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The Chronic lymphocytic leukemia/ small lymphocytic lymphoma treatment landscape is moving toward fixed-duration, chemotherapy-free regimens using targeted agents. BTK inhibitors combined with venetoclax offer deep remissions and undetectable MRD, with strong long-term outcomes and retreatment potential. This approach reflects a growing preference for time-limited yet effective therapies.
Durable Outcomes with Fixed-Duration Ibrutinib + Venetoclax: 97% OS at 5.5 Years in CLL/SLL
The Chronic lymphocytic leukemia/ small lymphocytic lymphoma treatment landscape is moving toward fixed-duration, chemotherapy-free regimens using targeted agents. BTK inhibitors combined with venetoclax offer deep remissions and undetectable MRD, with strong long-term outcomes and retreatment potential. This approach reflects a growing preference for time-limited yet effective therapies.
Extended IsaKRD vs. ASCT: MIDAS Trial Suggests Equivalent MRD Clearance in MRD-Negative Myeloma
The phase III MIDAS trial showed that IsaKRD consolidation and ASCT resulted in similar MRD negativity in MRD-negative NDMM patients. No clear benefit was seen with tandem ASCT in MRD-positive patients
Balanced Outcomes with Lower-Dose BESPONSA: 50.9% Remission and 12.2-Month OS in Early Responders Pre-HSCT
BESPONSA continues to be a practical choice in R/R B-ALL, particularly for older or transplant-ineligible patients needing rapid, off-the-shelf treatment. Despite SOS risks, it offers high remission rates and fills a crucial gap where CAR-T therapies may not be suitable.
Selective CD33 Deletion with Trem-cel Supports Novel Post-Transplant Strategy to Prevent Relapse in AML
Trem-cel, a gene-edited hematopoietic stem cell therapy, demonstrated high CD33-editing efficiency, rapid engraftment, and favorable safety in patients with CD33-positive AML or high-risk MDS undergoing allogeneic transplant. When combined with post-transplant gemtuzumab ozogamicin maintenance, trem-cel allowed therapeutic exposure with reduced toxicity, suggesting a novel relapse-prevention strategy.
BLINCYTO Outshines Chemo with 3-Year OS of 100% in BCR::ABL1-Like ALL, Reinforcing Its Role in High-Risk Disease.
BLINCYTO (blinatumomab), the first FDA-approved bispecific antibody, has transformed treatment for B-cell ALL, particularly in MRD-positive and relapsed/refractory cases. Its clinical success and targeted mechanism have positioned it as a foundational therapy in the bispecific space, including in pediatric ALL, where it competes with CAR-T therapies like KYMRIAH.
Progress in Waldenström Macroglobulinemia Treatment: Phase I/II CaDAnCe-101 Findings for BeiGene’s BTK Degrader
BeiGene presented the Phase I/II (CaDAnCe-101 study) data of BGB-16673, a BTK degrader, a potential first-in-class protein degrader that blocks BTK signaling by tagging BTK for degradation through the cell's proteasome pathway. Data from this ongoing study demonstrate that the novel BTK degrader BGB-16673 was well tolerated and continued to show substantial antitumor activity in pts with heavily pretreated BTK inhibitor-exposed R/R WM, including those with BTK, CXCR4, and TP53 mutations.

Currently, the AML sphere constitutes a robust pipeline with more than 250+ drugs under different phases of development. Even with the presence of so many therapeutic drugs, there is still a need for targeted palliative care interventions and therapies with lower toxicity and better efficacy. Learn about the recent happenings, ongoing research & development, and significant pharmaceutical companies involved in the AML treatment market.

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