Cargando…

Neoadjuvant chemotherapy followed by interval debulking surgery in patients with serous endometrial cancer with transperitoneal spread (stage IV): a new preferred treatment?

BACKGROUND: To investigate the value of neoadjuvant chemotherapy (NACT), followed by interval debulking surgery (IDS), in endometrial cancer with transperitoneal spread (stage IV). METHODS: Patients with endometrial cancer with transperitoneal spread, as determined by laparoscopy (±pleural effusion)...

Descripción completa

Detalles Bibliográficos
Autores principales: Vandenput, I, Van Calster, B, Capoen, A, Leunen, K, Berteloot, P, Neven, P, Moerman, Ph, Vergote, I, Amant, F
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2720217/
https://www.ncbi.nlm.nih.gov/pubmed/19568245
http://dx.doi.org/10.1038/sj.bjc.6605157
_version_ 1782170118833307648
author Vandenput, I
Van Calster, B
Capoen, A
Leunen, K
Berteloot, P
Neven, P
Moerman, Ph
Vergote, I
Amant, F
author_facet Vandenput, I
Van Calster, B
Capoen, A
Leunen, K
Berteloot, P
Neven, P
Moerman, Ph
Vergote, I
Amant, F
author_sort Vandenput, I
collection PubMed
description BACKGROUND: To investigate the value of neoadjuvant chemotherapy (NACT), followed by interval debulking surgery (IDS), in endometrial cancer with transperitoneal spread (stage IV). METHODS: Patients with endometrial cancer with transperitoneal spread, as determined by laparoscopy (±pleural effusion), were treated with NACT. Efficacy was determined according to the Response Evaluation Criteria in Solid Tumors, residual tumour at IDS and histopathological assessment of tumour regression. RESULTS: A total of 30 patients (median age: 65 years; range:44–81 years) received 3–4 cycles of NACT (83% paclitaxel/carboplatin). Histopathological subtypes were as follows: serous (90%), clear cell (3%) and endometrioid (6%) carcinoma. Response according to RECIST was as follows: 2 (7%) complete remission, 20 (67%) partial remission, 6 (20%) stable disease and 2 (7%) progressive disease (PD). Patients with PD were not operated upon. A total of 24 patients (80%) had optimal cytoreduction (R ⩽1 cm), of whom 22 (92%) were without residual tumour. Four patients were considered inoperable and were excluded from further analysis. The median progression-free survival and overall survival times were 13 and 23 months, respectively. Histopathological features of chemoresponse in both uterus and omentum were related to a better PFS (P=0.017, hazard ratio (HR) =0.785) and overall survival (P=0.014, HR=0.707). In particular, the absence of tumour infiltration and necrosis were associated with prognosis. CONCLUSION: The use of NACT resulted in a high rate (80%) of optimal IDS for the treatment of endometrial cancer with transperitoneal spread.
format Text
id pubmed-2720217
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-27202172010-07-21 Neoadjuvant chemotherapy followed by interval debulking surgery in patients with serous endometrial cancer with transperitoneal spread (stage IV): a new preferred treatment? Vandenput, I Van Calster, B Capoen, A Leunen, K Berteloot, P Neven, P Moerman, Ph Vergote, I Amant, F Br J Cancer Clinical Study BACKGROUND: To investigate the value of neoadjuvant chemotherapy (NACT), followed by interval debulking surgery (IDS), in endometrial cancer with transperitoneal spread (stage IV). METHODS: Patients with endometrial cancer with transperitoneal spread, as determined by laparoscopy (±pleural effusion), were treated with NACT. Efficacy was determined according to the Response Evaluation Criteria in Solid Tumors, residual tumour at IDS and histopathological assessment of tumour regression. RESULTS: A total of 30 patients (median age: 65 years; range:44–81 years) received 3–4 cycles of NACT (83% paclitaxel/carboplatin). Histopathological subtypes were as follows: serous (90%), clear cell (3%) and endometrioid (6%) carcinoma. Response according to RECIST was as follows: 2 (7%) complete remission, 20 (67%) partial remission, 6 (20%) stable disease