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A Phase II Trial of Atezolizumab Plus Carboplatin Plus Pemetrexed Plus Bevacizumab in the Treatment of Patients with Stage IV Non-Squamous Non-Small Cell Lung Cancer: Big Ten Cancer Research Consortium (BTCRC)- LUN 17-139.
Ardeshir-Larijani, Fatemeh; Althouse, Sandra K; Leal, Ticiana; Feldman, Lawrence Eric; Hejleh, Taher Abu; Patel, Malini; Gentzler, Ryan D; Miller, Adam Ryan; Hanna, Nasser H.
Affiliation
  • Ardeshir-Larijani F; Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN.
  • Althouse SK; Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN.
  • Leal T; Winship Cancer Institute, Emory University.
  • Feldman LE; University of Illinois Hospital & Health Sciences System, Chicago, IL.
  • Hejleh TA; University of Iowa Hospitals and Clinics, Iowa City, IA.
  • Patel M; Rutgers Cancer Institute of New Jersey, New Brunswick, NJ.
  • Gentzler RD; University of Virginia Cancer Center, Charlottesville, VA.
  • Miller AR; Massachusetts General Hospital, Boston, MA.
  • Hanna NH; Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN. Electronic address: nhanna@iu.edu.
Clin Lung Cancer ; 23(7): 578-584, 2022 11.
Article in En | MEDLINE | ID: mdl-36041949
ABSTRACT

INTRODUCTION:

LUN17-139 evaluated the safety and efficacy of Atezolizumab (A) plus Carboplatin (C) plus Pemetrexed (Pem) plus Bevacizumab (B) (ACBPem) in treatment naïve patients with stage IV non-squamous non-small cell lung cancer (Ns-NSCLC). PATIENTS AND

METHODS:

In this multicenter, single-arm phase II trial, all patients received A (1200-mg, D1) + C (AUC 5, D1) + Pem (500-mg/m2, D1) + B (15-mg/kg D1) q3 week x4. If no PD (progressive disease), patients received maintenance ABPem until PD or intolerable side effects. The primary endpoint was progression-free survival (PFS). The positive PFS result was considered as PFS>6m (historical control). Secondary endpoints included objective response rate (ORR), disease control rate (DCR) defined by complete response (CR) + partial response (PR) + stable disease (SD) ≥ 2 months, overall survival (OS), and safety.

RESULTS:

Thirty patients were enrolled from November 2018 to October 2020. The study was closed early due to 3 patient deaths, possibly related to treatment. Median age 64 (range 38-83); Men/Women 20/10; PD-L1 TPS < 1%/1-49%/ ≥ 50% (8/15/7). The median follow-up was 20.3 months ( 1-28.1). ORR 42.9% (95% CI, 24.5-62.8%), DCR 96.4% (95% CI, 81.7-99.9%). The median PFS and OS were 11.3m (5.5-14.9,P > .05) and 22.4m (22.4-NR), respectively. Four patients had G4 toxicity (anemia, febrile-neutropenia, severe neutropenia, sepsis), and 3 patients had G5 toxicity (thromboembolism, sepsis, colonic perforation).

CONCLUSION:

ABCPem was associated with increased PFS compared to historical controls but this difference did not meet the statistical significance. Three on-treatment deaths and 5 thromboembolic events prompted early closure.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Non-Small-Cell Lung / Sepsis / Lung Neoplasms / Neutropenia Type of study: Clinical_trials / Etiology_studies Limits: Female / Humans / Male / Middle aged Language: En Journal: Clin Lung Cancer Journal subject: NEOPLASIAS Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Non-Small-Cell Lung / Sepsis / Lung Neoplasms / Neutropenia Type of study: Clinical_trials / Etiology_studies Limits: Female / Humans / Male / Middle aged Language: En Journal: Clin Lung Cancer Journal subject: NEOPLASIAS Year: 2022 Document type: Article Affiliation country: