'Tomudex' (ZD1694): Results of a randomised trial in advanced colorectal cancer demonstrate efficacy and reduced mucositis and leucopenia

被引:141
作者
Cunningham, D
Zalcberg, JR
Rath, U
Olver, I
VanCutsem, E
Svensson, C
Seitz, JF
Harper, P
Kerr, D
PerezManga, G
Azab, M
Seymour, L
Lowery, K
Ackland, SP
Basser, RL
Clarke, SJ
Goldstein, D
Green, MD
Grygiel, JJ
McKendrick, JJ
Millward, MJ
Olver, IN
Tattersall, MHN
Thomson, DB
Jakesz, R
Buset, M
Tueni, EA
VanCutsem, EJD
Bauer, J
Beska, F
Adenis, A
Brunet, R
Francois, E
Paillot, B
Rougier, P
Fink, UFW
Knuth, KRA
Koenig, HJ
Bohme, MWJ
Wander, HE
Amadori, D
Frassineti, L
Cocconi, G
Passalacqua, R
Frigerio, F
Barni, S
Luporini, G
Labianca, R
Marini, G
Zaniboni, A
机构
[1] ROYAL MARSDEN HOSP, SUTTON, SURREY, ENGLAND
[2] HEIDELBERG REPATRIAT HOSP, HEIDELBERG, VIC, AUSTRALIA
[3] UNIV HEIDELBERG, MED KLIN, W-6900 HEIDELBERG, GERMANY
[4] ROYAL ADELAIDE HOSP, ADELAIDE, SA 5000, AUSTRALIA
[5] UZ GASTHUISBERG, LOUVAIN, BELGIUM
[6] SODER SJUKHUSET, STOCKHOLM, SWEDEN
[7] INST J PAOLI I CALMETTES, MARSEILLE, FRANCE
[8] GUYS HOSP, LONDON SE1 9RT, ENGLAND
[9] QUEEN ELIZABETH HOSP, BIRMINGHAM B15 2TH, W MIDLANDS, ENGLAND
[10] HOSP GEN GREGORIO MARANON, MADRID, SPAIN
[11] ZENECA PHARMACEUT LTD, MACCLESFIELD, CHESHIRE, ENGLAND
关键词
colorectal cancer; advanced colorectal cancer; thymidylate synthase inhibitor; chemotherapy; Tomudex; Phase III study; palliation;
D O I
10.1016/0959-8049(95)00502-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
'Tomudex' (ZD1694), a direct and specific thymidylate synthase (TS) inhibitor entered phase III studies in November 1993. We present here the first analysis of a randomised multicentre, international phase III study. 439 patients with previously untreated advanced colorectal cancer were randomised to Tomudex 3.0 mg/m(2) given once every 3 weeks or 5-fluorouracil (5-FU) 425 m/m(2) and leucovorin (LV) 20 mg/m(2) for 5 days (the Mayo regimen), given every 4-5 weeks. Patients were evaluated weekly for toxicity and every 12 weeks for objective response. The two groups were well matched in terms of demographic characteristics. The mean age of the patients was 61 years and most had either Liver (78%) or lung (25-29%) metastases. Ninety seven per cent of patients allocated to Tomudex and 94% of those allocated to 5-FU plus LV had measurable disease. Response was assessed using WHO/UICC criteria; all response data were source validated; 19.8% of patients who received Tomudex and 12.7% of patients who received 5-FU plus LV had complete or partial responses (P = 0.059, odds ratio 1.7, 95% confidence limits 0.98-2.81). There were no statistically significant differences in time to progression or survival between the two groups. Patients who received Tomudex spent a substantially shorter time in hospital for dosing and had significantly lower rates of grade 3 and 4 toxicities such as leucopenia and mucositis. Patients who received Tomudex had a significantly higher incidence of reversible grade 3 or 4 increase in transaminases, which appear to be of limited clinical significance. Improvement in quality of life, weight gain and performance status was seen in both groups. Tomudex has benefits in terms of higher response rates, reduced toxicity and more frequent palliative benefits when compared with 5-FU plus LV in the management of advanced colorectal cancer, and has a more convenient administration schedule.
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页码:1945 / 1954
页数:10
相关论文
共 35 条
[1]   THE EUROPEAN-ORGANIZATION-FOR-RESEARCH-AND-TREATMENT-OF-CANCER QLQ-C30 - A QUALITY-OF-LIFE INSTRUMENT FOR USE IN INTERNATIONAL CLINICAL-TRIALS IN ONCOLOGY [J].
AARONSON, NK ;
AHMEDZAI, S ;
BERGMAN, B ;
BULLINGER, M ;
CULL, A ;
DUEZ, NJ ;
FILIBERTI, A ;
FLECHTNER, H ;
FLEISHMAN, SB ;
DEHAES, JCJM ;
KAASA, S ;
KLEE, M ;
OSOBA, D ;
RAZAVI, D ;
ROFE, PB ;
SCHRAUB, S ;
SNEEUW, K ;
SULLIVAN, M ;
TAKEDA, F .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (05) :365-376
[2]   CANCER STATISTICS, 1994 [J].
BORING, CC ;
SQUIRES, TS ;
TONG, T ;
MONTGOMERY, S .
CA-A CANCER JOURNAL FOR CLINICIANS, 1994, 44 (01) :7-26
[3]   RANDOMIZED COMPARISON OF 2 SCHEDULES OF FLUOROURACIL AND LEUCOVORIN IN THE TREATMENT OF ADVANCED COLORECTAL-CANCER [J].
BUROKER, TR ;
OCONNELL, MJ ;
WIEAND, HS ;
KROOK, JE ;
GERSTNER, JB ;
MAILLIARD, JA ;
SCHAEFER, PL ;
LEVITT, R ;
KARDINAL, CG ;
GESME, DH .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (01) :14-20
[4]   TEMPORAL PATTERNS IN COLORECTAL-CANCER INCIDENCE, SURVIVAL, AND MORTALITY FROM 1950 THROUGH 1990 [J].
CHU, KC ;
TARONE, RE ;
CHOW, WH ;
HANKEY, BF ;
RIES, LAG .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (13) :997-1006
[5]  
CLARKE JS, 1994, ANN ONCOL, V5, P132
[6]  
CLARKE SJ, 1993, ADV EXP MED BIOL, V339, P277
[7]   PROSPECTIVE RANDOMIZED COMPARISON OF FLUOROURACIL VERSUS FLUOROURACIL AND HIGH-DOSE CONTINUOUS INFUSION LEUCOVORIN CALCIUM FOR THE TREATMENT OF ADVANCED MEASURABLE COLORECTAL-CANCER IN PATIENTS PREVIOUSLY UNEXPOSED TO CHEMOTHERAPY [J].
DOROSHOW, JH ;
MULTHAUF, P ;
LEONG, L ;
MARGOLIN, K ;
LITCHFIELD, T ;
AKMAN, S ;
CARR, B ;
BERTRAND, M ;
GOLDBERG, D ;
BLAYNEY, D ;
ODUJINRIN, O ;
DELAP, R ;
SHUSTER, J ;
NEWMAN, E .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (03) :491-501
[8]   A RANDOMIZED TRIAL OF FLUOROURACIL AND FOLINIC ACID IN PATIENTS WITH METASTATIC COLORECTAL-CARCINOMA [J].
ERLICHMAN, C ;
FINE, S ;
WONG, A ;
ELHAKIM, T .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (03) :469-475
[9]  
GRAF W, 1994, EUR J CANCER, V13, P89
[10]   ASSESSMENT OF RESPONSE TO THERAPY IN ADVANCED BREAST-CANCER - PROJECT OF PROGRAM ON CLINICAL ONCOLOGY OF "INTERNATIONAL-UNION-AGAINST-CANCER, GENEVA, SWITZERLAND [J].
HAYWARD, JL ;
CARBONE, PP ;
HEUSON, JC ;
KUMAOKA, S ;
SEGALOFF, A ;
RUBENS, RD .
EUROPEAN JOURNAL OF CANCER, 1977, 13 (01) :89-94