and 2 (7%) progressive disease (PD). Patients with PD were not operated upon. A total of 24 patients (80%) had optimal cytoreduction (R ⩽1 cm), of whom 22 (92%) were without residual tumour. Four patients were considered inoperable and were excluded from further analysis. The median progression-free survival and overall survival times were 13 and 23 months, respectively. Histopathological features of chemoresponse in both uterus and omentum were related to a better PFS (P=0.017, hazard ratio (HR) =0.785) and overall survival (P=0.014, HR=0.707). In particular, the absence of tumour infiltration and necrosis were associated with prognosis. CONCLUSION: The use of NACT resulted in a high rate (80%) of optimal IDS for the treatment of endometrial cancer with transperitoneal spread. Nature Publishing Group 2009-07-21 2009-06-30 /pmc/articles/PMC2720217/ /pubmed/19568245 http://dx.doi.org/10.1038/sj.bjc.6605157 Text en Copyright © 2009 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Clinical Study
Vandenput, I
Van Calster, B
Capoen, A
Leunen, K
Berteloot, P
Neven, P
Moerman, Ph
Vergote, I
Amant, F
Neoadjuvant chemotherapy followed by interval debulking surgery in patients with serous endometrial cancer with transperitoneal spread (stage IV): a new preferred treatment?
title Neoadjuvant chemotherapy followed by interval debulking surgery in patients with serous endometrial cancer with transperitoneal spread (stage IV): a new preferred treatment?
title_full Neoadjuvant chemotherapy followed by interval debulking surgery in patients with serous endometrial cancer with transperitoneal spread (stage IV): a new preferred treatment?
title_fullStr Neoadjuvant chemotherapy followed by interval debulking surgery in patients with serous endometrial cancer with transperitoneal spread (stage IV): a new preferred treatment?
title_full_unstemmed Neoadjuvant chemotherapy followed by interval debulking surgery in patients with serous endometrial cancer with transperitoneal spread (stage IV): a new preferred treatment?
title_short Neoadjuvant chemotherapy followed by interval debulking surgery in patients with serous endometrial cancer with transperitoneal spread (stage IV): a new preferred treatment?
title_sort neoadjuvant chemotherapy followed by interval debulking surgery in patients with serous endometrial cancer with transperitoneal spread (stage iv): a new preferred treatment?
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2720217/
https://www.ncbi.nlm.nih.gov/pubmed/19568245
http://dx.doi.org/10.1038/sj.bjc.6605157
work_keys_str_mv AT vandenputi neoadjuvantchemotherapyfollowedbyintervaldebulkingsurgeryinpatientswithserousendometrialcancerwithtransperitonealspreadstageivanewpreferredtreatment
AT vancalsterb neoadjuvantchemotherapyfollowedbyintervaldebulkingsurgeryinpatientswithserousendometrialcancerwithtransperitonealspreadstageivanewpreferredtreatment
AT capoena neoadjuvantchemotherapyfollowedbyintervaldebulkingsurgeryinpatientswithserousendometrialcancerwithtransperitonealspreadstageivanewpreferredtreatment
AT leunenk neoadjuvantchemotherapyfollowedbyintervaldebulkingsurgeryinpatientswithserousendometrialcancerwithtransperitonealspreadstageivanewpreferredtreatment
AT bertelootp neoadjuvantchemotherapyfollowedbyintervaldebulkingsurgeryinpatientswithserousendometrialcancerwithtransperitonealspreadstageivanewpreferredtreatment
AT nevenp neoadjuvantchemotherapyfollowedbyintervaldebulkingsurgeryinpatientswithserousendometrialcancerwithtransperitonealspreadstageivanewpreferredtreatment
AT moermanph neoadjuvantchemotherapyfollowedbyintervaldebulkingsurgeryinpatientswithserousendometrialcancerwithtransperitonealspreadstageivanewpreferredtreatment
AT vergotei neoadjuvantchemotherapyfollowedbyintervaldebulkingsurgeryinpatientswithserousendometrialcancerwithtransperitonealspreadstageivanewpreferredtreatment
AT amantf neoadjuvantchemotherapyfollowedbyintervaldebulkingsurgeryinpatientswithserousendometrialcancerwithtransperitonealspreadstageivanewpreferredtreatment