Phase I Trial of Pembrolizumab and Radiation Therapy after Induction Chemotherapy for Extensive-Stage Small Cell Lung Cancer.


Journal

Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
ISSN: 1556-1380
Titre abrégé: J Thorac Oncol
Pays: United States
ID NLM: 101274235

Informations de publication

Date de publication:
02 2020
Historique:
received: 26 08 2019
revised: 27 09 2019
accepted: 01 10 2019
pubmed: 13 10 2019
medline: 7 1 2021
entrez: 13 10 2019
Statut: ppublish

Résumé

Radiation and immunotherapy have separately been shown to confer survival advantages to patients with extensive-stage small cell lung cancer (ESCLC), but failure rates remain high and combination therapy has been understudied. In this single-arm phase I trial (NCT02402920), we assessed the safety of combining pembrolizumab with thoracic radiotherapy (TRT) after induction chemotherapy for SCLC. Patients with ESCLC who had completed chemotherapy received TRT with pembrolizumab. The maximum tolerated dose of pembrolizumab was assessed by 3+3 dose-escalation; doses began at 100 mg and increased in 50 mg increments to 200 mg. Pembrolizumab was given every 3 weeks for up to 16 cycles; TRT was prescribed as 45 Gy in 15 daily fractions. Toxicity was evaluated with the Common Terminology Criteria for Adverse Events v4.0. The primary endpoint was safety of the combined therapy based on the incidence of dose-limiting toxicity in the 35 days following initiation of treatment. Thirty-eight patients with ESCLC (median age 65 years, range: 37-79 years) were enrolled from September 2015 through September 2017; 33 received per-protocol treatment, and all tolerated pembrolizumab at 100 to 200 mg with no dose-limiting toxicity in the 35-day window. There were no grade 4-5 toxicities; 2 (6%) patients experienced grade 3 events (n = 1 rash, n = 1 asthenia/paresthesia/autoimmune disorder) that were unlikely/doubtfully related to protocol therapy. The median follow-up time was 7.3 months (range: 1-13 months); median progression-free and overall survival times were 6.1 months (95% confidence interval: 4.1-8.1) and 8.4 months (95% confidence interval: 6.7-10.1). Concurrent pembrolizumab-TRT was tolerated well with few high-grade adverse events in the short-term; progression-free and overall survival rates are difficult to interpret due to heterogeneity in eligibility criteria (e.g., enrolling progressors on induction chemotherapy). Although randomized studies have shown benefits to TRT alone and immunotherapy alone, the safety of the combined regimen supports further investigation as a foundational approach for future prospective studies.

Identifiants

pubmed: 31605794
pii: S1556-0864(19)33525-7
doi: 10.1016/j.jtho.2019.10.001
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
pembrolizumab DPT0O3T46P

Banques de données

ClinicalTrials.gov
['NCT02402920']

Types de publication

Clinical Trial, Phase I Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

266-273

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.

Auteurs

James W Welsh (JW)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas. Electronic address: jwelsh@mdanderson.org.

John V Heymach (JV)

Department of Thoracic Head & Neck Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Dawei Chen (D)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas; Department of Radiation Oncology, Shandong Cancer Hospital affiliated to Shandong University, Jinan, China.

Vivek Verma (V)

Department of Radiation Oncology, Alleghany General Hospital, Pittsburgh, Pennsylvania.

Taylor R Cushman (TR)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Kenneth R Hess (KR)

Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Girish Shroff (G)

Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Chad Tang (C)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Ferdinandos Skoulidis (F)

Department of Thoracic Head & Neck Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Melenda Jeter (M)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Hari Menon (H)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Quynh-Nhu Nguyen (QN)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Joe Y Chang (JY)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Mehmet Altan (M)

Department of Thoracic Head & Neck Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Vassiliki A Papadimitrakopoulou (VA)

Department of Thoracic Head & Neck Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

George R Simon (GR)

Department of Thoracic Head & Neck Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Uma Raju (U)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Lauren Byers (L)

Department of Thoracic Head & Neck Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Bonnie Glisson (B)

Department of Thoracic Head & Neck Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

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Classifications MeSH