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腔内长春新碱作为经典型卡波西肉瘤结节性病变的一线治疗:151 例患者的前瞻性研究。

Intralesional vincristine as first-line therapy for nodular lesions in classic Kaposi sarcoma: a prospective study in 151 patients.

机构信息

Department of Anesthesia, Intensive Care and Dermatologic Sciences, Università degli Studi di Milano, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, 20122 Milan, Italy.

出版信息

Br J Dermatol. 2010 Apr;162(4):854-9. doi: 10.1111/j.1365-2133.2009.09601.x. Epub 2009 Nov 25.

Abstract

BACKGROUND

Classic Kaposi sarcoma is a rare angioproliferative neoplasm with varying biological behaviour. Depending on the clinical stage, local or systemic therapy can be used. Vincristine has proven to be effective as systemic chemotherapy and in very few reports as intralesional treatment.

OBJECTIVES

Our aim was to determine the efficacy and safety of intralesional vincristine in the treatment of classic Kaposi sarcoma nodular lesions.

METHODS

We conducted a prospective, open-label, single-centre clinical trial in 151 patients with stage IB classic Kaposi sarcoma. Vincristine was injected in a single nodule (0.3-0.8 mm) on the lower limb. Another similar lesion on the same limb, at a distance of >or= 10 cm, or on the contralateral limb, was kept under clinical observation as control. Adverse effects were evaluated after 1 week, and efficacy after 4 and 12 weeks.

RESULTS

One hundred and fifty-one patients were enrolled. At final evaluation, 115 patients presented complete response (76.1%), 28 had partial response (18.5%), six had improvement (4%), one had stable disease (0.7%) and only one patient had tumour progression (0.7%). Therefore the total response rate was 98.7% (149 patients). Therapy was generally well tolerated. The most frequently registered adverse events, observed in 21 patients (13.9%), were erythema and itching.

CONCLUSIONS

Intralesional vincristine is an effective and safe treatment for nodular lesions in classic Kaposi sarcoma and can be recommended as first-line therapy in initial stages and as support therapy in advanced stages.

摘要

背景

经典型卡波西肉瘤是一种罕见的血管增生性肿瘤,具有不同的生物学行为。根据临床分期,可以采用局部或全身治疗。长春新碱已被证明在全身化疗中有效,并且在极少数报告中作为腔内治疗有效。

目的

我们旨在确定腔内长春新碱治疗经典型卡波西肉瘤结节性病变的疗效和安全性。

方法

我们在 151 例 IB 期经典型卡波西肉瘤患者中进行了一项前瞻性、开放标签、单中心临床试验。长春新碱在下肢的单个结节(0.3-0.8 毫米)中注射。同一肢体上距离>或= 10 厘米的另一个类似病变,或对侧肢体上的类似病变作为对照进行临床观察。在第 1 周评估不良反应,在第 4 和 12 周评估疗效。

结果

共纳入 151 例患者。最终评估时,115 例患者完全缓解(76.1%),28 例部分缓解(18.5%),6 例有改善(4%),1 例疾病稳定(0.7%),仅 1 例肿瘤进展(0.7%)。因此,总缓解率为 98.7%(149 例)。治疗通常耐受性良好。21 例(13.9%)患者最常出现的不良反应为红斑和瘙痒。

结论

腔内长春新碱是治疗经典型卡波西肉瘤结节性病变的有效且安全的方法,可推荐作为初始阶段的一线治疗方法,并作为晚期阶段的支持治疗方法。

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