with cancer, but most do not specifically complain of sleep problems unless they are explicitly asked. Insomnia and fatigue are most common sleep disorders in this cohort, although primary sleep disorders, including obstructive sleep apnea and restless legs syndrome, which are common in the general population, have not been carefully studied in the oncology setting despite significant their impairment of quality of life.

 

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(4)
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148-155
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people with cancer, sleep disorders, insomnia, restless legs syndrome, RLS, fatigue, quality of life, sleep-disordered breathing, obstructuve sleep apnea, excessive daytime sleepiness, Rapid eye movement sleep behavior
disorder
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Sleep disturbances are common among patients with cancer for many reasons. Sleep problems can be present at any stage during treatment for cancer and in some patients, sleep disturbance may be the presenting symptoms that lead to the diagnosis of some types of cancer. Poor sleep impairs quality of life In people with cancer, but most do not specifically complain of sleep problems unless they are explicitly asked. Insomnia and fatigue are most common sleep disorders in this cohort, although primary sleep disorders, including obstructive sleep apnea and restless legs syndrome, which are common in the general population, have not been carefully studied in the oncology setting despite significant their impairment of quality of life.

 

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

 

 

 

 

Sleep disturbances are common among patients with cancer for many reasons. Sleep problems can be present at any stage during treatment for cancer and in some patients, sleep disturbance may be the presenting symptoms that lead to the diagnosis of some types of cancer. Poor sleep impairs quality of life In people with cancer, but most do not specifically complain of sleep problems unless they are explicitly asked. Insomnia and fatigue are most common sleep disorders in this cohort, although primary sleep disorders, including obstructive sleep apnea and restless legs syndrome, which are common in the general population, have not been carefully studied in the oncology setting despite significant their impairment of quality of life.

 

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(4)
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The Journal of Community and Supportive Oncology - 13(4)
Page Number
148-155
Page Number
148-155
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Sleep disorders in patients with cancer
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Sleep disorders in patients with cancer
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people with cancer, sleep disorders, insomnia, restless legs syndrome, RLS, fatigue, quality of life, sleep-disordered breathing, obstructuve sleep apnea, excessive daytime sleepiness, Rapid eye movement sleep behavior
disorder
Legacy Keywords
people with cancer, sleep disorders, insomnia, restless legs syndrome, RLS, fatigue, quality of life, sleep-disordered breathing, obstructuve sleep apnea, excessive daytime sleepiness, Rapid eye movement sleep behavior
disorder
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