Impact of Metastasis Surgery and Alkylating-Agent-Based Chemotherapy on Outcomes of Metastatic Malignant Phyllodes Tumors: A Multicenter Retrospective Study.


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
May 2020
Historique:
received: 28 01 2019
pubmed: 28 11 2019
medline: 12 1 2021
entrez: 28 11 2019
Statut: ppublish

Résumé

Metastatic phyllodes tumors have poor prognosis with median overall survival of 11.5 months. The objective of this study is to identify prognostic factors and the best options for management of metastatic malignant phyllode tumors (MMPTs). A multicentric retrospective study, including cases of MMPT from 10 sarcoma centers, was conducted. The primary end-point was overall survival (OS), and the secondary end-point was the clinical benefit of chemotherapy (CBCT) rate. 51 MMPT patients were included. Median time from diagnosis to metastatic recurrence was 13 months. Management of MMPT consisted in surgery of the metastatic disease for 16 patients (31.3%), radiation therapy of the metastatic disease for 15 patients (31.9%), and chemotherapy for 37 patients (72.5%). Median follow-up was 62.1 months [95% confidence interval (CI) 31-80 months]. Median OS was 11.5 months (95% CI 7.5-18.7 months). On multivariate analysis, two or more metastatic sites [hazard ratio (HR) 2.81, 95% CI 1.27-6.19; p = 0.01] and surgery of metastasis (HR 0.33, 95% CI 0.14-0.78; p = 0.01) were independently associated with OS. The CBCT rate was 31.4% and 16.7% for the first and second lines. Polychemotherapy was not superior to single-agent therapy. Alkylating-agent-based chemotherapy, possibly associated with anthracyclines, was associated with a better CBCT rate than anthracyclines alone (p = 0.049). The results of this study emphasize the impact of the number of metastatic sites on survival of MMPT patients and the leading role of metastasis surgery in MMPT management. If systemic therapy is used, it should include alkylating agents, which are associated with a better clinical benefit.

Sections du résumé

BACKGROUND BACKGROUND
Metastatic phyllodes tumors have poor prognosis with median overall survival of 11.5 months. The objective of this study is to identify prognostic factors and the best options for management of metastatic malignant phyllode tumors (MMPTs).
PATIENTS AND METHODS METHODS
A multicentric retrospective study, including cases of MMPT from 10 sarcoma centers, was conducted. The primary end-point was overall survival (OS), and the secondary end-point was the clinical benefit of chemotherapy (CBCT) rate.
RESULTS RESULTS
51 MMPT patients were included. Median time from diagnosis to metastatic recurrence was 13 months. Management of MMPT consisted in surgery of the metastatic disease for 16 patients (31.3%), radiation therapy of the metastatic disease for 15 patients (31.9%), and chemotherapy for 37 patients (72.5%). Median follow-up was 62.1 months [95% confidence interval (CI) 31-80 months]. Median OS was 11.5 months (95% CI 7.5-18.7 months). On multivariate analysis, two or more metastatic sites [hazard ratio (HR) 2.81, 95% CI 1.27-6.19; p = 0.01] and surgery of metastasis (HR 0.33, 95% CI 0.14-0.78; p = 0.01) were independently associated with OS. The CBCT rate was 31.4% and 16.7% for the first and second lines. Polychemotherapy was not superior to single-agent therapy. Alkylating-agent-based chemotherapy, possibly associated with anthracyclines, was associated with a better CBCT rate than anthracyclines alone (p = 0.049).
CONCLUSIONS CONCLUSIONS
The results of this study emphasize the impact of the number of metastatic sites on survival of MMPT patients and the leading role of metastasis surgery in MMPT management. If systemic therapy is used, it should include alkylating agents, which are associated with a better clinical benefit.

Identifiants

pubmed: 31773519
doi: 10.1245/s10434-019-08097-x
pii: 10.1245/s10434-019-08097-x
doi:

Substances chimiques

Alkylating Agents 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1693-1699

Auteurs

Mathias Neron (M)

Department of Surgical Oncology, Institut du Cancer Montpellier (ICM), Univ Montpellier, Montpellier, France. mathias.neron@orange.fr.

Christophe Sajous (C)

Department of Medical Oncology, Centre Léon Bérard, Université Claude Bernard Lyon I, Lyon, France.

Simon Thezenas (S)

Department of Biostatistics, Institut du Cancer Montpellier, Univ Montpellier, Montpellier, France.

Sophie Piperno-Neumann (S)

Department of Medical Oncology, Institut Curie, Paris, France.

Fabien Reyal (F)

Department of Surgical Oncology, Institut Curie, Paris, France.

Marick Laé (M)

Department of Pathology, Institut Curie, Paris, France.

Camille Chakiba (C)

Department of Medical Oncology, Institut Bergonié, Bordeaux, France.

Nicolas Penel (N)

Department of Medical Oncology, Centre Oscar Lambret, Lille, France.

Thomas Ryckewaert (T)

Department of Medical Oncology, Centre Oscar Lambret, Lille, France.

Charles Honoré (C)

Department of Surgical Oncology, Institut Gustave Roussy, Villejuif, France.

François Bertucci (F)

Department of Medical Oncology, Institut Paoli-Calmettes, Marseille, France.

Audrey Monneur (A)

Department of Medical Oncology, Institut Paoli-Calmettes, Marseille, France.

Sébastien Salas (S)

Department of Medical Oncology, CHU La Timone, Marseille, France.

Florence Duffaud (F)

Department of Medical Oncology, CHU La Timone, Marseille, France.

Esma Saada-Bouzid (E)

Department of Medical Oncology, Centre Antoine Lacassagne, Nice, France.

Nicolas Isambert (N)

Department of Medical Oncology, Centre Georges François Leclerc, Dijon, France.

Mehdi Brahmi (M)

Department of Medical Oncology, Centre Léon Bérard, Université Claude Bernard Lyon I, Lyon, France.

Isabelle Ray-Coquard (I)

Department of Medical Oncology, Centre Léon Bérard, Université Claude Bernard Lyon I, Lyon, France.

Jean-Yves Blay (JY)

Department of Medical Oncology, Centre Léon Bérard, Université Claude Bernard Lyon I, Lyon, France.

Nelly Firmin (N)

Department of Medical Oncology, Institut du cancer Montpellier, Univ Montpellier, Montpellier, France.

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Classifications MeSH