Lymphoma in the News: Two Important Studies Take Us One Step Closer to Personalized Lymphoma Therapy

By Peter Martin, MD and Olivier Elemento, PhD

Based on multiple randomized phase 3 studies initiated over a decade ago, R-CHOP chemotherapy is the standard of care for first-line treatment of patients with diffuse large B-cell lymphoma (DLBCL). However, sometimes R-CHOP is not successful. Fortunately, our understanding of lymphoma has evolved over the past decade.

It is increasingly clear that “DLBCL” is a heterogeneous group of related tumors. Studies using gene expression profiling [1], have revealed that DLBCL can be divided into three subgroups based on the probable cell of origin (i.e., the cell from which the lymphoma was derived): activated B-cell like DLBCL (ABC), germinal center-like DLBCL (GCB), and a third group, termed “type 3”, that doesn’t possess any specific characteristics (click here to read the abstract). So far, the clinical relevance of differentiating between the ABC and GCB subtypes of DLBCL remains somewhat unclear. Nonetheless, studies done at Weill Cornell Medical College and elsewhere have suggested that certain treatments might preferentially benefit one subtype (see here and here). As a result, ongoing clinical trials are evaluating newer therapies targeted to the appropriate subgroup.

Just as we are beginning to understand the significance of DLBCL gene expression profiles, recent technological advances in DNA sequencing are making the rapid, high-resolution sequencing of a tumor’s entire genome (DNA code) possible and affordable [2]. Two recently published papers describe the results of long-term efforts by two different groups to sequence the genome of DLBCL tumors.

A Groundbreaking Study

In a paper entitled “Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma” published in the journal Nature, Gascoyne, Marra and colleagues describe the results of a groundbreaking study. The researchers sequenced the entire DNA code from lymphoma tumors and compared the results to normal DNA obtained from the same patients. They were able to identify several genes that were mutated in the tumors but not in the normal DNA. Using these data, they were able to identify 109 genes with a potential role in lymphoma. Continue reading “Lymphoma in the News: Two Important Studies Take Us One Step Closer to Personalized Lymphoma Therapy”

Upcoming Cancer Care Workshop: Update on Diffuse Large B-cell Lymphoma

Cancer Care will present a Connect Education Workshop titled, “Update on Diffuse Large B-cell Lymphoma” via telephone on Wednesday, October 5, 2011 from 1:30 to 2:30 pm, Eastern Time. Weill Cornell’s Dr. John Leonard will be on the panel of experts.

The workshop is free of charge; no phone charges apply. However, pre-registration is required to secure a place on the call. Click here for more information and to register for the workshop.

BioTime Licenses Weill Cornell-Developed Vascular Cells Technology; Anti-Cancer Tumor Potential

BioTime, Inc. announced today it has entered into an exclusive agreement with Cornell University for the worldwide development and commercialization of technology developed at Weill Cornell Medical College for the differentiation of human embryonic stem cells into vascular endothelial cells. Potential uses of this technology may include a new modality for targeting cancer tumors.

Vascular endothelial cells form the blood vessels that support the growth of cancerous tumors. The technology may be used to derive vascular endothelial cells engineered to “deliver a toxic payload to the developing blood vessels of a tumor to remove malignant tumors while not affecting nearby normal tissues.”

Click here to read the full article.