TY - JOUR
T1 - Experimental chemotherapy for xenograft cell lines of human bile duct and gall bladder cancers in nude mice
AU - Tsubono, Michihiko
AU - Nio, Yoshinori
AU - Tseng, Chen‐Chiu ‐C
AU - Kawabata, Kazuya
AU - Masai, Yoshikazu
AU - Hayashi, Hitoshi
AU - Fukumoto, Manabu
AU - Tobe, Takayoshi
PY - 1992/12
Y1 - 1992/12
N2 - Most biliary tract cancers are advanced and inoperable when first diagnosed. Even if surgery can be performed, the postsurgical prognosis of these diseases is poor. In the present study, we investigated effective chemotherapies for a human bile duct cancer xenograft cell line (undifferentiated carcinoma, BDC‐SN) and a gall bladder cancer xenograft cell line (well‐differentiated adenocarcinoma, GBC‐GN), which were transplanted into nude mice. Eight anticancer agents (CDDP, 5‐FU, VDS, MMC, ADR, EPIR, CQ, and VP‐16) and their various combinations were evaluated at 2–4 times the clinical dose. When used singly, CDDP, 5‐FU, and VDS were effective against BDC‐SN, and only CDDP was effective against GBC‐GN. Among the various 2‐agent combinations, CDDP + 5‐FU was the most effective against both BDC‐SN and GBC‐GN. However, 3‐agent combinations consisting of CDDP + 5‐FU + another agent were less effective than the CDDP + 5‐FU double regimen and caused significant loss of weight as well as high mortality. These results suggest that CDDP + 5‐FU may be the most useful regimen against biliary tract cancers in clinical application. © 1992 Wiley‐Liss, Inc.
AB - Most biliary tract cancers are advanced and inoperable when first diagnosed. Even if surgery can be performed, the postsurgical prognosis of these diseases is poor. In the present study, we investigated effective chemotherapies for a human bile duct cancer xenograft cell line (undifferentiated carcinoma, BDC‐SN) and a gall bladder cancer xenograft cell line (well‐differentiated adenocarcinoma, GBC‐GN), which were transplanted into nude mice. Eight anticancer agents (CDDP, 5‐FU, VDS, MMC, ADR, EPIR, CQ, and VP‐16) and their various combinations were evaluated at 2–4 times the clinical dose. When used singly, CDDP, 5‐FU, and VDS were effective against BDC‐SN, and only CDDP was effective against GBC‐GN. Among the various 2‐agent combinations, CDDP + 5‐FU was the most effective against both BDC‐SN and GBC‐GN. However, 3‐agent combinations consisting of CDDP + 5‐FU + another agent were less effective than the CDDP + 5‐FU double regimen and caused significant loss of weight as well as high mortality. These results suggest that CDDP + 5‐FU may be the most useful regimen against biliary tract cancers in clinical application. © 1992 Wiley‐Liss, Inc.
KW - 5‐fluorouracil
KW - Cisplatin
KW - bile duct cancer
KW - chemotherapy
KW - gall bladder cancer
KW - nude mouse
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U2 - 10.1002/jso.2930510415
DO - 10.1002/jso.2930510415
M3 - Article
C2 - 1434661
AN - SCOPUS:0026447740
SN - 0022-4790
VL - 51
SP - 274
EP - 280
JO - Journal of Surgical Oncology
JF - Journal of Surgical Oncology
IS - 4
ER -