SFCE METRO-01 four-drug metronomic regimen phase II trial for pediatric extracranial tumor.


Journal

Pediatric blood & cancer
ISSN: 1545-5017
Titre abrégé: Pediatr Blood Cancer
Pays: United States
ID NLM: 101186624

Informations de publication

Date de publication:
07 2019
Historique:
received: 07 10 2018
revised: 27 01 2019
accepted: 12 02 2019
pubmed: 29 3 2019
medline: 18 12 2019
entrez: 29 3 2019
Statut: ppublish

Résumé

To investigate the antitumor activity of a four-drug metronomic chemotherapy (MC) regimen in relapsed/progressing pediatric extracranial solid tumors (EST). The primary objective was clinical benefit (complete response /partial response/stable disease [SD]) after two cycles of therapy (four months). Patients aged ≥4 to 25 years with progressing EST and adequate organ function were eligible. Treatment consisted of an eight-week cycle of oral celecoxib b.i.d., weekly vinblastine, and oral cyclophosphamide for three weeks alternating with oral methotrexate for three weeks, with a two-week rest. The Kepner-Chang two-stage model was used with 10 patients in the first stage. If primary objective was reached in two or more patients, eight additional patients were included according to four groups: neuroblastoma (NBL), soft-tissue sarcoma (STS), bone sarcoma (BS), and miscellaneous (Misc.). Forty-four patients were evaluable. The NBL cohort could be expanded to 18 patients: 4 of 18 patients stabilized with MC treatment for 6 (n = 1) and 12 (n = 3) months. In STS, two of seven patients (metastatic hemangioendothelioma and angiosarcoma) had SD for > 2 cycles. One of nine Misc. (metastatic myoepithelial carcinoma) had SD for one year. All patients with BS had progressive disease. One-year progression-free survival of the whole cohort was 6.8% and one-year overall survival was 55.3%. Grade 3 toxicity occurred in 18 patients and grade 4 in 15 patients. The most frequent toxicity was hematologic, predominantly neutropenia. This MC has no activity in BS and limited though interesting activity in NBL with some patients being stable for > 1 year. It is not possible to conclude activity in STS and Misc.

Identifiants

pubmed: 30920117
doi: 10.1002/pbc.27693
doi:

Substances chimiques

Celecoxib JCX84Q7J1L

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e27693

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Marie-Amélie Heng-Maillard (MA)

Department of Pediatric Oncology, La Timone Children's Hospital, Marseille, France.

Arnauld Verschuur (A)

Department of Pediatric Oncology, La Timone Children's Hospital, Marseille, France.
Metronomics Global Health Initiative, Marseille, France.

Audrey Aschero (A)

Department of pediatric imaging, La Timone Children's Hospital, Marseille, France.

Alexia Dabadie (A)

Department of pediatric imaging, La Timone Children's Hospital, Marseille, France.

Elisabeth Jouve (E)

CIC-CPCET, La Timone Hospital, AP-HM, Marseille, France.

Pascal Chastagner (P)

Department of Pediatric Oncology, Children's Hospital, Nancy, France.

Pierre Leblond (P)

Pediatric Oncology Unit, Oscar Lambret Centre, Lille, France.

Isabelle Aerts (I)

Pediatric Department, Institut Curie, Paris, France.

Bénédicte De Luca (B)

Department of Clinical Pharmacy, AP-HM, La Timone Children's Hospital, Marseille, France.

Nicolas André (N)

Department of Pediatric Oncology, La Timone Children's Hospital, Marseille, France.
Metronomics Global Health Initiative, Marseille, France.
SMARTc Unit, Pharmacokinetics Laboratory, CRCM UMR U1068 CNRS UMR 7258 Aix Marseille Université, Marseille, France.

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