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New England Journal of Medicine· 2022Q1

Uyumsuzluk Onarımında Eksik, Lokal Olarak İleri Evre Rektal Kanserlerde PD-1 Blokajı

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

Andrea Cercek, Melissa Lumish, Jenna Sinopoli, Jill Weiss ve diğerleri

Kısa özet

Uyumsuzluk onarımında eksik, lokal olarak ileri evre rektal kanserli 10 hastanın tamamında neoadjuvan dostarlimab ile PD-1 blokajı, standart kemoradyoterapi ve cerrahiye gerek kalmadan klinik tam yanıt sağladı.

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Ana noktalar

  • Lokal olarak ileri evre, uyumsuzluk onarımında eksik rektal kanseri olan 10 hastanın tamamı, neoadjuvan dostarlimab tedavisinden sonra klinik tam yanıt elde etti.
  • Tedaviyi takiben hiçbir hasta standart kemoradyoterapi veya cerrahiye ihtiyaç duymadı veya almadı.
  • Takip süresi boyunca (6-25 ay) hastalık ilerlemesi veya nüks vakası bildirilmedi.
  • Çalışma sırasında 3. derece veya daha yüksek herhangi bir yan etki gözlenmedi.

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Özet (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.).

Yazarların özeti; kaynağından alınmıştır. New England Journal of Medicine, 2022 · DOI ↗

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