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Should MMMT still be treated with adjuvant taxane-based combination chemotherapy?

BACKGROUND: Malignant mixed Mullerian tumors of endometrial (MMMT-E) and ovarian (MMMT-O) origin are associated with poor prognosis. Suggestively epithelial-driven tumors, their treatment has shifted from anthracycline or ifosfamide-based towards taxane-based chemotherapy. It remains unclear whether...

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Autores principales: Heinzelmann-Schwarz, Viola, Kind, André B., Vetter, Marcus, Russell, Kenneth, Omar, Siti, Schoetzau, Andreas, Hoeck, Kerstin, Fink, Daniel, Friedlander, Michael L., Hacker, Neville F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039840/
https://www.ncbi.nlm.nih.gov/pubmed/31993743
http://dx.doi.org/10.1007/s00432-019-03091-y
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author Heinzelmann-Schwarz, Viola
Kind, André B.
Vetter, Marcus
Russell, Kenneth
Omar, Siti
Schoetzau, Andreas
Hoeck, Kerstin
Fink, Daniel
Friedlander, Michael L.
Hacker, Neville F.
author_facet Heinzelmann-Schwarz, Viola
Kind, André B.
Vetter, Marcus
Russell, Kenneth
Omar, Siti
Schoetzau, Andreas
Hoeck, Kerstin
Fink, Daniel
Friedlander, Michael L.
Hacker, Neville F.
author_sort Heinzelmann-Schwarz, Viola
collection PubMed
description BACKGROUND: Malignant mixed Mullerian tumors of endometrial (MMMT-E) and ovarian (MMMT-O) origin are associated with poor prognosis. Suggestively epithelial-driven tumors, their treatment has shifted from anthracycline or ifosfamide-based towards taxane-based chemotherapy. It remains unclear whether this change associates with better outcomes. PATIENTS AND METHODS: A conjoined Australian and Swiss patient cohort of MMMT-E (N = 103) and MMMT-O (N = 17) was compared to patients with adenocarcinoma of the endometrium (EC, N = 172) and ovary (OC, N = 189). Clinicopathological characteristics, FIGO stage, first-line treatment, and patient outcomes were analyzed. The generated hypothesis was verified in an US-American cohort with high-grade serous ovarian cancer (HGSOC, N = 1290) and MMMT-O (N = 450) using immunohistochemistry and next-generation sequencing. RESULTS: Early stage I/II MMMT-E showed a survival plateau after 2.5 years, with no recurrence or death observed afterwards. Relapse-free survival was significantly worse in MMMT-E treated with platinum/taxanes (P = 0.024) compared to non-taxane regimen. Hypothesizing that also MMMT-O might benefit from an adjuvant non-paclitaxel regimen, a second independent cohort of MMMT-O and HGSOC patients was examined. p53 mutations dominated in both cancers with comparable frequency. PI3KCA and KRAS mutations were less frequent: they were more frequent in MMMT-O than in HGSOC (P = 0.015 and P = 0.018, respectively). MMMT-O responded better to a combination of carboplatin with anthracyclines than with taxanes (73.9% vs. 39.4%). CONCLUSION: Early stage I/II MMMT-E patients have excellent prognosis if no recurrence has appeared within the first 2.5 years. In MMMT-E, platinum/anthracycline or ifosfamide regimen associated with better outcomes than platinum/taxanes regimens. This might also apply to MMMT-O. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00432-019-03091-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-70398402020-03-09 Should MMMT still be treated with adjuvant taxane-based combination chemotherapy? Heinzelmann-Schwarz, Viola Kind, André B. Vetter, Marcus Russell, Kenneth Omar, Siti Schoetzau, Andreas Hoeck, Kerstin Fink, Daniel Friedlander, Michael L. Hacker, Neville F. J Cancer Res Clin Oncol Original Article – Clinical Oncology BACKGROUND: Malignant mixed Mullerian tumors of endometrial (MMMT-E) and ovarian (MMMT-O) origin are associated with poor prognosis. Suggestively epithelial-driven tumors, their treatment has shifted from anthracycline or ifosfamide-based towards taxane-based chemotherapy. It remains unclear whether this change associates with better outcomes. PATIENTS AND METHODS: A conjoined Australian and Swiss patient cohort of MMMT-E (N = 103) and MMMT-O (N = 17) was compared to patients with adenocarcinoma of the endometrium (EC, N = 172) and ovary (OC, N = 189). Clinicopathological characteristics, FIGO stage, first-line treatment, and patient outcomes were analyzed. The generated hypothesis was verified in an US-American cohort with high-grade serous ovarian cancer (HGSOC, N = 1290) and MMMT-O (N = 450) using immunohistochemistry and next-generation sequencing. RESULTS: Early stage I/II MMMT-E showed a survival plateau after 2.5 years, with no recurrence or death observed afterwards. Relapse-free survival was significantly worse in MMMT-E treated with platinum/taxanes (P = 0.024) compared to non-taxane regimen. Hypothesizing that also MMMT-O might benefit from an adjuvant non-paclitaxel regimen, a second independent cohort of MMMT-O and HGSOC patients was examined. p53 mutations dominated in both cancers with comparable frequency. PI3KCA and KRAS mutations were less frequent: they were more frequent in MMMT-O than in HGSOC (P = 0.015 and P = 0.018, respectively). MMMT-O responded better to a combination of carboplatin with anthracyclines than with taxanes (73.9% vs. 39.4%). CONCLUSION: Early stage I/II MMMT-E patients have excellent prognosis if no recurrence has appeared within the first 2.5 years. In MMMT-E, platinum/anthracycline or ifosfamide regimen associated with better outcomes than platinum/taxanes regimens. This might also apply to MMMT-O. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00432-019-03091-y) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-01-28 2020 /pmc/articles/PMC7039840/ /pubmed/31993743 http://dx.doi.org/10.1007/s00432-019-03091-y Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article – Clinical Oncology
Heinzelmann-Schwarz, Viola
Kind, André B.
Vetter, Marcus
Russell, Kenneth
Omar, Siti
Schoetzau, Andreas
Hoeck, Kerstin
Fink, Daniel
Friedlander, Michael L.
Hacker, Neville F.
Should MMMT still be treated with adjuvant taxane-based combination chemotherapy?
title Should MMMT still be treated with adjuvant taxane-based combination chemotherapy?
title_full Should MMMT still be treated with adjuvant taxane-based combination chemotherapy?
title_fullStr Should MMMT still be treated with adjuvant taxane-based combination chemotherapy?
title_full_unstemmed Should MMMT still be treated with adjuvant taxane-based combination chemotherapy?
title_short Should MMMT still be treated with adjuvant taxane-based combination chemotherapy?
title_sort should mmmt still be treated with adjuvant taxane-based combination chemotherapy?
topic Original Article – Clinical Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039840/
https://www.ncbi.nlm.nih.gov/pubmed/31993743
http://dx.doi.org/10.1007/s00432-019-03091-y
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