Cargando…
Paclitaxel–ifosfamide–carboplatin combination chemotherapy regimen in advanced uterine and adnexal malignant mixed Mullerian tumours
BACKGROUND: Malignant mixed Mullerian tumours (MMMTs) of the uterus and adnexa represent aggressive gynaecologic malignancies with a high rate of loco-regional and distant failure. For that reason, we evaluated the paclitaxel–ifosfamide–carboplatin (TICb) combination in patients with advanced MMMTs....
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185936/ https://www.ncbi.nlm.nih.gov/pubmed/21847127 http://dx.doi.org/10.1038/bjc.2011.316 |
_version_ | 1782213279108562944 |
---|---|
author | Kosmas, C Vorgias, G Tsakonas, G Politis, P Daladimos, T Panagiotidi, E Papachrysanthou, T Moschovis, D Kalinoglou, N Tsavaris, N Karabelis, A Mylonakis, N |
author_facet | Kosmas, C Vorgias, G Tsakonas, G Politis, P Daladimos, T Panagiotidi, E Papachrysanthou, T Moschovis, D Kalinoglou, N Tsavaris, N Karabelis, A Mylonakis, N |
author_sort | Kosmas, C |
collection | PubMed |
description | BACKGROUND: Malignant mixed Mullerian tumours (MMMTs) of the uterus and adnexa represent aggressive gynaecologic malignancies with a high rate of loco-regional and distant failure. For that reason, we evaluated the paclitaxel–ifosfamide–carboplatin (TICb) combination in patients with advanced MMMTs. METHODS: Female patients with advanced MMMTs, WHO-PS 0–2, no prior chemotherapy for systemic disease, unimpaired haemopoietic and organ function were eligible. Chemotherapy was administered at the following doses; paclitaxel: 175 mg m(–2) on day 1, ifosfamide: 2.0g m(–2) day(–1) – days 1 and 2, and carboplatin at a target area under the curve 5 on day 2, with prophylactic G-CSF from day 3. RESULTS: Forty patients of a median age 61 (45–72) years, performance status 0–2 with advanced MMMTs of the uterus (n=34), tubes (n=2) or ovary (n=4) have entered and all were evaluable for response and toxicity. Responses were as follows: 27 out of 40 (67.5%) evaluable patients responded, with 11 complete responses and 16 partial responses, while 10 had stable disease, and 3 developed progressive disease. The median response duration was 9 months (range, 4–40 months), median progression-free survival 13 months (range, 3–42 months), while median overall survival 18 months (range, 4–48 months). Grade 3/4 neutropenia was recorded in 22 out of 40 (55%) – with 13 developing grade 4 (⩽7 days) and 7 out of 40 (17.5%) of patients at least one episode of febrile neutropenia. CONCLUSION: In this study, it appears that the TICb combination, yielded important activity with manageable toxicity in females with advanced MMMTs warranting further randomised comparison with current standard regimens. |
format | Online Article Text |
id | pubmed-3185936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-31859362012-09-27 Paclitaxel–ifosfamide–carboplatin combination chemotherapy regimen in advanced uterine and adnexal malignant mixed Mullerian tumours Kosmas, C Vorgias, G Tsakonas, G Politis, P Daladimos, T Panagiotidi, E Papachrysanthou, T Moschovis, D Kalinoglou, N Tsavaris, N Karabelis, A Mylonakis, N Br J Cancer Clinical Study BACKGROUND: Malignant mixed Mullerian tumours (MMMTs) of the uterus and adnexa represent aggressive gynaecologic malignancies with a high rate of loco-regional and distant failure. For that reason, we evaluated the paclitaxel–ifosfamide–carboplatin (TICb) combination in patients with advanced MMMTs. METHODS: Female patients with advanced MMMTs, WHO-PS 0–2, no prior chemotherapy for systemic disease, unimpaired haemopoietic and organ function were eligible. Chemotherapy was administered at the following doses; paclitaxel: 175 mg m(–2) on day 1, ifosfamide: 2.0g m(–2) day(–1) – days 1 and 2, and carboplatin at a target area under the curve 5 on day 2, with prophylactic G-CSF from day 3. RESULTS: Forty patients of a median age 61 (45–72) years, performance status 0–2 with advanced MMMTs of the uterus (n=34), tubes (n=2) or ovary (n=4) have entered and all were evaluable for response and toxicity. Responses were as follows: 27 out of 40 (67.5%) evaluable patients responded, with 11 complete responses and 16 partial responses, while 10 had stable disease, and 3 developed progressive disease. The median response duration was 9 months (range, 4–40 months), median progression-free survival 13 months (range, 3–42 months), while median overall survival 18 months (range, 4–48 months). Grade 3/4 neutropenia was recorded in 22 out of 40 (55%) – with 13 developing grade 4 (⩽7 days) and 7 out of 40 (17.5%) of patients at least one episode of febrile neutropenia. CONCLUSION: In this study, it appears that the TICb combination, yielded important activity with manageable toxicity in females with advanced MMMTs warranting further randomised comparison with current standard regimens. Nature Publishing Group 2011-09-27 2011-08-16 /pmc/articles/PMC3185936/ /pubmed/21847127 http://dx.doi.org/10.1038/bjc.2011.316 Text en Copyright © 2011 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 Kosmas, C Vorgias, G Tsakonas, G Politis, P Daladimos, T Panagiotidi, E Papachrysanthou, T Moschovis, D Kalinoglou, N Tsavaris, N Karabelis, A Mylonakis, N Paclitaxel–ifosfamide–carboplatin combination chemotherapy regimen in advanced uterine and adnexal malignant mixed Mullerian tumours |
title | Paclitaxel–ifosfamide–carboplatin combination chemotherapy regimen in advanced uterine and adnexal malignant mixed Mullerian tumours |
title_full | Paclitaxel–ifosfamide–carboplatin combination chemotherapy regimen in advanced uterine and adnexal malignant mixed Mullerian tumours |
title_fullStr | Paclitaxel–ifosfamide–carboplatin combination chemotherapy regimen in advanced uterine and adnexal malignant mixed Mullerian tumours |
title_full_unstemmed | Paclitaxel–ifosfamide–carboplatin combination chemotherapy regimen in advanced uterine and adnexal malignant mixed Mullerian tumours |
title_short | Paclitaxel–ifosfamide–carboplatin combination chemotherapy regimen in advanced uterine and adnexal malignant mixed Mullerian tumours |
title_sort | paclitaxel–ifosfamide–carboplatin combination chemotherapy regimen in advanced uterine and adnexal malignant mixed mullerian tumours |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185936/ https://www.ncbi.nlm.nih.gov/pubmed/21847127 http://dx.doi.org/10.1038/bjc.2011.316 |
work_keys_str_mv | AT kosmasc paclitaxelifosfamidecarboplatincombinationchemotherapyregimeninadvanceduterineandadnexalmalignantmixedmulleriantumours AT vorgiasg paclitaxelifosfamidecarboplatincombinationchemotherapyregimeninadvanceduterineandadnexalmalignantmixedmulleriantumours AT tsakonasg paclitaxelifosfamidecarboplatincombinationchemotherapyregimeninadvanceduterineandadnexalmalignantmixedmulleriantumours AT politisp paclitaxelifosfamidecarboplatincombinationchemotherapyregimeninadvanceduterineandadnexalmalignantmixedmulleriantumours AT daladimost paclitaxelifosfamidecarboplatincombinationchemotherapyregimeninadvanceduterineandadnexalmalignantmixedmulleriantumours AT panagiotidie paclitaxelifosfamidecarboplatincombinationchemotherapyregimeninadvanceduterineandadnexalmalignantmixedmulleriantumours AT papachrysanthout paclitaxelifosfamidecarboplatincombinationchemotherapyregimeninadvanceduterineandadnexalmalignantmixedmulleriantumours AT moschovisd paclitaxelifosfamidecarboplatincombinationchemotherapyregimeninadvanceduterineandadnexalmalignantmixedmulleriantumours AT kalinogloun paclitaxelifosfamidecarboplatincombinationchemotherapyregimeninadvanceduterineandadnexalmalignantmixedmulleriantumours AT tsavarisn paclitaxelifosfamidecarboplatincombinationchemotherapyregimeninadvanceduterineandadnexalmalignantmixedmulleriantumours AT karabelisa paclitaxelifosfamidecarboplatincombinationchemotherapyregimeninadvanceduterineandadnexalmalignantmixedmulleriantumours AT mylonakisn paclitaxelifosfamidecarboplatincombinationchemotherapyregimeninadvanceduterineandadnexalmalignantmixedmulleriantumours |