Exploring GPRC5D as an Important Target for Multiple Myeloma

Publication
Article
ONCOLOGY® CompanionONCOLOGY® Companion, Volume 38, Supplement 9
Volume 38
Issue 9
Pages: 3

Experts highlighted the use of GPRC5D therapy in patients with multiple myeloma.

Meet the experts

Meet the experts

A recent Training Academy highlighted the use of GPRC5D therapy in patients with multiple myeloma. The most common and only approved option is talquetamab-tgvs (Talvey). The panel highlighted the treatment in the phase 1/2 MonumenTAL-1 trial (NCT03399799; NCT04634552).

Using, Treating, and Sequencing GPRC5D Therapy

  • An important target because there needs to be a range of options developed to treat multiple myeloma.
    • This can be used prior to a B-cell maturation antigen (BCMA).
  • Can be considered to be used as a bridge to a BCMA or chimeric antigen receptor T-cell therapy.
  • GPRC5D is more commonly expressed in malignant plasma vs normal.
  • Combination therapies may produce higher efficacy rates than these monotherapies.
  • Talquetamab was assessed in the phase 1/2 MonumenTAL-3 trial (NCT05455320).
  • The most common toxicities include oral and skin.
    • Not as severe as with bispecific antibodies.
    • Hypothesized, as this is given one treatment at a time vs continuous bispecific use.
  • Dose de-escalation can be helpful to manage.
    • Monthly treatment may be an option to help lessen or avoid dysgeusia.
  • Talquetamab has not shown adverse effects (AEs) related to cardiac issues, pulmonary issues, renal issues, or neuropathy.
  • AEs typically happen at first onset and then lessen as the disease becomes better controlled.
  • As a GPRC5D target, there is less infectious toxicity involved.
    • Intravenous immunoglobulin supplementation is not needed as much.
Recent Videos
Younger and fitter patients with relapsed/refractory multiple myeloma were more likely to receive bispecific antibodies in community oncology settings.
Mechanistic treatment benefits were observed in the phase 2 STEM trial for patients with multiple myeloma.
Data from a retrospective cohort study showed that one-fifth of patients with multiple myeloma received bispecific antibodies in rural community settings.
Being able to treat patients with cevostamab who have multiple myeloma after 1 to 3 prior lines of therapy vs 4 lines may allow for better outcomes.
Using the monitoring of symptoms and quality of life platform may provide a quick and efficient system for patients to submit outcome data.
Current FDA expectations may allow patients to return to their community physicians at 2 weeks after administration of anitocabtagene autoleucel.
Based on its mechanism of action, anito-cel may cause fewer instances of cytokine release syndrome and delayed toxicities vs other therapies.
Combining daratumumab with other agents is one strategy that investigators are exploring in the smoldering multiple myeloma field.
A substantial portion of patients who received daratumumab in the AQUILA study were able to delay disease progression to active multiple myeloma.
The approval of daratumumab validates the notion of using limited therapy to help delay progression from smoldering disease to multiple myeloma.
Related Content