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Real-World Outcomes for Advanced Non-Small Cell Lung Cancer Patients Treated With a PD-L1 Inhibitor Beyond Progression.
Stinchcombe, Thomas E; Miksad, Rebecca A; Gossai, Anala; Griffith, Sandra D; Torres, Aracelis Z.
Afiliación
  • Stinchcombe TE; Duke Cancer Institute, Duke University School of Medicine, Durham, NC.
  • Miksad RA; Flatiron Health, Inc, New York, NY.
  • Gossai A; Flatiron Health, Inc, New York, NY.
  • Griffith SD; Flatiron Health, Inc, New York, NY.
  • Torres AZ; Flatiron Health, Inc, New York, NY. Electronic address: atorres@flatiron.com.
Clin Lung Cancer ; 21(5): 389-394.e3, 2020 09.
Article en En | MEDLINE | ID: mdl-32409266
ABSTRACT

BACKGROUND:

Clinical trials of anti-programmed cell death ligand 1 (PD-L1) inhibitor to treat advanced non-small-cell lung cancer (aNSCLC) have permitted treatment beyond progression (TBP). However, the outcomes of patients receiving TBP in routine clinical care are unknown. MATERIALS AND

METHODS:

The present retrospective, observational, multicenter analysis evaluated de-identified electronic health record-derived data from community-based clinics in the United States. The patients had confirmed aNSCLC, had started anti-PD-L1 inhibitor therapy (nivolumab, pembrolizumab, or atezolizumab) before October 1, 2018, and had experienced a real-world progression (rwP) event. The study period ended March 31, 2019. The primary objective was to compare the overall survival (OS) of patients who had discontinued immunotherapy ≤ 30 days (non-TBP) compared with > 30 days after rwP (TBP). Descriptive analyses were performed. The Kaplan-Meier method and log-rank test were conducted for OS. An adjusted multivariable Cox proportional hazards regression model was also used.

RESULTS:

Overall, the data from 4223 patients were analyzed; 2555 (60.5%) and 1668 (39.5%) in the non-TBP and TBP cohorts, respectively. The median treatment duration for the non-TBP and TBP patients was 2.8 and 9.1 months (log-rank test, P < .001), respectively. The TBP group experienced longer unadjusted OS compared with the non-TBP group (11.5 vs. 5.1 months; log-rank test, P < .001). After adjusting for clinically relevant patient characteristics, the TBP OS benefit persisted (adjusted hazard ratio, 0.69; P < .001).

CONCLUSIONS:

TBP with PD-L1 inhibitor therapy is common in aNSCLC routine care and is potentially effective. These results support clinical trial observations likely to affect practice patterns.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Carcinoma de Células Escamosas / Carcinoma de Pulmón de Células no Pequeñas / Antígeno B7-H1 / Adenocarcinoma del Pulmón / Inhibidores de Puntos de Control Inmunológico / Neoplasias Pulmonares Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Lung Cancer Asunto de la revista: NEOPLASIAS Año: 2020 Tipo del documento: Article País de afiliación: Nueva Caledonia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Carcinoma de Células Escamosas / Carcinoma de Pulmón de Células no Pequeñas / Antígeno B7-H1 / Adenocarcinoma del Pulmón / Inhibidores de Puntos de Control Inmunológico / Neoplasias Pulmonares Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Lung Cancer Asunto de la revista: NEOPLASIAS Año: 2020 Tipo del documento: Article País de afiliación: Nueva Caledonia