TY - JOUR
T1 - Hepatic arterial floxuridine and leucovorin for unresectable liver metastases from colorectal carcinoma. New dose schedules and survival update
AU - Kemeny, Nancy
AU - Seiter, Karen
AU - Conti, John A.
AU - Cohen, Alfred
AU - Bertino, Joseph R.
AU - Sigurdson, Elin R.
AU - Botet, Jose
AU - Chapman, Douglass
AU - Mazumdar, Madhu
AU - Budd, Andrew J.
PY - 1994/2/15
Y1 - 1994/2/15
N2 - Background. We studied three new dose schedules of hepatic arterial infusion of floxuridine (FUDR) and leucovorin and update survival analysis of a previously reported trial using these drugs by hepatic arterial infusion for patients with hepatic metastases from colorectal carcinoma. Methods. Untreated patients with hepatic metastases from colorectal cancer were treated with three dose schedules: Group D, FUDR (0.3 mg/kg/day) and leucovorin (30 mg/m2day) as a 14‐day continuous infusion through an implantable hepatic arterial pump alternating with a 4‐week rest period; Group E, a lower dose of FUDR (0.25 mg/kg/day) and leucovorin (30 mg/m2day) as a 14‐day infusion alternating with 2 weeks of saline; and Group F, FUDR (0.3 mg/kg/day) with a lower leucovorin dose (15 mg/m2/day) for 2 weeks followed by a 2‐week rest. Results. In 42 patients with unresectable hepatic metastases, the complete‐plus‐partial response rate was 56%, with a median survival of 24.2 months. Complete‐plus‐partial response rates for groups D, E, and F were 30%, 54%, and 75%, respectively. Twelve percent of the 42 patients developed biliary sclerosis; the percentages of patients per group were 17%, 15%, and 6%, respectively. Updated median survival of the original 24 patients treated with FUDR and leucovorin by hepatic arterial infusion and these 42 new patients (66 total) was 28.8 months. One‐, two‐, three‐, four‐, and five‐year survival rates were 86%, 62%, 31%, 15%, and 7%, respectively. Conclusions. Hepatic arterial chemotherapy with FUDR and leucovorin for patients with hepatic metastases from colorectal carcinoma yields a high response rate and 1‐ and 2‐year survivals of 86% and 62%, respectively. Although a lower dose of leucovorin (15 mg/m2) with FUDR produces a high response rate with less toxicity, before larger scale trials are initiated, further investigation is needed to reduce toxicity. A study of hepatic arterial dexamethasone with FUDR and leucovorin has been initiated for this purpose. Cancer.
AB - Background. We studied three new dose schedules of hepatic arterial infusion of floxuridine (FUDR) and leucovorin and update survival analysis of a previously reported trial using these drugs by hepatic arterial infusion for patients with hepatic metastases from colorectal carcinoma. Methods. Untreated patients with hepatic metastases from colorectal cancer were treated with three dose schedules: Group D, FUDR (0.3 mg/kg/day) and leucovorin (30 mg/m2day) as a 14‐day continuous infusion through an implantable hepatic arterial pump alternating with a 4‐week rest period; Group E, a lower dose of FUDR (0.25 mg/kg/day) and leucovorin (30 mg/m2day) as a 14‐day infusion alternating with 2 weeks of saline; and Group F, FUDR (0.3 mg/kg/day) with a lower leucovorin dose (15 mg/m2/day) for 2 weeks followed by a 2‐week rest. Results. In 42 patients with unresectable hepatic metastases, the complete‐plus‐partial response rate was 56%, with a median survival of 24.2 months. Complete‐plus‐partial response rates for groups D, E, and F were 30%, 54%, and 75%, respectively. Twelve percent of the 42 patients developed biliary sclerosis; the percentages of patients per group were 17%, 15%, and 6%, respectively. Updated median survival of the original 24 patients treated with FUDR and leucovorin by hepatic arterial infusion and these 42 new patients (66 total) was 28.8 months. One‐, two‐, three‐, four‐, and five‐year survival rates were 86%, 62%, 31%, 15%, and 7%, respectively. Conclusions. Hepatic arterial chemotherapy with FUDR and leucovorin for patients with hepatic metastases from colorectal carcinoma yields a high response rate and 1‐ and 2‐year survivals of 86% and 62%, respectively. Although a lower dose of leucovorin (15 mg/m2) with FUDR produces a high response rate with less toxicity, before larger scale trials are initiated, further investigation is needed to reduce toxicity. A study of hepatic arterial dexamethasone with FUDR and leucovorin has been initiated for this purpose. Cancer.
KW - Adult
KW - Aged
KW - Antineoplastic Combined Chemotherapy Protocols/administration & dosage
KW - Carcinoma/drug therapy
KW - Colorectal Neoplasms/pathology
KW - Drug Administration Schedule
KW - Female
KW - Floxuridine/administration & dosage
KW - Hepatic Artery
KW - Humans
KW - Infusion Pumps, Implantable
KW - Infusions, Intra-Arterial
KW - Leucovorin/administration & dosage
KW - Liver Neoplasms/drug therapy
KW - Male
KW - Middle Aged
KW - Survival Analysis
UR - http://www.scopus.com/inward/record.url?scp=0027972450&partnerID=8YFLogxK
U2 - 10.1002/1097-0142(19940215)73:4<1134::AID-CNCR2820730403>3.0.CO;2-V
DO - 10.1002/1097-0142(19940215)73:4<1134::AID-CNCR2820730403>3.0.CO;2-V
M3 - Article
C2 - 8313315
AN - SCOPUS:0027972450
SN - 0008-543X
VL - 73
SP - 1134
EP - 1142
JO - Cancer
JF - Cancer
IS - 4
ER -