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The predictive role of interim PET after the first chemotherapy cycle and sequential evaluation of response to ABVD in Hodgkin's lymphoma patients-the Polish Lymphoma Research Group (PLRG) Observational Study.
Zaucha, J M; Malkowski, B; Chauvie, S; Subocz, E; Tajer, J; Kulikowski, W; Fijolek-Warszewska, A; Biggi, A; Fallanca, F; Kobylecka, M; Dziuk, M; Woszczyk, D; Rybka, J; Kroll-Balcerzak, R; Bergesio, F; Romanowicz, A; Chamier-Cieminska, A; Kurczab, P; Giza, A; Lesniewski-Kmak, K; Zaucha, R; Swietlik, D; Wróbel, T; Knopinska-Posluszny, W; Walewski, J; Gallamini, A.
Afiliação
  • Zaucha JM; Gdynia Oncology Center, Gdynia.
  • Malkowski B; Departments of Oncological Propedeutics.
  • Chauvie S; Hematology and Transplantology, Medical University of Gdansk, Gdansk.
  • Subocz E; Nuclear Medicine Department, Oncology Center, Bydgoszcz.
  • Tajer J; Positron Emission Tomography and Molecular Imagining Department, Collegium Medicum N. Copernicus University, Bydgoszcz, Poland.
  • Kulikowski W; Medical Physics Department, Santa Croce e Carle Hospital, Cuneo, Italy.
  • Fijolek-Warszewska A; Department of Hematology, Military Institute of Medicine, Warszawa.
  • Biggi A; Department of Lymphoproliferative Diseases, Maria Sklodowska-Curie Memorial Institute, Warszawa.
  • Fallanca F; Clinical Department of Hematology, Interior Ministry Hospital, Warmia.
  • Kobylecka M; Mazury Medical University, Olsztyn.
  • Dziuk M; Affidea Mazovian PET/CT Center, Warszawa, Poland.
  • Woszczyk D; Nuclear Medicine Department, Santa Croce e Carle Hospital, Cuneo.
  • Rybka J; Nuclear Medicine Department, San Raffaele Hospital, Milano, Italy.
  • Kroll-Balcerzak R; Nuclear Medicine Department, Warsaw Medical University, Warszawa.
  • Bergesio F; Nuclear Medicine Department, Military Institute of Medicine, Warszawa.
  • Romanowicz A; Hematology Unit, Regional Hospital, Opole.
  • Chamier-Cieminska A; Department of Hematology, Blood Neoplasms and Bone Marrow Transplantation, Wroclaw Medical University, Wroclaw.
  • Kurczab P; Department of Hematology, University Medical School, Poznan.
  • Giza A; Medical Physics Department, Santa Croce e Carle Hospital, Cuneo, Italy.
  • Lesniewski-Kmak K; Department of Hematology, Central Clinical Hospital MSW, Warszawa.
  • Zaucha R; Department of Clinical Oncology, Oncology Center, Bydgoszcz.
  • Swietlik D; Poradnia Onkologiczna z Oddzialem Chemioterapii Dziennej NZOZ Mrukmed, Rzeszów.
  • Wróbel T; Department of Hematology, Jagiellonian University Medical College, Krakow.
  • Knopinska-Posluszny W; Gdynia Oncology Center, Gdynia.
  • Walewski J; Departments of Oncological Propedeutics.
  • Gallamini A; Hematology and Transplantology, Medical University of Gdansk, Gdansk.
Ann Oncol ; 28(12): 3051-3057, 2017 Dec 01.
Article em En | MEDLINE | ID: mdl-28950332
ABSTRACT

BACKGROUND:

Interim PET after two ABVD cycles (iPET2) predicts treatment outcome in classical Hodgkin's lymphoma. To test whether an earlier assessment of chemosensitivity would improve the prediction accuracy, we launched a prospective, multicenter observational study aimed at assessing the predictive value of iPET after one ABVD (iPET1) and the kinetics of response assessed by sequential PET scanning. PATIENTS AND

METHODS:

Consecutive patients with newly diagnosed classical Hodgkin's lymphoma underwent interim PET scan after one ABVD course (iPET1). PETs were interpreted according to the Deauville score (DS) as negative (-) (DS 1-3) and positive (+) (DS 4, 5). Patients with iPET1 DS 3-5 underwent iPET2.

RESULTS:

About 106 early (I-IIA) and 204 advanced (IIB-IV) patients were enrolled between January 2008 and October 2014. iPET1 was (-) in 87/106 (82%) or (+) in 19/106 (18%) of early, and (-) in 133/204 (65%) or (+) in 71/204 (35%) of advanced stage patients, respectively. Twenty-four patients were excluded from response analysis due to treatment escalation. After a median follow-up of 38.2 (3.2-90.2) months, 9/102 (9%) early and 43/184 (23%) advanced patients experienced a progression-free survival event. At 36 months, negative and positive predictive value for iPET1 were 94% and 41% (early) and 84% and 43% (advanced), respectively. The kinetics of PET response was assessed in 198 patients with both iPETs. All 116 patients with iPET1(-) remained iPET2(-) (fast responders), 41/82 with IPET1(+) became iPET2(-) (slow responders), and the remaining 41 stayed iPET2(+) (non-responders); progression-free survival at 36 months for fast, slow and non-responders was 0.88, 0.79 and 0.34, respectively.

CONCLUSION:

The optimal tool to predict ABVD outcome in HL remains iPET2 because it distinguishes responders, whatever their time to response, from non-responders. However, iPET1 identified fast responders with the best outcome and might guide early treatment de-escalation in both early and advanced-stage HL.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Hodgkin / Protocolos de Quimioterapia Combinada Antineoplásica / Tomografia por Emissão de Pósitrons Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Hodgkin / Protocolos de Quimioterapia Combinada Antineoplásica / Tomografia por Emissão de Pósitrons Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2017 Tipo de documento: Article