Advertisement
Cleveland Clinic's approach to the therapy
Cleveland Clinic Cancer Center is now accepting patients for the FDA-approved chimeric antigen receptor (CAR) T-cell therapy, Yescarta™ (axicabtagene ciloleucel).
Advertisement
Cleveland Clinic is a non-profit academic medical center. Advertising on our site helps support our mission. We do not endorse non-Cleveland Clinic products or services. Policy
Yescarta is a CD19-directed CAR T-cell therapy indicated for the treatment of adult patients with relapsed or refractory large B-cell lymphoma after two or more lines of systemic therapy (including autologous stem cell transplantation). This includes diffuse large B-cell lymphoma(DLBCL), primary mediastinal B-cell lymphoma, high grade B-cell lymphoma and DLBCL arising from follicular lymphoma.
Cleveland Clinic participated in the pivotal phase 2 trial that reported outcomes on 111 patients with relapsed or refractory large B-cell lymphomas. Yescarta was administered to 101 patients (91 percent) with an objective response rate of 82 percent and a complete response rate of 54 percent. At 18 months post-treatment, the overall survival rate was 52 percent.
Severe side effects have been noted, prompting the FDA to require any centers that dispense Yescarta to be specially certified. These serious potential side effects include cytokine release syndrome and neurologic toxicities, both of which can be life-threatening. Building on experience obtained from participation on Yescarta clinical trials, Cleveland Clinic has established a multidisciplinary expert team with training and familiarity in administering this therapy and managing its toxicities.
Patients with relapsed or refractory large B-cell lymphoma should be referred for a consultation preferably prior to initiating second-line therapy. Earlier referral allows us to expedite eligibility evaluation for Yescarta in case the patient does not respond to salvage therapy. Patients with more advanced disease should be referred as soon as possible, including patients whose lymphoma has relapsed or not responded after autologous or allogeneic stem cell transplantation.
Advertisement
For questions about our approach to this therapy, please contact Brian Hill, MD, PhD, Director of the Lymphoma Program at hillb2@ccf.org or 216.445.9451, or Navneet Majhail, MD, MS, Director of the Blood and Marrow Transplant Program at majhain@ccf.org or 216.444.2199.
Advertisement
Advertisement
Study measures real-world outcomes for relapsed or refractory large B-cell lymphoma
Optimized responses in transplant- and CAR T-cell therapy-eligible patients
Findings from large database important to inform clinical practice
Socioeconomic disparities have a notable influence on access to allogeneic hematopoietic cell transplant
What’s coming up at ASH and beyond
Blinatumomab plus chemotherapy improves overall survival and relapse-free survival over chemotherapy alone
First-ever U.S. population-level retrospective analysis reveals many patients with systemic mastocytosis need faster intervention
Global R&D efforts expanding first-line and relapse therapy options for patients