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Prognostic value of baseline total metabolic tumor volume (TMTV0) measured on FDG-PET/CT in patients with peripheral T-cell lymphoma (PTCL).
Cottereau, A S; Becker, S; Broussais, F; Casasnovas, O; Kanoun, S; Roques, M; Charrier, N; Bertrand, S; Delarue, R; Bonnet, C; Hustinx, R; Gaulard, P; de Leval, L; Vera, P; Itti, E; Mounier, N; Haioun, C; Tilly, H; Meignan, M.
Afiliação
  • Cottereau AS; Department of Nuclear Medicine, Centre H. Becquerel and Rouen University Hospital, Rouen Department of Hematology, Centre H. Becquerel, Rouen, France.
  • Becker S; Department of Nuclear Medicine, Centre H. Becquerel and Rouen University Hospital, Rouen.
  • Broussais F; Department of Hematology, Institut Paoli-Calmettes, Marseille.
  • Casasnovas O; Department of Hematology, Hopital Le Bocage, C.H.U Dijon.
  • Kanoun S; Department of Nuclear Medicine, Centre GF Leclerc, Dijon.
  • Roques M; Department of Hematology, Hopital Le Bocage, C.H.U Dijon.
  • Charrier N; Department of Nuclear Medicine, Institut Paoli-Calmettes, Marseille.
  • Bertrand S; Department of Nuclear Medicine, Institut Paoli-Calmettes, Marseille.
  • Delarue R; Department of Hematology, Hopital Necker, Paris, France.
  • Bonnet C; Departments of Hematology.
  • Hustinx R; Nuclear Medicine, C.H.U, ULg, Liège, Belgium.
  • Gaulard P; Department of Pathology, Groupe Henri Mondor-Albert Chenevier, Créteil Faculte de Medecine, Université Paris-Est, Créteil Unité U955, INSERM, Creteil, France.
  • de Leval L; Institute of Pathology, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
  • Vera P; Department of Nuclear Medicine, Centre H. Becquerel and Rouen University Hospital, Rouen QuantIF (Litis EA 418) University of Rouen, Rouen.
  • Itti E; Department of Nuclear Medicine, Groupe Henri Mondor-Albert Chenevier, Créteil.
  • Mounier N; Department of Hematology, Groupe hospitalier l'Archet, Nice.
  • Haioun C; Faculte de Medecine, Université Paris-Est, Créteil Unité U955, INSERM, Creteil, France Lymphoid Malignancies Unit, Department of Hematology, Groupe Henri Mondor-Albert Chenevier, Créteil.
  • Tilly H; Department of Hematology, Centre H. Becquerel, Rouen, France.
  • Meignan M; Department of Nuclear Medicine, Groupe Henri Mondor-Albert Chenevier, Créteil michel.meignan@hmn.aphp.fr.
Ann Oncol ; 27(4): 719-24, 2016 Apr.
Article em En | MEDLINE | ID: mdl-26787236
BACKGROUND: Most peripheral T-cell lymphoma (PTCL) patients have a poor outcome and the identification of prognostic factors at diagnosis is needed. PATIENTS AND METHODS: The prognostic impact of total metabolic tumor volume (TMTV0), measured on baseline [(18)F]2-fluoro-2-deoxy-d-glucose positron emission tomography/computed tomography, was evaluated in a retrospective study including 108 PTCL patients (27 PTCL not otherwise specified, 43 angioimmunoblastic T-cell lymphomas and 38 anaplastic large-cell lymphomas). All received anthracycline-based chemotherapy. TMTV0 was computed with the 41% maximum standardized uptake value threshold method and an optimal cut-off point for binary outcomes was determined and compared with others prognostic factors. RESULTS: With a median follow-up of 23 months, 2-year progression-free survival (PFS) was 49% and 2-year overall survival (OS) was 67%. High TMTV0 was significantly associated with a worse prognosis. At 2 years, PFS was 26% in patients with a high TMTV0 (>230 cm(3), n = 53) versus 71% for those with a low TMTV0, [P < 0.0001, hazard ratio (HR) = 4], whereas OS was 50% versus 80%, respectively, (P = 0.0005, HR = 3.1). In multivariate analysis, TMTV0 was the only significant independent parameter for both PFS and OS. TMTV0, combined with PIT, discriminated even better than TMTV0 alone, patients with an adverse outcome (TMTV0 >230 cm(3) and PIT >1, n = 33,) from those with good prognosis (TMTV0 ≤230 cm(3) and PIT ≤1, n = 40): 19% versus 73% 2-year PFS (P < 0.0001) and 43% versus 81% 2-year OS, respectively (P = 0.0002). Thirty-one patients (other TMTV0-PIT combinations) had an intermediate outcome, 50% 2-year PFS and 68% 2-year OS. CONCLUSION: TMTV0 appears as an independent predictor of PTCL outcome. Combined with PIT, it could identify different risk categories at diagnosis and warrants further validation as a prognostic marker.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prognóstico / Linfoma de Células T Periférico / Carga Tumoral Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2016 Tipo de documento: Article País de afiliação: França País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prognóstico / Linfoma de Células T Periférico / Carga Tumoral Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2016 Tipo de documento: Article País de afiliação: França País de publicação: Reino Unido