TUMOR-TARGETED CHEMOTHERAPY WITH LIPID CONTRAST-MEDIUM AND MACROMOLECULAR ANTICANCER DRUG (SMANCS) FOR RENAL-CELL CARCINOMA

被引:11
作者
KOBAYASHI, M
IMAI, K
SUGIHARA, S
MAEDA, H
KONNO, T
YAMANAKA, H
机构
[1] GUNMA UNIV,SCH MED,DEPT UROL,MAEBASHI,GUNMA 371,JAPAN
[2] GUNMA CANC CTR HOSP,DEPT PATHOL,OTA,JAPAN
[3] KUMAMOTO UNIV,SCH MED,DEPT SURG,KUMAMOTO 860,JAPAN
[4] KUMAMOTO UNIV,SCH MED,DEPT MICROBIOL,KUMAMOTO 860,JAPAN
关键词
D O I
10.1016/0090-4295(91)80308-T
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Twenty-five patients with renal cell carcinoma were treated with a lipophilic macromolecular drug, poly(stylene-co-maleic acid)-conjugated neocarzinostatin (SMANCS) dissolved in lipid contrast medium (Lipiodol). The drug was injected by catheterizing the renal artery and another feeding artery in 24 patients, and in the common hepatic artery in 1 patient with metastases to the liver after a radical nephrectomy. The procedure of selective arterial administration of 3-20 mg/mL of SMANCS/Lipiodol was simple to perform and was required once every two to three weeks. Total dose of SMANCS for each patient varied from 3 to 57 mg. Both SMANCS and Lipiodol accumulated more selectively in tumor than in any other tissue and remained in the neovasculature and extracapillary space for a long time. CT pattern of the remaining oil contrast medium in the tumor was characterized by the high-density area localized mainly in the periphery of the tumor around the central necrosis. When hyperviscosity Lipiodol (Lipiodol HV) was used as lipid contrast medium, it remained more persistently in the tumor and disappeared more slowly than Lipiodol. Moreover, the pronounced anticancer effect was recognized when SMANCS/Lipiodol HV was administered compared with only SMANCS/Lipiodol. Severe side effects, such as myelosuppression, unendurable pain, paralytic ileus, etc., were not observed. This targeting chemotherapy may be of great significance for advanced renal cell carcinoma.
引用
收藏
页码:288 / 294
页数:7
相关论文
共 18 条
[1]  
Almgard L E, 1973, Br J Urol, V45, P474, DOI 10.1111/j.1464-410X.1973.tb06806.x
[2]   TRANSCATHETER OCCLUSIVE THERAPY OF GENITO-URINARY ABNORMALITIES USING ISOBUTYL 2-CYANOACRYLATE (BUCRYLATE) [J].
FREENY, PC ;
BUSH, WH ;
KIDD, R .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1979, 133 (04) :647-656
[3]   MECHANICAL DEVICES FOR ARTERIAL-OCCLUSION [J].
GIANTURCO, C ;
ANDERSON, JH ;
WALLACE, S .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1975, 124 (03) :428-435
[4]   TRANSCATHETER EMBOLIZATION OF RENAL CELL-CARCINOMA [J].
GOLDSTEIN, HM ;
MEDELLIN, H ;
TALALBEYDOUN, M ;
WALLACE, S ;
BENMENACHEM, Y ;
BRACKEN, RB ;
JOHNSON, DE .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1975, 123 (03) :557-562
[5]  
KANAMORI H, 1957, J ANTIBIOT, V10, P120
[6]  
KONNO T, 1984, CANCER, V54, P2367, DOI 10.1002/1097-0142(19841201)54:11<2367::AID-CNCR2820541111>3.0.CO
[7]  
2-F
[8]  
Konno T, 1983, EUR J CANC CHN ONCOL, V19, P1058
[9]   TAILOR-MAKING OF PROTEIN DRUGS BY POLYMER CONJUGATION FOR TUMOR TARGETING - A BRIEF REVIEW ON SMANCS [J].
MAEDA, H ;
MATSUMOTO, T ;
KONNO, T ;
IWAI, K ;
UEDA, M .
JOURNAL OF PROTEIN CHEMISTRY, 1984, 3 (02) :181-193
[10]  
MAEDA H, 1981, ANTICANCER RES, V1, P175