RANDOMIZED PHASE-III STUDY OF 5-FLUOROURACIL PLUS HIGH-DOSE FOLINIC ACID VERSUS 5-FLUOROURACIL PLUS FOLINIC ACID PLUS METHYL-LOMUSTINE FOR PATIENTS WITH ADVANCED COLORECTAL-CANCER

被引:0
|
作者
JONES, DV
WINN, RJ
BROWN, BW
LEVY, LB
PUGH, RP
WADE, JL
GROSS, HM
PENDERGRASS, KB
LEVIN, B
ABBRUZZESE, JL
机构
[1] UNIV TEXAS, MD ANDERSON CANC CTR, DEPT MED ONCOL, HOUSTON, TX 77030 USA
[2] UNIV TEXAS, MD ANDERSON CANC CTR, DEPT BIOMATH, HOUSTON, TX 77030 USA
[3] ALLEGHENY COMMUNITY CLIN ONCOL PROGRAM, PITTSBURGH, PA USA
[4] CENT ILLINOIS CCOP, DECATUR, IL USA
[5] DAYTON CCOP, KETTERING, OH USA
[6] KANSAS CITY CCOP, KANSAS CITY, MO USA
关键词
COLON CANCER; METHYL-LOMUSTINE; NITROSOUREAS; 5-FLUOROURACIL; FOLINIC ACID; RANDOMIZED TRIAL;
D O I
10.1002/1097-0142(19951115)76:10<1709::AID-CNCR2820761006>3.0.CO;2-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Metastatic colorectal cancer is generally incurable. The most active regimen available, 5-fluorouracil (5-FU) and folinic acid (Leucovorin), produces response rates of approximately 25% to 30%. Methyl-lomustine is a nitrosourea with modest activity against colorectal cancer. A randomized trial was undertaken to evaluate the impact the addition of methyl-lomustine would have on response, duration of survival, and survival rates in patients with advanced colorectal cancer. Methods. The methyl-lomustine/5-FU/Leucovorin (MFL) regimen consisted of methyl-lomustine (110 mg/m(2)), administered on Day 1 of each 8-week cycle with six weekly boluses of 5-FU (600 mg/m(2)), and Leucovorin (500 mg/m(2)). The FL treatment arm consisted of the administration of 5-FU and Leucovorin as described above. Patients were evaluated for response and toxicity after each 8-week cycle. Results. Of 319 patients included in this trial, 297 (93.1%) had disease evaluable for response and toxicity: 145 received MFL, and 152 received FL. in this trial, 526 courses of MFL and 529 courses of FL were administered. Methyl-lomustine/5-FU/Leucovorin treatment resulted in 4 complete and 30 partial responses (response rate, 21.9%), and FL treatment resulted in 9 complete and 33 partial responses (response rate, 26.4%). There was no significant difference in median survival duration between patients in the two arms (MFL = 48 weeks, FL = 51 weeks). However, MFL was significantly more toxic with greater myelosuppression than was FL (Grade 3-4 neutropenia: MFL = 56 patients, FL = 27 patients, P < 0.001; Grade 3-4 thrombocytopenia: MFL = 49 patients, FL = 2 patients, P < 0.001; Grade 3-4 anemia: MFL = 15 patients, FL = 6 patients, P < 0.001; and more prolonged median duration of granulocytopenia: MFL = 9 days, FL = 7 days, P < 0.001; and thrombocytopenia: MFL = 14 days, FL = 7.5 days, P < 0.001). Conclusion. Because the addition of methyl-lomustine in the MFL schedule markedly increased the toxicity of the regimen and because the FL regimen was as effective as MFL, the authors recommend that Leucovorin and 5-FU remain the treatment choice for treating patients with metastatic colorectal cancer.
引用
收藏
页码:1709 / 1714
页数:6
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