Cai Jiaoyang, Liu Hu, Chen Yumei, Yu Jie, Gao Ju, Jiang Hua, Zhai Xiaowen, Ju Xiuli, Wu Xuedong, Wang Ningling, Tian Xin, Liang Changda, Fang Yongjun, Zhou Fen, Li Hong, Sun Lirong, Yang Liangchun, Guo Jing, Liu Aiguo, Li Chi-Kong, Zhu Yiping, Tang Jingyan, Yang Jun J, Shen Shuhong, Cheng Cheng, Pui Ching-Hon
Department of Hematology/Oncology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Key Laboratory of Pediatric Hematology & Oncology of China Ministry of Health, and National Children's Medical Center, Shanghai, China.
Department of Hematology/Oncology, Children's Hospital of Soochow University, Suzhou, China.
Lancet Reg Health West Pac. 2023 Jun 10;38:100818. doi: 10.1016/j.lanwpc.2023.100818. eCollection 2023 Sep.
First-generation ABL-targeted tyrosine kinase inhibitor (TKI) imatinib is known to retard growth in children but it is not known if the second-generation ABL-targeted TKI dasatinib has the same effect. We aimed to determine the impact of the first- or second-generation TKI on the growth of children treated for Philadelphia chromosome-positive (Ph) childhood acute lymphoblastic leukemia (ALL).
We evaluated the longitudinal growth changes in 140 children with Ph ALL treated with imatinib or dasatinib in additional to intensive cytotoxic chemotherapy and 280 matched controls treated with the same intensity of cytotoxic chemotherapy without TKI on Chinese Children's Cancer Group ALL-2015 protocol between 2015 and 2019. We retrospectively reviewed the height data obtained during routine clinic visits at 4 time points: at diagnosis, the end of therapy, 1 year and 2 years off therapy. Height z Scores were derived with the aid of WHO Anthro version 3.2.2 and WHO AnthroPlus version 1.0.4, global growth monitoring tool.
This study consisted only patients who have completed all treatment in continuous complete remission without major events, including 33 patients randomized to receive imatinib, 43 randomized to receive dasatinib, and 64 assigned to receive dasatinib. Similar degree of loss of height z scores from diagnosis to the end of therapy was observed for the 33 imatinib- and the 107 dasatinib-treated patients (median △ = -0.84 vs. -0.88, P = 0.41). Adjusting for height z score at diagnosis, puberty status, and sex, there was no significant difference in the longitudinal mean height z scores between patients treated with imatinib and those with dasatinib (0.08, 95% CI, -0.22 to 0.38, P = 0.60). The degree of loss of height z scores from diagnosis to end of therapy was significantly greater in the 140 TKI-treated patients than the 280 controls (median △ = -0.88 vs. -0.18, P < 0.001). The longitudinal mean height z scores in the TKI-treated patients were significantly lower than those of the controls (-0.84, 95% CI, -0.98 to -0.69; P < 0.001).
These data suggest that dasatinib and imatinib have the similar adverse impact on the growth of children with Ph ALL.
This study was supported by the National Natural Science Foundation of China (grant 81670136 [JCai and JT]), the fourth round of Three-Year Public Health Action Plan (2015-2017; GWIV-25 [SS]), Shanghai Health Commission Clinical Research Project (202140161 [JCai]), the US National Cancer institute (CA21765 [C-H Pui]), and the American Lebanese Syrian Associated Charities (CC, JJY, and C-HP). The content of this paper is solely the responsibility of the authors and does not necessarily represent the official views of the US National Institutes of Health.
已知第一代靶向ABL的酪氨酸激酶抑制剂(TKI)伊马替尼可延缓儿童生长,但尚不清楚第二代靶向ABL的TKI达沙替尼是否具有相同作用。我们旨在确定第一代或第二代TKI对接受费城染色体阳性(Ph)儿童急性淋巴细胞白血病(ALL)治疗的儿童生长的影响。
我们评估了140例接受伊马替尼或达沙替尼治疗的Ph ALL儿童以及280例接受相同强度细胞毒性化疗但未使用TKI的匹配对照的纵向生长变化,这些儿童均按照中国儿童癌症协作组ALL-2015方案在2015年至2019年期间接受治疗。我们回顾性分析了在4个时间点的常规门诊就诊时获得的身高数据:诊断时、治疗结束时、治疗结束后1年和2年。身高z评分借助全球生长监测工具WHO Anthro 3.2.2版和WHO AnthroPlus 1.0.4版得出。
本研究仅纳入了所有治疗均持续完全缓解且无重大事件发生的患者,其中33例随机接受伊马替尼治疗,43例随机接受达沙替尼治疗,64例分配接受达沙替尼治疗。在33例接受伊马替尼治疗的患者和107例接受达沙替尼治疗的患者中,从诊断到治疗结束观察到的身高z评分下降程度相似(中位数△=-0.84 vs. -0.88,P=0.41)。在对诊断时的身高z评分、青春期状态和性别进行校正后,接受伊马替尼治疗的患者与接受达沙替尼治疗的患者的纵向平均身高z评分无显著差异(0.08,95%CI,-0.22至0.38,P=0.60)。140例接受TKI治疗的患者从诊断到治疗结束时身高z评分的下降程度显著大于280例对照(中位数△=-0.88 vs. -0.18,P<0.001)。接受TKI治疗的患者的纵向平均身高z评分显著低于对照组(-0.84,95%CI,-0.98至-0.69;P<0.001)。
这些数据表明,达沙替尼和伊马替尼对Ph ALL儿童的生长具有相似的不良影响。
本研究得到了中国国家自然科学基金(81670136[蔡建和季涛])、第四轮三年公共卫生行动计划(2015 - 2017;GWIV - 25[施松])、上海市卫生健康委员会临床研究项目(202140161[蔡建])、美国国立癌症研究所(CA21765[普伊成浩])以及美国黎巴嫩叙利亚联合慈善机构(CC、JJY和普伊成浩)的支持。本文内容仅由作者负责,不一定代表美国国立卫生研究院的官方观点。