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New England Journal of Medicine· 2022Q1

PD-1 Blockade in Mismatch Repair–Deficient, Locally Advanced Rectal Cancer

Andrea Cercek, Melissa Lumish, Jenna Sinopoli, Jill Weiss et al.

Short summary

A neoadjuvant PD-1 blockade with dostarlimab resulted in a clinical complete response in all 10 patients with mismatch repair-deficient, locally advanced rectal cancer, eliminating the need for standard chemoradiotherapy and surgery.

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Key points

  • All 10 patients with mismatch repair-deficient, locally advanced rectal cancer achieved a clinical complete response after neoadjuvant dostarlimab therapy.
  • No patients required or received standard chemoradiotherapy or surgery following dostarlimab treatment.
  • No cases of disease progression or recurrence were reported during follow-up (6-25 months).
  • No adverse events of grade 3 or higher were observed during the study.

AI-generated from the title and abstract; the full text is not read.

Abstract

BACKGROUND: Neoadjuvant chemotherapy and radiation followed by surgical resection of the rectum is a standard treatment for locally advanced rectal cancer. A subset of rectal cancer is caused by a deficiency in mismatch repair. Because mismatch repair-deficient colorectal cancer is responsive to programmed death 1 (PD-1) blockade in the context of metastatic disease, it was hypothesized that checkpoint blockade could be effective in patients with mismatch repair-deficient, locally advanced rectal cancer. METHODS: We initiated a prospective phase 2 study in which single-agent dostarlimab, an anti-PD-1 monoclonal antibody, was administered every 3 weeks for 6 months in patients with mismatch repair-deficient stage II or III rectal adenocarcinoma. This treatment was to be followed by standard chemoradiotherapy and surgery. Patients who had a clinical complete response after completion of dostarlimab therapy would proceed without chemoradiotherapy and surgery. The primary end points are sustained clinical complete response 12 months after completion of dostarlimab therapy or pathological complete response after completion of dostarlimab therapy with or without chemoradiotherapy and overall response to neoadjuvant dostarlimab therapy with or without chemoradiotherapy. RESULTS: F-fluorodeoxyglucose-positron-emission tomography, endoscopic evaluation, digital rectal examination, or biopsy. At the time of this report, no patients had received chemoradiotherapy or undergone surgery, and no cases of progression or recurrence had been reported during follow-up (range, 6 to 25 months). No adverse events of grade 3 or higher have been reported. CONCLUSIONS: Mismatch repair-deficient, locally advanced rectal cancer was highly sensitive to single-agent PD-1 blockade. Longer follow-up is needed to assess the duration of response. (Funded by the Simon and Eve Colin Foundation and others; ClinicalTrials.gov number, NCT04165772.).

The authors' abstract, as published at the source. New England Journal of Medicine, 2022 · DOI ↗

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Field: Pathology and Forensic Medicine

Pathology and Forensic MedicineMedicine