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复发性淋巴瘤挽救治疗方案的结果:MINE方案与ESHAP方案联合巩固治疗

Results of a salvage treatment program for relapsing lymphoma: MINE consolidated with ESHAP.

作者信息

Rodriguez M A, Cabanillas F C, Velasquez W, Hagemeister F B, McLaughlin P, Swan F, Romaguera J E

机构信息

Department of Hematology, M.D. Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

J Clin Oncol. 1995 Jul;13(7):1734-41. doi: 10.1200/JCO.1995.13.7.1734.

Abstract

PURPOSE

We report the results of a prospective trial in which patients with relapsing non-Hodgkin's lymphomas were sequentially treated with two regimens (mesna, ifosfamide, mitoxantrone, and etoposide [MINE], and etoposide, methylprednisolone, cytarabine, and cisplatin [ESHAP]) if they had no history of disease resistance to these drugs.

PATIENTS AND METHODS

Ninety-two patients received MINE (mesna 4 g/m2, ifosfamide 4 g/m2, mitoxantrone 8 mg/m2, and etoposide 195 mg/m2) for a maximum of six courses followed by ESHAP (etoposide 240 mg/m2, methylprednisone 500 mg/d, high-dose cytarabine 2 g/m2, and cisplatin 100 mg/m2) for three courses to consolidate complete response (CR) or for a maximum of six cycles after a partial response (PR) or no response to MINE. Pretreatment serum levels of lactate dehydrogenase (LDH) and beta 2-microglobulin (beta 2M) were documented in 80 of 92 patients.

RESULTS

The response rate to MINE-ESHAP was 69% (48% CRs and 21% PRs), with a median survival time of 24 months and median time to treatment failure of 12 months. The median time to treatment failure according to histology was as follows: low-grade histologies, 16 months; low-grade transformed to intermediate-grade, 8 months; and intermediate-grade, 5 months. The most serious complication was myelosuppression, which resulted in two deaths due to neutropenic sepsis. A risk factor model based on beta 2M and LDH levels before salvage treatment showed three categories of risk, with 36-month survival rates as follows: low (beta 2M < 3 mg/dL and LDH normal), 61%; intermediate (beta 2M > or = 3 mg/dL or LDH above normal), 23%; and high (beta 2M > or = 3 mg/dL and LDH above normal), 0%.

CONCLUSION

MINE-ESHAP is an effective salvage strategy for patients with recurrent lymphoma. Toxicity was acceptable. Factors that determine prognostic categories at relapse merit further study.

摘要

目的

我们报告了一项前瞻性试验的结果,在该试验中,复发的非霍奇金淋巴瘤患者若对两种方案(美司钠、异环磷酰胺、米托蒽醌和依托泊苷[MINE],以及依托泊苷、甲泼尼龙、阿糖胞苷和顺铂[ESHAP])无耐药病史,则依次接受这两种方案治疗。

患者与方法

92例患者接受MINE方案(美司钠4 g/m²、异环磷酰胺4 g/m²、米托蒽醌8 mg/m²和依托泊苷195 mg/m²),最多六个疗程,随后接受ESHAP方案(依托泊苷240 mg/m²、甲泼尼龙500 mg/d、大剂量阿糖胞苷2 g/m²和顺铂100 mg/m²)三个疗程,以巩固完全缓解(CR),或者在部分缓解(PR)或对MINE方案无反应后最多进行六个周期的治疗。92例患者中的80例记录了预处理时的血清乳酸脱氢酶(LDH)和β2微球蛋白(β2M)水平。

结果

MINE-ESHAP方案的缓解率为69%(48%为CR,21%为PR),中位生存时间为24个月,中位治疗失败时间为12个月。根据组织学类型的中位治疗失败时间如下:低级别组织学类型为16个月;低级别转化为中级别的为8个月;中级别的为5个月。最严重的并发症是骨髓抑制,导致两例因中性粒细胞减少性败血症死亡。基于挽救治疗前β2M和LDH水平的危险因素模型显示有三类风险,36个月生存率如下:低风险(β2M<3 mg/dL且LDH正常)为61%;中风险(β2M≥3 mg/dL或LDH高于正常)为23%;高风险(β2M≥3 mg/dL且LDH高于正常)为0%。

结论

MINE-ESHAP是复发性淋巴瘤患者的一种有效挽救策略。毒性是可接受的。复发时决定预后类别的因素值得进一步研究。

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