RNOP-09: pegylated liposomal doxorubicine and prolonged temozolomide in addition to radiotherapy in newly diagnosed glioblastoma--a phase II study.


Autoria(s): Beier C.P.; Schmid C.; Gorlia T.; Kleinletzenberger C.; Beier D.; Grauer O.; Steinbrecher A.; Hirschmann B.; Brawanski A.; Dietmaier C.; Jauch-Worley T.; Kölbl O.; Pietsch T.; Proescholdt M.; Rümmele P.; Muigg A.; Stockhammer G.; Hegi M.; Bogdahn U.; Hau P.
Data(s)

2009

Resumo

BACKGROUND: Although Temozolomide is effective against glioblastoma, the prognosis remains dismal and new regimens with synergistic activity are sought for. METHODS: In this phase-I/II trial, pegylated liposomal doxorubicin (Caelyx, PEG-Dox) and prolonged administration of Temozolomide in addition to radiotherapy was investigated in 63 patients with newly diagnosed glioblastoma. In phase-I, PEG-Dox was administered in a 3-by-3 dose-escalation regimen. In phase-II, 20 mg/m2 PEG-Dox was given once prior to radiotherapy and on days 1 and 15 of each 28-day cycle starting 4 weeks after radiotherapy. Temozolomide was given in a dose of 75 mg/m2 daily during radiotherapy (60 Gy) and 150-200 mg/m2 on days 1-5 of each 28-day cycle for 12 cycles or until disease progression. RESULTS: The toxicity of the combination of PEG-Dox, prolonged administration of Temozolomide, and radiotherapy was tolerable. The progression free survival after 12 months (PFS-12) was 30.2%, the median overall survival was 17.6 months in all patients including the ones from Phase-I. None of the endpoints differed significantly from the EORTC26981/NCIC-CE.3 data in a post-hoc statistical comparison. CONCLUSION: Together, the investigated combination is tolerable and feasible. Neither the addition of PEG-Dox nor the prolonged administration of Temozolomide resulted in a meaningful improvement of the patient's outcome as compared to the EORTC26981/NCIC-CE.3 data.

Identificador

http://serval.unil.ch/?id=serval:BIB_852C93962248

isbn:1471-2407[electronic]

doi:10.1186/1471-2407-9-308

pmid:19725960

http://my.unil.ch/serval/document/BIB_852C93962248.pdf

http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_852C939622489

isiid:000270309200001

Idioma(s)

en

Direitos

info:eu-repo/semantics/openAccess

Fonte

BMC Cancer, vol. 9, no. 1, pp. 308

Tipo

info:eu-repo/semantics/article

article