Histological regression of peritoneal metastases of recurrent tubo-ovarian cancer after systemic chemotherapy.

Details

Ressource 1Download: fsurg-09-936613.pdf (569.20 [Ko])
State: Public
Version: Final published version
License: CC BY 4.0
Serval ID
serval:BIB_F38405596143
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Histological regression of peritoneal metastases of recurrent tubo-ovarian cancer after systemic chemotherapy.
Journal
Frontiers in surgery
Author(s)
Pache B. (co-first), Teixeira Farinha H. (co-first), Toussaint L., Demartines N., Hastir D., Mathevet P., Sempoux C., Hübner M.
ISSN
2296-875X (Print)
ISSN-L
2296-875X
Publication state
Published
Issued date
2022
Peer-reviewed
Oui
Volume
9
Pages
936613
Language
english
Notes
Publication types: Journal Article
Publication Status: epublish
Abstract
Post-treatment histological regression of peritoneal metastases (PM) is a new and potentially important predictor of oncological outcomes. Histology of PM from adnexal origin is usually evaluated by the Chemotherapy Response Score (CRS). The aim of this preliminary study was to quantify the response of PM of recurrent tubo-ovarian cancer (TOVC) after systemic chemotherapy by using the recently validated Peritoneal Regression Grading System (PRGS) and compare it with CRS. Correlation with per operative evaluation through Peritoneal Cancer Index (PCI) was performed.
Retrospective cohort study of all consecutive patients with recurrent PM from TOVC undergoing surgery after prior systemic chemotherapy from January 2015 to March 2019. Biopsies were assessed with the four-scale PRGS.
Thirty-eight patients were included. Patients had a median of 2 (range 1-2) lines and 12 (range 3-18) cycles of prior systemic chemotherapy. Overall mean (SD) PRGS was 2.3 (±1.1). Of the patients, 26% (10) had complete response (PRGS 1), 40% (15) had major response (PRGS 2), 26% (10) minor response (PRGS 3), and 8% (3) had no response (PRGS 4). Mean PRGS was positively correlated with the Peritoneal Cancer Index (ρ = 0.5302, p = 0.0003) and inversely correlated with CRS (ρ = -0.8403, p < 0.0001). No correlation was highlighted between mean PRGS and overall survival (ρ = -0.0195, p = 0.9073).
CRS and mean PRGS correlated with each other. Histological response of PM after systemic chemotherapy was quantifiable and variable. The role of PRGS for the evaluation of treatment response and as potential surrogate marker for oncological outcomes is part of ongoing and planned research.
Keywords
PRGS, chemotherapy, gynecology, histology, ovary, peritoneal metastasis, surgery
Pubmed
Web of science
Open Access
Yes
Create date
09/11/2022 11:17
Last modification date
28/10/2023 6:11
Usage data