FDA Grants Breakthrough Designation to Atezolizumab Combo for Advanced HCC
July 19th 2018The FDA has granted a breakthrough therapy designation to atezolizumab (Tecentriq) for use in combination with bevacizumab (Avastin) as a first-line treatment for patients with advanced or metastatic hepatocellular carcinoma (HCC).
FDA Grants Priority Review to Sacituzumab Govitecan for Metastatic Triple-Negative Breast Cancer
July 18th 2018The FDA has granted a priority review to antibody-drug conjugate sacituzumab govitecan for the treatment of patients with metastatic triple-negative breast cancer following at least 2 prior therapies for metastatic disease.
FDA Approves Ribociclib Combos for Advanced Breast Cancer Subtypes Using New Review Process
July 18th 2018The US Food and Drug Administration (FDA) approved two ribociclib (Kisqali) combination treatments for subsets of advanced breast cancer in less than a month using a pilot process called the Real-Time Oncology Review.
Genetic Variants Influence Treatment, Surveillance of Children with Medulloblastoma
July 13th 2018Based on the identification of 6 gene variations that make carriers susceptible to developing medulloblastoma and possibly other cancers, researchers have proposed subgroup-based counseling and screening recommendations.
Frontline Combination Improves PFS in Advanced Triple-Negative Breast Cancer
July 13th 2018The frontline combination use of atezolizumab (Tecentriq) plus nab-paclitaxel (Abraxane) yielded a significant reduction in the risk for disease progression or death compared with nab-paclitaxel alone in patients with metastatic or unresectable locally advanced triple-negative breast cancer (TNBC).
FDA Approves Nivolumab/Ipilimumab for Metastatic CRC Subgroup
July 11th 2018The FDA granted an accelerated approval to the immunotherapy combination of nivolumab (Opdivo) and ipilimumab (Yervoy) for use in adult and pediatric patients 12 years and older with microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) metastatic colorectal cancer (mCRC) following progression on a fluoropyrimidine, oxaliplatin, and irinotecan.
Apalutamide Significantly Lowers Risk of PSA Progression in Nonmetastatic CRPC
July 10th 2018Patients with nonmetastatic castration-resistant prostate cancer experienced a 94% reduction in their risk of PSA progression following apalutamide (Erleada) treatment, according to a posthoc analysis from the phase III SPARTAN trial.
TAS-102 Prolongs Survival in Patients With Advanced Gastric Cancer
July 6th 2018Patients with heavily pretreated metastatic or advanced gastric cancer who received TAS-102 (trifluridine/tipiracil; Lonsurf) saw a significant overall survival benefit, according to phase III study findings presented at the 2018 World Gastrointestinal Cancer Congress.
Fertility Preservation Guidelines Urge for Early Discussions with Young Patients with Cancer
July 2nd 2018Nurses treating young patients with cancer should be aware of the American Society of Clinical Oncology's updated guidelines and recommendations on fertility preservation, which were released in April 2018.
FDA Grants Priority Review to Frontline Pembrolizumab Combo in Metastatic NSCLC
July 2nd 2018The FDA granted a priority review to the anti-PD-1 agent pembrolizumab (Keytruda) in combination with chemotherapy as a first-line treatment for metastatic squamous non-small cell lung cancer (NSCLC), regardless of PD-L1 expression.
FDA Grants Priority Review to Glasdegib for Acute Myeloid Leukemia
June 28th 2018The FDA granted a priority review to a new drug application for glasdegib, an investigational oral smoothened inhibitor, for the treatment of adult patients with previously untreated acute myeloid leukemia in combination with low-dose cytarabine, a type of chemotherapy.
FDA Approves Binimetinib/Encorafenib for BRAF+ Melanoma
June 27th 2018The FDA has approved the combination of the BRAF inhibitor encorafenib (Braftovi) and the MEK inhibitor binimetinib (Mektovi) for the treatment of patients with BRAF-mutant unresectable or metastatic melanoma, as detected by an FDA-approved test.