Dr. Wojciech Jurczak on MOR208 in Non-Hodgkin's Lymphoma

​Wojciech Jurczak, MD
Published: Saturday, Jun 11, 2016



Wojciech Jurczak, MD Head of Lymphoma, Department of Hematology, Jagiellonian University, Kopernika, Poland, discuses a subgroup analyses of diffuse large b-cell lymphoma (DLBCL) and indolent lymphoma cohorts from a phase IIa study of single-agent MOR208 in patients with relapsed or refractory non-Hodgkin's lymphoma (NHL).
 
MOR208, a monoclonal antibody directed against the antigen CD19, was given to patients for at least 3 months. In the DLBCL subgroup a 30% objective response rate was achieved, with most responses being durable and some continuing beyond 2-years. MOR208 is a relatively non-toxic treatment and a potential target for future combinations regimens, said Jurczak. The 30% response rate was more than expected, he says.
 
In the indolent lymphoma cohort, the protocol was poorly designed, says Jurczak. Most of the patients responded, however nearly half had stable disease and as such therapy was not continued after the first cycle. Those who responded did have a prolonged progression-free-survival, he says.

<<< View more from the 2016 EHA Congress


Wojciech Jurczak, MD Head of Lymphoma, Department of Hematology, Jagiellonian University, Kopernika, Poland, discuses a subgroup analyses of diffuse large b-cell lymphoma (DLBCL) and indolent lymphoma cohorts from a phase IIa study of single-agent MOR208 in patients with relapsed or refractory non-Hodgkin's lymphoma (NHL).
 
MOR208, a monoclonal antibody directed against the antigen CD19, was given to patients for at least 3 months. In the DLBCL subgroup a 30% objective response rate was achieved, with most responses being durable and some continuing beyond 2-years. MOR208 is a relatively non-toxic treatment and a potential target for future combinations regimens, said Jurczak. The 30% response rate was more than expected, he says.
 
In the indolent lymphoma cohort, the protocol was poorly designed, says Jurczak. Most of the patients responded, however nearly half had stable disease and as such therapy was not continued after the first cycle. Those who responded did have a prolonged progression-free-survival, he says.

<<< View more from the 2016 EHA Congress

View Conference Coverage
Online CME Activities
TitleExpiration DateCME Credits
Oncology Best Practice™: Choosing Therapies for Patients with EGFR-Mutant Lung Cancers: More Options... More Decisions... Better OutcomesFeb 28, 20182.0
Clinical Vignette Series: 34th Annual Chemotherapy Foundation Symposium: Innovative Cancer Therapy for Tomorrow®Feb 28, 20182.0
Publication Bottom Border
Border Publication
x