November 27th 2024
LBS-007, a novel targeted therapy, has received FDA fast track designation for the treatment of acute myeloid leukemia.
November 25th 2024
November 15th 2024
November 14th 2024
November 12th 2024
Current Salvage Therapy Options for Relapsed/Refractory CLL
May 11th 2018Neil E. Kay, MD, professor of medicine at the Mayo Clinic, addresses the “Big 4” in salvage therapies for patients with relapsed/refractory chronic lymphocytic leukemia, including a newer therapy coming down the pipeline now.
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Survival Improved With Quizartinib in FLT3-ITD+ Relapsed/Refractory AML
May 9th 2018According to findings from the phase III QuANTUM-R study, overall survival was improved with quizartinib compared with chemotherapy in patients with <em>FLT3</em>-ITD–positive relapsed/refractory acute myeloid leukemia after first-line treatment with or without hematopoietic stem cell transplantation.<br />
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Rituximab/Bendamustine Combo Demonstrates Promising Results in Fludarabine-Ineligible CLL
May 7th 2018According to results from the MABLE trial, the combination of rituximab plus bendamustine demonstrated significant value as a frontline treatment option for fludarabine-ineligible patients with chronic lymphocytic leukemia.
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HCT Following CAR T-Cell Therapy May Improve Patient Outcomes in ALL
May 4th 2018Results of an interim analysis from a small phase I trial presented at the 2018 American Society of Pediatric Hematology/Oncology Conference showed that CAR T-cell therapy can induce next generation sequencing negativity in patients with relapsed/refractory acute lymphoblastic leukemia, suggesting a “synergistic” relationship with hematopoietic cell transplant that could enhance patient outcomes.
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Memory T Cells May Predict Response to CAR T-Cell Therapy in CLL
May 4th 2018Results from a recent study conducted at the University of Pennsylvania may demonstrate why some patients with chronic lymphocytic leukemia are resistant to tisagenlecleucel, while potentially providing a pathway to enhance patient response.
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Bendamustine/Rituximab is an Effective Salvage Therapy in CLL
May 2nd 2018The combination of bendamustine and rituximab induced a 12-month progression-free survival of 78.6% for patients with chronic lymphocytic leukemia, suggesting that the combination is an effective first salvage regimen.
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Selinexor Demonstrates Promising Results in Heavily Pretreated Myeloma
May 2nd 2018In top-line results from part 2 of the phase IIb STORM trial, selinexor induced an overall response rate of 25.4% in patients with penta-refractory multiple myeloma, according to Karyopharm Therapeutics, the manufacturer of the oral SINE compound.
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Tisagenlecleucel Granted FDA Approval for Large B-Cell Lymphoma
May 2nd 2018Based on data from the phase II JULIET study, tisagenlecleucel has received FDA approval for the treatment of adult patients with relapsed/refractory large B-cell lymphoma—including diffuse large B-cell lymphoma, high-grade B-cell lymphoma, and DLBCL arising from follicular lymphoma—after 2 or more lines of systemic therapy.
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A Look Back at FDA News in the Month of April
May 1st 2018The FDA approved several indications throughout the month of April 2018. A number of drugs were granted priority review and Fast Track designation. The FDA also halted all clinical trials using tazemetostat as treatment, and new initiatives were introduced to help ease the development of genetic and genomic-based tests. Check out our list of all FDA happenings from April 2018.
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Shingrix Prevents Herpes Zoster Episodes Following HSCT
May 1st 2018A herpes zoster subunit vaccine effectively prevented episodes of HZ and other related complications among patients who had recently underwent autologous hematopoietic stem cell transplant, according to the results of the phase III ZOE-HSCT trial presented at the 2018 BMT Tandem Meetings.
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A recommendation has been made by the European Medicines Agency’s Committee for Medicinal Products for Human Use to add final overall survival data from the open-label phase III ASPIRE trial to the label for carfilzomib for the treatment of patients with relapsed/refractory multiple myeloma.
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Chen Awarded Lurie Prize in Biomedical Sciences for Breakthrough Discovery
April 30th 2018Zhijian “James” Chen, PhD, has proudly been recognized by the Foundation for the National Institutes of Health for his breakthrough discovery of the enzyme cyclic GMP-AMP synthase and its corresponding pathway. He will receive the 2018 Lurie Prize in Biomedical Sciences during the FNIH Award Ceremony to be held on May 16 in Washington, DC.
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