Phase I-II trial of perioperative chemotherapy plus atezolizumab and tiragolumab in localized esophageal and gastroesophageal junction adenocarcinoma.

M Mariela A. Blum Murphy (The University of Texas MD Anderson Cancer Center, Houston, TX) L Lianchun Xiao X Xuemei Wang M Matheus Sewastjanow-Silva (The University of Texas MD Anderson Cancer Center, Houston, TX) W Wayne L. Hofstetter (The University of Texas MD Anderson Cancer Center, Houston, TX) S Stephen Swisher R Reza J. Mehran (Department of Thoracic and Cardiovascular Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX) K Kyle Gregory Mitchell (The University of Texas MD Anderson Cancer Center, Houston, TX) M Manoop S. Bhutani (Department of Gastroenterology, Hepatology, and Nutrition, The University of Texas MD Anderson Cancer Center, Houston, TX) B Brian Weston (The University of Texas MD Anderson Cancer Center, Houston, TX) E Emmanuel Coronel (The University of Texas MD Anderson Cancer Center, Houston, TX) J Jeannelyn Estrella (The University of Texas MD Anderson Cancer Center, Houston, TX) R Rebecca E. Waters (The University of Texas MD Anderson Cancer Center, Houston, TX) D Dipen M. Maru B Brian Justin Witt (The University of Texas MD Anderson Cancer Center, Houston, TX) J Jenny Jing Li (The University of Texas MD Anderson Cancer Center, Houston, TX) J James C. Yao J Jaffer A. Ajani

Abstract

418 Background: Management of esophageal and gastroesophageal junction (GEJ) adenocarcinoma focuses on perioperative strategies to increase pathological complete response rates, delay or eliminate metastases, and prolong overall survival. Atezolizumab is a humanized IgG1 monoclonal antibody that blocks PD-L1 from binding its inhibitory receptors, PD-1 and B7-1, thereby boosting tumor-specific T-cell responses and anti-tumor activity. Tiragolumab is a fully human IgG1/κ monoclonal antibody targeting TIGIT, an inhibitory receptor on activated T cells and NK cells that binds CD155. Blocking TIGIT could further enhance T-cell responses. Combining tiragolumab with atezolizumab and chemotherapy may improve outcomes in patients with localized esophageal and GEJ adenocarcinoma. Methods: We conducted a phase I/II study to evaluate the efficacy and safety of combining atezolizumab and tiragolumab with modified FOLFOX (oxaliplatin and 5-fluorouracil) in the perioperative treatment of localized esophageal and GEJ type I or II adenocarcinoma. Eligible patients were treatment naïve with T1N1 or T2-3 (any N) GEJ adeno. Treatment involved FOLFOX on days 1 and 15, followed by atezolizumab (840 mg IV) and tiragolumab (420 mg IV) on the same days of each 28-day cycle, for a total of six doses. Surgery was performed afterward, followed by adjuvant atezolizumab (1200 mg IV) plus tiragolumab (600 mg IV) on day 1 administered every 21 days for sixteen cycles. Results: Twenty-three patients (median age 67) were enrolled (stage IIb: n=6; stage III: n=13; stage IVa: n=4). Twenty patients were evaluated for efficacy. Thus far, 16 patients had undergone surgery. Pathological complete response (pCR, T0N0) has been observed in 18.8% (3/16; 95% CI: 4.1–45.7%), with 1 additional patient showing near-complete response (<1% viable tumor). R0 resection rate was 87.5%. There were no grade 4 treatment-related adverse events, deaths or treatment discontinuations. At a median follow-up of 21.1 months, four patients had died. Estimated 1- and 2-year survival rates were 94.1% and 74.0%, respectively. Conclusions: Results indicate that atezolizumab and tiragolumab in combination with oxaliplatin and 5-fluorouracil has an acceptable safety profile providing high rate of tumor regression. This trial supports further research checkpoint inhibition in patients with localized esophageal and GEJ adenocarcinomas in the perioperative setting. Clinical trial information: NCT03784326 .

Article Details

Volume / Issue Vol. 44, Issue 2_suppl
Published January 10, 2026
Pages 418-418
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (18)

M

Mariela A. Blum Murphy

The University of Texas MD Anderson Cancer Center, Houston, TX

L

Lianchun Xiao

X

Xuemei Wang

M

Matheus Sewastjanow-Silva

The University of Texas MD Anderson Cancer Center, Houston, TX

W

Wayne L. Hofstetter

The University of Texas MD Anderson Cancer Center, Houston, TX

S

Stephen Swisher

R

Reza J. Mehran

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

K

Kyle Gregory Mitchell

The University of Texas MD Anderson Cancer Center, Houston, TX

M

Manoop S. Bhutani

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

B

Brian Weston

The University of Texas MD Anderson Cancer Center, Houston, TX

E

Emmanuel Coronel

The University of Texas MD Anderson Cancer Center, Houston, TX

J

Jeannelyn Estrella

The University of Texas MD Anderson Cancer Center, Houston, TX

R

Rebecca E. Waters

The University of Texas MD Anderson Cancer Center, Houston, TX

D

Dipen M. Maru

B

Brian Justin Witt

The University of Texas MD Anderson Cancer Center, Houston, TX

J

Jenny Jing Li

The University of Texas MD Anderson Cancer Center, Houston, TX

J

James C. Yao

J

Jaffer A. Ajani