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ESHAP salvage therapy for relapsed or refractory non-Hodgkin's lymphoma.

机译:ESHAP挽救疗法用于复发性或难治性非霍奇金淋巴瘤。

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摘要

The ESHAP regimen, a combination of the chemotherapeutic drugs etoposide, methylprednisolone (solumedrol), high-dose cytarabine (ara-C), and cisplatin, has been shown to be active against refractory or relapsed non-Hodgkin's lymphoma (NHL) in therapeutic trials. We undertook this study to determine whether this regimen would be effective and tolerable in Korean patients. A total of 40 patients with refractory or relapsed NHL (8 indolent and 32 aggressive) were enrolled in this study. The overall response rate was 70% (95% confidence interval; 59.8-89.7%); 22.5% of patients achieved a complete response and 47.5% a partial response. The median survival duration was 12 months (95% confidence interval; 5.9-18.1 months) and the median duration of progression-free survival was 9 months (95% confidence interval; 1.1-16.9 months). The median survival duration of patients with relapsed NHL was longer than that of patients with refractory lymphoma (15 months vs 4 months, p=0.02). Myelosuppression was the most frequent complication and treatment-related mortality was noted in two patients. These results suggest that the ESHAP regimen is effective in patients with relapsed NHL who have a sensitive disease. The role of ESHAP chemotherapy in discriminating patients who are more likely to benefit from a subsequent transplant should be evaluated in the future.
机译:ESHAP方案是化疗药物依托泊苷,甲基泼尼松龙(solumedrol),大剂量阿糖胞苷(ara-C)和顺铂的组合,在治疗试验中已证明对难治性或复发性非霍奇金淋巴瘤(NHL)具有活性。我们进行了这项研究,以确定该方案对韩国患者是否有效和可耐受。本研究共纳入40例顽固性或复发性NHL患者(8例惰性和32例侵袭性)。总体回应率为70%(95%置信区间; 59.8-89.7%); 22.5%的患者完全缓解,部分缓解47.5%。中位生存期为12个月(95%置信区间; 5.9-18.1个月),无进展生存期中位数为9个月(95%置信区间; 1.1-16.9个月)。 NHL复发患者的中位生存期比难治性淋巴瘤患者的中位生存期长(15个月对4个月,p = 0.02)。骨髓抑制是最常见的并发症,在两名患者中发现与治疗相关的死亡率。这些结果表明,ESHAP方案对患有敏感疾病的复发性NHL患者有效。将来应评估ESHAP化疗在区分更可能受益于后续移植的患者中的作用。

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