Compassionate-use oxaliplatin with bolus 5-fluorouracil/leucovorin in heavily pretreated patients with advanced colorectal cancer

被引:3
作者
LaRocca, RV
Glisson, SD
Hargis, JB
Kosfeld, RE
Leaton, KE
Hicks, RM
Amin-Zimmerman, F
机构
[1] Univ Louisville, Dept Radiat Oncol, James Graham Brown Canc Ctr, Louisville, KY 40202 USA
[2] Kentuckiana Canc Inst, PLLC, Louisville, KY USA
关键词
bolus; 5-fluorouracil/leucovorin; colorectal cancer; compassionate use study; diarrhea; oxaliplatin; pretreated;
D O I
10.1097/01.SMJ.0000129793.35088.5C
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: The efficacy of a concomitant oxaliplatin/bolus 5-fluorouracil/leucovorin regimen in 123 heavily pretreated patients with advanced colorectal cancer was evaluated. Patients with an Eastern Cooperative Oncology Group performance status of 0 to 2 and radiographically progressive cancer which failed to respond to between two and five prior treatment modalities were consented and enrolled. Methods: Patients received oxaliplatin on day 1 of weeks 1, 3, and 5 of an 8-week cycle. 5-fluorouracil/leucovorin was administered on day 1 of weeks 1 through 6. Results: Grade 3 to 4 toxicities were as follows: diarrhea 30%; vomiting 11%; hematologic <3%; peripheral neuropathy 2.5%. Of the 101 patients evaluable for response, 7% achieved a partial response (median duration 4.25 mo), 1 patient achieved a minor response (7 mo), and 31% had stable disease (median duration 6.08 mo). The median time to progression was 3.6 months. Conclusion: This regimen in heavily pretreated patients with disseminated colorectal cancer is of modest benefit, often at the expense of considerable gastrointestinal toxicity. It appears that the use of oxaliplatin/bolus 5-fluorouracil/leucovorin is more toxic than oxaliplatin/infusional 5-fluorouracil and possibly less effective.
引用
收藏
页码:831 / 835
页数:5
相关论文
共 32 条
[1]  
*AM CANC SOC, 2001, ACS PUBL
[2]   Multicenter phase II study of bimonthly high-dose leucovorin, fluorouracil infusion, and oxaliplatin for metastatic colorectal cancer resistant to the same leucovorin and fluorouracil regimen [J].
André, T ;
Bensmaine, MA ;
Louvet, C ;
François, E ;
Lucas, V ;
Desseigne, F ;
Beerblock, K ;
Bouché, O ;
Carola, E ;
Merrouche, Y ;
Morvan, F ;
Dupon-André, G ;
de Gramont, A .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (11) :3560-3568
[3]  
BALCONI G, 1971, BRIT J CANCER, V64, P288
[4]  
BEHRENS BC, 1987, CANCER RES, V47, P414
[5]  
Bleiberg H, 1998, SEMIN ONCOL, V25, P32
[6]   Oxaliplatin added to 5-fluorouracil-based therapy (5-FU ± FA) in the treatment of 5-FU-pretreated patients with advanced colorectal carcinoma (ACRC):: Results from the European compassionate-use program [J].
Brienza, S ;
Bensmaïne, MA ;
Soulié, P ;
Louvet, C ;
Gamelin, E ;
François, E ;
Ducreux, M ;
Marty, M ;
André, T ;
de Braud, F ;
Bleiberg, H ;
Ségal, V ;
Itzhaki, M ;
Cvitkovic, E .
ANNALS OF ONCOLOGY, 1999, 10 (11) :1311-1316
[7]  
Cvitkovic E, 1998, SEMIN ONCOL, V25, P1
[8]   Leucovorin and fluorouracil with or without oxaliplatin as first-line treatment in advanced colorectal cancer [J].
de Gramont, A ;
Figer, A ;
Seymour, M ;
Homerin, M ;
Hmissi, A ;
Cassidy, J ;
Boni, C ;
Cortes-Funes, H ;
Cervantes, A ;
Freyer, G ;
Papamichael, D ;
Le Bail, N ;
Louvet, C ;
Hendler, D ;
de Braud, F ;
Wilson, C ;
Morvan, F ;
Bonetti, A .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (16) :2938-2947
[9]   Oxaliplatin as single agent in previously untreated colorectal carcinoma patients: A phase II multicentric study [J].
Diaz-Rubio, E ;
Sastre, J ;
Zaniboni, A ;
Labianca, R ;
Cortes-Funes, H ;
de Braud, F ;
Boni, C ;
Benavides, M ;
Dallavalle, G ;
Homerin, M .
ANNALS OF ONCOLOGY, 1998, 9 (01) :105-108
[10]   Phase III multicenter randomized trial of oxaliplatin added to chronomodulated fluorouracil-leucovorin as first-line treatment of metastatic colorectal cancer [J].
Giacchetti, S ;
Perpoint, B ;
Zidani, R ;
Le Bail, N ;
Faggiuolo, R ;
Focan, C ;
Chollet, P ;
Llory, JF ;
Letourneau, Y ;
Coudert, B ;
Bertheaut-Cvitkovic, F ;
Larregain-Fournier, D ;
Le Rol, A ;
Walter, S ;
Adam, R ;
Misset, JL ;
Lévi, F .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (01) :136-147