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Targeted Oncology
15 小时
Exploring Immunotherapy and Radiation Therapy in Cervical Cancer
ENGOT-cx11 is a randomized, double-blind, placebo-controlled trial that enrolled patients aged 18 years or older diagnosed ...
Targeted Oncology
17 小时
Improving the Transition From Inpatient to Outpatient Care in Oncology
A recent Targeted Oncology survey explores the challenges and best practices in transitioning patients with cancer from inpatient to outpatient care, featuring insights from Cristina Gasparetto, MD, ...
Targeted Oncology
19 小时
HBI-8000 Plus Nivolumab Is Safe, Active in Melanoma
The combination of HBI-8000 and nivolumab induced a response in nearly two-thirds of patients with advanced melanoma and no ...
Targeted Oncology
20 小时
FDA Grants Fast Track Designation to LBS-007 in AML
LBS-007, a novel targeted therapy, has received FDA fast track designation for the treatment of acute myeloid leukemia.
Targeted Oncology
1 天
Functional High-Risk is a Leading Rationale for Early CAR T in Myeloma
Samer A. Al’Hadidi, MD, discusses factors influencing early use of chimeric antigen receptor T-cell therapy in patients with ...
Targeted Oncology
1 天
The Clinical Utility of Genetic Risk Scores in Chronic Lymphocytic Leukemia
Susan L. Slager, PhD, discusses the background of her research on inherited germline genetics for risk of chronic lymphocytic ...
Targeted Oncology
1 天
Novel METTL3 Inhibitor Elicits Clinical Activity Across Tumor Types
STC-15, an investigational RNA methyltransferase inhibitor, has shown promising clinical activity and an encouraging safety ...
Targeted Oncology
1 天
Tiragolumab/Atezolizumab Combo Fails to Meet Primary End Point in NSCLC Trial
The phase 3 SKYSCRAPER-01 trial of tiragolumab and atezolizumab in PD-L1-high non–small cell lung cancer did not meet its ...
Targeted Oncology
1 天
FDA Receives BLA for RP1 and Nivolumab Combo in Advanced Melanoma
The FDA has received a biologics license application submission for RP1 plus nivolumab in patients with PD-1 ...
Targeted Oncology
1 天
LBL-024 Gains FDA Orphan Drug Status in Neuroendocrine Cancer
The FDA has granted LBL-024 orphan drug designation (ODD) for the treatment of neuroendocrine cancer. The agent has already ...
Targeted Oncology
2 天
Timing of MRD Testing in Lung Cancer Affects Patient Outcomes
Oleg Gligich, MD, assistant professor at the Columbia University Division of Hematology/Oncology at Mount Sinai Medical ...
Targeted Oncology
2 天
FDA Approves HER2 Test as Companion Diagnostic for Zanidatamab in Biliary Tract Cancer
Rabbit Monoclonal Primary Antibody test as a companion diagnostic to assess HER2+ status in patients with BTC.
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