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A Modified 2 Tier Chemotherapy Response Score (CRS) and Other Histopathologic Features for Predicting Outcomes of Patients with Advanced Extrauterine High-Grade Serous Carcinoma after Neoadjuvant Chemotherapy

Authors :
Jinsong Liu
Shannon N. Westin
Robert L. Coleman
Barrett C Lawson
Anil K. Sood
Anais Malpica
Yanping Zhong
Xiaoran Li
Nicole D. Fleming
Sanghoon Lee
Bryan Fellman
Source :
Cancers, Volume 13, Issue 4, Cancers, Vol 13, Iss 704, p 704 (2021)
Publication Year :
2021
Publisher :
MDPI AG, 2021.

Abstract

Background: The impact of chemotherapy response score (CRS) on prognosis has varied among studies. We addressed the prognostic significance of CRS and the prognostic value of previously undescribed histologic features using a cohort of 245 patients. Methods: Retrospective study in patients with advanced extrauterine high-grade serous carcinomas treated with neoadjuvant chemotherapy followed by interval tumor reductive surgery from 1990 to 2018 in our hospital. Gynecologic pathologists assessed tumor CRS and other histologic features. Clinical information was collected, and multivariate analyses were conducted. Results: A modified 2 tier CRS (CRS 1/2 versus CRS 3) was significantly associated, independent of scoring site (omental versus adnexal), with overall survival (OS) (omentum, p = 0.018<br />adnexa, p = 0.042<br />entire cohort, p = 0.002) and progression-free survival (PFS) (p = 0.021, p = 0.035, and p = 0.001, respectively). On multivariate survival analysis, 2 tier CRS, oncocytic change, inflammation, and desmoplasia were significant for OS (p = 0.034, p = 0.020, p = 0.007, and p = 0.010, respectively). Likewise, 2 tier CRS, inflammation, and desmoplasia were significant for PFS (p = 0.012, p = 0.003, p = 0.011, respectively). Conclusions: The modified 2 tier CRS was significantly associated with survival, independent of scoring site. Additional histologic features including oncocytic change, inflammation, and desmoplasia can also predict patient outcomes.

Details

ISSN :
20726694
Volume :
13
Database :
OpenAIRE
Journal :
Cancers
Accession number :
edsair.doi.dedup.....4d069c9861f29ffdf72dcfeff3dbf051
Full Text :
https://doi.org/10.3390/cancers13040704