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[借助长春新碱、阿霉素、地塞米松联合化疗(VAD)或仅用地塞米松对晚期多发性骨髓瘤治疗结果的比较评估]

[Comparative evaluation of treatment results in advanced multiple myeloma with the help of polychemotherapy with vincristine, doxorubicin, dexamethasone (VAD) or only with dexamethasone].

作者信息

Hansz J, Włodarczyk M, Psuja P

机构信息

Kliniki Hematologii Instytutu Chorób Wewnetrznych A.M., Poznaniu.

出版信息

Acta Haematol Pol. 1992;23(4):277-84.

PMID:1293910
Abstract

A prospective clinical trial was undertaken to determine the therapeutical effectiveness of multidrug chemotherapy consisting of vincristine, doxorubicin and dexamethasone (VAD) or only high dose of dexamethasone (D) in 56 patients with multiple myeloma (MM). The group of patients included 41 with intermediate (II) and 15 with high (III) tumor mass. The final evaluation was performed in 19 patients treated with D and in 19 receiving VAD regimen. Improvement was defined by at least 50% reduction of serum myeloma protein concentration or disappearance of light chain proteinuria. The VAD regimen was more effective giving improvement in 90% of patients with no prior therapy and in 44% of patients with reflectory myeloma. In this respect, cytoreduction of the same magnitude was noted both in stages II and III. Higher therapeutical effect of VAD regimen was observed independently of the immunological type of MM. The treatment with D has given the improvement in 56% of patients with no previous therapy. Our results support the usefulness of VAD regimen in MM-patients with no prior therapy and with refractory myeloma. High frequency of therapy-related complications, however, indicates that VAD treatment should rather be reserved for the patients with resistant MM.

摘要

进行了一项前瞻性临床试验,以确定由长春新碱、阿霉素和地塞米松(VAD)组成的多药化疗或仅高剂量地塞米松(D)对56例多发性骨髓瘤(MM)患者的治疗效果。患者组包括41例中度(II期)和15例高度(III期)肿瘤肿块患者。对19例接受D治疗的患者和19例接受VAD方案治疗的患者进行了最终评估。改善的定义为血清骨髓瘤蛋白浓度至少降低50%或轻链蛋白尿消失。VAD方案更有效,在90%的未接受过治疗的患者和44%的难治性骨髓瘤患者中产生了改善。在这方面,II期和III期患者的细胞减少程度相同。观察到VAD方案具有更高的治疗效果,与MM的免疫类型无关。D治疗使56%的未接受过治疗的患者得到改善。我们的结果支持VAD方案对未接受过治疗和难治性骨髓瘤的MM患者有用。然而,治疗相关并发症的高发生率表明,VAD治疗应优先用于耐药MM患者。

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