Detailed Information on Publication Record
2016
Prognostic relevance of DHAP dose-density in relapsed Hodgkin lymphoma: an analysis of the German Hodgkin-Study Group
SASSE, Stephanie, Magdalena ALRAM, Horst MÜLLER, Lenka ŠMARDOVÁ, Bernd METZNER et. al.Basic information
Original name
Prognostic relevance of DHAP dose-density in relapsed Hodgkin lymphoma: an analysis of the German Hodgkin-Study Group
Authors
SASSE, Stephanie (276 Germany), Magdalena ALRAM (276 Germany), Horst MÜLLER (276 Germany), Lenka ŠMARDOVÁ (203 Czech Republic, guarantor, belonging to the institution), Bernd METZNER (276 Germany), Hartmut DOEHNER (276 Germany), Thomas FISCHER (276 Germany), Dietger W. NIEDERWIESER (276 Germany), Norbert SCHMITZ (276 Germany), Kerstin SCHÄFER-ECKART (276 Germany), John M. M. RAEMAEKERS (528 Netherlands), Oliver SCHMALZ (276 Germany), Bastian V. TRESCKOW (276 Germany), Andreas ENGERT (276 Germany) and Peter BORCHMANN (276 Germany)
Edition
Leukemia & Lymphoma, Abingdon, Taylor & Francis LTD, 2016, 1042-8194
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30200 3.2 Clinical medicine
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 2.755
RIV identification code
RIV/00216224:14110/16:00089247
Organization unit
Faculty of Medicine
UT WoS
000375027000014
Keywords in English
DHAP; dose density; hematotoxicity; outcome; relapsed Hodgkin lymphoma
Tags
Tags
International impact, Reviewed
Změněno: 29/7/2016 15:10, Soňa Böhmová
Abstract
V originále
Only 50% of patients with relapsed Hodgkin lymphoma (HL) can be cured with intensive induction chemotherapy, followed by high-dose chemotherapy (HDCT) and autologous stem cell transplant (ASCT). Based on the results of the HDR2 trial two courses of DHAP and subsequent HDCT/ASCT are the current standard of care in relapsed HL. In order to assess the prognostic relevance of DHAP dose density, we performed a retrospective multivariate analysis of the HDR2 trial (N=266). In addition to four risk factors (early or multiple relapse, stage IV disease or anemia at relapse, and grade IV hematotoxicity during the first cycle of DHAP) a delayed start of the second cycle of DHAP>day 22 predicted a significantly poorer progression-free survival (PFS, p=0.0356) and overall survival (OS, p=0.0025). In conclusion, our analysis strongly suggests that dose density of DHAP has a relevant impact on the outcome of relapsed HL patients.