| Literature DB >> 29040054 |
Simone Storck1, Alyssa L Kennedy2, Karen J Marcus3, Lisa Teot4, Jennifer Vaughn5, Astrid K Gnekow1, Bruno Märkl6, Ivo Leuschner7, Steven G DuBois2, Christopher A French8, Michael C Frühwald1.
Abstract
A subset of poorly differentiated squamous cell carcinomas, NUT midline carcinomas (NMC) are characterized by a translocation t(15;19)(q13;p13) [ 1 ]. The prognosis is generally dismal [ 2 ] and therapeutic success has been limited to exceptional cases [ 3 ]. We present two cases of pediatric NMC from two different institutions treated according to a multimodal sarcoma approach involving surgery, chemotherapy, and focal radiotherapy. One patient has remained in complete continuous remission for over 6 years, while the other is in CR in early follow-up off therapy. Our proposed multimodal strategy apparently meets the aggressive biologic nature of NMC and should be considered for further evaluation in this context potentially in the setting of a clinical trial.Entities:
Keywords: NUT midline carcinoma; Rare tumors; multimodal therapy
Mesh:
Year: 2017 PMID: 29040054 DOI: 10.1080/08880018.2017.1363839
Source DB: PubMed Journal: Pediatr Hematol Oncol ISSN: 0888-0018 Impact factor: 1.969