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المؤلفElmakaty, Ibrahim
المؤلفSaglio, Giuseppe
المؤلفAl-Khabori, Murtadha
المؤلفElsayed, Abdelrahman
المؤلفElsayed, Basant
المؤلفElmarasi, Mohamed
المؤلفElsabagh, Ahmed A.
المؤلفAlshurafa, Awni
المؤلفAli, Elrazi
المؤلفYassin, Mohamed
تاريخ الإتاحة2024-04-24T09:53:23Z
تاريخ النشر2024
اسم المنشورCancers
المصدرScopus
الرقم المعياري الدولي للكتاب20726694
معرّف المصادر الموحدhttp://dx.doi.org/10.3390/cancers16040754
معرّف المصادر الموحدhttp://hdl.handle.net/10576/54199
الملخصHematopoietic stem cell transplantation (HSCT) for chronic myeloid leukemia (CML) patients has transitioned from the standard of care to a treatment option limited to those with unsatisfactory tyrosine kinase inhibitor (TKI) responses and advanced disease stages. In recent years, the threshold for undergoing HSCT has increased. Most CML patients now have life expectancies comparable to the general population, and therefore, the goal of therapy is shifting toward achieving treatment-free remission (TFR). While TKI discontinuation trials in CML show potential for achieving TFR, relapse risk is high, affirming allogeneic HSCT as the sole curative treatment. HSCT should be incorporated into treatment algorithms from the time of diagnosis and, in some patients, evaluated as soon as possible. In this review, we will look at some of the recent advances in HSCT, as well as its indication in the era of aiming for TFR in the presence of TKIs in CML.
راعي المشروعOpen Access funding provided by the Qatar National Library. This research did not receive any grants from funding agencies in the public, commercial, or not-for-profit sectors.
اللغةen
الناشرMultidisciplinary Digital Publishing Institute (MDPI)
الموضوعBCR-ABL1 gene fusion
chronic myeloid leukemia
hematopoietic stem cell transplant
survival
treatment-free remission
tyrosine kinase inhibitors
العنوانThe Contemporary Role of Hematopoietic Stem Cell Transplantation in the Management of Chronic Myeloid Leukemia: Is It the Same in All Settings?
النوعArticle Review
رقم العدد4
رقم المجلد16
dc.accessType Open Access


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