生物
trk受体
平滑肌肉瘤
原肌球蛋白受体激酶A
病理
癌症研究
肉瘤
纤维肉瘤
荧光原位杂交
受体
医学
神经营养素
染色体
遗传学
生物化学
基因
作者
Sarah Chiang,Paolo Cotzia,David M. Hyman,Alexander Drilon,William D. Tap,Lei Zhang,Jaclyn F. Hechtman,Denise Frosina,Achim A. Jungbluth,Rajmohan Murali,Kay J. Park,Robert A. Soslow,Esther Oliva,A. John Iafrate,Ryma Benayed,Marc Ladanyi,Cristina R. Antonescu
标识
DOI:10.1097/pas.0000000000001055
摘要
Tropomyosin receptor kinase (Trk) inhibitors have shown high response rates in patients with tumors harboring NTRK fusions. We identified 4 NTRK fusion-positive uterine sarcomas that should be distinguished from leiomyosarcoma and undifferentiated uterine sarcoma. NTRK rearrangements were detected by fluorescence in situ hybridization (FISH) and/or targeted RNA or DNA sequencing in 4 undifferentiated uterine sarcomas with spindle cell morphology. Because of histologic overlap with leiomyosarcoma, TrkA and pan-Trk immunohistochemistry was performed in 97 uterine leiomyosarcomas. NTRK1 and NTRK3 FISH was performed on tumors with TrkA or pan-Trk staining. We also performed whole transcriptome RNA sequencing of a leiomyosarcoma with TrkA expression and targeted RNA sequencing of 2 additional undifferentiated uterine sarcomas. FISH and/or targeted RNA or DNA sequencing in the study group showed TPM3-NTRK1 , LMNA-NTRK1 , RBPMS-NTRK3 , and TPR-NTRK1 fusions. All tumors were composed of fascicles of spindle cells. Mitotic index was 7 to 30 mitotic figures per 10 high power fields; tumor necrosis was seen in 2 tumors. Desmin, estrogen receptor, and progesterone receptor were negative in all tumors, while pan-Trk was expressed in all tumors with concurrent TrkA staining in 3 of them. TrkA and/or pan-Trk staining was also seen in 6 leiomyosarcomas, but these tumors lacked NTRK fusions or alternative isoforms by FISH or whole transcriptome sequencing. No fusions were detected in 2 undifferentiated uterine sarcomas. NTRK fusion-positive uterine spindle cell sarcomas constitute a novel tumor type with features of fibrosarcoma; patients with these tumors may benefit from Trk inhibition. TrkA and pan-Trk expression in leiomyosarcomas is rare and does not correlate with NTRK rearrangement.
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