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Patient-Reported Distress and Clinical Outcomes with Immuno-Oncology Agents in Metastatic Non-Small Cell Lung Cancer (mNSCLC): A Real-World Retrospective Cohort Study.
Bodd, Monica H; Locke, Susan C; Wolf, Steve P; Antonia, Scott; Crawford, Jeffrey; Hartman, John; Herring, Kris W; Ready, Neal E; Stinchcombe, Thomas E; Troy, Jesse D; Williams, Chakita; Clarke, Jeffrey M; LeBlanc, Thomas W.
Afiliação
  • Bodd MH; Duke University School of Medicine, Durham, NC, USA.
  • Locke SC; Duke Cancer Institute, Duke University, Durham, NC, USA.
  • Wolf SP; Division of Biostatistics, Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC 27710, USA.
  • Antonia S; Duke Cancer Institute, Duke University, Durham, NC, USA; Division of Medical Oncology, Duke University Medical Center, Durham, NC, USA.
  • Crawford J; Duke Cancer Institute, Duke University, Durham, NC, USA; Division of Medical Oncology, Duke University Medical Center, Durham, NC, USA.
  • Hartman J; Bristol Myers Squibb, Lawrenceville, NJ, USA.
  • Herring KW; Duke Cancer Institute, Duke University, Durham, NC, USA.
  • Ready NE; Duke Cancer Institute, Duke University, Durham, NC, USA; Division of Medical Oncology, Duke University Medical Center, Durham, NC, USA.
  • Stinchcombe TE; Duke Cancer Institute, Duke University, Durham, NC, USA; Division of Medical Oncology, Duke University Medical Center, Durham, NC, USA.
  • Troy JD; Division of Biostatistics, Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC 27710, USA.
  • Williams C; Bristol Myers Squibb, Lawrenceville, NJ, USA.
  • Clarke JM; Duke Cancer Institute, Duke University, Durham, NC, USA; Division of Medical Oncology, Duke University Medical Center, Durham, NC, USA.
  • LeBlanc TW; Duke Cancer Institute, Duke University, Durham, NC, USA; Division of Hematologic Malignancies and Cellular Therapy, Department of Medicine, Duke University School of Medicine, Durham, NC, USA. Electronic address: thomas.leblanc@duke.edu.
Lung Cancer ; 175: 17-26, 2023 01.
Article em En | MEDLINE | ID: mdl-36442383
OBJECTIVES: There are limited real-world data about patient-reported outcomes with immunotherapies (IO) in metastatic non-small cell lung cancer (mNSCLC). We describe patient-reported distress and clinical outcomes with IO-based treatments or cytotoxic chemotherapies (Chemo). METHODS: We conducted a single-institution retrospective chart review of adults with mNSCLC treated at Duke from 03/2015 to 06/2020. At each visit, patients self-reported their distress level and sources of distress using the NCCN Distress Thermometer (DT) and its 39-item Problem List. We abstracted demographic, clinical, distress, and investigator assessed-clinical response data, then analyzed these using descriptive statistics and generalized estimating equations. RESULTS: Data from 152 patients were analyzed in four groups: Chemo alone, IO + Chemo, single agent IO, dual agent IO. Distress was worse before treatment start in all groups, and the odds of actionable distress (DT score > 4) decreased by 10 % per month. The most frequent sources of distress were physical symptoms (e.g., fatigue, pain), which remained high longitudinally. Patients receiving IO had higher clinical response rates and a lower rate of unplanned healthcare encounters compared to patients treated with Chemo alone. Only one-third of all patients were seen by palliative care. CONCLUSIONS: This single-center, real-world evidence study demonstrates that patients with mNSCLC experience significant distress prior to starting first-line treatment. IO treatment was associated with higher clinical benefit rates and lower healthcare utilization compared to chemotherapy. Symptom distress persists over time, highlighting potential unmet palliative and supportive care needs in mNSCLC care in the IO treatment era.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Revista: Lung Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Revista: Lung Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos