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Enhanced Efficacy of Radioimmunotherapy Combined with Systemic Chemotherapy and Local Hyperthermia in Xenograft Model

We previously found that the efficacy of radioimmunotherapy (RIT) with (131)I‐A7, an IgG(1) against M(r) 45000 glycoprotein on colon cancer, was enhanced by local hyperthermia (HT) or chemotherapy with 5‐fluorouracil (5‐FU). In this study, we aimed to further enhance its efficacy by combining these...

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Detalles Bibliográficos
Autores principales: Kinuya, Seigo, Yokoyama, Kunihiko, Konishi, Shota, Hiramatsu, Takashi, Watanabe, Naoto, Shuke, Noriyuki, Aburano, Tamio, Takayama, Teruhiko, Michigishi, Takatoshi, Tonami, Norihisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926375/
https://www.ncbi.nlm.nih.gov/pubmed/10835504
http://dx.doi.org/10.1111/j.1349-7006.2000.tb00983.x
Descripción
Sumario:We previously found that the efficacy of radioimmunotherapy (RIT) with (131)I‐A7, an IgG(1) against M(r) 45000 glycoprotein on colon cancer, was enhanced by local hyperthermia (HT) or chemotherapy with 5‐fluorouracil (5‐FU). In this study, we aimed to further enhance its efficacy by combining these three modalities. Human colon cancer xenografts (146±12 mm(3)) in Balb/c nu/nu female mice were treated with 9.25 MBq (131)I‐A7 i.v. combined with HT (43°C for 1 h) and 5‐FU (30 mg/kg/day i.p. for 5 days). Tumor growth delay, (Tq(treated)‐Tq(control))/Tq(control) where Tq is tumor quadrupling time, in mice treated with RIT+HT+5‐FU was improved to 12.7 from 5.90, 7.55 and 10.1 with RIT alone, RIT+5‐FU and RIT+HT, respectively. Complete response was observed in 4 out of 8 tumors with RIT+HT+5‐FU and 3 out of 10 with RIT+HT. No tumor showed complete response with RIT+5‐FU or RIT alone. 5‐FU slightly increased myelotoxicity of RIT, but HT did not affect it. Body weight loss was not enhanced by the combination. These results indicate that the combination of three modalities is a feasible approach to enhance the antitumor efficacy of RIT without serious increase of toxicity.