Phase II trial of preirradiation and concurrent temozolomide in patients with newly diagnosed anaplastic oligodendrogliomas and mixed anaplastic oligoastrocytomas: RTOG BR0131

被引:48
作者
Vogelbaum, Michael A. [1 ]
Berkey, Brian [2 ]
Peereboom, David [1 ]
Macdonald, David [3 ]
Giannini, Caterina [4 ]
Suh, John H. [1 ]
Jenkins, Robert [4 ]
Herman, James [5 ]
Brown, Paul [4 ]
Blumenthal, Deborah T. [6 ]
Biggs, Christopher [7 ]
Schultz, Christopher [8 ]
Mehta, Minesh [9 ]
机构
[1] Cleveland Clin, Brain Tumor & NeuroOncol Ctr, Cleveland, OH 44195 USA
[2] Radiat Therapy Oncol Grp, Philadelphia, PA USA
[3] London Reg Canc Ctr, London, ON N6A 4L6, Canada
[4] Mayo Clin, Rochester, MN USA
[5] Johns Hopkins Sch Med, Baltimore, MD USA
[6] Univ Utah, Huntsman Canc Ctr, Salt Lake City, UT USA
[7] Arizona Oncol Serv, Phoenix, AZ USA
[8] Med Coll Wisconsin, Milwaukee, WI 53226 USA
[9] Univ Wisconsin, Dept Human Oncol, Madison, WI USA
关键词
1p/19q loss of heterozygosity; MGMT; oligodendroglioma; RTOG; temozolomide; CHROMOSOME ARMS 1P; EUROPEAN-ORGANIZATION; CHEMOTHERAPY; RADIOTHERAPY; PROCARBAZINE; SURVIVAL; TUMORS; 19Q; GLIOBLASTOMA; PREDICTORS;
D O I
10.1215/15228517-2008-073
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The primary objectives of this phase II study were to evaluate the use of preirradiation temozolomide followed by concurrent temozolomide and radiotherapy (RT) in patients with newly diagnosed anaplastic oligodendroglioma (AO) and mixed anaplastic oligoastrocytoma (MOA). Preirradiation temozolomide (150 mg/m(2)/day) was given on a 7-day-on/7-day-off schedule for up to six cycles. The primary end point was the response rate during the 6-month, pre-RT chemotherapy. Tumor tissue was analyzed for the presence of chromosomal deletions on 1p and 19q and for MGMT-promoter methylation. Forty-two patients were enrolled; 39 were eligible. The objective response rate was 32% (6% [complete response, CR], 26% [partial response PR]), and the rate of progression during pre-RT chemotherapy was 10%. The worst nonhematological toxicity was grade 4 in three patients (8%). Twenty-two patients completed concurrent chemotherapy and RT. There were no grade 4 nonhematological toxicities during the concurrent chemotherapy and RT. Seventeen of 28 (60.7%) evaluable cases had codeletion of 1p/19q; all 17 were free from progression at 6 months. Sixteen of 20 (80%) evaluable cases had MGMT-promoter methylation; all 16 were free from progression at 6 months. In conclusion, the rate of progression of 10% during pre-RT temozolomide chemotherapy for newly diagnosed AO and MAO compared favorably with prior experience with pre-RT PCV chemotherapy (20% in RTOG 9402). The toxicity of the dose-intense pre-RT regimen used in this study may warrant evaluation of other, less intense dosing strategies. Future studies will need to prospectively stratify patients according to the presence of deletions of chromosomes 1p and 19q. Neuro-Oncology 11, 167-175, 2009 (Posted to NeuroOncology [serial online], Doc. D08-00104, September 8, 2008. URL http://neuro-oncology.dukejournals.org; DOI: 10.1215/15228517-2008-073)
引用
收藏
页码:167 / 175
页数:9
相关论文
共 26 条
[21]   Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma [J].
