Departments of Pathology.
Medicine, Gynecologic Medical Oncology Service.
Am J Surg Pathol. 2018 Jun;42(6):791-798. doi: 10.1097/PAS.0000000000001055.
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.
原肌球蛋白受体激酶(Trk)抑制剂在携带 NTRK 融合的肿瘤患者中显示出高反应率。我们鉴定了 4 例 NTRK 融合阳性的子宫肉瘤,这些肿瘤应与平滑肌肉瘤和未分化的子宫肉瘤区分开来。在 4 例具有梭形细胞形态的未分化的子宫肉瘤中,通过荧光原位杂交(FISH)和/或靶向 RNA 或 DNA 测序检测到 NTRK 重排。由于与平滑肌肉瘤的组织学重叠,对 97 例子宫平滑肌肉瘤进行了 TrkA 和泛 Trk 免疫组化染色。在具有 TrkA 染色的肿瘤上进行了 NTRK1 和 NTRK3 FISH。我们还对具有 TrkA 表达的平滑肌肉瘤进行了全转录组 RNA 测序,并对另外 2 例未分化的子宫肉瘤进行了靶向 RNA 测序。在研究组中,FISH 和/或靶向 RNA 或 DNA 测序显示 TPM3-NTRK1、LMNA-NTRK1、RBPMS-NTRK3 和 TPR-NTRK1 融合。所有肿瘤均由梭形细胞束组成。有丝分裂指数为每 10 个高倍视野中有 7 至 30 个有丝分裂象;2 例肿瘤中可见肿瘤坏死。所有肿瘤的结蛋白、雌激素受体和孕激素受体均为阴性,而所有肿瘤均表达泛 Trk,其中 3 例同时存在 TrkA 染色。在 6 例平滑肌肉瘤中也观察到 TrkA 和/或泛 Trk 染色,但这些肿瘤通过 FISH 或全转录组测序缺乏 NTRK 融合或替代异构体。在 2 例未分化的子宫肉瘤中未检测到融合。NTRK 融合阳性的子宫梭形细胞肉瘤构成一种具有纤维肉瘤特征的新型肿瘤类型;这些肿瘤患者可能受益于 Trk 抑制。平滑肌肉瘤中 TrkA 和泛 Trk 的表达很少见,与 NTRK 重排无关。