Second-line chemotherapy with temozolomide in recurrent oligodendroglioma after PCV (procarbazine, lomustine and vincristine) chemotherapy: EORTC Brain Tumor Group phase II study 26972

被引:107
作者
van den Bent, MJ
Chinot, O
Boogerd, W
Marques, JB
Taphoorn, MJB
Kros, JM
van der Rijt, CCD
Vecht, CJ
De Beule, N
Baron, B
机构
[1] Univ Rotterdam Hosp, Dept Neurooncol, Rotterdam Canc Ctr, NL-3008 AE Rotterdam, Netherlands
[2] Univ Rotterdam Hosp, Dept Pathol, Rotterdam Canc Ctr, NL-3008 AE Rotterdam, Netherlands
[3] Univ Rotterdam Hosp, Dept Med Oncol, Rotterdam Canc Ctr, NL-3008 AE Rotterdam, Netherlands
[4] CHU Timone, Marseille, France
[5] Netherlands Canc Inst, Amsterdam, Netherlands
[6] IPO Francisco Gentil, Lisbon, Portugal
[7] Univ Utrecht, Med Ctr, Dept Neurol, Utrecht, Netherlands
[8] Med Ctr Haaglanden Westeinde, Dept Neurol, The Hague, Netherlands
[9] European Org Res Treatment Canc, Ctr Data, Brussels, Belgium
关键词
chemotherapy; oligoastrocytoma; oligodendroglioma; recurrent; second line; temozolomide;
D O I
10.1093/annonc/mdg157
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Oligodendroglial tumors are chemosensitive, with two-thirds of patients responding to PCV combination chemotherapy with procarbazine, lomustine (CCNU) and vincristine. Temozolomide (TMZ), a new alkylating and methylating agent has shown high response rates in recurrent anaplastic astrocytoma. We investigated this drug in recurrent oligodendroglial tumors (OD) and mixed oligoastrocytomas (OA) after prior PCV chemotherapy and radiation therapy. Patients and methods: In a prospective non-randomized multicenter phase H trial patients were treated with TMZ 150 mg/m(2) on days 1-5 in cycles of 28 days for 12 cycles. Eligible patients had a recurrence after prior PCV chemotherapy, with measurable and enhancing disease as shown by magnetic resonance imaging. Pathology and all responses were centrally reviewed. Results: Thirty-two eligible patients were included. In four patients the pathology review did not confirm the presence of an OD or OA. Twelve of 24 patients [50%, 95% confidence interval (CI) 29% to 71%] evaluable for response to first-line PCV chemotherapy had responded to PCV. Temozolomide was in general well tolerated; the most frequent side-effects were hematological. One patient discontinued treatment due to toxicity. In seven of 28 patients (25%, 95% CI 11% to 45%) with histologically confirmed OD an objective response to TMZ was observed. Median time to progression for responding patients was 8.0 months. After 6 and 12 months from the start of treatment, 29% and 11% of patients, respectively, were still free from progression. Conclusions: TMZ may be regarded as the preferred second-line treatment in OD after failure of PCV chemotherapy. Further studies on TMZ in OD are indicated.
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页码:599 / 602
页数:4
相关论文
共 20 条
[1]   Temozolomide as a second-line systemic regimen in recurrent high-grade glioma:: A phase II study [J].
Brandes, AA ;
Ermani, M ;
Basso, U ;
Amistà, P ;
Berti, F ;
Scienza, R ;
Rotilio, A ;
Pinna, G ;
Gardiman, M ;
Monfardini, S .
ANNALS OF ONCOLOGY, 2001, 12 (02) :255-257
[2]   CHEMOTHERAPY FOR ANAPLASTIC OLIGODENDROGLIOMA [J].
CAIRNCROSS, G ;
MACDONALD, D ;
LUDWIN, S ;
LEE, D ;
CASCINO, T ;
BUCKNER, J ;
FULTON, D ;
DROPCHO, E ;
STEWART, D ;
SCHOLD, C ;
WAINMAN, N ;
EISENHAUER, E .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (10) :2013-2021
[3]   Salvage chemotherapy with paclitaxel for recurrent oligodendrogliomas [J].
Chamberlain, MC ;
Kormanik, PA .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (12) :3427-3432
[4]   Salvage chemotherapy with CPT-11 for recurrent oligodendrogliomas [J].
Chamberlain, MC .
JOURNAL OF NEURO-ONCOLOGY, 2002, 59 (02) :157-163
[5]  
CHINOT O, 2001, P AN M AM SOC CLIN, V20, pB78
[6]   Safety and efficacy of temozolomide in patients with recurrent anaplastic oligodendrogliomas after standard radiotherapy and chemotherapy [J].
Chinot, OL ;
Honore, S ;
Dufour, H ;
Barrie, M ;
Figarella-Branger, D ;
Muracciole, X ;
Braguer, D ;
Martin, PM ;
Grisoli, F .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (09) :2449-2455
[7]  
Coons SW, 1997, CANCER, V79, P1381, DOI 10.1002/(SICI)1097-0142(19970401)79:7<1381::AID-CNCR16>3.0.CO
[8]  
2-W
[9]  
Ino Y, 2001, CLIN CANCER RES, V7, P839
[10]   NONPARAMETRIC-ESTIMATION FROM INCOMPLETE OBSERVATIONS [J].
KAPLAN, EL ;
MEIER, P .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1958, 53 (282) :457-481