Current management of neurotrophic receptor tyrosine kinase fusion-positive sarcoma: an updated review

被引:0
作者
Kubota, Yuta [1 ]
Kawano, Masanori [1 ]
Iwasaki, Tatsuya [1 ]
Itonaga, Ichiro [1 ]
Kaku, Nobuhiro [1 ]
Ozaki, Toshifumi [2 ]
Tanaka, Kazuhiro [1 ,3 ]
机构
[1] Oita Univ, Fac Med, Dept Orthopaed Surg, 1-1 Idaigaoka Hasama, Yufu City, Oita 8795593, Japan
[2] Okayama Univ, Fac Med Dent & Pharmaceut Sci, Dept Orthopaed Surg, Sci Funct Recovery & Reconstruct, 2-5-1 Shikata Cho,Kita Ku, Okayama 7008558, Japan
[3] Oita Univ, Fac Med, Dept Adv Med Sci, 1-1 Idaigaoka Hasama, Yufu City, Oita 8795593, Japan
关键词
NTRK fusion-positive sarcoma; larotrectinib; entrectinib; infantile fibrosarcoma; NTRK-rearranged spindle cell neoplasms; INFLAMMATORY MYOFIBROBLASTIC TUMORS; ETV6-NTRK3 GENE FUSION; SOFT-TISSUE SARCOMAS; INFANTILE FIBROSARCOMA; SOLID TUMORS; NTRK FUSION; NEXT-GENERATION; LAROTRECTINIB; SUBSET; RECOMMENDATIONS;
D O I
10.1093/jjco/hyaf015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In recent years, pembrolizumab has demonstrated significant efficacy in treating tumors characterized by a high tumor mutational burden and high microsatellite instability. Tropomyosin receptor kinase (TRK) inhibitors have shown considerable efficacy against tumors harboring neurotrophic receptor tyrosine kinase (NTRK) fusion genes, highlighting the growing importance of personalized medicine in cancer treatment. Advanced sequencing technologies enable the rapid analysis of numerous genetic abnormalities in tumors, facilitating the identification of patients with positive biomarkers. These advances have increased the likelihood of providing effective, tailored treatments. NTRK fusion genes are present in various cancer types, including sarcomas, and the TRK inhibitors larotrectinib and entrectinib have been effectively used for these malignancies. Consequently, the treatment outcomes for NTRK fusion-positive tumors have improved significantly, reflecting a shift toward more personalized therapeutic approaches. This review focuses on NTRK fusion-positive sarcomas and comprehensively evaluates their epidemiology, clinical features, and radiological and histological characteristics. We also investigated the treatment landscape, including the latest methodologies involving TRK inhibitors, and discussed the long-term efficacy of these inhibitors, and their optimal order of use. Notably, larotrectinib has demonstrated a high response rate in infantile fibrosarcoma, and its efficacy has been confirmed even in advanced cases. However, further research is warranted to optimize treatment duration and subsequent management strategies. The accumulation of clinical cases worldwide will play a pivotal role in refining the treatment approaches for tumors associated with NTRK fusion genes. This review focuses on NTRK fusion-positive sarcomas; evaluates their epidemiology, clinical features, and histological characteristics; explores treatments, including TRK inhibitors; and discusses the long-term efficacy and optimal order of action.
引用
收藏
页码:313 / 326
页数:14
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