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Use of a Cancer Registry to Evaluate Patient-Reported Outcomes of Immune Checkpoint Inhibitors.
Jim, Heather S L; Eisel, Sarah L; Hoogland, Aasha I; Shaw, Sandra; King, Jennifer C; Dicker, Adam P.
Afiliación
  • Jim HSL; Moffitt Cancer Center, Department of Health Outcomes and Behavior, Tampa, FL 33612, USA.
  • Eisel SL; Moffitt Cancer Center, Department of Health Outcomes and Behavior, Tampa, FL 33612, USA.
  • Hoogland AI; Moffitt Cancer Center, Department of Health Outcomes and Behavior, Tampa, FL 33612, USA.
  • Shaw S; GO2 Foundation for Lung Cancer, Washington, DC 20006, USA.
  • King JC; GO2 Foundation for Lung Cancer, Washington, DC 20006, USA.
  • Dicker AP; Jefferson Center for Digital Health, Department of Radiation Oncology, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Cancers (Basel) ; 13(1)2020 Dec 31.
Article en En | MEDLINE | ID: mdl-33396286
Immune checkpoint inhibitors (ICIs) are increasingly used for advanced lung cancer, but few studies have reported on patient-reported outcomes (PROs) outside the context of a clinical trial. The goal of the current study was to assess PROs in participants of a lung cancer registry who had been treated with an ICI. Patients participating in the GO2 Foundation's Lung Cancer Registry who reported receiving atezolizumab, durvalumab, nivolumab, or pembrolizumab were invited to participate in a survey about their experiences during treatment. Quality of life was evaluated using the Functional Assessment of Cancer Therapy-General (FACT-G). Common symptomatic adverse events were evaluated using an item bank generated for ICIs. Internationally, 226 patients (mean age 61, 75% female) participated. Patients reported worse quality of life at the time of assessment than U.S. population and cancer normative samples. The most common moderate to severe adverse events during ICI treatment were fatigue (41%), aching joints (27%), and aching muscles (20%). Due to toxicity, 25% reported a treatment delay, 11% an emergency room visit, and 9% a hospitalization. This study is among the first to our knowledge to report on PROs of ICIs outside the context of a clinical trial. Results suggest higher rates of adverse events than previously reported in clinical trials.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Aspecto: Patient_preference Idioma: En Revista: Cancers (Basel) Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Aspecto: Patient_preference Idioma: En Revista: Cancers (Basel) Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos
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