Only strongly enhanced residual FDG uptake in early response PET (Deauville 5 or qPET ≥ 2) is prognostic in pediatric Hodgkin lymphoma: Results of the GPOH-HD2002 trial.


Journal

Pediatric blood & cancer
ISSN: 1545-5017
Titre abrégé: Pediatr Blood Cancer
Pays: United States
ID NLM: 101186624

Informations de publication

Date de publication:
03 2019
Historique:
received: 23 04 2018
revised: 11 10 2018
accepted: 14 10 2018
pubmed: 15 11 2018
medline: 13 11 2019
entrez: 15 11 2018
Statut: ppublish

Résumé

In 2014, we published the qPET method to quantify fluorodeoxyglucose positron emission tomography (FDG-PET) responses. Analysis of the distribution of the quantified signals suggested that a clearly abnormal FDG-PET response corresponds to a visual Deauville score (vDS) of 5 and high qPET values ≥ 2. Evaluation in long-term outcome data is still pending. Therefore, we analyzed progression-free survival (PFS) by early FDG-PET response in a subset of the GPOH-HD2002 trial for pediatric Hodgkin lymphoma (PHL). Pairwise FDG-PET scans for initial staging and early response assessment after two cycles of chemotherapy were available in 93 PHL patients. vDS and qPET measurement were performed and related to PFS. Patients with a qPET value ≥ 2.0 or vDS of 5 had 5-year PFS rates of 44%, respectively 50%. Those with qPET values < 2.0 or vDS 1 to 4 had 5-year PFS rates of 90%, respectively 80%. The positive predictive value of FDG-PET response assessment increased from 18% (9%; 33%) using a qPET threshold of 0.95 (vDS ≤ 3) to 30% (13%; 54%) for a qPET threshold of 1.3 (vDS ≤ 4) and to 56% (23%; 85%) when the qPET threshold was ≥ 2.0 (vDS 5). The negative predictive values remained stable at ≥92% (CI: 82%; 98%). Only strongly enhanced residual FDG uptake in early response PET (vDS 5 or qPET ≥ 2, respectively) seems to be markedly prognostic in PHL when treatment according to the GPOH-HD-2002 protocol is given.

Identifiants

pubmed: 30426671
doi: 10.1002/pbc.27539
doi:

Substances chimiques

Radiopharmaceuticals 0
Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e27539

Informations de copyright

© 2018 Wiley Periodicals, Inc.

Auteurs

L Kurch (L)

Department of Nuclear Medicine, University Hospital of Leipzig, Leipzig, Germany.

D Hasenclever (D)

Institute of Medical Statistics, Informatics and Epidemiology, University of Leipzig, Leipzig, Germany.

R Kluge (R)

Department of Nuclear Medicine, University Hospital of Leipzig, Leipzig, Germany.

T Georgi (T)

Department of Nuclear Medicine, University Hospital of Leipzig, Leipzig, Germany.

L Tchavdarova (L)

Clinic of Nuclear Medicine, National Hospital for Active Treatment in Oncology, Sofia, Bulgaria.

M Golombeck (M)

Department of Nuclear Medicine, University Hospital of Leipzig, Leipzig, Germany.

O Sabri (O)

Department of Nuclear Medicine, University Hospital of Leipzig, Leipzig, Germany.

A Eggert (A)

Division of Pediatric Hematology and Oncology, Department of Pediatrics, Charité Berlin, Berlin, Germany.

W Brenner (W)

Department of Nuclear Medicine, Charité - Universitätsmedizin Berlin, Berlin, Germany.

K W Sykora (KW)

Department of Pediatric Hematology and Oncology, Medizinische Hochschule Hannover, Hannover, Germany.

F M Bengel (FM)

Department of Nuclear Medicine, Medizinische Hochschule Hannover, Hannover, Germany.

C Rossig (C)

University Children's Hospital Münster, Pediatric Hematology and Oncology, Münster, Germany.

D Körholz (D)

Division of Pediatric Hematology and Oncology, Department of Pediatrics, Justus-Liebig University of Giessen, Giessen, Germany.

M Schäfers (M)

Department of Nuclear Medicine, University Hospital of Münster, Münster, Germany.

T Feuchtinger (T)

Dr. von Hauner University Children's Hospital, LMU Munich, Munich, Germany.

P Bartenstein (P)

Department of Nuclear Medicine, LMU Munich, Munich, Germany.

R A Ammann (RA)

Division of Pediatric Hematology and Oncology, Department of Pediatrics (Inselspital) Bern University Hospital, University of Bern, Bern, Switzerland.

T Krause (T)

Department of Nuclear Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

C Urban (C)

Division of Pediatric Hematology and Oncology, Department of Pediatrics, University Hospital Graz, Graz, Austria.

R Aigner (R)

Department of Radiology, Medical University Graz, Graz, Austria.

S Gattenlöhner (S)

Department of Pathology, Justus-Liebig University of Giessen, Giessen, Germany.

W Klapper (W)

Department of Pathology, University Hospital of Kiel, Kiel, Germany.

C Mauz-Körholz (C)

Division of Pediatric Hematology and Oncology, Department of Pediatrics, Justus-Liebig University of Giessen, Giessen, Germany.
Medical Faculty, Martin-Luther-University of Halle-Wittenberg, Halle, Germany.

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