Sex-dependent Prognosis of Patients with Advanced Soft Tissue Sarcoma

Author:

Pan Minggui12ORCID,Zhou Maggie Yuxi1ORCID,Jiang Chen2ORCID,Zhang Zheyang3ORCID,Bui Nam Q.1ORCID,Bien Jeffrey1ORCID,Siy Amanda1ORCID,Achacoso Ninah2ORCID,Solorzano Aleyda V.2ORCID,Tse Pamela2ORCID,Chung Elaine2ORCID,Thomas Sachdev4ORCID,Habel Laurel A.2ORCID,Ganjoo Kristen N.1ORCID

Affiliation:

1. 1Sarcoma Program, Division of Oncology, Stanford University School of Medicine, Stanford, California.

2. 2Division of Research, Kaiser Permanente, Oakland, California.

3. 3State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Faculty of Medicine and Life Sciences, Xiamen University; and National Institute for Data Science in Health and Medicine, Xiamen University, Xiamen, Fujian, China.

4. 4Department of Oncology and Hematology, Kaiser Permanente, Vallejo, California.

Abstract

Abstract Purpose: To examine whether overall survival (OS) differs for male and female patients with advanced soft-tissue sarcoma (STS). Experimental Design: The study included patients from Kaiser Permanente Northern California and Stanford Cancer Center with grade 2 and 3 locally advanced or metastatic STS whose tumor underwent next-generation sequencing. We used Cox regression modeling to examine association of sex and OS adjusting for other important factors. Results: Among 388 eligible patients, 174 had leiomyosarcoma (LMS), 136 had undifferentiated pleomorphic sarcoma (UPS), and 78 had liposarcoma. OS for male versus female patients appeared to be slightly better among the full cohort [HR = 0.89; 95% confidence interval (CI), 0.66–1.20]; this association appeared to be stronger among the subsets of patients with LMS (HR = 0.76; 95% CI, 0.39–1.49) or liposarcoma (HR = 0.74; 95% CI, 0.32–1.70). Better OS for male versus female patients was also observed among all molecular subgroups except mutRB1 and mutATRX, especially among patients whose tumor retained wtTP53 (HR = 0.73; 95% CI, 0.44–1.18), wtCDKN2A (HR = 0.85; 95% CI, 0.59–1.23), wtRB1 (HR = 0.73; 95% CI, 0.51–1.04), and among patients whose tumor had mutPTEN (HR = 0.37; 95% CI, 0.09–1.62). OS also appeared to be better for males in the MSK-IMPACT and TCGA datasets. Conclusions: A fairly consistent pattern of apparent better OS for males across histologic and molecular subgroups of STS was observed. If confirmed, our results could have implications for clinical practice for prognostic stratification and possibly treatment tailoring as well as for future clinical trials design.

Funder

Stanford University

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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