Radiation plus Procarbazine, CCNU, and Vincristine in Low-Grade Glioma

被引:719
|
作者
Buckner, Jan C. [1 ]
Shaw, Edward G. [2 ]
Pugh, Stephanie L. [4 ]
Chakravarti, Arnab [5 ]
Gilbert, Mark R. [7 ]
Barger, Geoffrey R. [8 ]
Coons, Stephen [9 ]
Ricci, Peter [11 ]
Bullard, Dennis [3 ]
Brown, Paul D. [7 ]
Stelzer, Keith [12 ]
Brachman, David [10 ]
Suh, John H. [6 ]
Schultz, Christopher J. [13 ]
Bahary, Jean-Paul [14 ]
Fisher, Barbara J. [15 ]
Kim, Harold [8 ]
Murtha, Albert D. [16 ]
Bell, Erica H. [5 ]
Won, Minhee [4 ]
Mehta, Minesh P. [17 ]
Curran, Walter J., Jr. [18 ]
机构
[1] Mayo Clin, 200 First St SW, Rochester, MN 55905 USA
[2] Wake Forest Univ, Bowman Gray Sch Med, Winston Salem, NC USA
[3] Triangle Neurosurg, Raleigh, NC USA
[4] NRG Oncol Stat & Data Management Ctr, Philadelphia, PA USA
[5] Ohio State Univ, Columbus, OH 43210 USA
[6] Cleveland Clin, Cleveland, OH 44106 USA
[7] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[8] Wayne State Univ, Detroit, MI USA
[9] Barrow Neurol Inst, Phoenix, AZ USA
[10] Arizona Oncol Serv Fdn, Phoenix, AZ USA
[11] Radiol Imaging Associates, Englewood, CO USA
[12] Mid Columbia Med Ctr, The Dalles, OR USA
[13] Med Coll Wisconsin, Milwaukee, WI 53226 USA
[14] Ctr Hosp Univ Montreal, Montreal, PQ, Canada
[15] London Reg Canc Program, London, ON, Canada
[16] Cross Canc Inst, Edmonton, AB T6G 1Z2, Canada
[17] Univ Maryland, Baltimore, MD 21201 USA
[18] Emory Univ, Atlanta, GA 30322 USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2016年 / 374卷 / 14期
关键词
PHASE-II TRIAL; TERM-FOLLOW-UP; ANAPLASTIC OLIGODENDROGLIOMA; RECURRENT GLIOMA; CHEMOTHERAPY; LOMUSTINE; RADIOTHERAPY; THERAPY; CANCER;
D O I
10.1056/NEJMoa1500925
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Grade 2 gliomas occur most commonly in young adults and cause progressive neurologic deterioration and premature death. Early results of this trial showed that treatment with procarbazine, lomustine (also called CCNU), and vincristine after radiation therapy at the time of initial diagnosis resulted in longer progression-free survival, but not overall survival, than radiation therapy alone. We now report the long-term results. METHODS We included patients with grade 2 astrocytoma, oligoastrocytoma, or oligodendroglioma who were younger than 40 years of age and had undergone subtotal resection or biopsy or who were 40 years of age or older and had undergone biopsy or resection of any of the tumor. Patients were stratified according to age, histologic findings, Karnofsky performance-status score, and presence or absence of contrast enhancement on pre-operative images. Patients were randomly assigned to radiation therapy alone or to radiation therapy followed by six cycles of combination chemotherapy. RESULTS A total of 251 eligible patients were enrolled from 1998 through 2002. The median follow-up was 11.9 years; 55% of the patients died. Patients who received radiation therapy plus chemotherapy had longer median overall survival than did those who received radiation therapy alone (13.3 vs. 7.8 years; hazard ratio for death, 0.59; P = 0.003). The rate of progression-free survival at 10 years was 51% in the group that received radiation therapy plus chemotherapy versus 21% in the group that received radiation therapy alone; the corresponding rates of overall survival at 10 years were 60% and 40%. A Cox model identified receipt of radiation therapy plus chemotherapy and histologic findings of oligodendroglioma as favorable prognostic variables for both progression-free and overall survival. CONCLUSIONS In a cohort of patients with grade 2 glioma who were younger than 40 years of age and had undergone subtotal tumor resection or who were 40 years of age or older, progression-free survival and overall survival were longer among those who received combination chemotherapy in addition to radiation therapy than among those who received radiation therapy alone. (Funded by the National Cancer Institute and others; ClinicalTrials.gov number, NCT00003375.)
引用
收藏
页码:1344 / 1355
页数:12
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