Epirubicin-lipiodol chemotherapy versus131iodine-lipiodol radiotherapy in the treatment of unresectable hepatocellular carcinoma
- 1 December 1995
- Vol. 76 (11), 2202-2210
- https://doi.org/10.1002/1097-0142(19951201)76:11<2202::aid-cncr2820761105>3.0.co;2-8
Abstract
Background. Arterially administered iodized oil (Lipiodol) is selectively retained by hepatocellular carcinomas (HCCs), and has been used as a vehicle for delivery of therapeutic agents to these tumors. This study compared the efficacy of Lipiodol‐targeted epirubicin chemotherapy with Lipiodol‐131I radiotherapy. Methods. Ninety‐five patients with unresectable HCC confined to the liver were administered either Lipiodol‐epirubicin emulsion (n=69; 61 cirrhotics; Okuda tumor Stage I, 14; II, 37; III, 18; epirubicin dose, 75 mg/m2) or Lipiodol‐131I (131I) (n=26; 18 cirrhotics; Okuda tumor Stage I, 6; II, 19; III, 1; dose 750–1050 MBq). The last 28 patients (17 epirubicin, 11131I) were treated within a prospective randomized trial. Bolus drug or isotope was injected into the hepatic artery by transfemoral cannulation. Lipiodol and 131I uptake were gauged by 10th day computed tomography and 48‐hour scintiscan. Treatments were repeated two‐monthly when indicated. Results. Tumor size at 2 months remained static or diminished partially in 21 of 38 epirubicin recipients (55%) and 15/22 131I recipients (68%). Actuarial survival at 6, 12, and 24 months was 40%, 25%, and 6% with epirubicin, and 58%, 25%, and 0% with 131I; 30‐day mortality was 11% and 15%, respectively. Comparison with historic controls indicated survival benefit in Stages I and II. Similar findings were recorded in the 28 patients in the randomized trial. Conclusions. Patients with unresectable HCC receiving Lipiodol‐epirubicin or Lipiodol‐131I show good tumor localization, acceptable toxicity, and comparable survival benefit at 6 and 12 months with either modality. Cancer 1995; 76:2202–10.Keywords
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