Exceptional response to neoadjuvant targeted therapy with the selective RET inhibitor selpercatinib in RET-fusion-associated sarcoma

被引:4
|
作者
Schrenk, Karin G. [1 ]
Weschenfelder, Wolfram [2 ]
Spiegel, Christian [2 ]
Agaimy, Abbas [3 ]
Stoehr, Robert [3 ]
Hartmann, Arndt [3 ]
Gassler, Nikolaus [4 ]
Drescher, Robert [5 ]
Freesmeyer, Martin [5 ]
Malouhi, Amer [6 ]
Buerckenmeyer, Florian [6 ]
Aschenbach, Rene [6 ]
Teichgraeber, Ulf [6 ]
Koegler, Christine [7 ]
Vogt, Matthias [8 ]
Hofmann, Gunther O. [2 ]
Hochhaus, Andreas [1 ]
机构
[1] Univ Hosp Jena, Dept Hematol & Internal Oncol, Clin Internal Med 2, Klinikum 1, D-07747 Jena, Germany
[2] Univ Hosp Jena, Clin Trauma Hand & Reconstruct Surg, Jena, Germany
[3] Friedrich Alexander Univ Erlangen Nurnberg, Univ Hosp Erlangen, Comprehens Canc Ctr Erlangen EMN CCC ER EMN, Inst Pathol, Erlangen, Germany
[4] Univ Hosp Jena, Inst Forens Med, Sect Pathol, Jena, Germany
[5] Univ Hosp Jena, Clin Nucl Med, Jena, Germany
[6] Univ Hosp Jena, Inst Diagnost & Intervent Radiol, Jena, Germany
[7] Malteser Hosp St Marien, Clin Gen & Visceral Surg, Erlangen, Germany
[8] Clin Medictr PartGmbB, Erlangen, Germany
关键词
RET-fusion; Sarcoma; Selpercatinib; Targeted therapy; TRIM33; EFFICACY; CANCERS;
D O I
10.1007/s00432-022-04496-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
With the increasing use of next-generation sequencing, highly effective targeted therapies have been emerging as treatment options for several cancer types. Recurrent gene-fusions have been recognized in sarcomas; however, options for targeted therapy remain scarce. Here, we describe a case of a sarcoma, associated with a RET::TRIM33-fusion gene with an exceptional response to a neoadjuvant therapy with the selective RET inhibitor selpercatinib. Resected tumor revealed subtotal histopathologic response. This is the first report of successful targeted therapy with selpercatinib in RET-fusion-associated sarcomas. As new targeted therapies are under development, similar treatment options may become available for sarcoma patients.
引用
收藏
页码:5493 / 5496
页数:4
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