Use of doxorubicin is not associated with hemolytic complications in severely G6PD deficient patients with lymphoma.

IF 2.2 4区 医学 Q3 HEMATOLOGY
Shruti Prem Sudha, Atef Shehata, Fatima Al-Ali, Nabil Abdelfattah, Taif Najeebi, Cigdem Ozturk, Aly Rashed, Manu Venkatesan, Rehab Helmy, Eman Aljufairi
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引用次数: 0

Abstract

G6PD-deficiency is prevalent in the Middle East, and is linked to oxidative hemolysis with doxorubicin. Physicians substitute etoposide for doxorubicin in chemotherapy for G6PD-deficient lymphoma patients. We studied severely G6PD-deficient Hodgkin (HL) and diffuse large B cell lymphoma (DLBCL) patients. The primary outcome was the occurrence of hemolysis after doxorubicin, and secondary outcome was survival where etoposide was substituted for doxorubicin. Of 177 patients, 16% were severely G6PD-deficient. Eleven deficient HL patients had received ABVD, and seven deficient DLBCL patients had received R-CHOP, none had documented hemolysis. DLBCL patients who received R-CEOP had inferior survival compared to R-CHOP, while HL patients who received EBVD had comparable survival to ABVD. In the second part of the study, we prospectively monitored 39 severely G6PD-deficient lymphoma patients receiving doxorubicin, none had hemolysis. We conclude that doxorubicin is safe in severely G6PD-deficient patients. Substituting etoposide for doxorubicin in DLBCL was associated with decreased survival.

严重G6PD缺陷淋巴瘤患者使用阿霉素与溶血并发症无关。
g6pd缺乏症在中东地区很普遍,与阿霉素氧化溶血有关。在g6pd缺陷淋巴瘤患者的化疗中,医生用依托泊苷代替阿霉素。我们研究了严重g6pd缺陷霍奇金淋巴瘤(HL)和弥漫性大B细胞淋巴瘤(DLBCL)患者。主要终点是阿霉素治疗后溶血的发生,次要终点是依托泊苷替代阿霉素治疗后的生存。在177例患者中,16%为严重g6pd缺陷。11例HL缺陷患者接受了ABVD, 7例DLBCL缺陷患者接受了R-CHOP,无溶血记录。与R-CHOP相比,接受R-CEOP的DLBCL患者的生存期较差,而接受EBVD的HL患者的生存期与ABVD相当。在研究的第二部分,我们前瞻性监测了39例接受阿霉素治疗的严重g6pd缺陷淋巴瘤患者,无一例发生溶血。我们得出结论,阿霉素对严重g6pd缺陷患者是安全的。在DLBCL中用依托泊苷代替阿霉素与生存率降低相关。
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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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