Pemetrexed disodium in recurrent locally advanced or metastatic squamous cell carcinoma of the head and neck

被引:67
作者
Pivot, X
Raymond, E
Laguerre, B
Degardin, M
Cals, L
Armand, JP
Lefebvre, JL
Gedouin, D
Ripoche, V
Kayitalire, L
Niyikiza, C
Johnson, R
Latz, J
Schneider, M
机构
[1] Ctr Antoine Lacassagne, F-06054 Nice, France
[2] Inst Gustave Roussy, Villejuif, France
[3] Ctr Eugene Marquis, Rennes, France
[4] Inst Oscar Lambret, Lille, France
[5] Hop Font Pre, Toulon, France
[6] Eli Lilly & Co, Indianapolis, IN 46285 USA
关键词
LY231514; pemetrexed disodium; ALIMTA((R)); multitargeted antifolate; head and neck squamous cell carcinoma; chemotherapy;
D O I
10.1054/bjoc.2001.2010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This phase II study determined response rate of patients with locally advanced or metastatic head and neck cancer treated with pemetrexed disodium, a new multitargeted antifolate that inhibits thymidylate synthase, dihydrofolate reductase and glycinamide ribonucleotide formyl transferase. 35 patients with local or metastatic relapse of squamous cell carcinoma of the head and neck (31 male, 4 female; median age 53 years) were treated with pemetrexed 500 mg m(2) administered as a 10-minute infusion on day 1 of a 21-day cycle. Patients received 1 to 8 cycles of therapy. 9 patients (26.5%) had an objective response, with a median response duration of 5.6 months (range 2.9-20 months). 15 (44.1%) had stable disease, and 8 (23.5%) had progressive disease. 2 patients were not assessable for response. Median overall survival was 6.4 months (range 0.7-28.1 months; 95% CI: 3.9-7.7 months). 24 patients (68.6%) experienced grade 3/4 neutropenia, with febrile neutropenia in 4 (11.4%). Grade 3/4 anaemia and thrombocytopenia occurred in 11 (34.3%) and 6 (17.1%) patients, respectively. The most frequent non-haematological toxicity was grade 3/4 mucositis (17.1%; 6 patients). In conclusion, pemetrexed is active in squamous cell carcinoma of the head and neck. Although substantial haematological toxicities were experienced by patients, subsequent studies have shown that these toxicities can be proactively managed by folic acid and vitamin B-12 supplementation. (C) 2001 Cancer Research Campaign.
引用
收藏
页码:649 / 655
页数:7
相关论文
共 32 条
[21]  
Postmus PE, 1999, SEMIN ONCOL, V26, P31
[22]  
RECONDO G, 1991, LARYNGOSCOPE, V101, P494
[23]   A phase I evaluation of multitargeted antifolate (MTA, LY231514), administered every 21 days, utilizing the modified continual reassessment method for dose escalation [J].
Rinaldi, DA ;
Kuhn, JG ;
Burris, HA ;
Dorr, FA ;
Rodriguez, G ;
Eckhardt, SG ;
Jones, S ;
Woodworth, JR ;
Baker, S ;
Langley, C ;
Mascorro, D ;
Abrahams, T ;
Von Hoff, DD .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1999, 44 (05) :372-380
[24]   Multitargeted antifolate LY231514 as first-line chemotherapy for patients with advanced non-small-cell lung cancer: A phase II study [J].
Rusthoven, JJ ;
Eisenhauer, E ;
Butts, C ;
Gregg, R ;
Dancey, J ;
Fisher, B .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (04) :1194-1199
[25]   RANDOMIZED PHASE-III TRIAL OF EDATREXATE VERSUS METHOTREXATE IN PATIENTS WITH METASTATIC AND/OR RECURRENT SQUAMOUS-CELL CARCINOMA OF THE HEAD AND NECK - A EUROPEAN ORGANIZATION FOR RESEARCH AND TREATMENT OF CANCER HEAD AND NECK-CANCER COOPERATIVE GROUP-STUDY [J].
SCHORNAGEL, JH ;
VERWEIJ, J ;
DEMULDER, PHM ;
COGNETTI, F ;
VERMORKEN, JB ;
CAPPELAERE, P ;
ARMAND, JP ;
WILDIERS, J ;
DEGRAEFF, A ;
CLAVEL, M ;
SAHMOUD, T ;
KIRKPATRICK, A ;
LEFEBVRE, JL .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (07) :1649-1655
[26]  
Shih C, 1997, CANCER RES, V57, P1116
[27]  
SMITH GK, 1995, CANCER RES, V55, P6117
[28]  
STELL PM, 1990, BRIT J CANCER, V61, P311
[29]  
STELL PM, 1990, BRIT J CANCER, V62, P171
[30]  
VOGL SE, 1985, CANCER, V56, P432, DOI 10.1002/1097-0142(19850801)56:3<432::AID-CNCR2820560304>3.0.CO