Ponatynib w leczeniu przewlekłej białaczki szpikowej i ostrej białaczki limfoblastycznej z chromosomem Filadelfia

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• 作者：Tomasz Sacha ; ^{sachatom@gmail.com" class="auth_mail" title="E-mail the corresponding author}
• 关键词：przewlekła białaczka szpikowa ; ostra białaczka limfoblastyczna Ph+ ; mutacja T315I ; ponatynib ; wskazania ; leczenie
• 刊名：Acta Haematologica Polonica
• 出版年：2016
• 出版时间：April-June 2016
• 年：2016
• 卷：47
• 期：2
• 页码：128-138
• 全文大小：435 K

文摘

Ponatinib is a third generation tyrosine kinase inhibitor (TKI) active against wild type and mutant bcr/abl tyrosine kinase (including T315I). Ponatinib is approved for the treatment of adult patients with T315I mutation detected in CML (all phases) and in Ph+ ALL, for CML patients who are resistant to dasatinib or nilotinib and patients with Ph+ ALL who are intolerant or resistant to dasatinib and for whom subsequent imatinib treatment is not an optimal therapy. In phase II registration study (PACE), 267 patients with CML in chronic phase (CP), 83 in accelerated (AC) and 94 patients in blastic phase (BP) of CML or Ph+ALL were enrolled. T315I mutation was detected in 64, 18 and 46 patients, respectively. Two or more or three or more TKIs were used before ponatinib in 93% and 58% of patients, respectively for median period of 16.7 months. Major cytogenetic response (MCyR) by 12 months was achieved in 59% of CP CML patients (median follow-up 36 months), and major hematological response (MaHR) by 6 months in 55% of AC CML patients, and in 34% of BP CML and Ph+ALL patients (median follow-up 15.16 and 6 months, respectively). Efficacy of ponatinib as a first-line treatment for CP CML patients was shown in phase II and III trials. Serious adverse reactions have been reported with ponatinib, including vascular occlusion, heart failure and hepatotoxicity. Ponatinib is a valuable treatment option for patients with CML and Ph+ALL resistant or intolerant to previous therapy with TKIs and those with T315I mutation.