Stupp, R ;
Mason, WP ;
van den Bent, MJ ;
Weller, M ;
Fisher, B ;
Taphoorn, MJB ;
Belanger, K ;
Brandes, AA ;
Marosi, C ;
Bogdahn, U ;
Curschmann, J ;
Janzer, RC ;
Ludwin, SK ;
Gorlia, T ;
Allgeier, A ;
Lacombe, D ;
Cairncross, JG ;
Eisenhauer, E ;
Mirimanoff, RO ;
Van Den Weyngaert, D ;
Kaendler, S ;
Krauseneck, P ;
Vinolas, N ;
Villa, S ;
Wurm, RE ;
Maillot, MHB ;
Spagnolli, F ;
Kantor, G ;
Malhaire, JP ;
Renard, L ;
De Witte, O ;
Scandolaro, L ;
Vecht, CJ ;
Maingon, P ;
Lutterbach, J ;
Kobierska, A ;
Bolla, M ;
Souchon, R ;
Mitine, C ;
Tzuk-Shina, T ;
Kuten, A ;
Haferkamp, G ;
de Greve, J ;
Priou, F ;
Menten, J ;
Rutten, I ;
Clavere, P ;
Malmstrom, A ;
Jancar, B ;
Newlands, E .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (10) :987-996
[22]   Loss of heterozygosity for loci on chromosome arms 1p and 10q in oligodendroglial tumors: relationship to outcome and chemosensitivity [J].
Thiessen, B ;
Maguire, JA ;
McNeil, K ;
Huntsman, D ;
Martin, MA ;
Horsman, D .
JOURNAL OF NEURO-ONCOLOGY, 2003, 64 (03) :271-278
[23]   Adjuvant procarbazine, lomustine, and vincristine improves progression-free survival but not overall survival in newly diagnosed anaplastic oligodendrogliomas and oligoastrocytomas: A Randomized European Organisation for Research and Treatment of Cancer Phase III Trial [J].
van den Bent, Martin J. ;
Carpentier, Antoine F. ;
Brandes, Alba A. ;
Sanson, Marc ;
Taphoorn, Martin J. B. ;
Bernsen, Hans J. J. A. ;
Frenay, Marc ;
Tijssen, Cees C. ;
Grisold, Wolfgang ;
Sipos, Laslo ;
Haaxma-Reiche, Hanny ;
Kros, Johannes M. ;
van Kouwenhoven, Mathilde C. M. ;
Vecht, Charles J. ;
Allgeier, Anouk ;
Lacombe, Denis ;
Gorlia, Thierry .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (18) :2715-2722
[24]   Phase II study of first-line chemotherapy with temozolomide in recurrent oligodendroglial tumors: The European Organization for Research and Treatment of Cancer Brain Tumor Group study 26971 [J].
van den Bent, MJ ;
Taphoorn, MJB ;
Brandes, AA ;
Menten, J ;
Stupp, R ;
Frenay, M ;
Chinot, O ;
Kros, JM ;
van der Rijt, CCD ;
Vecht, CJ ;
Allgeier, A ;
Gorlia, T .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (13) :2525-2528
[25]   Temozolomide chemotherapy in recurrent oligodendroglioma [J].
van den Bent, MJ ;
Keime-Guibert, F ;
Brandes, AA ;
Taphoorn, MJB ;
Kros, JM ;
Eskens, FALM ;
Carpentier, AF .
NEUROLOGY, 2001, 57 (02) :340-342
[26]   A phase II study of temozolomide vs. procarbazine in patients with glioblastoma multiforme at first relapse [J].
Yung, WKA ;
Albright, RE ;
Olson, J ;
Fredericks, R ;
Fink, K ;
Prados, MD ;
Brada, M ;
Spence, A ;
Hohl, RJ ;
Shapiro, W ;
Glantz, M ;
Greenberg, H ;
Selker, RG ;
Vick, NA ;
Rampling, R ;
Friedman, H ;
Phillips, P ;
Bruner, J ;
Yue, N ;
Osoba, D ;
Zaknoen, S ;
Levin, VA .
BRITISH JOURNAL OF CANCER, 2000, 83 (05) :588-593