Efficacy and Safety of Atezolizumab and Bevacizumab in Appendiceal Adenocarcinoma

Author:

Hornstein Nicholas J.1ORCID,Zeineddine Mohammad A.2ORCID,Gunes Betul B.23ORCID,Pellatt Andrew J.1ORCID,Knafl Mark4ORCID,Zhu Haifeng4ORCID,Willett Anneleis F.2ORCID,Yousef Abdelrahman2ORCID,Liu Suyu4ORCID,Sun Ryan4ORCID,Futreal Andrew5ORCID,Woodman Scott E.4ORCID,Taggart Melissa W.6ORCID,Overman Michael J.2ORCID,Halperin Daniel M.2ORCID,Raghav Kanwal P.2ORCID,Shen John Paul2ORCID

Affiliation:

1. 1Medical Oncology Fellowship, University of Texas MD Anderson Cancer Center, Houston, Texas.

2. 2GI Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas.

3. 3Faculty of Medicine, Biruni University, Zeytinburnu, Istanbul, Turkey.

4. 4Biostatistics, University of Texas MD Anderson Cancer Center, Houston, Texas.

5. 5Genomic Medicine, University of Texas M. D. Anderson Cancer Center, Houston, Texas.

6. 6Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.

Abstract

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. 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. 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). 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. 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.

Funder

HHS | NIH | National Cancer Institute

Cancer Prevention and Research Institute of Texas

American Society of Clinical Oncology

Publisher

American Association for Cancer Research (AACR)

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