Chemotherapy Plus Atezolizumab Pre- and Post-Resection in Localized Esophageal or Gastroesophageal Junction Adenocarcinomas: A Phase I/II Single-Arm Study

Author:

Sewastjanow-Silva Matheus1ORCID,Xiao Lianchun2,Gonzalez Graciela N.2ORCID,Wang Xuemei2,Hofstetter Wayne3,Swisher Stephen3,Mehran Reza3,Sepesi Boris3,Bhutani Manoop S.4,Weston Brian4,Coronel Emmanuel4,Waters Rebecca E.5,Rogers Jane E.6ORCID,Smith Jackie1,Lyons Larry7,Reilly Norelle7,Yao James C.1,Ajani Jaffer A.1,Murphy Mariela Blum1

Affiliation:

1. Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

2. Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

3. Department of Thoracic and Cardiovascular Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

4. Department of Gastroenterology, Hepatology and Nutrition, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

5. Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

6. Department of Pharmacy Clinical Programs, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

7. Genentech Inc., South San Francisco, CA 94080, USA

Abstract

Efforts to improve the prognosis for patients with locally advanced esophageal or gastroesophageal junction (GEJ) adenocarcinoma have focused on neoadjuvant approaches to increase the pathological complete response (pathCR) rate, improve surgical resection, and prolong event-free and overall survival (OS). Building on the recent evidence that PD-1 inhibition plus chemotherapy improves the OS of patients with metastatic GEJ adenocarcinoma, we evaluated whether the application of this strategy in the neoadjuvant setting would improve the pathological response. This single-center phase I/II trial evaluated the safety, toxicity, and efficacy of neoadjuvant atezolizumab with oxaliplatin and 5-fluorouracil (modified FOLFOX) followed by esophagectomy followed by atezolizumab. The primary objective goal was to achieve 20% pathCR. From the twenty enrolled patients, eighteen underwent resection and two (10%, 95% CI: 1.24–31.7%) achieved pathCR. After a median follow-up duration of 40.7 months, 11 patients had disease recurrence and 10 had died. The median disease-free and OS were 28.8 (95% CI: 14.7, NA) and 38.6 months (95% CI: 30.5, NA), respectively. No treatment-related adverse events led to death. Although modified FOLFOX plus atezolizumab did not achieve the expected pathCR, an acceptable safety profile was observed. Our results support the continued development of a more refined strategy (neoadjuvant chemotherapy plus perioperative immunotherapy/targeted agents) with molecular/immune profiling in parallel.

Funder

Genentech Inc.

Publisher

MDPI AG

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