Efficacy and safety of neoadjuvant ICI-based regimens in resectable gastric and GEJ cancer: Updated systematic review and meta-analysis.

S Sana Arif Khan (Aga Khan University Hospital, Karachi, Pakistan) M Mohammad Dawar Zahid (Aga Khan University Hospital, Karachi, Pakistan) M Mazhar Ali A Anushah Faheem Ilyas (Karachi Medical and Dental College, Karachi, Pakistan) M Muhammad Junaid A Abdul Muqsit (Liaquat National University, Karachi, Pakistan) S Sadia Qazi (Al Faisal University, Riyadh, Saudi Arabia) M Muhammad Atif Mazhar (Al Faisal University, Riyadh, Saudi Arabia) S Safia Bibi (Quetta Institute of Medical Sciences, Quetta, Pakistan)

Abstract

e16124 Background: Gastric and gastroesophageal junction (GEJ) cancers remain highly lethal, and durable cure relies on curative resection and deep pathologic response. Despite neoadjuvant chemotherapy, relapse is frequent. With newly published, more mature studies reporting resection, downstaging, and perioperative safety for neoadjuvant immune checkpoint inhibitor (ICI) based therapy, we updated prior limited syntheses to refine contemporary efficacy and toxicity estimates. Methods: We performed a PRISMA-compliant systematic review and meta-analysis of studies comparing neoadjuvant ICI-based therapy versus non-ICI regimens in resectable gastric/GEJ cancer, using the most mature reports. Outcomes were overall survival (HR), resection rate, pCR, ypT-0, ypT-1, ypT-2 downstaging, any-grade adverse events, and grade 3–4 adverse events (all pooled as ORs) with random-effects models and I² heterogeneity. Results: We performed a PRISMA-compliant systematic review and meta-analysis of studies comparing neoadjuvant ICI-based therapy versus non-ICI regimens in resectable gastric/GEJ cancer, using the most mature reports. Outcomes were overall survival (HR), resection rate, pCR, ypT-0, ypT-1, ypT-2 downstaging, any-grade adverse events, and grade 3–4 adverse events (all pooled as ORs) with random-effects models and I² heterogeneity. Conclusions: Neoadjuvant ICI-based therapy improved resection and pathological response without clear excess toxicity, but OS benefit was not demonstrated. Prospective trials and standardized reporting are needed to determine whether pathological gains translate into durable survival.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (9)

S

Sana Arif Khan

Aga Khan University Hospital, Karachi, Pakistan

M

Mohammad Dawar Zahid

Aga Khan University Hospital, Karachi, Pakistan

M

Mazhar Ali

A

Anushah Faheem Ilyas

Karachi Medical and Dental College, Karachi, Pakistan

M

Muhammad Junaid

A

Abdul Muqsit

Liaquat National University, Karachi, Pakistan

S

Sadia Qazi

Al Faisal University, Riyadh, Saudi Arabia

M

Muhammad Atif Mazhar

Al Faisal University, Riyadh, Saudi Arabia

S

Safia Bibi

Quetta Institute of Medical Sciences, Quetta, Pakistan