Immune-Hot tumor features associated with recurrence in early-stage ovarian clear cell carcinoma.
Ruby Yun-Ju HuangKuan-Ju HuangKo-Chen ChenSheng-Mou HsiaoTuan Zea TanChin-Jui WuChing HsuWen-Chun ChangChen-Yu PanBor-Ching SheuLin-Hung WeiPublished in: International journal of cancer (2023)
Ovarian 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.
Keyphrases
- free survival
- early stage
- prognostic factors
- end stage renal disease
- ejection fraction
- newly diagnosed
- clear cell
- chronic kidney disease
- peritoneal dialysis
- type diabetes
- high throughput
- deep learning
- sentinel lymph node
- radiation therapy
- single cell
- quality improvement
- neoadjuvant chemotherapy
- patient reported
- data analysis