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阿霉素与α-2b干扰素治疗晚期非髓样甲状腺癌的II期试验。

A phase II trial of doxorubicin and interferon alpha 2b in advanced, non-medullary thyroid cancer.

作者信息

Argiris Athanassios, Agarwala Sanjiv S, Karamouzis Michalis V, Burmeister Lynn A, Carty Sally E

机构信息

Division of Hematology-Oncology, Department of Medicine, University of Pittsburgh, UPMC Cancer Pavilion, 5th Floor, Pittsburgh, PA 15232, USA.

出版信息

Invest New Drugs. 2008 Apr;26(2):183-8. doi: 10.1007/s10637-007-9091-2. Epub 2007 Oct 2.

Abstract

BACKGROUND

The combination of doxorubicin and interferon alpha is supported by preclinical data. We sought to evaluate the efficacy of this combination in patients with advanced thyroid cancer.

PATIENTS AND METHODS

Patients with locally recurrent or metastatic, radioiodine- refractory thyroid cancer, excluding medullary carcinoma, were treated with interferon alpha-2b 12 million units/m2 subcutaneously on days 1-5 and doxorubicin 40 mg/m2 intravenously, on day 3, every 28 days.

RESULTS

17 patients, 15 with well differentiated and 2 with anaplastic thyroid carcinoma, were enrolled; median age was 69 years. Three patients had received radiation plus low dose doxorubicin previously. In 16 patients assessable for response, 1 patient (6%), who had follicular carcinoma, achieved a partial response and 10 patients (62.5%) stable disease as best response. Median time to progression was 5.9 months and median overall survival 26.4 months. In 14 evaluable patients, 5 (36%) had a thyroglobulin response (30% or more reduction in serum levels). Grade 3/4 neutropenia occurred in 76% of patients and neutropenic fever in 24%. Other grade 3/4 adverse events included fatigue (41%), rigors (18%), fever (6%), nausea/vomiting (29%), anorexia (29%), stomatitis (24%), vision disturbances (18%), neuropathy (18%), and hyponatremia (6%). One patient developed heart failure.

CONCLUSIONS

Doxorubicin and interferon alpha was associated with considerable toxicities but modest antitumor activity in patients with advanced, non-medullary thyroid cancer.

摘要

背景

阿霉素与α干扰素联合使用有临床前数据支持。我们试图评估这种联合用药对晚期甲状腺癌患者的疗效。

患者与方法

局部复发或转移性、放射性碘难治性甲状腺癌患者(不包括髓样癌),于第1 - 5天皮下注射α - 2b干扰素1200万单位/平方米,第3天静脉注射阿霉素40毫克/平方米,每28天重复一次。

结果

共纳入17例患者,其中15例为高分化甲状腺癌,2例为未分化甲状腺癌;中位年龄69岁。3例患者先前接受过放疗加小剂量阿霉素治疗。在16例可评估疗效的患者中,1例滤泡状癌患者(6%)获得部分缓解,10例患者(62.5%)最佳疗效为病情稳定。中位疾病进展时间为5.9个月,中位总生存期为26.4个月。在14例可评估的患者中,5例(36%)甲状腺球蛋白水平有反应(血清水平降低30%或更多)。76%的患者出现3/4级中性粒细胞减少,24%的患者出现中性粒细胞减少性发热。其他3/4级不良事件包括疲劳(41%)、寒战(18%)、发热(6%)、恶心/呕吐(29%)、厌食(29%)、口腔炎(24%)、视力障碍(18%)、神经病变(18%)和低钠血症(6%)。1例患者发生心力衰竭。

结论

阿霉素与α干扰素联合使用对晚期非髓样甲状腺癌患者毒性较大,但抗肿瘤活性一般。

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