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转移性肾上腺皮质癌联合化疗与手术切除的II期试验:持续输注阿霉素、长春新碱和依托泊苷,每日服用米托坦作为P-糖蛋白拮抗剂。

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.

作者信息

Abraham Jame, Bakke Susan, Rutt Ann, Meadows Beverly, Merino Maria, Alexander Richard, Schrump David, Bartlett David, Choyke Peter, Robey Rob, Hung Elizabeth, Steinberg Seth M, Bates Susan, Fojo Tito

机构信息

Medicine Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Cancer. 2002 May 1;94(9):2333-43. doi: 10.1002/cncr.10487.

Abstract

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 microg/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.

摘要

背景

肾上腺皮质癌(ACC)较为罕见,几乎总是致命的,据作者所知,其非手术治疗选择很少。基于体外研究显示米托坦作为P-糖蛋白(Pgp)拮抗剂的疗效,以及ACC中高水平Pgp的表达,作者开展了一项针对转移性ACC患者的研究,采用静脉输注阿霉素、长春新碱和依托泊苷联合口服米托坦,±手术切除。

方法

36例转移性ACC患者接受每日口服米托坦(平均4.6g/天)以及96小时静脉输注阿霉素(10mg/m²/天)、依托泊苷(75mg/m²/天)和长春新碱(0.4mg/m²/天)。4例有反应的患者(11%)接受了手术。

结果

35例患者可评估;均有转移性疾病。11例患者未切除原发肿瘤。约53%的患者有功能性肿瘤。共对36例患者进行了190个周期的治疗。8例患者(22%)出现反应:1例完全缓解,4例部分缓解,3例轻微缓解。平均反应持续时间为12.4个月。采用标志性方法,对化疗无反应的患者从治疗开始后4个月起的中位生存期为11.6个月,而8例对化疗有反应的患者从同一标志性时间起的中位生存期为34.3个月。9个肿瘤中有9个检测到高水平的Pgp表达。36例患者中有25例(69%)米托坦水平>10μg/mL,此前体外研究表明该水平可拮抗Pgp。然而,CD56阳性细胞的罗丹明外流未受损害,提示体内Pgp抑制效果不佳。主要的3/4级毒性(根据美国国立癌症研究所通用毒性标准)在66%的周期中为中性粒细胞减少;然而,发热仅出现在3%的周期中。36例患者中有31例(86%)每日服用米托坦出现1/2级恶心、腹泻、疲劳和神经精神变化。

结论

在转移性ACC患者中使用每日米托坦联合静脉输注阿霉素、长春新碱和依托泊苷的联合方案,22%的患者出现反应。该联合方案相对于单药米托坦的优越性尚不确定。米托坦的副作用使治疗困难。需要更有效的Pgp拮抗剂。

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