# The Charité protocol for surveillance, treatment and after-care management in women with Lynch syndrome

**Authors:** Lukas Chinczewski, Radoslav Chekerov, Severin Daum, Claus-Eric Ott, Jalid Sehouli

PMC · DOI: 10.1007/s00404-025-08112-5 · Archives of Gynecology and Obstetrics · 2025-08-28

## TL;DR

This paper introduces a new gynecological care program for women with Lynch syndrome, focusing on surveillance, treatment, and follow-up to manage cancer risks.

## Contribution

The first structured gynecological outpatient consultation program for Lynch syndrome patients in Germany is developed and evaluated.

## Key findings

- Among 40 LS patients, 21 had cancer and 19 were cancer-free but undergoing surveillance.
- Surveillance identified urothelial carcinoma and endometrial hyperplasia in the non-affected group.
- 61.1% of tumors in the affected group were MSI-positive, and 33.3% of patients received immunotherapy.

## Abstract

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.

## Linked entities

- **Genes:** MLH1 (mutL homolog 1) [NCBI Gene 4292], MSH2 (mutS homolog 2) [NCBI Gene 4436], MSH6 (mutS homolog 6) [NCBI Gene 2956], PMS2 (PMS1 homolog 2, mismatch repair system component) [NCBI Gene 5395]
- **Diseases:** Lynch syndrome (MONDO:0005835), colorectal cancer (MONDO:0005575), endometrial cancer (MONDO:0002447), ovarian cancer (MONDO:0005140), urothelial carcinoma (MONDO:0040679), endometrial hyperplasia (MONDO:0041161), breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** MLH1 (mutL homolog 1) [NCBI Gene 4292] {aka COCA2, FCC2, HNPCC, HNPCC2, LYNCH2, MLH-1}, MSH2 (mutS homolog 2) [NCBI Gene 4436] {aka COCA1, FCC1, HNPCC, HNPCC1, LCFS2, LYNCH1}, MSH6 (mutS homolog 6) [NCBI Gene 2956] {aka GTBP, GTMBP, HNPCC5, HSAP, LYNCH5, MMRCS3}, PMS2 (PMS1 homolog 2, mismatch repair system component) [NCBI Gene 5395] {aka HNPCC4, LYNCH4, MLH4, MMRCS4, PMS-2, PMSL2}
- **Diseases:** breast cancers (MESH:D001943), endometrial (MESH:D014591), ovarian (MESH:D010049), urothelial carcinoma (MESH:D014523), LS (MESH:D003123), cancer (MESH:D009369), endometrial and ovarian cancers (MESH:D004714), colorectal cancer (MESH:D015179), inherited cancer syndrome (MESH:D009386)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

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Source: https://tomesphere.com/paper/PMC12589233