
Articles
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2 days ago |
oncologynewscentral.com | Leah Lawrence
Combining two bispecific antibodies, talquetamab and teclistamab, led to a higher overall response rate (ORR) with deep, durable responses among patients with multiple myeloma and extramedullary disease (EMD), according to the results of the phase 2 RedirecTT-1 trial presented at the European Hematology Association 2025 Congress (Abstract LB4001).
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3 days ago |
ascopost.com | Leah Lawrence
ASCO has released a clinical practice guideline update on the role of sentinel lymph node biopsy (SLNB) in early-stage breast cancer.1 The update includes recommendations based on findings from trials released after the published guideline in 2017, including data from nine randomized trials comparing SLNB alone against SLNB with complete axillary lymph node dissection (ALND) and two trials comparing SLNB against no axillary surgery.2 “Several decades ago, we felt that we needed to know...
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1 week ago |
oncologynewscentral.com | Leah Lawrence
Post-transplant cyclophosphamide (PTCy) combined with cyclosporin significantly improved outcomes for patients with acute leukemia or myelodysplastic syndrome undergoing stem cell transplantation with a matched sibling donor, according to data from the BM12 CAST trial presented at the European Hematology Association 2025 Congress (Abstract S103) and published in the New England Journal of Medicine.
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1 week ago |
oncologynewscentral.com | Leah Lawrence
The combination of polatuzumab vedotin, rituximab, gemcitabine, and oxaliplatin (Pola-R-GemOx) significantly improved overall survival (OS) compared with rituximab, gemcitabine, and oxaliplatin (R-GemOx) alone in patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL), according to the results of the POLARGO trial presented at the European Hematology Association 2025 Congress (Abstract S101).
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1 week ago |
oncologynewscentral.com | Leah Lawrence
Treatment with ropeginterferon alfa-2b (ropeg; Besremi) showed superior efficacy to anagrelide as a second-line treatment for patients with high-risk essential thrombocythemia (ET) who were intolerant or resistant to hydroxyurea, according to results of the phase 3 SURPASS ET trial presented at the European Hematology Association 2025 Congress (S102).
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