A phase II trial of combination chemotherapy and surgical resection for the treatment of metastatic adrenocortical carcinoma - Continuous infusion doxorubicin, vincristine, and etoposide with daily mitotane as a p-glycoprotein antagonist

被引:74
作者
Abraham, J
Bakke, S
Rutt, A
Meadows, B
Merino, M
Alexander, R
Schrump, D
Bartlett, D
Choyke, P
Robey, R
Hung, E
Steinberg, SM
Bates, S
Fojo, T
机构
[1] NCI, Med Branch, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[2] NCI, Surg Pathol Branch, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[3] NCI, Surg Branch, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[4] NIH, Dept Radiol, Ctr Clin, Bethesda, MD 20892 USA
[5] NCI, Biostat & Data Management Sect, NIH, Bethesda, MD 20892 USA
关键词
combination chemotherapy; drug resistance reversal; adrenocortical carcinoma (ACC); P-glycoprotein (Pgp); mitotane; doxorubicin; etoposide; vincristine;
D O I
10.1002/cncr.10487
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Adrenocortical carcinoma (ACC) is rare, nearly always fatal, and to the authors' knowledge has few nonsurgical treatment options, Based on in vitro studies demonstrating the efficacy of mitotane as a P-glycoprotein (Pgp) antagonist, and expression of high levels of Pgp in ACC, the authors conducted a study of infusional doxorubicin, vincristine, and etoposide with oral mitotane +/- surgical resection in patients with metastatic ACC. METHODS. Thirty-six patients with metastatic ACC received daily oral mitotane (mean, 4.6 g/day) and 96-hour infusional doxorubicin (10 mg/m(2)/day), etoposide (75 mg/m(2)/day), and vincristine (0.4 mg/m(2)/day). Four responding patients (11%) underwent surgery. RESULTS. Thirty-five patients were evaluable; all had metastatic disease. Eleven patients had not undergone resection of the primary tumor. Approximately 53% of patients had functional tumors. A total of 190 cycles were administered to 36 patients. Responses were observed in 8 patients (22%): 1 complete, 4 partial, and 3 minor responses. The mean duration of response was 12.4 months. Using a landmark method, the median survival of patients who did not respond to chemotherapy was 11.6 months from a point 4 months after the initiation of therapy, whereas that of 8 patients who demonstrated a response to chemotherapy was 34.3 months from that same landmark. High levels of Pgp expression were documented in nine of nine tumors. Mitotane levels > 10 mug/mL, previously shown to antagonize Pgp in vitro, were achieved in 25 of 36 patients (69%). However, rhodamine efflux from CD56-positive cells was not impaired, suggesting poor in vivo Pgp inhibition. The predominant Grade 3/4 toxicity (according to the Common Toxicity Criteria of the National Cancer Institute) was neutropenia. in 66% of cycles; however, fever occurred in only 3% of cycles. Daily mitotane was associated with Grade 1/2 nausea, diarrhea, fatigue, and neuropsychiatric changes in 31 of 36 patients (86%). CONCLUSIONS. Using a combination regimen of daily mitotane with infusional doxorubicin, vincristine, and etoposide in patients with metastatic ACC, responses were observed in 22% of patients. The superiority of this combination over single-agent mitotane is uncertain. The side effects of mitotane made treatment difficult. More effective Pgp antagonists are needed. (C) 2002 American Cancer Society.
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收藏
页码:2333 / 2343
页数:11
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