Kako Shinichi, Akahoshi Yu, Harada Naonori, Nakano Hirofumi, Kameda Kazuaki, Ugai Tomotaka, Wada Hidenori, Yamasaki Ryoko, Ishihara Yuko, Kawamura Koji, Sakamoto Kana, Sato Miki, Ashizawa Masahiro, Terasako-Saito Kiriko, Kimura Shun-Ichi, Kikuchi Misato, Nakasone Hideki, Yamazaki Rie, Kanda Junya, Nishida Junji, Kanda Yoshinobu
Division of Hematology, Department of Internal Medicine, Saitama Medical Center, Jichi Medical University, 1-847 Amanuma, Omiya-ku, Saitama-city, Saitama, 330-8503, Japan.
Ann Hematol. 2016 Jan;95(1):87-92. doi: 10.1007/s00277-015-2510-0. Epub 2015 Sep 22.
The effects of intensive regimens and the roles of drugs used might differ between T- and B-lineage acute lymphoblastic leukemia (ALL). We performed a literature search for clinical studies published from January 1998 to March 2013. Studies were eligible for inclusion in the analyses if they included more than 80 patients with adult ALL who were treated with a uniform regimen and compared T- and B-lineage ALL. Studies that included only adolescent or elderly patients were excluded. We identified 11 clinical studies, which included a total of 381 and 1366 patients with T- and B-lineage ALL, respectively, and performed meta-analyses using the selected studies. Nine studies included patients with Philadelphia chromosome-positive (Ph+) ALL. A meta-analysis using the random-effect model demonstrated superior survival in patients with T-lineage ALL compared to those with B-lineage ALL (hazard ratio 1.78, 95 % confidence interval 1.50-2.11), though the inclusion of patients with Ph+ ALL in B-lineage ALL must have influenced this result strongly. We performed meta-regression analyses, adjusted according to whether or not patients with Ph+ ALL were included in each study. Use of dexamethasone (Dex), higher dose of methotrexate (MTX), and higher dose of L-asparaginase (L-asp) were associated with a significant trend toward a better outcome in T-lineage ALL. A meta-regression analysis including Dex and the dose of L-asp or MTX together as covariates showed that these factors were independently significant. In conclusion, the use of Dex and high-dose L-asp or MTX may improve the outcome of T-lineage ALL. This hypothesis should be tested in a prospective study including only patients with Ph-negative ALL.
强化治疗方案的效果以及所用药物的作用在T系和B系急性淋巴细胞白血病(ALL)中可能有所不同。我们对1998年1月至2013年3月发表的临床研究进行了文献检索。如果研究纳入了80多名接受统一方案治疗的成人ALL患者,并对T系和B系ALL进行了比较,则这些研究符合纳入分析的条件。仅纳入青少年或老年患者的研究被排除。我们确定了11项临床研究,分别包括总共381例T系ALL患者和1366例B系ALL患者,并使用所选研究进行了荟萃分析。9项研究纳入了费城染色体阳性(Ph+)ALL患者。使用随机效应模型进行的荟萃分析表明,与B系ALL患者相比,T系ALL患者的生存率更高(风险比1.78,95%置信区间1.50 - 2.11),尽管B系ALL中纳入Ph+ ALL患者肯定对这一结果产生了强烈影响。我们进行了荟萃回归分析,并根据每项研究是否纳入Ph+ ALL患者进行了调整。地塞米松(Dex)的使用、更高剂量的甲氨蝶呤(MTX)和更高剂量的L-天冬酰胺酶(L-asp)与T系ALL更好的预后显著相关。将Dex与L-asp或MTX的剂量一起作为协变量进行的荟萃回归分析表明,这些因素具有独立的显著性。总之,Dex以及高剂量L-asp或MTX的使用可能改善T系ALL的预后。这一假设应在仅纳入Ph阴性ALL患者的前瞻性研究中进行检验。