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DOI 10.1210/jc.2013-2281

Медицинская библиотека · The Journal of clinical endocrinology and metabolism · 2013

Comparison of two mitotane starting dose regimens in patients with advanced adrenocortical carcinoma.

Kerkhofs T M, Baudin E, Terzolo M, Allolio B, Chadarevian R, Mueller H H, Skogseid B, Leboulleux S, Mantero F, Haak H R, Fassnacht M

Клиническое исследованиеСравнительное исследованиеСтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

CONTEXT: Mitotane is the only approved drug for treatment of adrenocortical carcinoma. Its pharmacokinetic properties are not fully elucidated and different dosing regimens have never been compared head to head.

OBJECTIVE

The objective of the study was to investigate the relationship between mitotane dose and plasma concentration comparing two dosing regimens.

DESIGN/

SETTING

This was a prospective, open-label, multicenter trial of a predefined duration of 12 weeks.

PATIENTS/INTERVENTIONS: Forty mitotane-naïve patients with metastatic adrenocortical carcinoma were assigned to a predefined low- or high-dose regimen by the local investigator. Thirty-two patients could be evaluated in detail.

MAIN OUTCOME MEASURE: The difference in median mitotane plasma levels between both treatment groups was measured.

RESULTS

Despite a difference in mean cumulative dose (440 ± 142 g vs 272 ± 121 g), median maximum plasma levels were not significantly different between the two groups [high dose 14.3 mg/L (range 6.3-29.7, n = 20) vs 11.3 mg/L (range 5.5-20.0, n = 12), P = .235]. Ten of 20 patients on the high-dose regimen reached plasma concentrations of 14 mg/L or greater after 46 days (range 18-81 d) compared with 4 of 12 patients on the low-dose regimen after 55 days (range 46-74 d, P = .286). All patients who reached 14 mg/L at 12 weeks displayed a level of 4.1 mg/L or greater on day 33 (100% sensitivity). There were no significant differences in frequency and severity of adverse events. Among patients not receiving concomitant chemotherapy mitotane exposure was higher in the high-dose group: 1013 ± 494 mg/L · d vs 555 ± 168 mg/L · d (P = .080).

CONCLUSIONS

The high-dose starting regimen resulted in neither significantly different mitotane levels nor a different rate of adverse events, but concomitant chemotherapy influenced these results. Thus, for mitotane monotherapy the high-dose approach is favorable, whereas for combination therapy a lower dose seems reasonable.

Для цитирования: Kerkhofs T M, Baudin E, Terzolo M, Allolio B, Chadarevian R, Mueller H H, Skogseid B, Leboulleux S, Mantero F, Haak H R, Fassnacht M. Comparison of two mitotane starting dose regimens in patients with advanced adrenocortical carcinoma.. The Journal of clinical endocrinology and metabolism. 2013. DOI: 10.1210/jc.2013-2281.

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