医学
子宫内膜癌
免疫疗法
癌
外科
内科学
肿瘤科
舒尼替尼
肾细胞癌
肾癌
生物标志物
放射科
切除术
完全响应
靶向治疗
癌症
病态的
子宫内膜
疾病
妇科肿瘤学
索拉非尼
不利影响
子宫切除术
卵巢癌
醋酸甲地孕酮
护理标准
作者
Huijiao Fu,Bo Yang,Jing Li,Xingxin Zhu,Yunjun Yang,Songhua Yuan
标识
DOI:10.1007/s12672-026-04917-1
摘要
Mismatch repair-deficient (dMMR) advanced or recurrent endometrial carcinoma presents a therapeutic challenge, and the role of preoperative immunotherapy prior to its guideline incorporation (2020–2022) remained unexplored. We report three patients with dMMR endometrial carcinoma who received preoperative anti‑PD‑1 therapy (sintilimab). Case 1 (locally recurrent vaginal mass) was treated with sintilimab monotherapy, achieving a pathological complete response. Case 2 (stage IVB with bulky uterine and osseous metastases) received sintilimab combined with carboplatin/docetaxel, attaining partial response. Case 3 (recurrent disease with renal impairment) received sintilimab plus megestrol acetate, which yielded a marked biochemical response (98.6% CA125 reduction) enabling resection despite radiographic stable disease. All patients underwent R0 resection and remained recurrence‑free after a median follow‑up of 36 months, with no grade ≥ 3 adverse events. Exploratory biomarker analysis revealed cGAS‑STING pathway activation in all tumors. These findings provide early real‑world evidence that preoperative anti‑PD‑1 therapy is a feasible and effective strategy for converting unresectable dMMR endometrial carcinoma to resectable disease, supporting further investigation in larger studies.
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