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“Larotrectinib is extremely well-tolerated, and when we look at the poster from ASCO, we can actually see there are very few grade 3 toxicities that are attributed to larotrectinib. With a 10% complete response rate and all the patients getting really deep responses, it just blows almost all of the comparative chemotherapies in each of these cancers out of the park."

In an interview with Targeted Oncology, Raajit K. Rampal, MD, PhD, hematologic oncologist, Memorial Sloan Kettering Cancer Center, discussed the novel agent, APR-246, and its significance for use in the patients with myelodysplastic syndrome and acute myeloid leukemia

The FDA granted approval to pegfilgrastim-apgf, a biosimilar of pegfilgrastim, which is indicated to decrease the incidence of infection due to febrile neutropenia in patients with non-myeloid malignancies who are receiving myelosuppressive anti-cancer agents associated with a clinically significant incidence of febrile neutropenia.