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Hematologic Malignancy Treatment: Community Oncology Updates - News Directory 3

Hematologic Malignancy Treatment: Community Oncology Updates

January 12, 2026 Jennifer Chen Health
News Context
At a glance
  • The‌ treatment landscape for hematologic malignancies like multiple myeloma (MM) adn chronic lymphocytic leukemia (CLL) is rapidly evolving, bringing new targeted therapies‌ to the community ‍setting.
  • One study reviewed the rapid uptake of bispecific antibodies for relapsed/refractory MM, noting that real-world patients tend⁢ to be older‌ than those in clinical trials.1 The other ‌analysis...
  • The data suggest a tendency away from continuous therapy, particularly among patients with varying health and performance statuses.
Original source: ajmc.com

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The‌ treatment landscape for hematologic malignancies like multiple myeloma (MM) adn chronic lymphocytic leukemia (CLL) is rapidly evolving, bringing new targeted therapies‌ to the community ‍setting. In an interview​ wiht The American Journal of Managed Care®(AJMC®)that ‌took place during the 67th American Society of Hematology Annual Meeting and Exposition, Ira Zackon, MD, senior medical director, Ontada, discussed findings from 2 major analyses that explored the real-world adoption, patient characteristics, and treatment paradigms associated with⁣ these novel⁣ agents.1,2

One study reviewed the rapid uptake of bispecific antibodies for relapsed/refractory MM, noting that real-world patients tend⁢ to be older‌ than those in clinical trials.1 The other ‌analysis highlighted meaningful real-world‌ discontinuation ​rates for ⁢covalent Bruton tyrosine kinase (BTK) inhibitors in CLL, primarily due to adverse effects (AEs), suggesting advantages for time-limited therapy approaches.2 These essential insights into community-based oncology care

A significant discontinuation rate was observed with all covalent ⁢BTK inhibitors, with approximately ‍two-thirds of patients discontinuing treatment during the study period, even with second-generation drugs like acalabrutinib and zanubrutinib. These newer drugs had become preferred first-line options due to their improved safety⁤ profiles ⁣- specifically, lower rates of cardiovascular adverse ⁢events like atrial ⁣fibrillation or⁢ hypertension – and comparable or superior efficacy. However, the study found that nearly 40% of patients discontinued acalabrutinib, around 50% discontinued zanubrutinib, and 56% discontinued ibrutinib. The primary reason for discontinuation was toxicity or adverse⁢ events, though documentation was lacking for about a ​third of discontinuations.

The data suggest a tendency away from continuous therapy, particularly among patients with varying health and performance statuses. This presents a potential limitation to the continuous therapy paradigm, which currently has the most mature follow-up data.Time-limited therapy may offer advantages, and treatment paradigms⁤ are increasingly moving in that direction, both in clinical practice and ongoing trials. Shorter times to discontinuation were linked to lower performance status, more comorbidities, and specific adverse events,⁢ highlighting factors common in real-world settings.

Currently, patients have the option of ‌continuous covalent BTK inhibitor therapy or a time-limited, fixed-duration approach, such as venetoclax (a BCL-2 inhibitor) combined with obinutuzumab (an anti-CD20 ‌monoclonal antibody). The National Comprehensive Cancer Network supports​ combinations like acalabrutinib and venetoclax. Time-limited⁣ approaches‍ offer potential⁤ benefits, including shorter ⁤overall treatment ⁢duration, the possibility of a ‍treatment-free interval to ⁢improve quality of life, and reduced⁢ costs for⁣ both⁤ patients and payers.Combinations are becoming more prevalent, and ongoing clinical trials⁤ will continue to refine treatment strategies.

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