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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[21]   Gemcitabine (GEM) plus oxaliplatin, folinic acid, and 5-fluorouracil (FOLFOX-4) in patients with advanced gastric cancer [J].
Correale, P ;
Fulfaro, F ;
Marsili, S ;
Cicero, G ;
Bajardi, E ;
Intrivici, C ;
Vuolo, G ;
Carli, AF ;
Caraglia, M ;
Del Prete, S ;
Greco, E ;
Gebbia, N ;
Francini, G .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2005, 56 (06) :563-568
[22]   Influence of intraperitoneal 5-fluorouracil plus folinic acid on the healing of colonic anastomoses in rats [J].
Kanellos, I ;
Kavouni, A ;
Zaraboukas, T ;
Odisseos, C ;
Galovatsea, K ;
Dadoukis, I .
EUROPEAN SURGICAL RESEARCH, 1996, 28 (05) :374-379
[23]   Randomised phase II study of standard versus chronomodulated CPT-11 plus chronomodulated 5-fluorouracil and folinic acid in advanced colorectal cancer patients [J].
Garufi, C ;
Vanni, B ;
Aschelter, AM ;
Zappalà, AR ;
Bria, E ;
Nisticò, C ;
Sperduti, I ;
Cognetti, F ;
Terzoli, E .
EUROPEAN JOURNAL OF CANCER, 2006, 42 (05) :608-616
[24]   Increasing doses of 5-fluorouracil and high-dose folinic acid in the treatment of metastatic colorectal cancer [J].
Meregalli, M ;
Martignoni, G ;
Frontini, L ;
Zonato, S ;
Pavia, G ;
Beretta, G .
TUMORI, 1998, 84 (06) :662-665
[25]   Intravenous weekly high-dose infusion of 5-fluorouracil and folinic acid in pretreated patients with metastatic colorectal cancer [J].
Lorenz, M ;
StaibSebler, E ;
Gog, C ;
Petrowsky, H ;
Encke, A .
ONKOLOGIE, 1997, 20 (03) :222-225
[26]   5-fluorouracil versus folinic acid and 5-fluorouracil in advanced, hormone-resistant prostate cancer: A prospective, randomized pilot trial [J].
Breul, J ;
Jakse, G ;
Forster, G ;
Lampel, A ;
Rohani, A ;
Hartung, R .
EUROPEAN UROLOGY, 1997, 32 (03) :280-283
[27]   HIGH-DOSE FOLINIC ACID AND 5-FLUOROURACIL BOLUS AND CONTINUOUS-INFUSION IN ADVANCED COLORECTAL-CANCER - POOR RESPONSE RATE IN UNSELECTED PATIENTS [J].
HANNA, CL ;
MCKINNA, FE ;
WILLIAMS, LB ;
MORREY, D ;
ADAMS, M ;
MASON, MD ;
MAUGHAN, TS .
BRITISH JOURNAL OF CANCER, 1995, 72 (03) :774-776
[28]   Phase II evaluation of 5-fluorouracil plus folinic acid and alpha 2b-interferon in metastatic colorectal cancer [J].
Kohne, CH ;
Wilke, H ;
Hiddemann, W ;
Bokemeyer, C ;
Lohrmann, HP ;
Bodenstein, H ;
Preiss, J ;
Rauschecker, H ;
Hill, H ;
Kaufer, C ;
Fischer, JT ;
Ohl, U ;
Urbanitz, D ;
Balleisen, L ;
Schmoll, HJ .
ONCOLOGY, 1997, 54 (02) :96-101
[29]   WEEKLY HIGH-DOSE 5-FLUOROURACIL AND FOLINIC ACID AS SALVAGE TREATMENT IN ADVANCED GASTRIC-CANCER [J].
VANHOEFER, U ;
WILKE, H ;
WEH, HJ ;
CLEMENS, M ;
HARSTRICK, A ;
STAHL, M ;
HOSSFELD, DK ;
SEEBER, S .
ANNALS OF ONCOLOGY, 1994, 5 (09) :850-851
[30]   A phase III study of 5-fluorouracil versus 5-fluorouracil plus interferon alpha 2b versus 5-fluorouracil plus leucovorin in patients with advanced colorectal cancer - A Hellenic Cooperative Oncology Group (HeCOG) study [J].
Kalofonos, HP ;
Nicolaides, C ;
Samantas, E ;
Mylonakis, N ;
Aravantinos, G ;
Dimopoulos, MA ;
Gennatas, C ;
Kouvatseas, G ;
Giannoulis, E ;
Dervenis, C ;
Basdanis, G ;
Pavlidis, N ;
Androulakis, I ;
Fountzilas, G .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2002, 25 (01) :23-30