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恶性嗜铬细胞瘤:环磷酰胺、长春新碱和达卡巴嗪联合治疗有效

Malignant pheochromocytoma: effective treatment with a combination of cyclophosphamide, vincristine, and dacarbazine.

作者信息

Averbuch S D, Steakley C S, Young R C, Gelmann E P, Goldstein D S, Stull R, Keiser H R

机构信息

National Cancer Institute, Uniformed Services, University of the Health Sciences, Bethesda, Maryland.

出版信息

Ann Intern Med. 1988 Aug 15;109(4):267-73. doi: 10.7326/0003-4819-109-4-267.

Abstract

STUDY OBJECTIVE

To determine the efficacy and toxicity of combination chemotherapy in patients with advanced, malignant pheochromocytoma.

DESIGN

Nonrandomized, single-arm trial.

SETTING

Governmental medical referral center.

PATIENTS

Fourteen patients with malignant pheochromocytoma confirmed by histologic tests. All patients had metastatic disease and elevated urinary catecholamine secretion.

INTERVENTIONS

After optimization of antihypertensive therapy, patients received cyclophosphamide, 750 mg/m2 body surface area on day 1; vincristine, 1.4 mg/m2 on day 1, and dacarbazine, 600 mg/m2 on days 1 and 2, every 21 days.

MEASUREMENTS AND MAIN RESULTS

Combination chemotherapy with cyclophosphamide, vincristine, and dacarbazine produced a complete and partial response rate of 57% (median duration, 21 months; range, 7 to more than 34). Complete and partial biochemical responses were seen in 79% of patients (median duration, more than 22 months; range, 6 to more than 35). All responding patients had objective improvement in performance status and blood pressure. Toxicity included expected hematologic, neurologic, and gastrointestinal effects of chemotherapy without serious sequelae. There were four minor hypotensive episodes and one minor hypertensive episode.

CONCLUSIONS

Combination chemotherapy with cyclophosphamide, vincristine, and dacarbazine is effective for advanced malignant pheochromocytoma. Urinary catecholamines are useful to ascertain biochemical response to therapy.

摘要

研究目的

确定联合化疗对晚期恶性嗜铬细胞瘤患者的疗效和毒性。

设计

非随机单臂试验。

地点

政府医疗转诊中心。

患者

14例经组织学检查确诊为恶性嗜铬细胞瘤的患者。所有患者均有转移性疾病且尿儿茶酚胺分泌升高。

干预措施

在优化抗高血压治疗后,患者接受环磷酰胺,第1天剂量为750mg/m²体表面积;长春新碱,第1天剂量为1.4mg/m²;达卡巴嗪分别于第1天和第2天给予600mg/m²,每21天重复一次。

测量指标及主要结果

环磷酰胺、长春新碱和达卡巴嗪联合化疗的完全缓解率和部分缓解率为57%(中位持续时间21个月;范围7至超过34个月)。79%的患者出现完全和部分生化缓解(中位持续时间超过22个月;范围6至超过35个月)。所有有反应的患者在身体状况和血压方面都有客观改善。毒性包括化疗预期的血液学、神经学和胃肠道影响,但无严重后遗症。有4次轻度低血压发作和1次轻度高血压发作。

结论

环磷酰胺、长春新碱和达卡巴嗪联合化疗对晚期恶性嗜铬细胞瘤有效。尿儿茶酚胺有助于确定对治疗的生化反应。

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