A phase Ib/II dose expansion study of subcutaneous sasanlimab in patients with locally advanced or metastatic non-small-cell lung cancer and urothelial carcinoma.


Journal

ESMO open
ISSN: 2059-7029
Titre abrégé: ESMO Open
Pays: England
ID NLM: 101690685

Informations de publication

Date de publication:
08 2023
Historique:
received: 14 12 2022
revised: 15 05 2023
accepted: 23 05 2023
medline: 29 8 2023
pubmed: 30 6 2023
entrez: 29 6 2023
Statut: ppublish

Résumé

Sasanlimab is an antibody to the programmed cell death protein 1 receptor. We report updated data of subcutaneous sasanlimab in non-small-cell lung cancer (NSCLC) and urothelial carcinoma dose expansion cohorts from a first-in-human phase Ib/II study. Patients were ≥18 years of age with NSCLC or urothelial carcinoma, and no prior immunotherapies, who progressed on or were intolerant to systemic therapy, or for whom systemic therapy was refused or unavailable. Patients received subcutaneous sasanlimab at 300 mg every 4 weeks (q4w). Primary objectives were to evaluate safety, tolerability, and clinical efficacy by objective response rate (ORR). Sixty-eight and 38 patients with NSCLC and urothelial carcinoma, respectively, received subcutaneous sasanlimab. Overall, sasanlimab was well tolerated; 13.2% of patients experienced grade ≥3 treatment-related adverse events. Confirmed ORR was 16.4% and 18.4% in the NSCLC and urothelial carcinoma cohorts, respectively. ORR was generally higher in patients with high programmed death-ligand 1 (PD-L1) expression (≥25%) and high tumor mutational burden (TMB; >75%). In the NSCLC and urothelial carcinoma cohorts, median progression-free survival (PFS) was 3.7 and 2.9 months, respectively; corresponding median overall survival (OS) was 14.7 and 10.9 months. Overall, longer median PFS and OS correlated with high PD-L1 expression and high TMB. Longer median PFS and OS were also associated with T-cell inflamed gene signature in the urothelial carcinoma cohort. Subcutaneous sasanlimab at 300 mg q4w was well tolerated with promising clinical efficacy observed. Phase II and III clinical trials of sasanlimab are ongoing to validate clinical benefit. Subcutaneous sasanlimab may be a potential treatment option for patients with NSCLC or urothelial carcinoma.

Sections du résumé

BACKGROUND
Sasanlimab is an antibody to the programmed cell death protein 1 receptor. We report updated data of subcutaneous sasanlimab in non-small-cell lung cancer (NSCLC) and urothelial carcinoma dose expansion cohorts from a first-in-human phase Ib/II study.
PATIENTS AND METHODS
Patients were ≥18 years of age with NSCLC or urothelial carcinoma, and no prior immunotherapies, who progressed on or were intolerant to systemic therapy, or for whom systemic therapy was refused or unavailable. Patients received subcutaneous sasanlimab at 300 mg every 4 weeks (q4w). Primary objectives were to evaluate safety, tolerability, and clinical efficacy by objective response rate (ORR).
RESULTS
Sixty-eight and 38 patients with NSCLC and urothelial carcinoma, respectively, received subcutaneous sasanlimab. Overall, sasanlimab was well tolerated; 13.2% of patients experienced grade ≥3 treatment-related adverse events. Confirmed ORR was 16.4% and 18.4% in the NSCLC and urothelial carcinoma cohorts, respectively. ORR was generally higher in patients with high programmed death-ligand 1 (PD-L1) expression (≥25%) and high tumor mutational burden (TMB; >75%). In the NSCLC and urothelial carcinoma cohorts, median progression-free survival (PFS) was 3.7 and 2.9 months, respectively; corresponding median overall survival (OS) was 14.7 and 10.9 months. Overall, longer median PFS and OS correlated with high PD-L1 expression and high TMB. Longer median PFS and OS were also associated with T-cell inflamed gene signature in the urothelial carcinoma cohort.
CONCLUSIONS
Subcutaneous sasanlimab at 300 mg q4w was well tolerated with promising clinical efficacy observed. Phase II and III clinical trials of sasanlimab are ongoing to validate clinical benefit. Subcutaneous sasanlimab may be a potential treatment option for patients with NSCLC or urothelial carcinoma.

Identifiants

pubmed: 37385154
pii: S2059-7029(23)00823-2
doi: 10.1016/j.esmoop.2023.101589
pmc: PMC10485400
pii:
doi:

Substances chimiques

B7-H1 Antigen 0
Immune Checkpoint Inhibitors 0

Types de publication

Clinical Trial, Phase I Clinical Trial, Phase II Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

101589

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Ltd.. All rights reserved.

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Auteurs

B C Cho (BC)

Division of Medical Oncology, Yonsei Cancer Center, Seoul, Republic of Korea. Electronic address: cbc1971@yuhs.ac.

K Penkov (K)

Private Healthcare Institution Clinical Hospital "RZhD-Medicine", St Petersburg, Russian Federation.

I Bondarenko (I)

Department of Oncology and Medical Oncology, Dnipropetrovsk City Multiple-Discipline Clinical Hospital, Dnipro, Ukraine.

A Kurochkin (A)

Municipal Non-profit Enterprise of Sumy Regional Council, Sumy Regional Clinical Oncology Dispensary, Sumy, Ukraine.

J Pikiel (J)

Poradnia Onkologiczna, Szpitale Pomorskie Sp. z o.o, Gdynia, Poland.

H K Ahn (HK)

Division of Medical Oncology, Gachon University Gil Medical Center, Incheon, Republic of Korea.

M E Korożan (ME)

Oddzial Onkologii Klinicznej, Szpital Grudziądz, Grudziądz, Poland.

M Osipov (M)

Sbhi "Lrcod", Vsevolozhsky District, Leningrad Region, Russian Federation.

S Odintsova (S)

Current Medical Technology, St Petersburg, Russian Federation.

F Braiteh (F)

Comprehensive Cancer Centers of Nevada, Las Vegas, USA.

A Ribas (A)

Jonsson Comprehensive Cancer Center, The University of California Los Angeles, Los Angeles, USA.

J E Grilley-Olson (JE)

Duke Cancer Institute, Duke University, Durham, USA.

I Lugowska (I)

Early Phase Clinical Trials Unit, Maria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

V Bonato (V)

Pfizer Inc, San Diego, USA.

M A Damore (MA)

Pfizer Inc, San Diego, USA.

W Yang (W)

Pfizer Inc, San Diego, USA.

I A Jacobs (IA)

Pfizer Inc, New York, USA.

M Bowers (M)

Pfizer Inc, Arnold, USA.

M Li (M)

Pfizer Inc, San Francisco, USA.

M L Johnson (ML)

Sarah Cannon Research Institute, Tennessee Oncology PLLC, Nashville, USA. Electronic address: mjohnson@tnonc.com.

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