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

<p>Abstract</p> <p>Background</p> <p>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 re...

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Main Authors: Dimmler A, Doerfer J, Pelz Joerg OW, Hohenberger W, Meyer T
Format: Article
Language:English
Published: BMC 2006-06-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/6/162
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spelling doaj-d653f954890a439293209a093e2f664f2020-11-25T02:35:00ZengBMCBMC Cancer1471-24072006-06-016116210.1186/1471-2407-6-162Histological response of peritoneal carcinomatosis after hyperthermic intraperitoneal chemoperfusion (HIPEC) in experimental investigationsDimmler ADoerfer JPelz Joerg OWHohenberger WMeyer T<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Methods</p> <p>CC531 colon carcinoma (2,5 × 10<sup>6 </sup>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<sup>2 </sup>(n = 6), group V: mitomycin C i.p. alone in a concentration of 10 mg/m<sup>2 </sup>(n = 6). After 10 days the extent of tumor spread and histological outcome were analysed by autopsy.</p> <p>Results</p> <p>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.</p> <p>Conclusion</p> <p>These findings indicate that HIPEC is an effective treatment for peritoneal carcinomatosis in this animal model. HIPEC reduced macroscopic and microscopic intraperitoneal tumor spread.</p> http://www.biomedcentral.com/1471-2407/6/162
collection DOAJ
language English
format Article
sources DOAJ
author Dimmler A
Doerfer J
Pelz Joerg OW
Hohenberger W
Meyer T
spellingShingle Dimmler A
Doerfer J
Pelz Joerg OW
Hohenberger W
Meyer T
Histological response of peritoneal carcinomatosis after hyperthermic intraperitoneal chemoperfusion (HIPEC) in experimental investigations
BMC Cancer
author_facet Dimmler A
Doerfer J
Pelz Joerg OW
Hohenberger W
Meyer T
author_sort Dimmler A
title 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_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_sort histological response of peritoneal carcinomatosis after hyperthermic intraperitoneal chemoperfusion (hipec) in experimental investigations
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2006-06-01
description <p>Abstract</p> <p>Background</p> <p>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.</p> <p>Methods</p> <p>CC531 colon carcinoma (2,5 × 10<sup>6 </sup>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<sup>2 </sup>(n = 6), group V: mitomycin C i.p. alone in a concentration of 10 mg/m<sup>2 </sup>(n = 6). After 10 days the extent of tumor spread and histological outcome were analysed by autopsy.</p> <p>Results</p> <p>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.</p> <p>Conclusion</p> <p>These findings indicate that HIPEC is an effective treatment for peritoneal carcinomatosis in this animal model. HIPEC reduced macroscopic and microscopic intraperitoneal tumor spread.</p>
url http://www.biomedcentral.com/1471-2407/6/162
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AT doerferj histologicalresponseofperitonealcarcinomatosisafterhyperthermicintraperitonealchemoperfusionhipecinexperimentalinvestigations
AT pelzjoergow histologicalresponseofperitonealcarcinomatosisafterhyperthermicintraperitonealchemoperfusionhipecinexperimentalinvestigations
AT hohenbergerw histologicalresponseofperitonealcarcinomatosisafterhyperthermicintraperitonealchemoperfusionhipecinexperimentalinvestigations
AT meyert histologicalresponseofperitonealcarcinomatosisafterhyperthermicintraperitonealchemoperfusionhipecinexperimentalinvestigations
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