Article

Gazyva Boosts Outcomes in Follicular Lymphoma

Gazyva is an engineered monoclonal antibody designed to attach to CD20.

Obinutuzumab (Gazyva) demonstrated superior progression-free survival (PFS) compared with rituximab (Rituxan) in previously untreated follicular lymphoma patients.

Gazyva is an engineered monoclonal antibody designed to attach to CD20. The drug is thought to work by attacking targeted cells, both directly and together with the body’s immune system, according to a press release.

The global, open-label, multicenter, randomized, phase 3 GALLIUM study examined the safety and efficacy of Gazyva plus chemotherapy, followed by Gazyva alone for up to 2 years, as compared head-to-head against Rituxan plus chemotherapy, followed by Rituxan alone for up to 2 years.

Data from the pivotal study was presented for the first time during the American Society of Hematology Annual Meeting’s Plenary Scientific Session. This was the third positive phase 3 study for Gazyva, following the CLL11 and GADOLIN studies.

In the study, investigators evaluated 1401 patients with previously untreated indolent non-Hodgkin’s lymphoma (iNHL), of whom 1202 had follicular lymphoma. The primary endpoint was investigator-assessed PFS in patients with follicular lymphoma, with secondary endpoints including PFS as assessed by an independent review committee, PFS in the overall study population (iNHL), response rate (overall response and complete response), overall survival, and safety.

The results of the study showed that the Gazyva-based treatment reduced the risk of disease worsening or death (PFS) by 34% compared with Rituxan-based treatment (HR=0.66; 95% CI 0.51-0.85, p=0.0012). The median PFS was not yet reached.

“Follicular lymphoma, the most common slow-growing form of non-Hodgkin’s lymphoma, is an incurable blood cancer characterized by cycles of remission and disease progression, and becomes harder to treat with every relapse,” said Sandra Horning, MD, chief medical officer and head of Global Product Development for Genentech. “This study of Gazyva-based treatment is the first and only phase 3 trial to date to show superior progression-free survival compared to Rituxan-based treatment, the current standard of care, in previously untreated follicular lymphoma.”

Related Videos
Anthony Perissinotti, PharmD, BCOP, discusses unmet needs and trends in managing chronic lymphocytic leukemia (CLL), with an emphasis on the pivotal role pharmacists play in supporting medication adherence and treatment decisions.
Image Credit: © alenamozhjer - stock.adobe.com
pharmacogenetics testing, adverse drug events, personalized medicine, FDA collaboration, USP partnership, health equity, clinical decision support, laboratory challenges, study design, education, precision medicine, stakeholder perspectives, public comment, Texas Medical Center, DNA double helix
pharmacogenetics challenges, inter-organizational collaboration, dpyd genotype, NCCN guidelines, meta census platform, evidence submission, consensus statements, clinical implementation, pharmacotherapy improvement, collaborative research, pharmacist role, pharmacokinetics focus, clinical topics, genotype-guided therapy, critical thought
Image Credit: © Andrey Popov - stock.adobe.com
Image Credit: © peopleimages.com - stock.adobe.com
TRUST-I and TRUST-II Trials Show Promising Results for Taletrectinib in ROS1+ NSCLC
Image Credit: © Krakenimages.com - stock.adobe.com