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低剂量化疗联合酪氨酸激酶抑制剂诱导治疗Ph染色体阳性急性淋巴细胞白血病的疗效和安全性

OBJECTIVE: The study aims to explore the efficacy and safety of low-dose chemotherapy combined with tyrosine kinase inhibitor (TKI) as an induction therapy for Philadelphia-chromosomal-positive acute lymphoblastic leukemia (Ph(+) ALL). METHODS: The data of the consecutive newly diagnosed patients wi...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395566/
https://www.ncbi.nlm.nih.gov/pubmed/36709131
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2022.07.004
Descripción
Sumario:OBJECTIVE: The study aims to explore the efficacy and safety of low-dose chemotherapy combined with tyrosine kinase inhibitor (TKI) as an induction therapy for Philadelphia-chromosomal-positive acute lymphoblastic leukemia (Ph(+) ALL). METHODS: The data of the consecutive newly diagnosed patients with Ph(+) ALL were reviewed. The efficacy and safety of low-dose chemotherapy and conventional-dose chemotherapy combined with TKI were compared. RESULTS: A total of 217 patients with a median age of 38(10–69)years old were included in this study. 78 patients were in the low-dose chemotherapy group, and 139 patients were in the conventional-dose chemotherapy group. There were no significant differences in the 4-week complete remission(CR)rate(98.7% vs 97.0%, P=0.766)and overall CR rate(100% vs 100%, P=1.000)between the two groups. Multivariate analyses showed that the chemotherapy intensity was not related to the disease-free survival rate and overall survival rate. However, the lower incidence of infection(P=0.017), the shorter duration of neutropenia(P=0.001)and PLT<20×10(9)/L(P=0.057), and the lower red blood cell transfusion volume(P=0.002)were more common in the low-dose chemotherapy group than in the conventional-dose chemotherapy group. CONCLUSION: The low-dose chemotherapy is superior to the conventional-dose chemotherapy combined with TKI as induction therapy in Ph(+) ALL with similar efficacy but is safer.