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Erschienen in: Investigational New Drugs 5/2009

01.10.2009 | PHASE III STUDIES

Phase III trial of standard versus dose-intensified doxorubicin, ifosfamide and dacarbazine (MAID) in the first-line treatment of metastatic and locally advanced soft tissue sarcoma

verfasst von: Jérôme Fayette, Nicolas Penel, Christine Chevreau, Jean-Yves Blay, Didier Cupissol, Antoine Thyss, Cécile Guillemet, Maria Rios, Frédéric Rolland, Pierre Fargeot, Jacques Olivier Bay, Simone Mathoulin-Pelissier, Jean Michel Coindre, Binh Bui-Nguyen

Erschienen in: Investigational New Drugs | Ausgabe 5/2009

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Summary

Multidrug chemotherapy increases responses in advanced soft tissues sarcoma. Can a 20% increase of relative dose intensity of the MAID regimen, more improve responses? From 1994 to 1997, 162 patients were randomized in a phase III study to the conventional drug combination (6 cycles of MAID: 60, 7,500, 900 mg/m2 for doxorubicin, ifosfamide and dacarbazine respectively), or at doses 20–33% higher per cycle (5 cycles of intensified MAID for similar cumulative doses) with systematic G-CSF. Primary endpoint was response rate; secondary were toxicity, event-free and overall survival. The objective response rate in assessable patients was 38% with intensified MAID and 35% with MAID (p = 0.72). Event-free and overall survivals were similar in both arms. Only grade 3–4 thrombocytopenia and anemia were significantly higher in intensified arm. Treatment with intensified MAID did not improve response rate neither survival and cannot be recommended for advanced or metastatic soft tissue sarcoma.
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Metadaten
Titel
Phase III trial of standard versus dose-intensified doxorubicin, ifosfamide and dacarbazine (MAID) in the first-line treatment of metastatic and locally advanced soft tissue sarcoma
verfasst von
Jérôme Fayette
Nicolas Penel
Christine Chevreau
Jean-Yves Blay
Didier Cupissol
Antoine Thyss
Cécile Guillemet
Maria Rios
Frédéric Rolland
Pierre Fargeot
Jacques Olivier Bay
Simone Mathoulin-Pelissier
Jean Michel Coindre
Binh Bui-Nguyen
Publikationsdatum
01.10.2009
Verlag
Springer US
Erschienen in
Investigational New Drugs / Ausgabe 5/2009
Print ISSN: 0167-6997
Elektronische ISSN: 1573-0646
DOI
https://doi.org/10.1007/s10637-008-9217-1

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