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Prevalence and characteristics of moderate to severe fatigue: A multicenter study in cancer patients and survivors

Cancer, 2014-02, Vol.120 (3), p.425-432

2014

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Recommended Patient-Reported Core Set of Symptoms to Measure in Adult Cancer Treatment Trials

JNCI : Journal of the National Cancer Institute, 2014-07, Vol.106 (7), p.dju129-dju129

2014

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The symptom burden of cancer: Evidence for a core set of cancer‐related and treatment‐related symptoms from the Eastern Cooperative Oncology Group Symptom Outcomes and Practice Patterns study

Cancer, 2013-12, Vol.119 (24), p.4333-4340

2013

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Chemotherapy‐induced peripheral neuropathy: Identifying the research gaps and associated changes to clinical trial design

Cancer, 2020-10, Vol.126 (20), p.4602-4613

2020

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Longitudinal Trajectory and Characterization of Cancer-Related Cognitive Impairment in a Nationwide Cohort Study

Journal of clinical oncology, 2018-11, Vol.36 (32), p.JCO2018786624-3239

2018

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Fatigue, anxiety, and quality of life in breast cancer patients compared to non-cancer controls: a nationwide longitudinal analysis

Breast cancer research and treatment, 2021-05, Vol.187 (1), p.275-285

2021

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Feasibility of Patient Reporting of Symptomatic Adverse Events via the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) in a Chemoradiotherapy Cooperative Group Multicenter Clinical Trial

International journal of radiation oncology, biology, physics, 2017-06, Vol.98 (2), p.409-418

2017

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Patient free text reporting of symptomatic adverse events in cancer clinical research using the National Cancer Institute’s Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)

Journal of the American Medical Informatics Association : JAMIA, 2019-04, Vol.26 (4), p.276-285

2019

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ASCPRO Recommendations for the Assessment of Fatigue as an Outcome in Clinical Trials

Journal of pain and symptom management, 2010-06, Vol.39 (6), p.1086-1099

2010

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Enrollment of adolescents and young adults onto SWOG cancer research network clinical trials: A comparative analysis by treatment site and era

Cancer medicine (Malden, MA), 2020-03, Vol.9 (6), p.2146-2152

2020

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Patient-Reported Outcomes Assessment in Cancer Trials: Taking Stock, Moving Forward

Journal of clinical oncology, 2007-11, Vol.25 (32), p.5133-5140

2007

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Development of the National Cancer Institute's patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCAE)

JNCI : Journal of the National Cancer Institute, 2014-09, Vol.106 (9), p.dju244-dju244

2014

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Challenges to and Lessons Learned from Conducting Palliative Care Research

Journal of pain and symptom management, 2009-03, Vol.37 (3), p.387-394

2009

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Quality-of-Life Assessment in the Symptom Management Trials of the National Cancer Institute-Supported Community Clinical Oncology Program

Journal of clinical oncology, 2005-01, Vol.23 (3), p.591-598

2005

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Research-Design Issues in Cancer-Symptom–Management Trials Using Complementary and Alternative Medicine: Lessons From the National Cancer Institute Community Clinical Oncology Program Experience

Journal of clinical oncology, 2005-09, Vol.23 (27), p.6682-6689

2005

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Clinical research education: perspectives of nurses, employers, and educators

The Journal of nursing education, 2014-08, Vol.53 (8), p.466

2014

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Translating Research Into Evidence-Based Practice: The National Cancer Institute Community Clinical Oncology Program

Cancer, 2010-10, Vol.116 (19), p.4440-4449

2010

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Accrual to clinical trials: let's look at the physicians

JNCI : Journal of the National Cancer Institute, 2011-03, Vol.103 (5), p.357-358

2011

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Low Enrollment of Adolescents and Young Adults Onto Cancer Trials: Insights From the Community Clinical Oncology Program

Journal of oncology practice, 2016-04, Vol.12 (4), p.e388

2016

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Predictors of significant worsening of patient‐reported fatigue over a 1‐month timeframe in ambulatory patients with common solid tumors

Cancer, 2014-02, Vol.120 (3), p.442-450

2014

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Minority Representation, Prevalence of Symptoms, and Utilization of Services in a Large Metropolitan Hospice

Journal of pain and symptom management, 2001-04, Vol.21 (4), p.290-297

2001

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"Will I suffer?"

Journal of clinical oncology, 2007-05, Vol.25 (13), p.1645-1646

O'Mara, Ann M

2007

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Challenges and recommendations for advancing the state‐of‐the‐science of quality of life assessment in symptom management trials

Cancer, 2007-10, Vol.110 (7), p.1621-1628

2007

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Prevalence and characteristics of moderate to severe fatigue: A multicenter study in cancer patients and survivors

Recommended Patient-Reported Core Set of Symptoms to Measure in Adult Cancer Treatment Trials

The symptom burden of cancer: Evidence for a core set of cancer‐related and treatment‐related symptoms from the Eastern Cooperative Oncology Group Symptom Outcomes and Practice Patterns study

Chemotherapy‐induced peripheral neuropathy: Identifying the research gaps and associated changes to clinical trial design

Longitudinal Trajectory and Characterization of Cancer-Related Cognitive Impairment in a Nationwide Cohort Study

Fatigue, anxiety, and quality of life in breast cancer patients compared to non-cancer controls: a nationwide longitudinal analysis

Validity and Reliability of the US National Cancer Institute's Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)

Feasibility of Patient Reporting of Symptomatic Adverse Events via the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) in a Chemoradiotherapy Cooperative Group Multicenter Clinical Trial

Feasibility Assessment of Patient Reporting of Symptomatic Adverse Events in Multicenter Cancer Clinical Trials

Patient free text reporting of symptomatic adverse events in cancer clinical research using the National Cancer Institute’s Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)

ASCPRO Recommendations for the Assessment of Fatigue as an Outcome in Clinical Trials

Enrollment of adolescents and young adults onto SWOG cancer research network clinical trials: A comparative analysis by treatment site and era

Patient-Reported Outcomes Assessment in Cancer Trials: Taking Stock, Moving Forward

Development of the National Cancer Institute's patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCAE)

Challenges to and Lessons Learned from Conducting Palliative Care Research

Quality-of-Life Assessment in the Symptom Management Trials of the National Cancer Institute-Supported Community Clinical Oncology Program

Research-Design Issues in Cancer-Symptom–Management Trials Using Complementary and Alternative Medicine: Lessons From the National Cancer Institute Community Clinical Oncology Program Experience

Clinical research education: perspectives of nurses, employers, and educators

Translating Research Into Evidence-Based Practice: The National Cancer Institute Community Clinical Oncology Program

Accrual to clinical trials: let's look at the physicians

Low Enrollment of Adolescents and Young Adults Onto Cancer Trials: Insights From the Community Clinical Oncology Program

Predictors of significant worsening of patient‐reported fatigue over a 1‐month timeframe in ambulatory patients with common solid tumors

Minority Representation, Prevalence of Symptoms, and Utilization of Services in a Large Metropolitan Hospice

"Will I suffer?"

Challenges and recommendations for advancing the state‐of‐the‐science of quality of life assessment in symptom management trials

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