Exploring the role of BTK inhibitors in mantle cell lymphoma: sequencing & managing adverse events
Oct 30, 2024
auto_awesome
Join experts Krish Patel, MD, specializing in mantle cell lymphoma treatment, Marek Trněný, MD, PhD, a key contributor to BTK inhibitor trials, and Michael Wang, MD, who offers insights on therapeutic sequencing. They delve into groundbreaking trials like ECHO and SHINE, discussing the role of BTK inhibitors and their effectiveness for older patients. Notably, they address optimal sequencing methods to prevent cross-resistance and strategies for managing cardiac toxicities. Their collaboration underscores a comprehensive approach to enhancing patient care.
BTK inhibitors are effective for mantle cell lymphoma, particularly in older or non-chemo candidates, with ongoing trials enhancing treatment protocols.
Managing adverse effects of BTK inhibitors, especially cardiac toxicities and infections, requires careful sequencing and monitoring to prevent resistance.
Deep dives
Role of BTK Inhibitors in Treatment
BTK inhibitors have proven to be highly effective in the treatment of mantle cell lymphoma, particularly for older patients or those who are not good chemotherapy candidates. Recent trials indicate that these agents can be used either as monotherapy or in combination with rituximab, with ongoing studies like the Mangrove trial evaluating their benefit versus traditional chemoimmunotherapy. Furthermore, ibrutinib has shown improvement in progression-free survival when combined with BR (bendamustine and rituximab), enhancing the time between treatments. Additionally, for younger patients, data suggests that using BTK inhibitors as consolidation therapy might effectively replace autologous stem cell transplants, establishing a new treatment standard in Europe where these approaches are being actively investigated.
Managing Adverse Events and Sequencing Therapies
Managing the adverse effects of BTK inhibitors is crucial, particularly cardiac toxicities and the risk of infections, as these drugs can lead to immunosuppression. When a patient progresses on a BTK inhibitor, it is essential to avoid moving to another covalent BTK inhibitor, as this can perpetuate resistance; instead, non-covalent options should be considered. Physicians employ numerous strategies to monitor and mitigate side effects, including cardiac assessments and offering immunoglobulin therapy for patients experiencing infections. Furthermore, the approach to sequencing therapies for relapsed patients hinges on prior treatments, with BTK inhibitors remaining standard options post-chemotherapy, while alternative therapies like CAR T-cell therapy or non-covalent BTK inhibitors are considered based on individual patient responses to previous therapies.
Today’s podcast focuses on the role of BTK inhibitors (BTKis) in the treatment of mantle cell lymphoma (MCL). You will hear from experts Krish Patel, MD, Providence Swedish Cancer Institute, Seattle, WA, Marek Trněný, MD, PhD, Charles University Hospital, Prague, Czech Republic, Michael Wang, MD, The University of Texas MD Anderson Cancer Center, Houston, TX, and Craig Portell, MD, University of Virginia, Charlottesville, VA. They share updates on trials investigating BTKis in the frontline treatment of MCL, including the ECHO (NCT02972840), SHINE (NCT01776840), and TRIANGLE (NCT02858258) studies. They then go on to discuss how these agents are optimally sequenced and give advice for managing cardiac toxicities associated with BTKis.