J 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.