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Histological regression of gastrointestinal peritoneal metastases after systemic chemotherapy

OBJECTIVES: Peritoneal metastases (PM) are relatively resistant to systemic chemotherapy, and data on histological response to therapy is rare. The aim of this study was to quantify the treatment response of PM after systemic chemotherapy. METHODS: Retrospective monocentric cohort study of 47 consec...

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Autores principales: Toussaint, Laura, Teixeira Farinha, Hugo, Barras, Jean-Luc, Demartines, Nicolas, Sempoux, Christine, Hübner, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8482450/
https://www.ncbi.nlm.nih.gov/pubmed/34676284
http://dx.doi.org/10.1515/pp-2021-0118
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author Toussaint, Laura
Teixeira Farinha, Hugo
Barras, Jean-Luc
Demartines, Nicolas
Sempoux, Christine
Hübner, Martin
author_facet Toussaint, Laura
Teixeira Farinha, Hugo
Barras, Jean-Luc
Demartines, Nicolas
Sempoux, Christine
Hübner, Martin
author_sort Toussaint, Laura
collection PubMed
description OBJECTIVES: Peritoneal metastases (PM) are relatively resistant to systemic chemotherapy, and data on histological response to therapy is rare. The aim of this study was to quantify the treatment response of PM after systemic chemotherapy. METHODS: Retrospective monocentric cohort study of 47 consecutive patients with PM from gastrointestinal origin undergoing surgery (cytoreduction: CRS + Hyperthermic IntraPEritoneal Chemotherapy [HIPEC] or Pressurized IntraPeritoneal Aerosol Chemotherapy [PIPAC]) after prior systemic chemotherapy from 1.2015 to 3.2019. Tumor response was assessed using the 4-scale Peritoneal Regression Grading System (PRGS) (4: vital tumor to 1: complete response). RESULTS: Patients had a median of 2 (range: 1–7) lines and 10 (3–39) cycles of prior systemic chemotherapy. A median of four biopsies (range: 3–8) was taken with a total of 196 analyzed specimens. Twenty-four biopsies (12%) showed no histological regression (PRGS4), while PRGS 3, two and one were diagnosed in 37 (19%), 39 (20%), and 69 (49%) specimens, respectively. A significant heterogeneity was found between peritoneal biopsies in 51% patients. PRGS correlated strongly with peritoneal spread (PCI, p<0.0001), and was improved in patients with more than nine cycles of systemic chemotherapy (p=0.04). Median survival was higher in patients with PRGS < 1.8 (Quartiles one and 2) than higher (Q3 and Q4), but the difference did not reach significance in this small cohort. CONCLUSIONS: PRGS is an objective too to describe histological response of PM of GI origin after systemic chemotherapy. This response differs significantly between patients, allowing to distinguish between chemosensitive and chemoresistant tumors.
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spelling pubmed-84824502021-10-20 Histological regression of gastrointestinal peritoneal metastases after systemic chemotherapy Toussaint, Laura Teixeira Farinha, Hugo Barras, Jean-Luc Demartines, Nicolas Sempoux, Christine Hübner, Martin Pleura Peritoneum Research Article OBJECTIVES: Peritoneal metastases (PM) are relatively resistant to systemic chemotherapy, and data on histological response to therapy is rare. The aim of this study was to quantify the treatment response of PM after systemic chemotherapy. METHODS: Retrospective monocentric cohort study of 47 consecutive patients with PM from gastrointestinal origin undergoing surgery (cytoreduction: CRS + Hyperthermic IntraPEritoneal Chemotherapy [HIPEC] or Pressurized IntraPeritoneal Aerosol Chemotherapy [PIPAC]) after prior systemic chemotherapy from 1.2015 to 3.2019. Tumor response was assessed using the 4-scale Peritoneal Regression Grading System (PRGS) (4: vital tumor to 1: complete response). RESULTS: Patients had a median of 2 (range: 1–7) lines and 10 (3–39) cycles of prior systemic chemotherapy. A median of four biopsies (range: 3–8) was taken with a total of 196 analyzed specimens. Twenty-four biopsies (12%) showed no histological regression (PRGS4), while PRGS 3, two and one were diagnosed in 37 (19%), 39 (20%), and 69 (49%) specimens, respectively. A significant heterogeneity was found between peritoneal biopsies in 51% patients. PRGS correlated strongly with peritoneal spread (PCI, p<0.0001), and was improved in patients with more than nine cycles of systemic chemotherapy (p=0.04). Median survival was higher in patients with PRGS < 1.8 (Quartiles one and 2) than higher (Q3 and Q4), but the difference did not reach significance in this small cohort. CONCLUSIONS: PRGS is an objective too to describe histological response of PM of GI origin after systemic chemotherapy. This response differs significantly between patients, allowing to distinguish between chemosensitive and chemoresistant tumors. De Gruyter 2021-07-15 /pmc/articles/PMC8482450/ /pubmed/34676284 http://dx.doi.org/10.1515/pp-2021-0118 Text en © 2021 Laura Toussaint et al., published by De Gruyter, Berlin/Boston https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License.
spellingShingle Research Article
Toussaint, Laura
Teixeira Farinha, Hugo
Barras, Jean-Luc
Demartines, Nicolas
Sempoux, Christine
Hübner, Martin
Histological regression of gastrointestinal peritoneal metastases after systemic chemotherapy
title Histological regression of gastrointestinal peritoneal metastases after systemic chemotherapy
title_full Histological regression of gastrointestinal peritoneal metastases after systemic chemotherapy
title_fullStr Histological regression of gastrointestinal peritoneal metastases after systemic chemotherapy
title_full_unstemmed Histological regression of gastrointestinal peritoneal metastases after systemic chemotherapy
title_short Histological regression of gastrointestinal peritoneal metastases after systemic chemotherapy
title_sort histological regression of gastrointestinal peritoneal metastases after systemic chemotherapy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8482450/
https://www.ncbi.nlm.nih.gov/pubmed/34676284
http://dx.doi.org/10.1515/pp-2021-0118
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