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Positron emission tomography has a high negative predictive value for progression or early relapse for patients with residual disease after first-line chemotherapy in advanced-stage Hodgkin lymphoma
C Kobe, M Dietlein, J Franklin, J Markova, A Lohri, H Amthauer, S Klutmann, WH Knapp, JM Zijlstra, A Bockisch, M Weckesser, R Lorenz, M Schreckenberger, R Bares, HT Eich, RP Mueller, M Fuchs, P Borchmann, H Schicha, V Diehl, A Engert
Jazyk angličtina Země Spojené státy americké
Typ dokumentu multicentrická studie, randomizované kontrolované studie
Grantová podpora
NR8033
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
Free Medical Journals
od 1946 do Před 1 rokem
Freely Accessible Science Journals
od 1946 do Před 1 rokem
Open Access Digital Library
od 1946-01-01
Open Access Digital Library
od 1946-01-01
ROAD: Directory of Open Access Scholarly Resources
- MeSH
- bleomycin aplikace a dávkování MeSH
- cyklofosfamid aplikace a dávkování MeSH
- dospělí MeSH
- doxorubicin aplikace a dávkování MeSH
- etoposid aplikace a dávkování MeSH
- fluorodeoxyglukosa F18 * aplikace a dávkování MeSH
- Hodgkinova nemoc * farmakoterapie mortalita radiografie MeSH
- lidé středního věku MeSH
- lidé MeSH
- míra přežití MeSH
- mladiství MeSH
- pozitronová emisní tomografie * metody MeSH
- prediktivní hodnota testů MeSH
- prednison aplikace a dávkování MeSH
- přežití bez známek nemoci MeSH
- prokarbazin aplikace a dávkování MeSH
- protokoly protinádorové kombinované chemoterapie * aplikace a dávkování MeSH
- radiofarmaka * aplikace a dávkování MeSH
- reziduální nádor MeSH
- rizikové faktory MeSH
- vinkristin aplikace a dávkování MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- Publikační typ
- multicentrická studie MeSH
- randomizované kontrolované studie MeSH
In the HD15 trial of the German Hodgkin Study Group, the negative predictive value (NPV) of positron emission tomography (PET) using [(18)F]-fluorodeoxyglucose in advanced-stage Hodgkin lymphoma (HL) was evaluated. A total of 817 patients were enrolled and randomly assigned to receive BEACOPP-based chemotherapy. After completion of chemotherapy, residual disease measuring more than or equal to 2.5 cm in diameter was assessed by PET in 311 patients. The NPV of PET was defined as the proportion of PET(-) patients without progression, relapse, or irradiation within 12 months after PET review panel. The progression-free survival was 96% for PET(-) patients (95% confidence interval [CI], 94%-99%) and 86% for PET(+) patients (95% CI, 78%-95%, P = .011). The NPV for PET in this analysis was 94% (95% CI, 91%-97%). Thus, consolidation radiotherapy can be omitted in PET(-) patients with residual disease without increasing the risk for progression or early relapse compared with patients in complete remission. The impact of this finding on the overall survival at 5 years must be awaited. Until then, response adapted therapy guided by PET for HL patients seems to be a promising approach that should be further evaluated in clinical trials. This trial is registered at http://isrctn.org study as #ISRCTN32443041.
Department Nuclear Medicine University Medical Center Hamburg Eppendorf Hamburg Germany
Department of Hematology VU University Medical Centre Amsterdam The Netherlands
Department of Internal Medicine University of Cologne Cologne Germany
Department of Nuclear Medicine Gutenberg University Hospital Mainz Germany
Department of Nuclear Medicine Hanover University Medical School Hanover Germany
Department of Nuclear Medicine Universilsity Hospital Muenster Muenster Germany
Department of Nuclear Medicine University of Cologne Cologne Germany
Department of Nuclear Medicine University of Duisburg Essen Essen Germany
Department of Nuclear Medicine University of Tuebingen Tuebingen Germany
Department of Nuclear Medicine University of Wuerzburg Wuerzburg Germany
Department of Radiation Oncology University of Cologne Cologne Germany
German Hodgkin Study Group University of Cologne Cologne Germany
Schweizer Arbeitsgruppe fúr Klinische ebsforschung Bern Switzerland
Citace poskytuje Crossref.org
Literatura
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