A case of NUT midline carcinoma with complete response to gemcitabine following cisplatin and docetaxel

J Pediatr Hematol Oncol. 2014 Nov;36(8):e476-80. doi: 10.1097/MPH.0000000000000082.

Abstract

Background: NUT midline carcinoma (NMC) is recognized as a very rare tumor that most often occurs around the midline and shows NUT rearrangement. This tumor affects children and younger adults, progresses rapidly, and shows an extremely poor prognosis, even with intensive chemotherapy. Very few reports have described effective treatment for this tumor.

Methods: A 12-year-old girl with NMC was treated using cisplatin (CDDP), docetaxel, gemcitabine, pemetrexed, and vinorelbine.

Results: Imaging showed partial response with CDDP and docetaxel, and complete response with gemcitabine. After reexacerbation of the tumor, although partial response was achieved with vinorelbine, the patient died 89 weeks after onset because of reexacerbation.

Conclusions: NMC is a very rare disease with poor prognosis. This study is the first to report response of NMC to gemcitabine and vinorelbine. The findings suggest that combination chemotherapies including CDDP, docetaxel, gemcitabine, and vinorelbine may be a choice in the treatment for NMC.

Publication types

  • Case Reports

MeSH terms

  • Antimetabolites, Antineoplastic / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Carcinoma, Squamous Cell / diagnosis
  • Carcinoma, Squamous Cell / drug therapy*
  • Carcinoma, Squamous Cell / genetics
  • Child
  • Cisplatin / therapeutic use
  • Deoxycytidine / analogs & derivatives
  • Deoxycytidine / therapeutic use
  • Docetaxel
  • Fatal Outcome
  • Female
  • Gemcitabine
  • Humans
  • Nuclear Proteins / genetics*
  • Oncogene Proteins, Fusion / genetics*
  • Remission Induction
  • Taxoids / therapeutic use
  • Thoracic Neoplasms / diagnosis
  • Thoracic Neoplasms / drug therapy*
  • Thoracic Neoplasms / genetics

Substances

  • Antimetabolites, Antineoplastic
  • BRD4-NUT fusion oncogene protein, human
  • Nuclear Proteins
  • Oncogene Proteins, Fusion
  • Taxoids
  • Deoxycytidine
  • Docetaxel
  • Cisplatin
  • Gemcitabine