Cognitive interviewing of the US National Cancer Institute’s Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)

Capturing Acute Toxicity Data During Lung Radiotherapy by Using a Patient-Reported Assessment Tool

(2012) Brooke Tang et al.   Clinical Lung Cancer

Web-Based Patient-Reported Outcomes in Drug Safety and Risk Management

(2012) Anjan K. Banerjee et al.   DRUG SAFETY

Managing symptoms during cancer treatments: evaluating the implementation of evidence-informed remote support protocols

(2012) Dawn Stacey et al.   Implementation Science

Methodological Standards and Patient-Centeredness in Comparative Effectiveness Research

(2012)   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Electronic Symptom Reporting Between Patient and Provider for Improved Health Care Service Quality: A Systematic Review of Randomized Controlled Trials. Part 1: State of the Art

(2012) Monika Alise Johansen et al.   JOURNAL OF MEDICAL INTERNET RESEARCH

Beyond the FDA PRO Guidance: Steps toward Integrating Meaningful Patient-Reported Outcomes into Regulatory Trials and US Drug Labels

(2012) Ethan Basch   VALUE IN HEALTH

Integrating cancer survivors' experiences into UK cancer registries: design and development of the ePOCS system (electronic Patient-reported Outcomes from Cancer Survivors)

(2011) L Ashley et al.   BRITISH JOURNAL OF CANCER

Electronic Toxicity Monitoring and Patient-Reported Outcomes

(2011) Ethan M. Basch et al.   CANCER JOURNAL

Perspectives of Patients on the Utility of Electronic Patient-Reported Outcomes on Cancer Care

(2011) Hsien Seow et al.   JOURNAL OF CLINICAL ONCOLOGY

Patient Self-Reports of Symptoms and Clinician Ratings as Predictors of Overall Cancer Survival

(2011) Chantal Quinten et al.   JNCI-Journal of the National Cancer Institute

Can We Rely on Patientsʼ Reports of Adverse Events?

(2011) Junya Zhu et al.   MEDICAL CARE

Reliability of adverse symptom event reporting by clinicians

(2011) Thomas M. Atkinson et al.   QUALITY OF LIFE RESEARCH

Content Validity—Establishing and Reporting the Evidence in Newly Developed Patient-Reported Outcomes (PRO) Instruments for Medical Product Evaluation: ISPOR PRO Good Research Practices Task Force Report: Part 2—Assessing Respondent Understanding

(2011) Donald L. Patrick et al.   VALUE IN HEALTH

The Missing Voice of Patients in Drug-Safety Reporting

(2010) Ethan Basch   NEW ENGLAND JOURNAL OF MEDICINE

Time to listen: a review of methods to solicit patient reports of adverse events

(2010) A. King et al.   QUALITY & SAFETY IN HEALTH CARE

Development of a patient-reported questionnaire for collecting toxicity data following prostate brachytherapy

(2010) Damian J.J. Farnell et al.   RADIOTHERAPY AND ONCOLOGY

Toxicity and quality of life outcomes in ovarian cancer patients participating in randomized controlled trials

(2010) Elfriede R. Greimel et al.   SUPPORTIVE CARE IN CANCER

How well does the MESTT correlate with CTCAE scale for the grading of dermatological toxicities associated with oral tyrosine kinase inhibitors?

(2010) Alexandre Chan et al.   SUPPORTIVE CARE IN CANCER

Optimal recall periods for patient-reported outcomes: challenges and potential solutions

(2009) Donald E. Stull et al.   CURRENT MEDICAL RESEARCH AND OPINION

Adverse Symptom Event Reporting by Patients vs Clinicians: Relationships With Clinical Outcomes

(2009) Ethan Basch et al.   JNCI-Journal of the National Cancer Institute

Multinational Trials—Recommendations on the Translations Required, Approaches to Using the Same Language in Different Countries, and the Approaches to Support Pooling the Data: The ISPOR Patient-Reported Outcomes Translation and Linguistic Validation Good Research Practices Task Force Report

(2008) Diane Wild et al.   VALUE IN HEALTH

Recommendations on Evidence Needed to Support Measurement Equivalence between Electronic and Paper-Based Patient-Reported Outcome (PRO) Measures: ISPOR ePRO Good Research Practices Task Force Report

(2008) Stephen Joel Coons et al.   VALUE IN HEALTH