Remission and survival following monthly intraarterial cisplatinum in nonresectable hepatoma

被引:35
作者
Court, WS
Order, SE
Siegel, JA
Johnson, E
DeNittis, AS
Principato, R
Martz, K
Zeiger, LS
机构
[1] Ctr Mol Med, Garden City, NY 11530 USA
[2] Nucl Phys Enterprises, Cherry Hill, NJ 08003 USA
[3] Mayo Clin, Jacksonville, FL 32224 USA
[4] Univ Penn, Dept Radiat Oncol, Philadelphia, PA USA
[5] Cooper Univ Hosp, Dept Radiol, Camden, NJ 08103 USA
[6] Cooper Univ Hosp, Dept Nucl Med, Camden, NJ 08103 USA
[7] Ridgeview Stat, Bluemont, VA 20135 USA
关键词
hepatoma; hepatocellular; carcinoma; cisplatin; cisplatinum; (195m)cisplatinum; radioisotopes; intraarterial;
D O I
10.1081/CNV-120002486
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Precis: Intraarterial delivery of 50 mg/m(2) cisplatinum on a monthly basis is a well-tolerated regimen for patients with nonresectable hepatoma. The selective uptake of cisplatinum delivered intraarterially suggests other selective intraarterial protocols would be of use in regional cancers treated with cisplatinum. Background: Sixty-seven patients with nonresectable hepatoma were treated with hepatic artery infusions (HAI) of 50 mg/m(2) cisplatinum on a monthly basis. Methods: Forty-eight patients received an initial course of whole liver external radiation with intravenous (IV) cisplatinum 50 mg/m(2). Nineteen patients did not receive radiation and received HAI cisplatinum only. All patients then received HAI cisplatinum at 50 mg/m(2) on a monthly basis. Six patients were given a tracer dose of radioactive (195m)cisplatinum for quantitation by the HAI and IV routes. Results: Monthly HAI cisplatinum was well tolerated and could be repeated indefinitely. Median survival for primarily treated nonresectable hepatomas was 12 months [alpha fetoprotein (AFP) elevated] and 17.5 months (AFP negative). Radioactive cisplatinum given by HAI yielded 34-55% tumor uptake of cisplatinum vs. <5% by IV delivery. Conclusions: Hepatic intraarterial cisplatinum at 50 mg/m(2) is a well-tolerated monthly regimen for patients with nonresectable hepatoma.
引用
收藏
页码:613 / 625
页数:13
相关论文
共 68 条
[1]  
*AM JOINT COMM CAN, 1998, CANC STAG MAN
[2]   A NEW, SEMIAUTOMATED SYSTEM FOR THE MICROSCALE SYNTHESIS OF PT-195M]CIS PLATIN SUITABLE FOR CLINICAL-STUDIES [J].
ANAND, D ;
WOLF, W .
APPLIED RADIATION AND ISOTOPES, 1992, 43 (06) :809-814
[3]   Intra-hepatic arterial drug delivery [J].
Blesing, CH ;
Kerr, DJ .
JOURNAL OF DRUG TARGETING, 1996, 3 (05) :341-347
[4]   Epirubicin and etoposide combination chemotherapy to treat hepatocellular carcinoma patients: A phase II study [J].
BobbioPallavicini, E ;
Porta, C ;
Moroni, M ;
Bertulezzi, G ;
Civelli, L ;
Pugliese, P ;
Nastasi, G .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (11) :1784-1788
[5]  
CARR BI, 1996, ASCO P, V15, P198
[6]  
CARR BI, 1992, HEPATOLOGY, V16, P60
[7]  
Chao Y, 1996, CANCER, V77, P635, DOI 10.1002/(SICI)1097-0142(19960215)77:4<635::AID-CNCR8>3.0.CO
[8]  
2-F
[9]   PREPARATION AND METABOLISM OF A CISPLATIN-SERUM PROTEIN COMPLEX [J].
COLE, WC ;
WOLF, W .
CHEMICO-BIOLOGICAL INTERACTIONS, 1980, 30 (02) :223-235
[10]   Suppression of bursting [J].
Coller, BD ;
Holmes, P .
AUTOMATICA, 1997, 33 (01) :1-11