Abstract

BackgroundImmune checkpoint inhibitors (ICIs) have a significant therapeutic effect in patients with microsatellite instability-high (MSI-H) early-stage and metastatic colorectal cancer (CRC). However, data are rare on neoadjuvant immunotherapy for patients with MSI-H or DNA polymerase ε (POLE)-mutated locally advanced colorectal cancer (LACRC) with bulky tumors (> 8 cm). ObjectiveTo evaluate the efficacy and safety of neoadjuvant immunotherapy for patients with MSI-H or POLE-mutated LACRC with bulky tumors. DesignThis was a retrospective observational study. SettingsTertiary referral cancer center in China. PatientsWe retrospectively reviewed 22 consecutive patients with MSI-H or POLE-mutated LACRC with bulky tumors (> 8 cm in diameter) who received preoperative programmed death-1 blockade, with or without CapOx chemotherapy. All these patients had bulky tumor scheduled for multivisceral resection, or potentially local resectable metastatic lesions, or could not undergo initial R0 resection. Main Outcome MeasuresPathological complete response (pCR), clinical complete response (cCR), toxicity, R0 resection rate, and complications were evaluated. Survival outcomes were analyzed using the Kaplan–Meier method. Multiplex immunofluorescence analysis were performed before and after treatment. ResultsThe incidence of immune-related adverse events (irAEs) was 36.4% (8/22). Five of 22 patients presented with surgical emergencies, most commonly perforation or obstruction. The 22 patients underwent a median 4 (1-8) cycles. Two patients were evaluated as cCR and underwent a watch and wait strategy. The R0 resection rate was 100.0% (20/20) and pCR rate was 70.0% (14/20). Twelve of 14 cT4b patients (85.7%) avoided multivisceral resection, and 10 of them achieved pCR or cCR. In the 2 patients with POLE mutations, 1 each achieved pCR and cCR. No Grade III/IV postoperative complications occurred, and the most common complication was Grade I/II chylous leakage in 3 patients after radical right hemicolectomy. The median follow-up was 16.0 months. Two-year event-free and overall survival for the whole cohort was both 100%. LimitationsRetrospective study, small sample size, and short follow-up. ConclusionsPreoperative ICI therapy is the optimal option for MSI-H or POLE-mutated LACRC with bulky tumors, especially cT4b. Preoperative immunotherapy in patients with T4b CRC can reduce multivisceral resection and achieve high CR.

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