Phase 2 Study of Radiation Therapy Plus Low-Dose Temozolomide Followed by Temozolomide and Irinotecan for Glioblastoma: NRG Oncology RTOG Trial 0420.


Journal

International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616

Informations de publication

Date de publication:
15 03 2019
Historique:
received: 29 03 2018
revised: 19 10 2018
accepted: 05 11 2018
pubmed: 30 11 2018
medline: 7 9 2019
entrez: 30 11 2018
Statut: ppublish

Résumé

To evaluate the toxicity and efficacy of adjuvant temozolomide (TMZ) and irinotecan (CPT-11) for 12 months after concurrent chemoradiation in patients with newly diagnosed glioblastoma (GBM). Trial RTOG 04-20, a single-arm, multi-institutional phase 2 trial, was designed to determine the efficacy and toxicity of concomitant TMZ and radiation therapy (RT) followed by adjuvant TMZ combined with CPT-11 given for 12 cycles compared with historical controls of adjuvant TMZ alone given for 6 cycles. A total of 170 patients were enrolled, 152 of whom were eligible. Adjuvant CPT-11 combined with TMZ was more toxic than expected. A higher rate of hematologic and gastrointestinal toxicities was more frequently noted with the combination regimen compared with adjuvant TMZ alone. Grade 3/4 hematologic toxicity was 38% compared with 14% reported in the Stupp trial. After an early interim analysis, the adjuvant CPT-11 dose was reduced to 100 mg/m Although irinotecan and TMZ for 12 cycles given after chemoradiation for patients with newly diagnosed glioblastoma significantly improved median survival compared with historical control data at the time the study was conducted, the historical control median survival time of 13.7 months does not represent the current benchmark for this patient population. Treatment intensification does prolong overall survival compared with the current standard.

Identifiants

pubmed: 30496882
pii: S0360-3016(18)33955-5
doi: 10.1016/j.ijrobp.2018.11.008
pmc: PMC7034757
mid: NIHMS1526965
pii:
doi:

Substances chimiques

Irinotecan 7673326042
Temozolomide YF1K15M17Y

Types de publication

Clinical Trial, Phase II Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

878-886

Subventions

Organisme : NCI NIH HHS
ID : U10 CA021661
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180822
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180868
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233323
Pays : United States

Informations de copyright

Copyright © 2018. Published by Elsevier Inc.

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Auteurs

Frank S Lieberman (FS)

University of Pittsburgh Medical Center, University of Pittsburgh Physicians, Department of Neurology, Department of Medicine, Pittsburgh, Pennsylvania. Electronic address: liebermanf@upmc.edu.

Meihua Wang (M)

Merck & Co, Kenilworth, New Jersey.

H Ian Robins (HI)

University of Wisconsin, Madison, Wisconsin.

Christina I Tsien (CI)

Washington University School of Medicine, St Louis, Missouri.

Walter J Curran (WJ)

Emory University, Atlanta, Georgia.

Maria Werner-Wasik (M)

Thomas Jefferson University Hospital, Philadelphia, Pennsylvania.

Ryan P Smith (RP)

University of Pittsburgh UPMC Shadyside, Pittsburgh, Pennsylvania.

Christopher Schultz (C)

Medical College of Wisconsin, Milwaukee, Wisconsin.

Alan C Hartford (AC)

Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.

Peixin Zhang (P)

NRG Oncology Statistics and Data Management Center-American College of Radiology, Philadelphia, Pennsylvania.

Minesh P Mehta (MP)

University of Maryland Medical Systems, Baltimore, Maryland.

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Classifications MeSH