Top Myeloma Research Presented at ASH 2025

Описание: Key Highlights from ASH 2025 – Myeloma Updates

0:00:00 Event Overview:
ASH (American Society of Hematology) hosted its largest annual meeting with over 9,000 abstracts submitted, including 1,500+ related to multiple myeloma.
Attendance: 27,500 in-person and 3,500 virtual participants.

0:07:58 Top 10 Abstracts:
0:09:30 CAR T Cell Therapy (5 abstracts)
0:09:43 - In vivo CAR T (LBA-1) – novel gene therapy approach.
0:14:07 - Long-term follow-up of cilta-cel shows sustained progression-free survival.
0:18:28 - Safety enhancements for cilta-cel to reduce neurotoxicity.
0:21:27 - Dual-target FasTCAR-T for frontline therapy.
0:23:22 - Anito-cel (D-domain CAR T) demonstrates deep responses and manageable safety.

0:25:31 CAR T Cell Therapy Insights
Most effective therapy for multiple myeloma with remarkable long-term outcomes.
Novel approaches include:In vivo CAR T delivery (simplifies logistics, reduces cost).
Dual-targeting CAR T for deeper responses.
D-domain CAR T for improved safety and efficiency.
Key considerations:Effective bridging therapy reduces toxicity.
Earlier use in standard-risk patients improves survival.

0:39:21 Bispecific Antibodies (5 abstracts)
0:39:37 - Teclistamab + Daratumumab in early relapse
0:43:40 - Teclistamab + Daratumumab frontline settings.
0:45:41 - Linvoseltamab for MRD-positive patients post-induction.
0:50:12 - Cevostamab consolidation after CAR T therapy.
0:52:01 - Teclistamab + Talquetamab for aggressive extramedullary disease.
0:54:15 - Elranatamab + Iberdomide combination shows high ORR.

0:55:33 Bispecific Antibody Advances
Potent combinations (e.g., Teclistamab + Daratumumab) in both frontline and relapse settings.
Fixed-duration strategies (Linvoseltamab, Cevostamab) post-CAR T therapy.
Dual bispecific combinations (Teclistamab + Talquetamab) highly effective in aggressive disease.
Integration with CelMods for enhanced efficacy.

1:04:52 Future Directions in Myeloma Therapy
Continued evolution toward:Novel CAR T platforms (dual-target, in vivo).
Bispecific/Trispecific antibodies.
Next-gen immunomodulators (Iberdomide, Mezigdomide).
Targeted small molecules for specific genetic subtypes.

Patient-Centered Questions:
Should CAR T move to earlier lines for standard-risk patients?
How to manage infection risk with bispecific antibodies?
Is fixed-duration therapy the future for bispecifics?
Will dual bispecific combinations become standard?


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