Mohammed Rahman, MD
The pan-HER TKI neratinib (Nerlynx) demonstrates efficacy as an adjuvant therapy for patients with HER2-positive breast cancer; however, the associated adverse events (AEs) provide some patient selection challenges, explained Mohammed Rahman, MD.
“I think all-in-all, it’s an attractive treatment. The only downside of it is gastrointestinal toxicity—the diarrhea rate in the ExteNET trial was almost 90%, but more importantly, grade 3 diarrhea was close to 39% or 40%,” said Rahman. “However, if doctors are very aggressive with antidiarrheal management, these [events] can be managed easily and effectively. We can actually get the numbers down with various remedies to maybe single-digit figures in terms of grade 3 diarrhea toxicity.”
The FDA approved neratinib (Nerlynx) in July 2017 to prevent recurrence in patients with early-stage HER2-positive breast cancer who had completed at least 1 year of adjuvant therapy with trastuzumab (Herceptin).
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