Literature DB >> 32143966

Prognostic Variables Associated With Improved Outcomes in Patients With Stage III NSCLC Treated With Chemoradiation Followed by Consolidation Pembrolizumab: A Subset Analysis of a Phase II Study From the Hoosier Cancer Research Network LUN 14-179.

Bilal Anouti1, Sandra Althouse2, Greg Durm3, Nasser Hanna4.   

Abstract

INTRODUCTION: The Hoosier Cancer Research Network (HCRN) LUN 14-179 is a phase II trial of consolidation pembrolizumab after concurrent chemoradiation for the treatment of patients with stage III non-small-cell lung cancer (NSCLC). Time to metastatic disease or death (TMDD), progression-free survival (PFS), and overall survival (OS) appear to be superior to that in historical controls of chemoradiation alone. Unfortunately, not all patients benefit from consolidation immunotherapy. We performed a univariate analysis to evaluate variables associated with PFS, metastatic disease, and OS. PATIENTS AND METHODS: We conducted a retrospective analysis of patients enrolled in HCRN LUN 14-179. Data collected included age, sex, stage, smoking status, programmed death ligand 1 status, Grade (G) ≥ 2 versus G ≤ 1 adverse event, G ≤ 2 versus G ≥ 3 pneumonitis, duration of pembrolizumab (< 4 vs. ≥ 4 cycles), chemotherapy regimen, performance status 0 versus 1, time to start pembrolizumab (4-6 vs. 6-8 weeks from radiation), volume of lung receiving at least 20 Gy of radiation (V20; < 20% vs. ≥ 20%). Univariable Cox regression was performed to determine the variables associated with 3 end points: TMDD, PFS, and OS.
RESULTS: From April 2015 to December 2016, 93 patients were enrolled and 92 were included in the efficacy analysis (1 patient was ineligible). For TMDD, improved outcomes might be associated (P < .1) with stage IIIA and ≥ 4 cycles of pembrolizumab. For PFS, improved outcomes (P < .1) might be seen for ≥ 4 cycles of pembrolizumab, stage IIIA and V20 < 20%. For OS, improved outcomes (P < .1) might be seen for stage IIIA and ≥ 4 cycles of pembrolizumab.
CONCLUSION: Stage IIIA and longer duration of pembrolizumab treatment might be associated with prolonged TMDD, PFS, and OS for patients with stage III NSCLC treated with chemoradiation followed by pembrolizumab.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Adjuvant therapy; Consolidation; Immunotherapy; Non–small-cell lung cancer; Prognosis

Mesh:

Substances:

Year:  2019        PMID: 32143966     DOI: 10.1016/j.cllc.2019.06.009

Source DB:  PubMed          Journal:  Clin Lung Cancer        ISSN: 1525-7304            Impact factor:   4.785


  6 in total

1.  Association of Personal Characteristics and Effectiveness of Immunotherapy in Late-Stage Non-Small Cell Lung Cancer: A Systematic Review.

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Review 2.  Immunotherapy in non-small cell lung cancer: Update and new insights.

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Review 3.  Chemoradioimmunotherapy of inoperable stage III non-small cell lung cancer: immunological rationale and current clinical trials establishing a novel multimodal strategy.

Authors:  Lukas Käsmann; Chukwuka Eze; Julian Taugner; Olarn Roengvoraphoj; Maurice Dantes; Nina-Sophie Schmidt-Hegemann; Sanziana Schiopu; Claus Belka; Farkhad Manapov
Journal:  Radiat Oncol       Date:  2020-07-09       Impact factor: 3.481

4.  NICOLAS, DETERRED and KEYNOTE 799: focus on escalation of conventionally fractionated chemoradiotherapy by immune checkpoint inhibition in unresectable stage III non-small cell lung cancer.

Authors:  Farkhad Manapov; Saskia Kenndoff; Lukas Käsmann
Journal:  Transl Lung Cancer Res       Date:  2022-04

5.  A Multicenter Retrospective Study on the Prognosis of Stage III Unresectable Mutant Non-Small Cell Lung Cancer With Tyrosine Kinase Inhibitors Therapy.

Authors:  Ranpu Wu; Shaorong Yu; Jinjun Ye; Yimin Wang; Zhiting Zhao; Hongbing Liu; Yong Song
Journal:  Front Oncol       Date:  2021-07-12       Impact factor: 6.244

6.  Planning target volume as a predictor of disease progression in inoperable stage III non-small cell lung cancer patients treated with chemoradiotherapy and concurrent and/or sequential immune checkpoint inhibition.

Authors:  Julian Taugner; Lukas Käsmann; Monika Karin; Chukwuka Eze; Benedikt Flörsch; Julian Guggenberger; Minglun Li; Amanda Tufman; Niels Reinmuth; Thomas Duell; Claus Belka; Farkhad Manapov
Journal:  Invest New Drugs       Date:  2021-08-05       Impact factor: 3.850

  6 in total

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