CHEMOTHERAPY FOR ANAPLASTIC OLIGODENDROGLIOMA

被引:336
作者
CAIRNCROSS, G
MACDONALD, D
LUDWIN, S
LEE, D
CASCINO, T
BUCKNER, J
FULTON, D
DROPCHO, E
STEWART, D
SCHOLD, C
WAINMAN, N
EISENHAUER, E
机构
[1] UNIV WESTERN ONTARIO,DEPT CLIN NEUROL SCI,LONDON,ON,CANADA
[2] UNIV WESTERN ONTARIO,DEPT ONCOL,LONDON,ON,CANADA
[3] UNIV WESTERN ONTARIO,DEPT RADIOL,LONDON,ON,CANADA
[4] UNIV ALBERTA,CROSS CANC INST,EDMONTON,AB,CANADA
[5] UNIV OTTAWA,DEPT MED,OTTAWA,ON,CANADA
[6] QUEENS UNIV,DEPT PATHOL,KINGSTON K7L 3N6,ON,CANADA
[7] NATL CANC INST CANADA,CLIN TRIALS GRP,KINGSTON,ON,CANADA
[8] MAYO CLIN & MAYO FDN,DEPT NEUROL,ROCHESTER,MN 55905
[9] MAYO CLIN & MAYO FDN,DEPT ONCOL,ROCHESTER,MN 55905
[10] UNIV ALABAMA,DEPT NEUROL,BIRMINGHAM,AL 35294
[11] DUKE UNIV,DEPT MED,DURHAM,NC
关键词
D O I
10.1200/JCO.1994.12.10.2013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To examine the rate and duration of response of anaplastic oligodendrogliomas to a dose-escalated combination chemotherapy regimen consisting of procarbazine, lomustine (CCNU), and vincristine (PCV) and to evaluate the side effects of this treatment. Methods: In this single-arm multicentered phase II study, patients with measurable, newly diagnosed or recurrent contrast-enhancing anaplastic oligodendrogliomas were treated with up to six cycles of PCV. Central pathology and radiology review were mandatory, and rigorous response criteria based on imaging were used. Results: Thirty-three patients entered the trial; nine were excluded subsequently, seven due to ineligible pathology. Eighteen of 24 eligible patients (75%) responded, nine completely (38%), four had stable disease (SD), and two progressed during the first cycle of PCV. Responses were observed in nine of 10 patients (90%) with a preexisting low-grade oligodendroglioma and 10 of 15 (67%) with necrotic tumors, called glioblastoma multiforme by some. previously irradiated patients were as likely to respond to PCV as those newly diagnosed (11 of 15 [73%] v seven of nine [78%]). The median time to progression will be at least 25.2 months for complete responders, and was 14.2 months for partial responders and 6.8 months for stable patients. four ineligible patients also responded to PCV; all had gliomas with oligodendroglial differentiation. All responders, eligible or ineligible, were stable or improved neurologically, but nine of 22 (41%) experienced a decline in Eastern Cooperative Oncology Group (ECOG) performance status of one grade while on PCV. Adverse events on treatment included ct death from Pneumocystis pneumonia, ct severe reversible encephalopathy due to procarbazine, an intratumoral hemorrhage, and a subdural hematoma. All other acute toxicities were anticipated and manageable. Conclusion: Anaplastic oligodendrogliomas are chemosensitive cancers. Patients with these tumors respond predictably, durably, and often completely to PCV, and many tolerate a dose-escalated formulation, Cooperative group and randomized trials will be necessary to explore fully the role of chemotherapy in the treatment of aggressive oligodendrogliomas.
引用
收藏
页码:2013 / 2021
页数:9
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