Developing a System-Wide Protocol for Talquetamab Toxicity Management

Opinion
Video

Panelists discuss how health care providers can develop comprehensive management protocols for talquetamab-related toxicities by consulting with specialists, gathering patient feedback, and creating detailed handouts that empower patients to proactively manage adverse effects before they begin treatment.

Samantha Shenoy, NP, MSN, developed a comprehensive toxicity management protocol based on 5 years of clinical experience with patients on talquetamab, beginning with clinical trial participants. The protocol evolved through consultation with dermatologists, dietitians, colleagues at other institutions, and direct patient feedback about effective management strategies. This collaborative approach resulted in a 3- to 4-page handout covering taste changes, dry mouth, skin changes, nail changes, and weight loss management.

The handout provides practical, actionable recommendations organized by toxicity type, including specific product recommendations for managing each adverse effect category. For skin toxicities, recommendations include using emollients, ammonium lactate cream, and topical steroids for palmar-plantar peeling, along with lukewarm showers and immediate post-shower moisturizing. Nail care strategies involve nail hardeners, vitamin E cuticle oil, protective coverings such as finger cots, and trauma prevention through proper footwear and activity modifications.

The proactive distribution of educational materials before treatment initiation empowers patients to prepare by purchasing recommended products and understanding what to expect during therapy. The protocol emphasizes patient empowerment through preparation, suggesting patients keep materials accessible for ongoing reference rather than attempting to absorb all information at once. This systematic approach to toxicity management represents a scalable model for other institutions implementing bispecific antibody programs.

Recent Videos
4 experts are featured in this series.
4 experts are featured in this series.
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.
Related Content