Dual-Target Annihilation: New Hope Against Myeloma's Most Vicious Form

Ava ChenJun 16, 2025
An artistic rendering of two distinct antibodies (TALVEY® and TECVAYLI®) converging on and neutralizing a rogue multiple myeloma cell that has spread outside the bone marrow, perhaps with a subtle glow indicating successful targeting.
  • A groundbreaking combination of two first-in-class antibody therapies, TALVEY® (talquetamab) and TECVAYLI® (teclistamab), is showing remarkable success against a notoriously aggressive form of multiple myeloma.
  • Patients with extramedullary disease (EMD), where cancer spreads to soft tissues and organs, demonstrated deep and lasting responses in the pivotal RedirecTT-1 study.
  • These findings, presented at the 2025 European Hematology Association (EHA) Congress, signal a potential paradigm shift for those facing the poorest prognoses.

For patients battling relapsed or refractory multiple myeloma (RRMM), particularly the formidable extramedullary disease (EMD), the fight has often been a losing one. EMD, where myeloma cells form tumours beyond the bone marrow, has historically defied standard treatments, leaving patients with bleak outlooks and an average overall response rate below 40%7.

But now, a beacon of hope emerges. The investigational combination of TALVEY®, targeting the novel GPRC5D, and TECVAYLI®, targeting BCMA, has delivered stunning results in the RedirecTT-1 study – the largest of its kind for EMD patients2, 5, 7. This dual-pronged attack achieved an extraordinary overall response rate (ORR) of 78.9% in these heavily pretreated individuals, with over half experiencing a complete response or better7. Even more critically, these responses are proving durable, with 66.2% of responders still holding the disease at bay after a median follow-up of 13.4 months7.

This innovative approach, harnessing two distinct mechanisms, aims to outsmart the cancer's escape routes. "Dual targeting of GPRC5D and BCMA may lead to a higher ORR and greater depth of response by mitigating target antigen-related escape," stated Dr. Yael Cohen. The safety profile remained manageable, consistent with individual drug reports, offering a potent new strategy for patients who have exhausted other options, including prior CAR-T therapy2, 7, 8. This heralds a new era in the offensive against one of cancer's most challenging fronts.


References

  1. ashpublications.org
  2. pubmed.ncbi.nlm.nih.gov
  3. www.jnj.com
  4. trials.ohsu.edu
  5. www.cancernetwork.com
  6. www.myeloma.org
  7. innovativemedicine.jnj.com
  8. ascopost.com

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