费城染色体阳性急性淋巴细胞白血病首次完全缓解后接受或不接受异基因造血干细胞移植的酪氨酸激酶抑制剂维持治疗的疗效:一项系统评价和荟萃分析
Outcomes of Tyrosine Kinase Inhibitors Maintenance Therapy with or without Allogeneic Hematopoietic Stem Cell Transplantation in Philadelphia Chromosome Positive Acute Lymphoblastic Leukemia in First Complete Remission: A Systematic Review and Meta-Analysis.
作者信息
Shahzad Moazzam, Hussain Ali, Tariq Ezza, Anwar Iqra, Faisal Muhammad S, Syed Leena, Karam Alvina, Chaudhary Sibgha Gull, Ahmed Nausheen, Bansal Rajat, Khurana Sharad, Singh Anurag K, Byrd Kenneth P, Hematti Peiman, Abhyankar Sunil H, McGuirk Joseph P, Mushtaq Muhammad Umair
机构信息
Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS; Moffitt Cancer Center, University of South Florida, Tampa, FL.
Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS.
出版信息
Clin Lymphoma Myeloma Leuk. 2023 Mar;23(3):178-187. doi: 10.1016/j.clml.2023.01.002. Epub 2023 Jan 12.
We conducted a systematic review and meta-analysis to compare outcomes of tyrosine kinase inhibitor (TKI) maintenance therapy with or without allogeneic hematopoietic stem cell transplantation (HSCT) in Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) in first remission (CR1). A literature search was performed on PubMed, Cochrane, and Clinical trials.gov. After screening 1720 articles, 12 studies were included. Proportions and odds ratios (OR) with 95% confidence intervals (CI) were computed. I provides an estimate of the percentage of variability in results across studies that is due to real differences and not due to chance. Of 1039 patients, 635 (61%) had TKI alone and 404 (39%) patients had HSCT followed by TKI. At 3 years, a trend towards poor overall survival (OS; OR 0.67, 95% CI 0.39-1.15, I = 68%), (disease-free survival; OR 0.58, 95% CI 0.26-1.29, I = 76%), and higher relapse rate (RR; OR = 2.52, 95% CI = 1.66-3.83, I = 26%) was seen with TKI alone compared to HSCT-TKI. Although HSCT followed by TKI maintenance in Ph+ ALL has long been considered standard of care, the introduction of potent third-generation TKIs and bispecific T-cell engagers such as Blinatumomab has significantly improved outcomes while sparing the need for HSCT in newly diagnosed patients.
我们进行了一项系统评价和荟萃分析,以比较在费城染色体阳性(Ph+)急性淋巴细胞白血病(ALL)首次缓解期(CR1)接受或不接受异基因造血干细胞移植(HSCT)的酪氨酸激酶抑制剂(TKI)维持治疗的疗效。在PubMed、Cochrane和Clinical trials.gov上进行了文献检索。在筛选了1720篇文章后,纳入了12项研究。计算了比例和比值比(OR)以及95%置信区间(CI)。I提供了研究结果变异性的百分比估计,该变异性是由于实际差异而非偶然因素造成的。在1039例患者中,635例(61%)仅接受TKI治疗,404例(39%)患者接受HSCT后再接受TKI治疗。3年时,与HSCT-TKI相比,单纯TKI治疗的总生存期(OS;OR 0.67,95%CI 0.39-1.15,I=68%)、无病生存期(OR 0.58,95%CI 0.26-1.29,I=76%)有变差的趋势,复发率更高(RR;OR=2.52,95%CI=1.66-3.83,I=26%)。尽管长期以来,Ph+ ALL患者在HSCT后接受TKI维持治疗一直被视为标准治疗方案,但强效第三代TKI和双特异性T细胞衔接器(如博纳吐单抗)的引入显著改善了疗效,同时使新诊断患者无需进行HSCT。