布仑妥昔单抗维多汀
间变性淋巴瘤激酶
间变性大细胞淋巴瘤
癌症研究
肿瘤科
医学
长春新碱
移植
淋巴瘤
化疗
内科学
环磷酰胺
CD30
恶性胸腔积液
肺癌
作者
Xue Sun,Xiaosheng Fang,Yahan Li,Dongyue Lu,Xin Wang
标识
DOI:10.3892/ijo.2021.5232
摘要
Anaplastic large cell lymphoma (ALCL) is a rare and highly invasive non‑Hodgkin's lymphoma. In the past few decades, traditional chemotherapy regimens, such as as the cyclophosphamide, vincristine, doxorubicin and prednisone regimen, have been recommended for first‑line treatment. In order to improve the survival of patients, dose‑intensive chemotherapy and hematopoietic stem cell transplantation have been deeply studied and some progress has been made. Recently, with the accumulation of clinical cases and the development of clinical trials, as well improvements to our in‑depth understanding of the biological behavior of ALCL, the signaling pathways and the immunotherapy involved, research on this topic is in full swing. The emergence of several targeted drugs and immunotherapies, including anaplastic lymphoma kinase inhibitors, brentuximab vedotin, mTOR inhibitors, programmed cell death protein 1/programmed death ligand 1 inhibitors and chimeric antigen receptor‑T cell therapy, seems to provide new opportunities for certain patients with ALCL. The present review focuses on the current use of traditional therapy and the treatment prospects of these new drugs in ALCL.
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