Immune‐Hot tumor features associated with recurrence in early‐stage ovarian clear cell carcinoma

Author:

Huang Ruby Yun‐Ju1,Huang Kuan‐Ju23ORCID,Chen Ko‐Chen1,Hsiao Sheng‐Mou45,Tan Tuan Zea6,Wu Chin‐Jui7,Hsu Ching2,Chang Wen‐Chun2,Pan Chen‐Yu2,Sheu Bor‐Ching2,Wei Lin‐Hung2

Affiliation:

1. School of Medicine National Taiwan University College of Medicine Taipei Taiwan

2. Department of Obstetrics and Gynecology National Taiwan University Hospital & National Taiwan University College of Medicine Taipei Taiwan

3. National Taiwan University Hospital Yunlin Branch Douliu City Taiwan

4. Department of Obstetrics and Gynecology Far Eastern Memorial Hospital New Taipei Taiwan

5. Graduate School of Biotechnology and Bioengineering Yuan Ze University Taoyuan Taiwan

6. Cancer Science Institute of Singapore National University of Singapore, Center for Translational Medicine Singapore

7. National Taiwan University Hospital Hsin‐Chu Branch Hsin‐Chu Taiwan

Abstract

AbstractOvarian clear cell carcinoma (OCCC) is a distinct histotype of ovarian cancer, which usually presages a worse prognosis upon recurrence. Identifying patients at risk for relapse is an unmet need to improve outcomes. A retrospective cohort analysis of 195 early‐stage OCCC patients diagnosed between January 2011 and December 2019 at National Taiwan University Hospital was conducted to identify prognostic factors for recurrence, progression‐free survival (PFS) and overall survival (OS). Molecular profiling of tumors was performed in a case‐controlled cohort matched for adjuvant therapy for biomarker discovery. Multivariate Cox proportional hazard model revealed that paclitaxel‐based chemotherapy was associated with better PFS than nonpaclitaxel chemotherapy (HR = 0.19, P = .006). The addition of bevacizumab was associated with better PFS, compared to no bevacizumab (HR = 0.09, P = .02). Neither showed significant improvement in OS. Recurrence is associated with an Immune‐Hot tumor feature (P = .03), the CTLA‐4‐high subtype (P = .01) and increased infiltration of immune cells in general. The Immune‐Hot feature (HR = 3.39, P = .005) and the CTLA‐4‐high subtype (HR = 2.13, P = .059) were associated with worse PFS. Immune‐Hot tumor features could prognosticate recurrence in early‐stage OCCC.

Publisher

Wiley

Subject

Cancer Research,Oncology

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