Phase 2 study of temozolomide in children and adolescents with recurrent central nervous system tumors - A report from the children's oncology group

被引:145
作者
Nicholson, H. Stacy
Kretschmar, Cynthia S.
Krailo, Mark
Bernstein, Mark
Kadota, Richard
Fort, Daniel
Friedman, Henry
Harris, Michael B.
Tedeschi-Blok, Nicole
Mazewski, Claire
Sato, Judith
Reaman, Gregory H.
机构
[1] Oregon Hlth & Sci Univ, Dept Pediat, Portland, OR 97201 USA
[2] Boston Floating Hosp Infants & Children, Dept Pediat Oncol, Boston, MA USA
[3] Univ So Calif, Keck Sch Med, Dept Prevent Med, Los Angeles, CA USA
[4] Hop St Justine, Dept Pediat Hematol Oncol, Montreal, PQ H3T 1C5, Canada
[5] Childrens Hosp, Dept Hematol Oncol, San Diego, CA USA
[6] Univ Virginia, Div Pediat Hematol Oncol, Charlottesville, VA USA
[7] Duke Univ, Div Pediat Neurooncol, Durham, NC USA
[8] Tomorrows Childrens Inst, Dept Pediat Hematol Oncol, Hackensack, NJ USA
[9] Childrens Oncol Grp, Arcadia, CA USA
[10] Childrens Healthcare Atlanta, Dept Hematol Oncol, Atlanta, GA USA
[11] City Hope Natl Med Ctr, Div Pediat, Duarte, CA 91010 USA
[12] Childrens Natl Med Ctr, Dept Hematol Oncol, Washington, DC 20010 USA
关键词
temozolomide; childhood cancer; central nervous system tumors; brain tumors; phase; 2; trials; imidazotetrazine;
D O I
10.1002/cncr.22961
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Effective chemotherapy is lacking for most types of central nervous system (CNS) tumors in children. Temozolomide, an agent with activity against adult brain tumors, was investigated in children and adolescents with recurrent CNS tumors. METHODS. Temozolomide was administered orally as monthly 5-day courses at doses of 200 mg/m(2)/d (patients with no prior craniospinal irradiation [CSI]) or 180 mg/m(2)/d (prior CSI). Patients with a complete (CR) or partial (PR) response or stable disease (SD) could continue temozolomide for up to 12 cycles. RESULTS. The cohort comprised 122 patients, including 113 with CNS tumors. Median age was 11 years (range, 1-23 years). Among 104 evaluable patients with CNS tumors, 5 PRs and 1 CR were observed. PRs occurred in 1 of 23 evaluable patients with high-grade astrocytoma, 1 of 21 with low-grade astrocytoma, and 3 of 25 with medulloblastoma/primitive neuroectodermal tumor (PNET). The CR occurred in an additional patient with medulloblastoma/PNET. No responses were observed in patients with ependymoma, brain-stem glioma, or other CNS tumors. Notably, 41% of patients with low-grade astrocytoma had SD through 12 courses. The most frequent toxicities were grade 3 or 4 neutropenia (19%) and thrombocytopenia (25%); nonhematologic toxicity was infrequent. CONCLUSIONS. Although overall objective responses were limited, further exploration of temozolomide may be warranted in children with medulloblastoma and other PNETs, or in patients with low-grade astrocytoma, perhaps in a setting of less pretreatment than the patients in the current study, or in the context of multiagent therapy.
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收藏
页码:1542 / 1550
页数:9
相关论文
共 47 条
[1]  
[Anonymous], NIH PUBLICATION
[2]   A first feasibility study of temozolomide for Japanese patients with recurrent anaplastic astrocytoma and glioblastoma multiforme [J].
Tomokazu Aoki ;
Tomohiko Mizutani ;
Masatsune Ishikawa ;
Kazuhiko Sugiyama ;
Nobuo Hashimoto .
International Journal of Clinical Oncology, 2003, 8 (5) :301-304
[3]   Randomized phase II study of temozolomide and radiotherapy compared with radiotherapy alone in newly diagnosed glioblastoma multiforme [J].
Athanassiou, H ;
Synodinou, M ;
Maragoudakis, E ;
Paraskevaidis, M ;
Verigos, C ;
Misailidou, D ;
Antonadou, D ;
Saris, G ;
Beroukas, K ;
Karageorgis, P .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (10) :2372-2377
[4]   Multicentre CRC phase II trial of temozolomide in recurrent or progressive high-grade glioma [J].
Bower, M ;
Newlands, ES ;
Bleehen, NM ;
Brada, M ;
Begent, RJH ;
Calvert, H ;
Colquhoun, I ;
Lewis, P ;
Brampton, MH .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1997, 40 (06) :484-488
[5]   Phase II study of primary temozolomide chemotherapy in patients with WHO grade II gliomas [J].
Brada, M ;
Viviers, L ;
Abson, C ;
Hines, F ;
Britton, J ;
Ashley, S ;
Sardell, S ;
Traish, D ;
Gonsalves, A ;
Wilkins, P ;
Westbury, C .
ANNALS OF ONCOLOGY, 2003, 14 (12) :1715-1721
[6]   Multicenter phase II trial of temozolomide in patients with glioblastoma multiforme at first relapse [J].
Brada, M ;
Hoang-Xuan, K ;
Rampling, R ;
Dietrich, PY ;
Dirix, LY ;
Macdonald, D ;
Heimans, JJ ;
Zonnenberg, BA ;
Bravo-Marques, JM ;
Henriksson, R ;
Stupp, R ;
Yue, N ;
Bruner, J ;
Dugan, M ;
Rao, S ;
Zaknoen, S .
ANNALS OF ONCOLOGY, 2001, 12 (02) :259-266
[7]   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
[8]   Correlations between O6-methylguanine DNA methyltransferase promoter methylation status, 1p and 19q deletions, and response to temozolomide in anaplastic and recurrent oligodendroglioma: A prospective GICNO study [J].
Brandes, Alba A. ;
Tosoni, Alicia ;
Cavallo, Giovanna ;
Reni, Michele ;
Franceschi, Enrico ;
Bonaldi, Laura ;
Bertorelle, Roberta ;
Gardiman, Marina ;
Ghimenton, Claudio ;
Iuzzolino, Paolo ;
Pession, Annalisa ;
Blatt, Valeria ;
Ermani, Mario .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (29) :4746-4753
[9]  
Brock CS, 1998, CANCER RES, V58, P4363
[10]   Role of temozolomide after radiotherapy for newly diagnosed diffuse brainstem glioma in children - Results of a multiinstitutional study (SJHG-98) [J].
Broniscer, A ;
Iacono, L ;
Chintagumpala, M ;
Fouladi, M ;
Wallace, D ;
Bowers, DC ;
Stewart, C ;
Krasin, MJ ;
Gajjar, A .
CANCER, 2005, 103 (01) :133-139