The HER2 paradox in ovarian clear cell carcinoma: Expression and intrinsic resistance to trastuzumab deruxtecan (T-DXd).
Abstract
5563 Background: Trastuzumab deruxtecan (T-DXd) shows potent activity in HER2-expressing ovarian cancer (OC). However, efficacy across histologic subtypes remains under-characterized. Specifically, data on T-DXd response in ovarian clear cell carcinoma (OCCC), a distinct chemo-resistant entity, are lacking. This study aimed to evaluate T-DXd efficacy in recurrent OC across different histologic subtypes. Methods: We retrospectively analyzed 59 patients with recurrent OC who received T-DXd treatment between 2020 and 2025 at Yonsei Cancer Center. HER2 status (IHC), objective response rate (ORR), progression-free survival (PFS), duration of response, and safety were assessed by histology. Results: Patients included HGSC (n=38), Mucinous (n=9), OCCC (n=10), and Endometrioid (n=2). Median age was 55; median prior lines of therapy was 3. Notably, 100% of OCCC, mucinous, and endometrioid tumors were HER2 2+/3+, vs. 89.5% in HGSC. Despite high HER2 expression, outcomes diverged. ORR was 55.3% (26/47) for HGSC/Mucinous vs. 0% (0/12) for OCCC/Endometrioid ( P <0.001). Specifically, HGSC achieved 57.9% ORR (2 CRs) vs. 0% in OCCC. PFS was significantly shorter in the OCCC/Endometrioid group (median 1.2 vs 6.9 months; HR 18.3; P <0.0001). OCCC patients showed rapid progression. Regarding safety, among 54 evaluable patients, 36 (66.7%) experienced Grade 3-4 adverse events, and 5 cases (9.3%) of ILD occurred; however, no new safety signals or treatment-related deaths were reported. Conclusions: T-DXd showed robust efficacy in recurrent HGSC and mucinous OC but no response in OCCC and endometrioid OC. Thus, HER2 expression alone does not guarantee T-DXd response in OCCC, possibly due to its chemo-refractory nature. Mechanisms of T-DXd resistance in OCCC warrant investigation. Tumor response. Histology HGSC (n=38) Mucinous (n=9) Endometrioid (n=2) Clear cell (n=10) Objective response 1 (n, %) 22 (58%) 4 (44%) 0 (0%) 0 (0%) CR 2 (5%) 0 (0%) 0 (0%) 0 (0%) PR 20 (53%) 4 (44%) 0 (0%) 0 (0%) SD 14 (37%) 4 (44%) 0 (0%) 0 (0%) PD 2 (5%) 1 (11%) 2 (100%) 10 (100%) 1 P =0.0006.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (7)
Junsik Park
Department of Obstetrics and Gynecology, Soonchunhyang University Bucheon Hospital, Bucheon, South Korea
Soyeon Kim
Jeong-Hyun Kim
Department of Advanced Battery Convergence Engineering
Yoo Na Kim
Department of Obstetrics and Gynecology, Yonsei University College of Medicine, Seoul, South Korea
Yong Jae Lee
Cell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology
Sunghoon Kim
Jung-Yun Lee