# Recent therapeutic advances in gynecologic oncology: evolving roles of immunotherapy, antibody–drug conjugates, and clinical trial innovations

**Authors:** Gaukhar Koshkimbayeva, Akerke Amirkhanova, Aiken Orazymbetova, Alma Nurakhova, Akmaral Maimakova, Altyn Duisenbayeva, Nurgulim Akhmad, Altyn Abilova, Arailym Abilbayeva, Sholpan Akhelova, Dana Akhmentayeva, Aida Seitaliyeva, Zaure Dushimova, Zhanserik Shynykul, Sandugash Yerkenova

PMC · DOI: 10.3389/fonc.2025.1697180 · 2026-01-15

## TL;DR

New treatments like immunotherapy and antibody-drug conjugates are improving outcomes for gynecologic cancers by overcoming drug resistance and enabling personalized care.

## Contribution

This review highlights recent clinical advances in immunotherapy and ADCs, emphasizing their integration into treatment and the role of genomic profiling and AI.

## Key findings

- Checkpoint inhibitors and ADCs show clinical benefits in advanced endometrial and cervical cancers.
- Combination therapies with ICIs, PARP inhibitors, and antiangiogenic agents are effective in first-line and maintenance settings.
- Molecular profiling and AI are improving treatment precision in gynecologic oncology.

## Abstract

Gynecologic cancers, including cervical, endometrial, and ovarian malignancies, remain among the leading causes of cancer-related illness and death in women worldwide. Despite progress in surgery and chemotherapy, resistance to conventional cytotoxic drugs continues to limit durable outcomes. The introduction of immune checkpoint inhibitors (ICIs) and antibody–drug conjugates (ADCs) has created new therapeutic opportunities by improving survival and overcoming resistance mechanisms. This review summarizes the latest clinical evidence on immunotherapy and ADC-based regimens, emphasizing their integration into current treatment strategies and the expanding roles of genomic profiling and artificial intelligence (AI) in personalized therapy.

Recent findings from major clinical trials such as RUBY, NRG-GY018, DUO-O, SORAYA, and DESTINY-PanTumor02 were evaluated along with updated FDA and NCCN recommendations. The analysis focuses on treatments that have demonstrated clinical benefit in advanced or recurrent disease, including pembrolizumab, dostarlimab, tisotumab vedotin, and mirvetuximab soravtansine. Combination strategies incorporating PARP inhibitors, antiangiogenic agents, and immune checkpoint blockade were also reviewed.

Checkpoint inhibitors have achieved meaningful clinical benefits in patients with advanced or recurrent endometrial and cervical cancers, particularly in those with mismatch repair deficiency or PD-L1 expression. ADCs directed against tissue factor (TF) and folate receptor alpha have shown effectiveness in platinum-resistant cervical and ovarian cancers. Combination regimens that include ICIs, PARP inhibitors, or antiangiogenic therapy are yielding encouraging results in both first-line and maintenance settings. Advances in molecular profiling and biomarker-based patient selection, supported by AI applications, are further improving treatment precision in gynecologic oncology.

Immunotherapy and ADCs represent major advances in the treatment of gynecologic cancers. Their growing integration into clinical practice has reshaped therapeutic approaches, while ongoing research continues to refine optimal combinations, address resistance, and enhance biomarker-guided selection. Future developments are expected to unite immunologic, genomic, and computational strategies to achieve personalized and durable outcomes for patients with gynecologic malignancies.

## Linked entities

- **Diseases:** cervical cancer (MONDO:0002974), endometrial cancer (MONDO:0002447), ovarian cancer (MONDO:0005140)

## Full-text entities

- **Genes:** F3 (coagulation factor III, tissue factor) [NCBI Gene 2152] {aka CD142, TF, TFA}, COL11A2 (collagen type XI alpha 2 chain) [NCBI Gene 1302] {aka DFNA13, DFNB53, FBCG2, HKE5, OSMEDA, OSMEDB}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, FOLR1 (folate receptor alpha) [NCBI Gene 2348] {aka FBP, FOLR, FR-alpha, FRalpha, NCFTD}
- **Diseases:** cervical, endometrial, and ovarian malignancies (MESH:D002575), endometrial and cervical cancers (MESH:D002583), death (MESH:D003643), cervical and ovarian cancers (MESH:D010051), Gynecologic cancers (MESH:D009369), gynecologic malignancies (MESH:D005833)
- **Chemicals:** tisotumab vedotin (MESH:C000707142), dostarlimab (MESH:C000719628), mirvetuximab soravtansine (MESH:C000607289), platinum (MESH:D010984), pembrolizumab (MESH:C582435)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12851983/full.md

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Source: https://tomesphere.com/paper/PMC12851983