Ascites and resistance to immune checkpoint inhibition in dMMR/MSI-H metastatic colorectal and gastric cancers

Giovanni Fucà(Tumori Foundation), Romain Cohen(Inserm), Sara Lonardi(Istituto Oncologico Veneto), Kohei Shitara(National Cancer Center Hospital East), María Elena Elez(Universitat Autònoma de Barcelona), Marwan Fakih(City of Hope), Joseph Chao(City of Hope), Samuel J. Klempner(Harvard University), Matthew J. Emmett(Harvard University), Priya Jayachandran(University of Southern California), Francesca Bergamo(Istituto Oncologico Veneto), M. Díez García(Universitat Autònoma de Barcelona), Giacomo Mazzoli(Tumori Foundation), Leonardo Provenzano(Tumori Foundation), Raphaël Colle(Inserm), Magali Svrcek(Inserm), Margherita Ambrosini(Tumori Foundation), Giovanni Randon(Tumori Foundation), Aakash Tushar Shah(Baylor College of Medicine), Massimiliano Salati(University of Modena and Reggio Emilia), Elisabetta Fenocchio(Candiolo Cancer Institute), Lisa Salvatore(Agostino Gemelli University Polyclinic), Keigo Chida(National Cancer Center Hospital East), Akihito Kawazoe(National Cancer Center Hospital East), Veronica Conca(University of Pisa), Giuseppe Curigliano(University of Milan), Francesca Corti(Tumori Foundation), Chiara Cremolini(University of Pisa), Michael J. Overman(The University of Texas MD Anderson Cancer Center), Thierry André(Inserm), Filippo Pietrantonio(Tumori Foundation)
Journal for ImmunoTherapy of Cancer
February 1, 2022
Cited by 117Open Access
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Abstract

BACKGROUND: Despite unprecedented benefit from immune checkpoint inhibitors (ICIs) in patients with mismatch repair deficient (dMMR)/microsatellite instability high (MSI-H) advanced gastrointestinal cancers, a relevant proportion of patients shows primary resistance or short-term disease control. Since malignant effusions represent an immune-suppressed niche, we investigated whether peritoneal involvement with or without ascites is a poor prognostic factor in patients with dMMR/MSI-H metastatic colorectal cancer (mCRC) and gastric cancer (mGC) receiving ICIs. METHODS: We conducted a global multicohort study at Tertiary Cancer Centers and collected clinic-pathological data from a cohort of patients with dMMR/MSI-H mCRC treated with anti-PD-(L)1 ±anti-CTLA-4 agents at 12 institutions (developing set). A cohort of patients with dMMR/MSI-high mGC treated with anti-PD-1 agents±chemotherapy at five institutions was used as validating dataset. RESULTS: The mCRC cohort included 502 patients. After a median follow-up of 31.2 months, patients without peritoneal metastases and those with peritoneal metastases and no ascites had similar outcomes (adjusted HR (aHR) 1.15, 95% CI 0.85 to 1.56 for progression-free survival (PFS); aHR 0.96, 95% CI 0.65 to 1.42 for overall survival (OS)), whereas inferior outcomes were observed in patients with peritoneal metastases and ascites (aHR 2.90, 95% CI 1.70 to 4.94; aHR 3.33, 95% CI 1.88 to 5.91) compared with patients without peritoneal involvement. The mGC cohort included 59 patients. After a median follow-up of 17.4 months, inferior PFS and OS were reported in patients with peritoneal metastases and ascites (aHR 3.83, 95% CI 1.68 to 8.72; aHR 3.44, 95% CI 1.39 to 8.53, respectively), but not in patients with only peritoneal metastases (aHR 1.87, 95% CI 0.64 to 5.46; aHR 2.15, 95% CI 0.64 to 7.27) when compared with patients without peritoneal involvement. CONCLUSIONS: Patients with dMMR/MSI-H gastrointestinal cancers with peritoneal metastases and ascites should be considered as a peculiar subgroup with highly unfavorable outcomes to current ICI-based therapies. Novel strategies to target the immune-suppressive niche in malignant effusions should be investigated, as well as next-generation ICIs or intraperitoneal approaches.


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