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EPCORE NHL-2 Trial Shows Promise Combining Chemotherapy and Immunotherapy for DLBCL

• A phase Ib/II clinical trial led by Mount Sinai researchers demonstrates successful outcomes in combining chemotherapy with immunotherapy for diffuse large B-cell lymphoma treatment.

• The groundbreaking research, published in Blood journal, was conducted under the leadership of Dr. Joshua Brody, director of the Lymphoma Immunotherapy Program at the Tisch Cancer Institute.

• The study represents a significant advancement in lymphoma treatment, supported by the Leukemia & Lymphoma Society's research initiatives, which have invested over $600 million in hematologic oncology research.

In a significant advancement for lymphoma treatment, researchers have demonstrated promising results from combining chemotherapy with immunotherapy in patients with diffuse large B-cell lymphoma (DLBCL). The findings, published in the prestigious journal Blood, emerge from the EPCORE NHL-2 phase Ib/II clinical trial.
The study, spearheaded by Dr. Joshua Brody, director of the Lymphoma Immunotherapy Program at the Tisch Cancer Institute at Mount Sinai, marks a notable step forward in improving treatment outcomes for DLBCL patients. This research represents part of a broader initiative in hematologic oncology, supported by significant funding from the Leukemia & Lymphoma Society (LLS).

Strategic Research Investment

The Leukemia & Lymphoma Society has played a crucial role in advancing hematologic oncology research, contributing over $600 million to more than 1,000 research projects. These investments have been channeled through various initiatives, including biomedical research grant programs and the Society's venture philanthropy arm, the Therapy Acceleration Program (TAP).

Clinical Trial Impact

The EPCORE NHL-2 trial's findings underscore the potential of combination therapy approaches in treating aggressive lymphomas. By integrating immunotherapy with traditional chemotherapy regimens, researchers aim to enhance treatment efficacy while potentially reducing resistance to single-agent approaches.
This research aligns with the growing trend toward combination therapies in oncology, particularly in addressing complex hematological malignancies. The study's results suggest a promising direction for future treatment protocols in DLBCL, which remains one of the most common and aggressive forms of lymphoma.

Future Implications

The success of this trial opens new avenues for research in lymphoma treatment, potentially influencing treatment guidelines and clinical practice. The findings were recently presented at the 66th annual ASH Annual Meeting and Exposition in San Diego, highlighting their significance to the broader oncology community.
As research continues, these results may pave the way for more personalized treatment approaches, combining the precision of immunotherapy with the established efficacy of chemotherapy regimens. This development represents a significant step forward in the ongoing effort to improve outcomes for lymphoma patients.
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