Bogani G, Monk B J, Powell M A, Westin S N, Slomovitz B, Moore K N, Eskander R N, Raspagliesi F, Barretina-Ginesta M-P, Colombo N, Mirza M R
Gynecological Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.
GOG Foundation, Florida Cancer Specialists and Research Institute, West Palm Beach.
Ann Oncol. 2024 May;35(5):414-428. doi: 10.1016/j.annonc.2024.02.006. Epub 2024 Feb 29.
Immunotherapy has transformed the endometrial cancer treatment landscape, particularly for those exhibiting mismatch repair deficiency [MMRd/microsatellite instability-hypermutated (MSI-H)]. A growing body of evidence supports the integration of immunotherapy with chemotherapy as a first-line treatment strategy. Recently, findings from ongoing trials such as RUBY (NCT03981796), NRG-GY018 (NCT03914612), AtTEnd (NCT03603184), and DUO-E (NCT04269200) have been disclosed.
This paper constitutes a review and meta-analysis of phase III trials investigating the role of immunotherapy in the first-line setting for advanced or recurrent endometrial cancer.
The pooled data from 2320 patients across these trials substantiate the adoption of chemotherapy alongside immunotherapy, revealing a significant improvement in progression-free survival compared to chemotherapy alone [hazard ratio (HR) 0.70, 95% confidence interval (CI) 0.62-0.79] across all patient groups. Progression-free survival benefits are more pronounced in MMRd/MSI-H tumors (n = 563; HR 0.33, 95% CI 0.23-0.43). This benefit, albeit less robust, persists in the MMR-proficient/microsatellite stable group (n = 1757; HR 0.74, 95% CI 0.60-0.91). Pooled data further indicate that chemotherapy plus immunotherapy enhances overall survival compared to chemotherapy alone in all patients (HR 0.75, 95% CI 0.63-0.89). However, overall survival data maturity remains low.
The incorporation of immunotherapy into the initial treatment for advanced and metastatic endometrial cancer brings about a substantial improvement in oncologic outcomes, especially within the MMRd/MSI-H subset. This specific subgroup is currently a focal point of investigation for evaluating the potential of chemotherapy-free regimens. Ongoing exploratory analyses aim to identify non-responding patients eligible for inclusion in clinical trials.
免疫疗法已经改变了子宫内膜癌的治疗格局,尤其是对于那些表现出错配修复缺陷[错配修复缺陷/微卫星高度不稳定(MSI-H)]的患者。越来越多的证据支持将免疫疗法与化疗联合作为一线治疗策略。最近,如RUBY(NCT03981796)、NRG-GY018(NCT03914612)、AtTEnd(NCT03603184)和DUO-E(NCT04269200)等正在进行的试验结果已经公布。
本文对研究免疫疗法在晚期或复发性子宫内膜癌一线治疗中作用的III期试验进行了综述和荟萃分析。
这些试验中2320例患者的汇总数据证实了化疗联合免疫疗法的应用,显示与单纯化疗相比,所有患者组的无进展生存期均有显著改善[风险比(HR)0.70,95%置信区间(CI)0.62-0.79]。无进展生存期的获益在错配修复缺陷/微卫星高度不稳定肿瘤中更为明显(n = 563;HR 0.33,95%CI 0.23-0.43)。这种获益虽然不那么显著,但在错配修复功能正常/微卫星稳定组(n = 1757;HR 0.74,95%CI 0.60-0.91)中仍然存在。汇总数据进一步表明,与单纯化疗相比,化疗联合免疫疗法可提高所有患者的总生存期(HR 0.75,95%CI 0.63-0.89)。然而,总生存期数据的成熟度仍然较低。
将免疫疗法纳入晚期和转移性子宫内膜癌的初始治疗可显著改善肿瘤学结局,尤其是在错配修复缺陷/微卫星高度不稳定亚组中。这个特定的亚组目前是评估无化疗方案潜力的研究重点。正在进行的探索性分析旨在确定有资格纳入临床试验的无反应患者。