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1.
Int J Hyperthermia ; 34(5): 545-550, 2018 08.
Artículo en Inglés | MEDLINE | ID: mdl-28893108

RESUMEN

OBJECTIVES: The choice of an optimal administration route for intraperitoneal (IP) chemotherapy and a suitable chemotherapeutic regime in the treatment of ovarian cancer remains a controversy. We investigated survival outcomes according to catheter intraperitoneal chemotherapy (CIPC), normothermic and hyperthermic chemoperfusion (NIPEC and HIPEC) with cytostatic drugs dioxadet and cisplatin in rats with transplantable ascitic ovarian cancer. METHODS: Ascitic liquid containing 1 × 107 tumour cells was inoculated to female Wistar rats and 48 hours after rats received dioxadet and cisplatin at the maximum tolerated doses. Dioxadet at doses 1.5, 30 and 15 mg/kg and cisplatin at doses 4, 40 and 20 mg/kg body weight were administered for CIPC, NIPEC and HIPEC, respectively. Rats in the control groups received physiological saline and CIPC with physiological saline was regarded as the untreated control. The antitumor activity of the drugs was evaluated as an increase in average life expectancy (ALE). Analysis of the data was based primarily on Bayesian statistics and included Kaplan-Meier method, log-rank test and hazard ratio (HR) estimation. RESULTS: Compared to the untreated control CIPC, NIPEC and HIPEC with dioxadet significantly increased ALE by 101316, 61524 and 1.71735 days, whereas with cisplatin by 61013, 122437 and -13523 days, respectively. CONCLUSIONS: Dioxadet and cisplatin show similar efficacy in the CIPC route. Compared with CIPC IP chemotherapy by chemoperfusions is more effective for both the drugs. Dioxadet in HIPEC showed highest survival benefit whereas largest effect during NIPEC is achieved with cisplatin.


Asunto(s)
Ascitis/tratamiento farmacológico , Infusiones Parenterales/métodos , Neoplasias Ováricas/tratamiento farmacológico , Animales , Ascitis/patología , Quimioterapia del Cáncer por Perfusión Regional/métodos , Modelos Animales de Enfermedad , Femenino , Humanos , Hipertermia Inducida , Neoplasias Ováricas/mortalidad , Neoplasias Ováricas/patología , Ratas , Ratas Wistar , Análisis de Supervivencia
2.
J Surg Oncol ; 113(4): 438-42, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26710749

RESUMEN

BACKGROUND AND OBJECTIVES: Hyperthermic Intraperitoneal Chemotherapy (HIPEC) at the time of Cytoreductive Surgery (CRS) is an actively researched treatment in patients with advanced ovarian cancer. Relative contribution of heat and chemotherapeutic agents during HIPEC as well as efficacy of a new agent dioxadet for regional chemotherapy in a rat model of ovarian cancer was studied. METHODS: Sixty rats were divided into three groups: no treatment control group (n = 19), hyperthermia without chemotherapy (HIPEP) (n = 14), HIPEC + cisplatin (n = 14), HIPEC + dioxadet (n = 13). The intra-abdominal tumor was not resected. End points were: median survival (primary), cause of death (secondary). RESULTS: The median survival of the animals in the control group, HIPEP group, HIPEC + cisplatin, HIPEC + dioxadet were 9 (CI; 8-23), 22.5 (CI; 12-43), 25.5 (CI; 13-62), 49 (Cl; 28-70) days, respectively. The P-values control versus HIPEP, HIPEC + cisplatin versus HIPEC + dioxadet were 0.006, 0.002, and 0.001, respectively. CONCLUSION: During HIPEC both the heat and the cytotoxic drug had antitumor effects in a rat ovarian cancer model. Dioxadet showed potential as a drug for regional chemotherapy. J. Surg. Oncol. 2016;113:438-442. © 2015 Wiley Periodicals, Inc.


Asunto(s)
Antineoplásicos Alquilantes/administración & dosificación , Hipertermia Inducida/métodos , Neoplasias Ováricas/terapia , Triazinas/administración & dosificación , Animales , Quimioterapia del Cáncer por Perfusión Regional/métodos , Cisplatino/administración & dosificación , Terapia Combinada , Modelos Animales de Enfermedad , Femenino , Infusiones Parenterales , Neoplasias Ováricas/tratamiento farmacológico , Distribución Aleatoria , Ratas
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