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Durvalumab Outcomes in Stage III Non-small Cell Lung Cancer: A Single-institution Study.
Trinh, Jonathan Q; Xiong, Ying; Smith, Lynette M; Abughanimeh, Omar; Marr, Alissa S; Ganti, Apar K.
Afiliación
  • Trinh JQ; Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, U.S.A.; jtrinh@unmc.edu.
  • Xiong Y; Department of Biostatistics, University of Nebraska Medical Center, Omaha, NE, U.S.A.
  • Smith LM; Department of Biostatistics, University of Nebraska Medical Center, Omaha, NE, U.S.A.
  • Abughanimeh O; Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, U.S.A.
  • Marr AS; Fred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE, U.S.A.
  • Ganti AK; Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, U.S.A.
Anticancer Res ; 44(2): 605-612, 2024 Feb.
Article en En | MEDLINE | ID: mdl-38307589
ABSTRACT
BACKGROUND/

AIM:

The PACIFIC trial demonstrated improved survival in patients with unresectable stage III non-small cell lung cancer (NSCLC) treated with durvalumab following definitive concurrent chemoradiotherapy (CRT). This study sought to explore real-world outcomes with durvalumab consolidation therapy at our institution. PATIENTS AND

METHODS:

We retrospectively identified patients diagnosed with stage III NSCLC at our institution from January 2012 to January 2022. We created two cohorts one who received durvalumab following definitive CRT and a historical one who did not. Primary outcomes of interest included median progression-free survival (PFS) and overall survival (OS). Additionally, we performed subgroup analysis on the durvalumab cohort to explore the associations between survival and time to durvalumab initiation, PD-L1 expression, and neutrophil-to-lymphocyte ratio (NLR).

RESULTS:

We identified 79 patients with locally advanced NSCLC who were not surgical candidates. Patients treated with durvalumab (n=44) had significantly improved survival compared to the historical cohort (n=35) including a median PFS of 17.4 months versus 8.0 months (p=0.0019) and a median OS of 37.0 months versus 17.0 months (log-rank p-value=0.07, Wilcoxon p-value=0.02). Within the durvalumab group, outcomes did not significantly differ between those who initiated therapy before or after 42 days of finishing CRT, between various PD-L1 expression levels, or between high or low NLR.

CONCLUSION:

Patients who received durvalumab as consolidation therapy following definitive CRT demonstrated significantly improved survival compared to a historical cohort who did not receive durvalumab. Furthermore, durvalumab appears to benefit patients regardless of time to initiation, PD-L1 expression, or NLR.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares / Anticuerpos Monoclonales Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Anticancer Res Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares / Anticuerpos Monoclonales Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Anticancer Res Año: 2024 Tipo del documento: Article