‘Major step forward’ for adult patients as new blood cancer drug receives FDA approval

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‘Major step forward’ for adult patients as new blood cancer drug receives FDA approval
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A cancer specialist discussed the FDA's approval of Johnson & Johnson’s new drug, Talvey, an antibody-based therapy for adult patients with tough-to-treat blood cancers.

In clinical studies, Talvey showed"impressive response rates" in myeloma patients who had received prior treatments, said Landgren, who is a renowned hematologist/oncologist specializing in multiple myeloma, smoldering myeloma and related plasma cell disorders."The overall response rate is 70% in patients who failed four prior lines of myeloma therapy," he said.

The most common adverse effects included an altered or impaired sense of taste, dry mouth and difficulty swallowing. , skin reactions, serious infections, low white blood cell count and low blood platelets, per the press release. "Trained health care providers know what to look for clinically and how to do lab work to monitor the individual patient’s immune status," Landgren told Fox News Digital."If everything is done correctly, these drugs are overall very safe and effective."

"Ongoing studies are seeking to define optimal ways to pre-medicate patients for the first few doses to limit side effects such as fever and immunological reactions, so these drugs can be given outpatient from day one," he said. With the large number of new, effective and safe drugs, Landgren said"the future is bright" for patients with multiple myeloma.

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