间变性淋巴瘤激酶
中性粒细胞减少症
医学
克里唑蒂尼
肺癌
肿瘤科
内科学
化疗
淋巴瘤
碱性抑制剂
恶性胸腔积液
作者
Fabien Moinard‐Butot,Simon Nannini,Cathie Fischbach,Safa Abdallahoui,Martin Demarchi,Thierry Petit,Laura Bender,Roland Schött
出处
期刊:Cancers
[Multidisciplinary Digital Publishing Institute]
日期:2023-10-11
卷期号:15 (20): 4940-4940
被引量:1
标识
DOI:10.3390/cancers15204940
摘要
Lung cancers with ALK rearrangement represent less than 5% of all lung cancers. ALK inhibitors are currently used to treat first-line metastatic non-small cell lung cancer with ALK rearrangement. Compared to chemotherapy, ALK inhibitors have improved progression-free survival, overall survival, and quality of life for patients. The results of several phase 3 studies with a follow-up of over 6 years suggest that the life expectancy of these patients treated with targeted therapies is significantly higher than 5 years and could approach 10 years. Nevertheless, these treatments induce haematological toxicities, including neutropenia. Few data are available on neutropenia induced by ALK inhibitors and on the pathophysiological mechanism and therapeutic adaptations necessary to continue the treatment. Given the high efficacy of these treatments, managing side effects to avoid treatment interruptions is essential. Here, we have reviewed the data from published clinical studies and case reports to provide an overview of neutropenia induced by ALK inhibitors.
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