Beaziz Jessica, Battistella Maxime, Delyon Julie, Farges Cécile, Marco Oren, Pages Cécile, Le Maignan Christine, Da Meda Laetitia, Basset-Seguin Nicole, Resche-Rigon Matthieu, Walter Petrich Anouk, Kérob Delphine, Lebbé Céleste, Baroudjian Barouyr
Department of Dermatology, AP-HP Saint-Louis Hospital, F-75010 Paris, France.
Department of Pathology, AP-HP Saint-Louis Hospital, F-75010 Paris, France.
Cancers (Basel). 2021 May 6;13(9):2224. doi: 10.3390/cancers13092224.
In locally advanced dermatofibrosarcoma protuberans (DFSP), imatinib mesylate has been described as an efficient neoadjuvant therapy. This retrospective study included patients with locally advanced DFSP who received neoadjuvant TKI (imatinib or pazopanib) from 2007 to 2017 at Saint Louis Hospital, Paris. The primary endpoint was the evaluation of the long-term status. A total of 27 patients were included, of whom nine had fibrosarcomatous transformation. The median duration of treatment was 7 months. The best response to TKI treatment before surgery, evaluated according to RECIST1.1 on MRI, consisted of complete/partial response (38.5%) or stability (46.2%). DFSP was surgically removed in 24 (89%) patients. A total of 23 patients (85%) were disease-free after 64.8 months of median follow-up (95% confidence interval 47.8; 109.3). One patient developed distant metastases 37 months after surgical tumor resection and finally died. Two patients (7%) did not get surgery because of metastatic progression during TKI treatment, and one patient refused surgery even though the tumor decreased by 30%. Treatment-related adverse events (AE) occurred in 23 patients (85%). Only four patients (imatinib: = 3, pazopanib: = 1) had grade ≥3 AE requiring temporary treatment disruption. Neoadjuvant TKI followed by complete surgery with micrographic analysis is an effective strategy for locally advanced and unresectable DFSP, with durable local recurrence disease-free survival.
在局部晚期隆突性皮肤纤维肉瘤(DFSP)中,甲磺酸伊马替尼已被描述为一种有效的新辅助治疗方法。这项回顾性研究纳入了2007年至2017年在巴黎圣路易医院接受新辅助酪氨酸激酶抑制剂(TKI,伊马替尼或帕唑帕尼)治疗的局部晚期DFSP患者。主要终点是评估长期状况。共纳入27例患者,其中9例发生了纤维肉瘤转化。治疗的中位持续时间为7个月。术前根据MRI上的RECIST1.1评估,对TKI治疗的最佳反应包括完全/部分缓解(38.5%)或病情稳定(46.2%)。24例(89%)患者的DFSP通过手术切除。中位随访64.8个月后,共有23例患者(85%)无疾病(95%置信区间47.8;109.3)。1例患者在手术切除肿瘤37个月后发生远处转移,最终死亡。2例患者(7%)因TKI治疗期间发生转移进展而未接受手术,1例患者尽管肿瘤缩小了30%但仍拒绝手术。23例患者(85%)发生了与治疗相关的不良事件(AE)。只有4例患者(伊马替尼:3例,帕唑帕尼:1例)发生了≥3级AE,需要暂时中断治疗。新辅助TKI治疗后进行完整手术及显微镜分析是治疗局部晚期和不可切除DFSP的有效策略,可实现持久的无局部复发生存。