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吉西他滨、依托泊苷、顺铂和地塞米松用于难治性或复发性非霍奇金淋巴瘤患者。

Gemcitabine, etoposide, cisplatin, and dexamethasone in patients with refractory or relapsed non-Hodgkin's lymphoma.

作者信息

Kim Ki Hyang, Joo Young Don, Sohn Chang Hak, Shin Ho Jin, Chung Joo Seop, Cho Goon Jae, Shin Sung Hoon, Kim Yang Soo, Lee Won Sik

机构信息

Department of Hematology & Oncology, Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.

出版信息

Korean J Intern Med. 2009 Mar;24(1):37-42. doi: 10.3904/kjim.2009.24.1.37.

Abstract

BACKGROUND/AIMS: To date, an effective salvage chemotherapy regimen for the treatment of refractory or relapsing non-Hodgkin's lymphoma (NHL) has not been discovered. This study was conducted to evaluate the efficacy and safety of gemcitabine, etoposide, cisplatin, and dexamethasone in relapsed or refractory NHL patients.

METHODS

All patients had histologically proven relapsed or refractory NHL. Treatments consisted of gemcitabine 700 mg/m(2) by continuous i.v. on days 1 and 8; etoposide 40 mg/m(2) by i.v. on days 1-4; cisplatin 60 mg/m(2) by i.v. on day 1; or dexamethasone 40 mg by i.v. on days 1-4 (GEPD) every 21 days. The primary end point was the patient response rate following two cycles of treatment. After two cycles, stem cells were harvested using mobilizing regimens (ESHAP or GEPD plus filgrastim), and this was followed by autologous stem cell transplantation or four additional cycles of GEPD.

RESULTS

Between January 2005 and January 2006, 20 patients (13 males and 7 females) were enrolled in the study. The median age was 53 (range 16-75) years. The most common histology was diffuse large B-cell lymphoma (n=10). The median follow-up duration was 5.2 (range 1.0-16.0) months. After two cycles, the overall response rate was 50.0% (10/20), including two complete responses and eight partial responses. The dose-limiting toxicity was myelosuppression. Grade IV neutropenia and thrombocytopenia occurred in 13 (65.0%) and 6 patients (30.0%), respectively. The median number of CD34-positive cells collected was 6.0 (range, 2.8-11.6)x10(6)/kg. Of the 17 patients < 66 years of age, 4 (23.5%) proceeded to autologous stem cell transplantation.

CONCLUSIONS

GEPD chemotherapy in patients with refractory or relapsed NHL was effective as a salvage therapy and helpful for stem cell harvest followed by autologous transplantation.

摘要

背景/目的:迄今为止,尚未发现一种有效的挽救性化疗方案用于治疗难治性或复发性非霍奇金淋巴瘤(NHL)。本研究旨在评估吉西他滨、依托泊苷、顺铂和地塞米松用于复发性或难治性NHL患者的疗效和安全性。

方法

所有患者均经组织学证实为复发性或难治性NHL。治疗方案为第1天和第8天静脉持续输注吉西他滨700mg/m²;第1 - 4天静脉输注依托泊苷40mg/m²;第1天静脉输注顺铂60mg/m²;或第1 - 4天静脉输注地塞米松40mg(GEPD方案),每21天重复一次。主要终点为两个周期治疗后的患者缓解率。两个周期后,采用动员方案(ESHAP或GEPD加非格司亭)采集干细胞,随后进行自体干细胞移植或再进行四个周期的GEPD方案治疗。

结果

2005年1月至2006年1月,20例患者(13例男性和7例女性)纳入本研究。中位年龄为53岁(范围16 - 75岁)。最常见的组织学类型为弥漫性大B细胞淋巴瘤(n = 10)。中位随访时间为5.2个月(范围1.0 - 16.0个月)。两个周期后,总缓解率为50.0%(10/20),包括2例完全缓解和8例部分缓解。剂量限制性毒性为骨髓抑制。13例(65.0%)患者发生IV级中性粒细胞减少,6例(30.0%)患者发生IV级血小板减少。采集的CD34阳性细胞中位数为6.0(范围2.8 - 11.6)×10⁶/kg。17例年龄<66岁的患者中,4例(23.5%)进行了自体干细胞移植。

结论

GEPD化疗方案用于难治性或复发性NHL患者作为挽救性治疗有效,且有助于采集干细胞以便进行自体移植。

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