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Efficacy and Safety of Atezolizumab and Bevacizumab in Appendiceal Adenocarcinoma.

Authors :
Hornstein NJ
Zeineddine MA
Gunes BB
Pellatt AJ
Knafl M
Zhu H
Willett AF
Yousef A
Liu S
Sun R
Futreal A
Woodman SE
Taggart MW
Overman MJ
Halperin DM
Raghav KP
Shen JP
Source :
Cancer research communications [Cancer Res Commun] 2024 May 29; Vol. 4 (5), pp. 1363-1368.
Publication Year :
2024

Abstract

Purpose: Appendiceal adenocarcinoma (AA) remains an orphan disease with limited treatment options for patients unable to undergo surgical resection. Evidence supporting the efficacy of combined VEGF and PD-1 inhibition in other tumor types provided a compelling rationale for investigating this combination in AA, where immune checkpoint inhibitors have not been explored previously.<br />Experimental Design: We conducted a prospective, single-arm phase II study evaluating efficacy and safety of atezolizumab in conjunction with bevacizumab (Atezo+Bev) in advanced, unresectable AA.<br />Results: Patients treated with the Atezo+Bev combination had 100% disease control rate (1 partial response, 15 stable disease) with progression-free survival (PFS) of 18.3 months and overall survival not-yet-reached with median duration of follow-up of 40 months. These survival intervals were significantly longer relative to a clinically and molecularly matched synthetic control cohort treated with cytotoxic chemotherapy designed for colorectal cancer (PFS of 4.4 months, P = 0.041).<br />Conclusions: In light of recent data demonstrating a lack of efficacy of 5-fluorouracil-based chemotherapy, Atezo+Bev is a promising treatment option for patients with low-grade unresectable AA; further study is warranted.<br />Significance: AA remains an orphan disease with limited systemic therapy options for patients who are not candidates for surgical resection. These data suggest activity from combined VEGF and PD-L1 inhibition that warrants further study.<br /> (© 2024 The Authors; Published by the American Association for Cancer Research.)

Details

Language :
English
ISSN :
2767-9764
Volume :
4
Issue :
5
Database :
MEDLINE
Journal :
Cancer research communications
Publication Type :
Academic Journal
Accession number :
38709066
Full Text :
https://doi.org/10.1158/2767-9764.CRC-24-0019