U.S. Food and Drug Administration Approves CAR T Cell Therapy for Large B-Cell Lymphoma
The U.S. Food and Drug Administration Approves Axicabtagene Ciloeucel (YESCARTA) for Diffuse Large B-Cell Lymphoma…
Lymphoma News
U.S. Food and Drug Administration Approves Rituximab (RITUXAN) Plus Chemotherapy for Pediatric B-cell Lymphomas
Rituximab (RITUXAN, Genentech, Inc.), a monoclonal antibody, has been approved in combination with chemotherapy for pediatric patients 6-18 months with previously untreated, advanced staged, CD20-positive diffuse large B-cell lymphoma (DLBCL), Burkitt lymphoma (BL), and Burkitt-like lymphoma (BLL).
COVID-19 Vaccine Updates and FAQs
The Lymphoma Research Foundation (LRF) encourages patients, survivors, and their caregivers to take information and questions back to their individual health care providers as a way of creating a dialogue and partnership about their lymphoma and treatment.
Hope Forever and a Day
For more than 23 years, Marla Briskman faced her lymphoma—enduring five relapses and six different treatments. What gave her hope? Incredible treatment advancements and the support of family, friends, and her husband and caregiver, Rickey.
Caregiver Perspectives: Managing The Responsibilities of Caring for a Loved One
A lymphoma diagnosis not only affects the patient, but their caregivers too. LRF Scientific Advisory Board member, Thomas M. Habermann, MD shares some helpful strategies on how to help cope with some of the pressures of caregiving.
Three Healthy Ways to Navigate the Internet While Coping with a Lymphoma Diagnosis
Here are some ways lymphoma patients, survivors and caregivers can best navigate the internet for information, emotional and social support needs.
U.S. Food and Drug Administration Approves Ruxolitinib (Jakafi) for Chronic Graft-Versus-Host Disease
Belumosudil (REZUROCK, Kadmon Pharmaceuticals, LLC), is a kinase inhibitor for chronic graft-versus-host disease (chronic GVHD) in adult and pediatric patients 12 years and older.
The U.S. Food and Drug Administration Approves Zanubrutinib for Marginal Zone Lymphoma
On September 14, 2021, the U.S. Food and Drug Administration (FDA) announced it has approved zanubrutinib (BRUKINSA, BeiGene), for adult patients with relapsed or refractory marginal zone lymphoma (MZL) who have received at least one anti-CD20-based regimen.
Survivor: Africa Winner, Humanitarian and Cancer Survivor Ethan Zohn Named an Official Ambassador for the Lymphoma Research Foundation
Zohn joins a national LRF Ambassador program in which individuals from around the country share their stories of hope. With more than 100 types of lymphoma, many LRF Ambassadors’ diagnoses are different.
Ask the Doctor: What is the difference between primary cutaneous, systemic, and breast-implant associated ALCL?
Milos Miljkovic, MD MSc of the National Cancer Institute Center for Cancer Research discusses the main differences between these types of ALCL, how they are diagnosed, and typical frontline therapies.
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