Results of API-AI based regimen in osteosarcoma adult patients included in the French OS2006/Sarcome-09 study.


Journal

International journal of cancer
ISSN: 1097-0215
Titre abrégé: Int J Cancer
Pays: United States
ID NLM: 0042124

Informations de publication

Date de publication:
15 01 2020
Historique:
received: 27 12 2018
accepted: 28 05 2019
pubmed: 28 6 2019
medline: 20 2 2020
entrez: 28 6 2019
Statut: ppublish

Résumé

In the OS2006 study, patients younger than 18 years were treated with a methotrexate-based regimen (MTX), patients older than 25 years with a doxorubicin-cisplatin-ifosfamide-based regimen (API-AI), whereas patients aged 18-25 years received either API-AI or MTX. We herein report the prespecified subgroup analysis of the outcome of 106 patients treated with API-AI. Preoperative chemotherapy combined three doxorubicin-ifosfamide-cisplatin (API) and two doxorubicin-ifosfamide (AI) courses. Postoperative chemotherapy was assigned by risk group: localised patients with a good histological response (<10% viable cells) received two AI and two cisplatin-ifosfamide (PI) courses; patients with synchronous metastases, poor histological response or unresectable primary received five cycles of etoposide-ifosfamide (EI). Of the 106 patients, 61 were randomised to receive or not zoledronate. Median age was 30 years (range 18-67), 66 (62%) patients were >25 years. The primary tumours were axial in 28 patients (26%), and 28 (26%) presented with metastases. Ninety-six patients (91%) had surgery, conservative in 82 (85%); 36 patients (38%, 95% CI 28-48%) were good responders. Toxicity was manageable, with no significant difference in severe acute toxicity between patients aged >25 years and those younger. With a median follow-up of 4.8 years, the 5-year event-free survival and overall survival rates were 46% (95% CI 36-56) and 57% (95% CI 47-67), respectively. The primary tumour size and initial metastases correlated with a higher risk of event. In these 106 osteosarcoma adult patients, API-AI proved feasible with no excess of toxicity, and favourable activity despite poor-prognosis factors.

Identifiants

pubmed: 31246277
doi: 10.1002/ijc.32526
doi:

Substances chimiques

Etoposide 6PLQ3CP4P3
Zoledronic Acid 6XC1PAD3KF
Doxorubicin 80168379AG
Cisplatin Q20Q21Q62J
Ifosfamide UM20QQM95Y
Methotrexate YL5FZ2Y5U1

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

413-423

Informations de copyright

© 2019 UICC.

Références

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Auteurs

Sophie Piperno-Neumann (S)

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

Isabelle Ray-Coquard (I)

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

Bob-Valéry Occean (BV)

Biostatistics Unit, Gustave Roussy, Villejuif, France.

Valérie Laurence (V)

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

Didier Cupissol (D)

Department of Medicine, Val d'Aurelle Institute, Montpellier, France.

Christophe Perrin (C)

Department of Medical Oncology, Centre Eugène Marquis, Rennes, France.

Nicolas Penel (N)

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

Emmanuelle Bompas (E)

Medical Oncology Department, Institut de Cancérologie de l'Ouest, Saint-Herblain, France.

Maria Rios (M)

Department of Oncology, Institut de Cancérologie de Lorraine, Vandoeuvre-Lès-Nancy, France.

Axel Le Cesne (A)

Department of Medicine and Surgery, Gustave Roussy, Villejuif, France.

Antoine Italiano (A)

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

Philippe Anract (P)

Orthopaedic Department, Cochin University hospital, Paris, France.

Gonzague de Pinieux (G)

Department of Anatomopathology, University Hospital, Tours, France.

Olivier Collard (O)

Medical Oncology Department, Institut de Cancérologie de la Loire Lucien Neuwirth, St Priest en Jarez, France.

François Bertucci (F)

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

Florence Duffaud (F)

Department of Medical Oncology, Timone University Hospital, Marseille, France.

Marie-Cécile Le Deley (MC)

Biostatistics Unit, Gustave Roussy, Villejuif, France.
Paris-Saclay University, Paris-Sud University, CESP, INSERM, Villejuif, France.

Jessy Delaye (J)

UNICANCER, Paris, France.

Laurence Brugieres (L)

Department of Children and Adolescents Oncology, Gustave Roussy, Villejuif, France.

Jean-Yves Blay (JY)

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

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