Cargando…

Histological response of peritoneal carcinomatosis after hyperthermic intraperitoneal chemoperfusion (HIPEC) in experimental investigations

BACKGROUND: In selected patients with peritoneal carcinomatosis from colorectal cancer prognosis can be improved by hyperthermic intraperitoneal chemotherapy (HIPEC) after cytoreductive surgery. The aim of this study was to evaluate the tumor response of peritoneal carcinomatosis in tumor-bearing ra...

Descripción completa

Detalles Bibliográficos
Autores principales: Pelz, Joerg OW, Doerfer, J, Dimmler, A, Hohenberger, W, Meyer, T
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1552087/
https://www.ncbi.nlm.nih.gov/pubmed/16792796
http://dx.doi.org/10.1186/1471-2407-6-162
_version_ 1782129343394217984
author Pelz, Joerg OW
Doerfer, J
Dimmler, A
Hohenberger, W
Meyer, T
author_facet Pelz, Joerg OW
Doerfer, J
Dimmler, A
Hohenberger, W
Meyer, T
author_sort Pelz, Joerg OW
collection PubMed
description BACKGROUND: In selected patients with peritoneal carcinomatosis from colorectal cancer prognosis can be improved by hyperthermic intraperitoneal chemotherapy (HIPEC) after cytoreductive surgery. The aim of this study was to evaluate the tumor response of peritoneal carcinomatosis in tumor-bearing rats treated with HIPEC. METHODS: CC531 colon carcinoma (2,5 × 10(6 )cells), implanted intraperitoneally in Wag/Rija rats, was treated by hyperthermic intraperitoneal chemotherapy. After 10 days of tumor growth the animals were randomized into five groups of six animals each: group I: control (n = 6), group II: sham operated animals (n = 6), group III: hyperthermic intraperitoneal perfusion (HIP) without cytostatic drugs, group IV: HIPEC with mitomycin C in a concentration of 15 mg/m(2 )(n = 6), group V: mitomycin C i.p. alone in a concentration of 10 mg/m(2 )(n = 6). After 10 days the extent of tumor spread and histological outcome were analysed by autopsy. RESULTS: All control animals developed extensive intraperitoneal tumor growth. Histological tumor load was significantly reduced in group III and group V and was lowest in group IV. In group II tumor load was significantly higher than in group I. Implanted metastases were significantly decreased in group IV compared with group I and group II. CONCLUSION: These findings indicate that HIPEC is an effective treatment for peritoneal carcinomatosis in this animal model. HIPEC reduced macroscopic and microscopic intraperitoneal tumor spread.
format Text
id pubmed-1552087
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-15520872006-08-23 Histological response of peritoneal carcinomatosis after hyperthermic intraperitoneal chemoperfusion (HIPEC) in experimental investigations Pelz, Joerg OW Doerfer, J Dimmler, A Hohenberger, W Meyer, T BMC Cancer Research Article BACKGROUND: In selected patients with peritoneal carcinomatosis from colorectal cancer prognosis can be improved by hyperthermic intraperitoneal chemotherapy (HIPEC) after cytoreductive surgery. The aim of this study was to evaluate the tumor response of peritoneal carcinomatosis in tumor-bearing rats treated with HIPEC. METHODS: CC531 colon carcinoma (2,5 × 10(6 )cells), implanted intraperitoneally in Wag/Rija rats, was treated by hyperthermic intraperitoneal chemotherapy. After 10 days of tumor growth the animals were randomized into five groups of six animals each: group I: control (n = 6), group II: sham operated animals (n = 6), group III: hyperthermic intraperitoneal perfusion (HIP) without cytostatic drugs, group IV: HIPEC with mitomycin C in a concentration of 15 mg/m(2 )(n = 6), group V: mitomycin C i.p. alone in a concentration of 10 mg/m(2 )(n = 6). After 10 days the extent of tumor spread and histological outcome were analysed by autopsy. RESULTS: All control animals developed extensive intraperitoneal tumor growth. Histological tumor load was significantly reduced in group III and group V and was lowest in group IV. In group II tumor load was significantly higher than in group I. Implanted metastases were significantly decreased in group IV compared with group I and group II. CONCLUSION: These findings indicate that HIPEC is an effective treatment for peritoneal carcinomatosis in this animal model. HIPEC reduced macroscopic and microscopic intraperitoneal tumor spread. BioMed Central 2006-06-22 /pmc/articles/PMC1552087/ /pubmed/16792796 http://dx.doi.org/10.1186/1471-2407-6-162 Text en Copyright © 2006 Pelz et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Pelz, Joerg OW
Doerfer, J
Dimmler, A
Hohenberger, W
Meyer, T
Histological response of peritoneal carcinomatosis after hyperthermic intraperitoneal chemoperfusion (HIPEC) in experimental investigations
title Histological response of peritoneal carcinomatosis after hyperthermic intraperitoneal chemoperfusion (HIPEC) in experimental investigations
title_full Histological response of peritoneal carcinomatosis after hyperthermic intraperitoneal chemoperfusion (HIPEC) in experimental investigations
title_fullStr Histological response of peritoneal carcinomatosis after hyperthermic intraperitoneal chemoperfusion (HIPEC) in experimental investigations
title_full_unstemmed Histological response of peritoneal carcinomatosis after hyperthermic intraperitoneal chemoperfusion (HIPEC) in experimental investigations
title_short Histological response of peritoneal carcinomatosis after hyperthermic intraperitoneal chemoperfusion (HIPEC) in experimental investigations
title_sort histological response of peritoneal carcinomatosis after hyperthermic intraperitoneal chemoperfusion (hipec) in experimental investigations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1552087/
https://www.ncbi.nlm.nih.gov/pubmed/16792796
http://dx.doi.org/10.1186/1471-2407-6-162
work_keys_str_mv AT pelzjoergow histologicalresponseofperitonealcarcinomatosisafterhyperthermicintraperitonealchemoperfusionhipecinexperimentalinvestigations
AT doerferj histologicalresponseofperitonealcarcinomatosisafterhyperthermicintraperitonealchemoperfusionhipecinexperimentalinvestigations
AT dimmlera histologicalresponseofperitonealcarcinomatosisafterhyperthermicintraperitonealchemoperfusionhipecinexperimentalinvestigations
AT hohenbergerw histologicalresponseofperitonealcarcinomatosisafterhyperthermicintraperitonealchemoperfusionhipecinexperimentalinvestigations
AT meyert histologicalresponseofperitonealcarcinomatosisafterhyperthermicintraperitonealchemoperfusionhipecinexperimentalinvestigations