
Articles
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Mar 17, 2024 |
ajmc.com | Laura Joszt |Justina Petrullo
Typically, patients with acute myeloid leukemia (AML) or myelodysplastic syndromes (MDS) receive aggressive chemotherapy treatment that requires long hospital stays, but it is possible to put the foundation in place for these patients to receive support in the outpatient setting in order for them to maintain quality of life and remain close to the people who matter to them, explained Jennifer Vaughn, MD, of The Ohio State University Comprehensive Cancer Center – James Cancer Hospital.
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Mar 1, 2024 |
ajmc.com | Laura Joszt |Justina Petrullo
With most patients with myeloproliferative neoplasms (MPNs) and myelodysplastic syndromes (MDS) experiencing long-term, chronic disease, it’s important to discuss their priorities and set up the relationship with their providers upfront, explained Jennifer Vaughn, MD, assistant professor in the division of hematology at The Ohio State University Comprehensive Cancer Center – James Cancer Hospital and Solove Research Institute.
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Oct 29, 2023 |
centerforbiosimilars.com | Skylar Jeremias |Justina Petrullo
Stephen Hanauer, MD, professor of medicine, Feinberg School of Medicine, Northwestern University, comments on concerning data from Cardinal Health and Spherix Global Insights regarding the potential growth of the US adalimumab market, including providers’ views on interchangeability and payers’ influence on utilization.
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Oct 22, 2023 |
centerforbiosimilars.com | Skylar Jeremias |Justina Petrullo
There are many steps that health systems can take to prevent the nocebo effect when transitioning patients from Humira (reference adalimumab) to an adalimumab biosimilar, according to Stephen Hanauer, MD, professor of medicine, Feinberg School of Medicine, Northwestern University. TranscriptCan you discuss the importance of pharmacovigilance in populations with Crohn disease and ulcerative colitis since there haven’t been many studies evaluating adalimumab biosimilars in these patients?
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Oct 17, 2023 |
formularywatch.com | Justina Petrullo
No difference was found in the safety profiles or immunogenicity rates in patients who were switched and those who stayed on a reference biologic or biosimilar, according to the first systematic review using statistical methods to address switching risk in patients between reference biologics and biosimilars in PLoS One.
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