TremelImumab and Durvalumab Combination for the Non-OperatIve Management (NOM) of Microsatellite InstabiliTY (MSI)-High Resectable Gastric or Gastroesophageal Junction Cancer: The Multicentre, Single-Arm, Multi-Cohort, Phase II INFINITY Study

Author:

Raimondi Alessandra,Palermo Federica,Prisciandaro MicheleORCID,Aglietta Massimo,Antonuzzo Lorenzo,Aprile Giuseppe,Berardi RossanaORCID,Cardellino Giovanni G.,De Manzoni Giovanni,De Vita Ferdinando,Di Maio MassimoORCID,Fornaro Lorenzo,Frassineti Giovanni L.,Granetto Cristina,Iachetta Francesco,Lonardi Sara,Murialdo Roberto,Ongaro Elena,Pucci Francesca,Ratti Margherita,Silvestris NicolaORCID,Smiroldo Valeria,Spallanzani AndreaORCID,Strippoli Antonia,Tamberi Stefano,Tamburini Emiliano,Zaniboni Alberto,Di Bartolomeo Maria,Cremolini Chiara,Sposito Carlo,Mazzaferro Vincenzo,Pietrantonio FilippoORCID

Abstract

In resectable gastric or gastroesophageal junction cancer (GC/GEJC), the powerful positive prognostic effect and the potential predictive value for a lack of benefit from the combination of adjuvant/peri-operative chemotherapy for the MSI-high status was demonstrated. Given the high sensitivity of MSI-high tumors for immunotherapy, exploratory trials showed that combination immunotherapy induces a high rate of complete pathological response (pCR), potentially achieving cancer cure without surgery. INFINITY is an ongoing phase II, multicentre, single-arm, multi-cohort trial investigating the activity and safety of tremelimumab and durvalumab as neoadjuvant (Cohort 1) or potentially definitive (Cohort 2) treatment for MSI-high/dMMR/EBV-negative, resectable GC/GEJC. About 310 patients will be pre-screened, to enroll a total of 31 patients, 18 and 13 in Cohort 1 and 2, at 25 Italian Centres. The primary endpoint of Cohort 1 is rate of pCR (ypT0N0) and negative ctDNA after neoadjuvant immunotherapy, of Cohort 2 is 2-year complete response rate, defined as absence of macroscopic or microscopic residual disease (locally/regionally/distantly) at radiological examinations, tissue and liquid biopsy, during non-operative management without salvage gastrectomy. The ongoing INFINITY proof-of-concept study may provide evidence on immunotherapy and the potential omission of surgery in localized/locally advanced GC/GEJC patients selected for dMMR/MSI-high status eligible for radical resection.

Funder

AstraZeneca

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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