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Intensified therapies improve survival and identification of novel prognostic factors for placental-site and epithelioid trophoblastic tumours.
Froeling, Fieke E M; Ramaswami, Ramya; Papanastasopoulos, Panagiotis; Kaur, Baljeet; Sebire, Neil J; Short, Dee; Fisher, Rosemary A; Sarwar, Naveed; Wells, Michael; Singh, Kam; Ellis, Laura; Horsman, Janet M; Winter, Matthew C; Tidy, John; Hancock, Barry W; Seckl, Michael J.
Afiliación
  • Froeling FEM; Department of Medical Oncology, Charing Cross Gestational Trophoblastic Disease Centre, Imperial College NHS Healthcare Trust and Imperial College London, London, UK.
  • Ramaswami R; Department of Medical Oncology, Charing Cross Gestational Trophoblastic Disease Centre, Imperial College NHS Healthcare Trust and Imperial College London, London, UK.
  • Papanastasopoulos P; Department of Medical Oncology, Charing Cross Gestational Trophoblastic Disease Centre, Imperial College NHS Healthcare Trust and Imperial College London, London, UK.
  • Kaur B; Department of Medical Oncology, Charing Cross Gestational Trophoblastic Disease Centre, Imperial College NHS Healthcare Trust and Imperial College London, London, UK.
  • Sebire NJ; Department of Medical Oncology, Charing Cross Gestational Trophoblastic Disease Centre, Imperial College NHS Healthcare Trust and Imperial College London, London, UK.
  • Short D; Department of Medical Oncology, Charing Cross Gestational Trophoblastic Disease Centre, Imperial College NHS Healthcare Trust and Imperial College London, London, UK.
  • Fisher RA; Department of Medical Oncology, Charing Cross Gestational Trophoblastic Disease Centre, Imperial College NHS Healthcare Trust and Imperial College London, London, UK.
  • Sarwar N; Department of Medical Oncology, Charing Cross Gestational Trophoblastic Disease Centre, Imperial College NHS Healthcare Trust and Imperial College London, London, UK.
  • Wells M; Trophoblastic Disease Centre, Weston Park Hospital, Sheffield, UK.
  • Singh K; Trophoblastic Disease Centre, Weston Park Hospital, Sheffield, UK.
  • Ellis L; Trophoblastic Disease Centre, Weston Park Hospital, Sheffield, UK.
  • Horsman JM; Trophoblastic Disease Centre, Weston Park Hospital, Sheffield, UK.
  • Winter MC; Trophoblastic Disease Centre, Weston Park Hospital, Sheffield, UK.
  • Tidy J; Trophoblastic Disease Centre, Weston Park Hospital, Sheffield, UK.
  • Hancock BW; Trophoblastic Disease Centre, Weston Park Hospital, Sheffield, UK.
  • Seckl MJ; Department of Medical Oncology, Charing Cross Gestational Trophoblastic Disease Centre, Imperial College NHS Healthcare Trust and Imperial College London, London, UK. m.seckl@imperial.ac.uk.
Br J Cancer ; 120(6): 587-594, 2019 03.
Article en En | MEDLINE | ID: mdl-30792530
ABSTRACT

BACKGROUND:

Placental-site trophoblastic (PSTT) and epithelioid trophoblastic tumours (ETT) are the rarest malignant forms of gestational trophoblastic disease (GTD). Our prior work demonstrated that an interval of ≥48 months from the antecedent pregnancy was associated with 100% death rate, independent of the stage. Here, we assess whether modified treatments for these patients have increased survival and identify new prognostic factors.

METHODS:

The United Kingdom GTD database was screened to identify all PSTT/ETT cases diagnosed between 1973 and 2014. Data and survival outcomes from our prior patient cohort (1976-2006) were compared to our new modern cohort (2007-2014), when intensified treatments were introduced.

RESULTS:

Of 54,743 GTD patients, 125 (0.23%) were diagnosed with PSTT and/or ETT. Probability of survival at 5 and 10 years following treatment was 80% (95% CI 72.8-87.6%) and 75% (95% CI 66.3-84.3%), respectively. Univariate analysis identified five prognostic factors for reduced overall survival (age, FIGO stage, time since antecedent pregnancy, hCG level, mitotic index) of which stage IV disease (HR 6.18, 95% CI 1.61-23.81, p = 0.008) and interval ≥48 months since antecedent pregnancy (HR 14.57, 95% CI 4.17-50.96, p < 0.001) were most significant on multivariable analysis. No significant differences in prognostic factors were seen between the old and new patient cohort. However, the new cohort received significantly more cisplatin-based and high-dose chemotherapy, and patients with an interval ≥48 months demonstrated an improved median overall survival (8.3 years, 95% CI 1.53-15.1, versus 2.6 years, 95% CI 0.73-4.44, p = 0.·005).

CONCLUSION:

PSTT/ETT with advanced FIGO stage or an interval ≥48 months from their last known pregnancy have poorer outcomes. Platinum-based and high-dose chemotherapy may help to improve survival in poor-prognosis patients.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Uterinas / Tumor Trofoblástico Localizado en la Placenta / Neoplasias Trofoblásticas Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Br J Cancer Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Uterinas / Tumor Trofoblástico Localizado en la Placenta / Neoplasias Trofoblásticas Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Br J Cancer Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido