Shruti Prem Sudha, Atef Shehata, Fatima Al-Ali, Nabil Abdelfattah, Taif Najeebi, Cigdem Ozturk, Aly Rashed, Manu Venkatesan, Rehab Helmy, Eman Aljufairi
{"title":"严重G6PD缺陷淋巴瘤患者使用阿霉素与溶血并发症无关。","authors":"Shruti Prem Sudha, Atef Shehata, Fatima Al-Ali, Nabil Abdelfattah, Taif Najeebi, Cigdem Ozturk, Aly Rashed, Manu Venkatesan, Rehab Helmy, Eman Aljufairi","doi":"10.1080/10428194.2025.2521654","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":18047,"journal":{"name":"Leukemia & Lymphoma","volume":" ","pages":"1-7"},"PeriodicalIF":2.2000,"publicationDate":"2025-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Use of doxorubicin is not associated with hemolytic complications in severely G6PD deficient patients with lymphoma.\",\"authors\":\"Shruti Prem Sudha, Atef Shehata, Fatima Al-Ali, Nabil Abdelfattah, Taif Najeebi, Cigdem Ozturk, Aly Rashed, Manu Venkatesan, Rehab Helmy, Eman Aljufairi\",\"doi\":\"10.1080/10428194.2025.2521654\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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.</p>\",\"PeriodicalId\":18047,\"journal\":{\"name\":\"Leukemia & Lymphoma\",\"volume\":\" \",\"pages\":\"1-7\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-06-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Leukemia & Lymphoma\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/10428194.2025.2521654\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Leukemia & Lymphoma","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/10428194.2025.2521654","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"HEMATOLOGY","Score":null,"Total":0}
Use of doxorubicin is not associated with hemolytic complications in severely G6PD deficient patients with lymphoma.
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.
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