Multi-omic paired analysis reveals chemotherapy-associated immunosuppressive changes and therapeutic insights in recurrent endometrial carcinoma

Combination chemotherapy with immune checkpoint blockade has reshaped the treatment landscape for recurrent endometrial carcinoma (EC). However, subgroup analyses have demonstrated limited efficacy in patients previously treated with platinum-based adjuvant chemotherapy. To investigate how prior adjuvant chemotherapy affects the tumor microenvironment (TME) at recurrence, we analyzed 32 matched primary–recurrent EC pairs by performing multi-omic profiling in 20 pairs and multiplex immunohistochemistry (mIHC) in all cases. Recurrent tumors with prior platinum-based adjuvant chemotherapy exhibited increased variant allele frequencies of mutations in MYC signaling-related genes, with enrichment of glycolysis, regulatory T (Treg) cells, and M2 macrophage polarization. mIHC demonstrated increased Treg-cell infiltration and the M2/M1 macrophage ratio in recurrent tumors compared with matched primary tumors. Moreover, progression-free survival after recurrence correlated more strongly with the TME of recurrent tumors than with that of the primary tumors. Platinum-based adjuvant chemotherapy is associated with the emergence of immunosuppressive TME features in recurrent EC.

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Publication Details

Journal
npj Precision Oncology
Published
2026-09-01
DOI
https://doi.org/10.1038/s41698-026-01668-8
Primary Topic
Endometrial and Cervical Cancer Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

Multi-omic paired analysis reveals chemotherapy-associated immunosuppressive changes and therapeutic insights in recurrent endometrial carcinoma

Kenichi Harano, Takuma Irie, Yuki Koike, Shogo Kumagai et al.
npj Precision Oncology
Endometrial and Cervical Cancer Treatments
article

Multi-omic paired analysis reveals chemotherapy-associated immunosuppressive changes and therapeutic insights in recurrent endometrial carcinoma

Kenichi Harano, Takuma Irie, Yuki Koike, Shogo Kumagai, Tadaaki Nishikawa, Masataka Takenaka, Misato Kamii, Kyosuke Yamada, Aikou Okamoto, Tetsuro Taki, Hirokuni Takano, Suguru Odajima, Shin Takenaka, Hiroshi Tanabe, Nozomu Yanaihara, Motoaki Saito, Hiroyoshi Nishikawa, Toru Mukohara, Shohei Koyama, Jiro Suzuki
article en

Abstract

Combination chemotherapy with immune checkpoint blockade has reshaped the treatment landscape for recurrent endometrial carcinoma (EC). However, subgroup analyses have demonstrated limited efficacy in patients previously treated with platinum-based adjuvant chemotherapy. To investigate how prior adjuvant chemotherapy affects the tumor microenvironment (TME) at recurrence, we analyzed 32 matched primary–recurrent EC pairs by performing multi-omic profiling in 20 pairs and multiplex immunohistochemistry (mIHC) in all cases. Recurrent tumors with prior platinum-based adjuvant chemotherapy exhibited increased variant allele frequencies of mutations in MYC signaling-related genes, with enrichment of glycolysis, regulatory T (Treg) cells, and M2 macrophage polarization. mIHC demonstrated increased Treg-cell infiltration and the M2/M1 macrophage ratio in recurrent tumors compared with matched primary tumors. Moreover, progression-free survival after recurrence correlated more strongly with the TME of recurrent tumors than with that of the primary tumors. Platinum-based adjuvant chemotherapy is associated with the emergence of immunosuppressive TME features in recurrent EC.

npj Precision Oncology
Jikei University School of Medicine (JP), Immunité et Cancer (FR), Chiba Cancer Center (JP), National Cancer Center Hospital East (JP), National Cancer Research Institute (GB), Nagoya University (JP), Kindai University (JP)
Takeda Science Foundation, National Cancer Center Japan, Mitsubishi Foundation, Jikei University School of Medicine, MSD K.K., Japan Society for the Promotion of Science, Japan Science and Technology Agency
Good health and well-being
Openalex Percentile: Top 8%
Endometrial and Cervical Cancer Treatments
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