Chinczewski Lukas, Chekerov Radoslav, Daum Severin, Ott Claus-Eric, Sehouli Jalid
Department of Gynecology With Centre of Oncologic Surgery, Charité - Campus Virchow-Klinikum, Charité - Universitätsmedizin Berlin, Augustenburger Platz 1, 13353, Berlin, Germany.
Department of Gastroenterology, Infectious Diseases and Rheumatology, Charité - Universitätsmedizin Berlin, Hindenburgdamm 40, 12200, Berlin, Germany.
Arch Gynecol Obstet. 2025 Aug 28. doi: 10.1007/s00404-025-08112-5.
Lynch syndrome (LS) is the most common inherited cancer syndrome, caused by germline mutations in mismatch repair (MMR) genes such as MLH1, MSH2, MSH6, and PMS2. While primarily associated with colorectal cancer, LS significantly impacts gynecological oncology, with increased risks for endometrial and ovarian cancers. Despite its clinical relevance, structured counseling and surveillance programs tailored to LS patients in gynecology are lacking.
This study presents the first structured gynecological outpatient consultation program for LS patients in Germany, established at Charité-Universitätsmedizin Berlin in August 2021. The aim was to develop an individualized, multidisciplinary framework for surveillance, therapy, and follow-up care, addressing the specific needs of different patient cohorts. Between August 2021 and December 2023, clinical data from 40 LS patients were collected and analyzed descriptively. From this experience, we furthermore concluded a guideline for the care of individuals with Lynch syndrome.
Among the 40 patients, 21 had been diagnosed with cancer (affected group), while 19 were cancer-free and undergoing routine surveillance (non-affected group). The distribution of MMR gene mutations was 40% MSH2, 25% MSH6, 25% PMS2, and 15% MLH1. In the non-affected group, the median age was 38 years, with a BMI of 21.4. Surveillance identified one urothelial carcinoma and one case of endometrial hyperplasia. In the affected group, the mean age was 55.2 years, and the BMI was 24.7. Twenty-three gynecological cancers were diagnosed, of which 52% were endometrial, 26% ovarian, and 18% breast cancers. 61.1% of tumors were MSI-positive, and 33.3% of patients received immunotherapy.
A holistic, multidisciplinary approach is essential for the management of LS patients in gynecological oncology. The structured consultation model developed at Charité facilitates personalized surveillance, risk-adapted prevention, and evidence-based therapy strategies. Future studies and clinical trials should further investigate screening protocols, therapeutic interventions, and the role of LS patients in targeted treatment approaches. This guideline serves as a preliminary framework and will be continuously adapted as new research emerges.
林奇综合征(LS)是最常见的遗传性癌症综合征,由错配修复(MMR)基因(如MLH1、MSH2、MSH6和PMS2)的种系突变引起。虽然LS主要与结直肠癌相关,但它对妇科肿瘤学有重大影响,会增加子宫内膜癌和卵巢癌的发病风险。尽管其具有临床相关性,但针对妇科LS患者的结构化咨询和监测项目仍很缺乏。
本研究介绍了德国首个针对LS患者的结构化妇科门诊咨询项目,该项目于2021年8月在柏林夏里特大学医学中心设立。目的是制定一个针对监测、治疗和后续护理的个性化多学科框架,以满足不同患者群体的特定需求。在2021年8月至2023年12月期间,收集并对40例LS患者的临床数据进行了描述性分析。基于这一经验,我们还总结了一份林奇综合征患者护理指南。
在这40例患者中,21例已被诊断患有癌症(患病组),而19例未患癌症且正在接受常规监测(未患病组)。MMR基因突变的分布情况为:MSH2占40%,MSH6占25%,PMS2占25%,MLH1占15%。在未患病组中,中位年龄为38岁,体重指数为21.4。监测发现1例尿路上皮癌和1例子宫内膜增生。在患病组中,平均年龄为55.2岁,体重指数为24.7。共诊断出23例妇科癌症,其中52%为子宫内膜癌,26%为卵巢癌,18%为乳腺癌。61.1%的肿瘤为微卫星高度不稳定(MSI)阳性,33.3%的患者接受了免疫治疗。
整体多学科方法对于妇科肿瘤学中LS患者的管理至关重要。夏里特大学制定的结构化咨询模式有助于个性化监测、风险适应性预防和循证治疗策略。未来的研究和临床试验应进一步调查筛查方案、治疗干预措施以及LS患者在靶向治疗方法中的作用。本指南作为一个初步框架,将随着新研究的出现而不断调整。