Brief Report: Safety and Antitumor Activity of Alectinib Plus Atezolizumab From a Phase 1b Study in Advanced

ALK-positive Alectinib Atezolizumab Non–small cell lung cancer Phase 1b study

Journal

JTO clinical and research reports
ISSN: 2666-3643
Titre abrégé: JTO Clin Res Rep
Pays: United States
ID NLM: 101769967

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 20 03 2022
revised: 10 06 2022
accepted: 15 06 2022
entrez: 25 7 2022
pubmed: 26 7 2022
medline: 26 7 2022
Statut: epublish

Résumé

Alectinib is a preferred first-line treatment option for advanced Adults with treatment-naive, stage IIIB/IV, or recurrent In total, 21 patients received more than or equal to 1 dose of alectinib or atezolizumab. As no dose-limiting toxicities were observed in stage 1 (n = 7), the starting dose and schedule were continued into stage 2 (n = 14). Median duration of follow-up was 29 months (range: 1-39). Grade 3 treatment-related adverse events occurred in 57% of the patients, most often rash (19%). No grade 4 or 5 treatment-related adverse events were reported. Confirmed objective response rate was 86% (18 of 21; 95% confidence interval [CI]: 64-97). Median progression-free survival was not estimable (NE) (95% CI: 13 mo-NE), neither was median overall survival (95% CI: 33 mo-NE). The combination of alectinib and atezolizumab is feasible, but increased toxicity was found compared with the individual agents. With small sample sizes and relatively short follow-up, definitive conclusions regarding antitumor activity cannot be made.

Identifiants

pubmed: 35875467
doi: 10.1016/j.jtocrr.2022.100367
pii: S2666-3643(22)00091-1
pmc: PMC9304608
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100367

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States

Informations de copyright

© 2022 The Authors.

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Auteurs

Dong-Wan Kim (DW)

Department of Internal Medicine, Seoul National University College of Medicine and Seoul National University Hospital, Seoul, South Korea.

Shirish Gadgeel (S)

Department of Internal Medicine, Henry Ford Cancer Institute, Henry Ford Health System, Detroit, Michigan.

Scott N Gettinger (SN)

Department of Medicine (Medical Oncology), Yale School of Medicine, New Haven, Connecticut.

Gregory J Riely (GJ)

Division of Solid Tumor Oncology, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

Geoffrey R Oxnard (GR)

Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts.

Tarek Mekhail (T)

AdventHealth Cancer Institute, Orlando, Florida.

Peter Schmid (P)

Centre for Experimental Cancer Medicine, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.

Afshin Dowlati (A)

Division of Hematology and Oncology, University Hospitals Seidman Cancer Center and Case Western Reserve University, Cleveland, Ohio.

Rebecca S Heist (RS)

Massachusetts General Hospital Cancer Center, Boston, Massachusetts.

Antoinette J Wozniak (AJ)

UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, Pennsylvania.

Jatinder Singh (J)

Genentech, Inc., South San Francisco, California.

Edward Cha (E)

Genentech, Inc., South San Francisco, California.

Jessica Spahn (J)

Genentech, Inc., South San Francisco, California.

Sai-Hong Ignatius Ou (SI)

University of California Irvine School of Medicine, Orange, California.

Classifications MeSH