Results from the phase 3 EVOKE-03 trial demonstrated that adding sacituzumab govitecan to pembrolizumab did not significantly improve progression-free or overall survival in untreated patients with PD-L1–high metastatic non-small cell lung...
Results from the phase 3 EVOKE-03 trial demonstrated that adding sacituzumab govitecan to pembrolizumab did not significantly improve progression-free or overall survival in untreated patients with PD-L1–high metastatic non-small cell lung...
The FDA updated the prescribing information for tarlatamab to substantially shorten monitoring following the first 2 doses in patients with extensive-stage small cell lung cancer, potentially reducing treatment burden and facilitating...
The FDA updated the prescribing information for tarlatamab to substantially shorten monitoring following the first 2 doses in patients with extensive-stage small cell lung cancer, potentially reducing treatment burden and facilitating...
Topline results from the phase 3 DeLLphi-305 trial showed that adding tarlatamab to durvalumab significantly improved overall and progression-free survival compared with durvalumab alone as first-line maintenance therapy for patients with...
Topline results from the phase 3 DeLLphi-305 trial showed that adding tarlatamab to durvalumab significantly improved overall and progression-free survival compared with durvalumab alone as first-line maintenance therapy for patients with...
Real-world findings associated GLP-1 receptor agonist use with improved survival and lower rates of thrombotic, cardiovascular, and infectious complications among patients with essential thrombocythemia, supporting prospective investigation...
Real-world findings associated GLP-1 receptor agonist use with improved survival and lower rates of thrombotic, cardiovascular, and infectious complications among patients with essential thrombocythemia, supporting prospective investigation...
Extended results from the phase 3 SURPASS-ET trial showed that ropeginterferon alfa-2b provided durable hematologic responses and progressively reduced JAK2 V617F variant allele frequency in patients with high-risk essential thrombocythemia,...
Extended results from the phase 3 SURPASS-ET trial showed that ropeginterferon alfa-2b provided durable hematologic responses and progressively reduced JAK2 V617F variant allele frequency in patients with high-risk essential thrombocythemia,...
Results from a real-world study demonstrated that ropeginterferon alfa-2b produced increasing complete hematologic responses over time in patients with myeloproliferative neoplasms, including essential thrombocythemia, with tolerability...
Results from a real-world study demonstrated that ropeginterferon alfa-2b produced increasing complete hematologic responses over time in patients with myeloproliferative neoplasms, including essential thrombocythemia, with tolerability...
Real-world findings suggest that cardiovascular comorbidities, particularly hyperlipidemia and potentially hypertension, may contribute to thrombotic risk in essential thrombocythemia beyond conventional disease-related factors, supporting...
Real-world findings suggest that cardiovascular comorbidities, particularly hyperlipidemia and potentially hypertension, may contribute to thrombotic risk in essential thrombocythemia beyond conventional disease-related factors, supporting...
INCA033989 demonstrated rapid and durable hematologic responses with molecular evidence of reduced mutant CALR burden in patients with CALR-mutant essential thrombocythemia resistant or intolerant to cytoreductive therapy, supporting further...
INCA033989 demonstrated rapid and durable hematologic responses with molecular evidence of reduced mutant CALR burden in patients with CALR-mutant essential thrombocythemia resistant or intolerant to cytoreductive therapy, supporting further...
The FDA has approved BEXLUTRY, a lutetium Lu 177 dotatate radioligand therapy, for adults with somatostatin receptor-positive gastroenteropancreatic neuroendocrine tumors, introducing the first radioligand equivalent to LUTATHERA and...
The FDA has approved BEXLUTRY, a lutetium Lu 177 dotatate radioligand therapy, for adults with somatostatin receptor-positive gastroenteropancreatic neuroendocrine tumors, introducing the first radioligand equivalent to LUTATHERA and...
MRI-adapted M-RECIST identified more complete and partial responses than conventional RECIST following percutaneous cryoablation for progressing extra-abdominal desmoid-type fibromatosis, supporting viability-based imaging as a potentially...
MRI-adapted M-RECIST identified more complete and partial responses than conventional RECIST following percutaneous cryoablation for progressing extra-abdominal desmoid-type fibromatosis, supporting viability-based imaging as a potentially...