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An Anatomical Site and Genetic-Based Prognostic Model for Patients With Nuclear Protein in Testis (NUT) Midline Carcinoma: Analysis of 124 Patients.
Chau, Nicole G; Ma, Clement; Danga, Kristina; Al-Sayegh, Hasan; Nardi, Valentina; Barrette, Ryan; Lathan, Christopher S; DuBois, Steven G; Haddad, Robert I; Shapiro, Geoffrey I; Sallan, Stephen E; Dhar, Arindam; Nelson, Jeanenne J; French, Christopher A.
Afiliação
  • Chau NG; Dana-Farber Cancer Institute, Boston, MA.
  • Ma C; Harvard Medical School, Boston, MA.
  • Danga K; Harvard Medical School, Boston, MA.
  • Al-Sayegh H; Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA.
  • Nardi V; Brigham and Women's Hospital, Boston, MA.
  • Barrette R; Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA.
  • Lathan CS; Harvard Medical School, Boston, MA.
  • DuBois SG; Massachusetts General Hospital, Boston, MA.
  • Haddad RI; Brigham and Women's Hospital, Boston, MA.
  • Shapiro GI; Dana-Farber Cancer Institute, Boston, MA.
  • Sallan SE; Harvard Medical School, Boston, MA.
  • Dhar A; Harvard Medical School, Boston, MA.
  • Nelson JJ; Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA.
  • French CA; Dana-Farber Cancer Institute, Boston, MA.
JNCI Cancer Spectr ; 4(2): pkz094, 2020 Apr.
Article em En | MEDLINE | ID: mdl-32328562
ABSTRACT

BACKGROUND:

NUT midline carcinoma, renamed NUT carcinoma (NC), is an aggressive squamous cancer defined by rearrangement of the NUTM1 gene. Although a subset of patients can be cured, for the majority of patients the prognosis is grim. We sought to classify patients into risk groups based on molecular and clinicopathologic factors at the time of diagnosis.

METHODS:

Clinicopathologic variables and survival outcomes were extracted for a total of 141 NC patients from the NUT midline carcinoma Registry using questionnaires and medical records. Translocation type was identified by molecular analyses. Survival tree regression analysis was performed to determine risk factors associated with overall survival (OS).

RESULTS:

For 141 patients, the median age at diagnosis was 23.6 years. Fifty-one percent had thoracic origin compared with 49% nonthoracic sites (41% head and neck, 6% bone or soft tissue, 1% other). The median OS was 6.5 months (95% confidence interval [CI] = 5.8 to 9.1 months). Most patients had the BRD4-NUTM1 fusion (78%), followed by BRD3-NUTM1 (15%) and NSD3-NUTM1 (6%). Survival tree regression identified three statistically distinct risk groups among 124 patients classified by anatomical site and genetics group A is nonthoracic primary, BRD3-, or NSD3-NUT (n = 12, median OS = 36.5 months, 95% CI = 12.5 to not reported months); group B is nonthoracic primary, BRD4-NUT (n = 45, median OS = 10 months, 95% CI = 7 to 14.6 months); and group C is thoracic primary (n = 67, median OS = 4.4 months, 95% CI = 3.5 to 5.6 months). Only groups A and B had long-term (≥3 years, n = 12) survivors.

CONCLUSIONS:

We identify three risk groups defined by anatomic site and NUT fusion type. Nonthoracic primary with non-BRD4-NUT fusion confers the best prognosis, followed by nonthoracic primary with BRD4-NUT. Thoracic NC patients, regardless of the NUT fusion, have the worst survival.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: JNCI Cancer Spectr Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Marrocos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: JNCI Cancer Spectr Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Marrocos