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Treatment of fluorouracil-refractory patients with liver metastases from colorectal cancer by using yttrium-90 resin microspheres plus concomitant systemic irinotecan chemotherapy.
van Hazel, Guy A; Pavlakis, Nick; Goldstein, David; Olver, Ian N; Tapner, Michael J; Price, David; Bower, Geoffrey D; Briggs, Gregory M; Rossleigh, Monica A; Taylor, D James; George, Jacob.
Afiliação
  • van Hazel GA; Perth Radiologic Clinic, Mount Medical Centre, Perth, Western Australia, Australia.
J Clin Oncol ; 27(25): 4089-95, 2009 Sep 01.
Article em En | MEDLINE | ID: mdl-19652069
ABSTRACT

PURPOSE:

Liver metastases are the principal cause of death in patients with advanced colorectal cancer (CRC). Irinotecan is a chemotherapeutic agent used in the treatment of CRC and has demonstrated synergistic potential when used with radiation. Radioembolization with yttrium-90 microspheres has demonstrated increased response and survival rates when given with fluorouracil chemotherapy. This study's goal was to evaluate the maximum-tolerated dose of concomitant irinotecan and radioembolization in fluorouracil-refractory patients with CRC hepatic metastases. PATIENTS AND

METHODS:

Twenty-five irinotecan-naive patients who had experienced relapse after previous chemotherapy were enrolled onto three dose-escalating groups. Irinotecan was administered at 50, 75, or 100 mg/m(2) on days 1 and 8 of a 3-week cycle for the first two cycles, and full irinotecan doses (ie, 100 mg/m(2)) were administered during cycles 3 to 9. Radioembolization was administered during the first chemotherapy cycle.

RESULTS:

Most patients experienced acute, self-limiting abdominal pain and nausea. Mild lethargy and anorexia were common. Grades 3 to 4 events were seen in three of six patients at 50 mg/m(2) (obstructive jaundice, thrombocytopenia, diarrhea), in five of 13 patients at 75 mg/m(2) (neutropenia, leukopenia, thrombocytopenia, elevated alkaline phosphatase, abdominal pain, ascites, fatigue) and in four of six patients at 100 mg/m(2) (diarrhea, deep vein thrombosis, constipation, leukopenia). Eleven (48%) of 23 patients had a partial response, and nine patients (39%) had stable disease. The median progression-free survival was 6.0 months; the median survival was 12.2 months.

CONCLUSION:

Concomitant use of radioembolization plus irinotecan did not reach a maximum-tolerated dose. The recommended dose of irinotecan in this setting is 100 mg/m(2) on days 1 and 8 of a 3-week cycle.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Isótopos de Ítrio / Braquiterapia / Camptotecina / Neoplasias Colorretais / Resistencia a Medicamentos Antineoplásicos / Compostos Radiofarmacêuticos / Inibidores Enzimáticos / Neoplasias Hepáticas Tipo de estudo: Clinical_trials Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Oceania Idioma: En Revista: J Clin Oncol Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Isótopos de Ítrio / Braquiterapia / Camptotecina / Neoplasias Colorretais / Resistencia a Medicamentos Antineoplásicos / Compostos Radiofarmacêuticos / Inibidores Enzimáticos / Neoplasias Hepáticas Tipo de estudo: Clinical_trials Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Oceania Idioma: En Revista: J Clin Oncol Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Austrália