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Regorafenib Use Beyond Progression Explored in Colorectal Cancer Case Study
June 28th 2016Many patients with metastatic colorectal cancer (CRC) will ultimately progress on standard first- and second-line therapy while maintaining a good performance status, placing importance on the optimal use of third-line treatments.
Osteoporosis Drug Shows Promise for Breast Cancer Prevention in BRCA1 Carriers
June 23rd 2016TNFSF11, also known as RANKL, shows potential as a genetic pathway in the prevention of breast cancer for women carrying BRCA1 mutations. Early study findings, published in Nature Medicine, show that a drug currently used in the treatment of osteoporosis, denosumab (Xgeva)-an inhibitor of RANKL-could also be used for the prevention and delay of tumor growth for BRCA1-mutation carriers.
Considerations for Single-Agent Versus Combo Melanoma Immunotherapy
June 22nd 2016The combination of ipilimumab (Yervoy) and nivolumab (Opdivo) continues to show promise, with recent data demonstrating a 26% improvement in overall survival (OS) with the 2 drugs compared with ipilimumab alone for patients with advanced melanoma.
Nivolumab/Ipilimumab Combo Gains NICE Approval for Melanoma Treatment
June 22nd 2016The National Institute for Health and Care Excellence (NICE) has approved the combination of nivolumab (Opdivo) and ipilimumab (Yervoy) for patients with metastatic melanoma, which allows the combination to be used within the National Health Service (NHS).
USPSTF Expands Recommendation for Colorectal Cancer Screening Methods
June 21st 2016The United States Preventative Services Task Force (USPSTF) has updated its 2008 recommendation for colorectal cancer (CRC) screening to include 7 CRC screening tests for average-risk, asymptomatic adults between the ages of 50 and 75 to reduce the risk of CRC mortality.
Expert Explains Remaining Questions With Checkpoint Inhibitors in Melanoma
June 21st 2016Although nivolumab (Opdivo) and ipilimumab (Yervoy) are approved in combination for the first-line treatment of patients with metastatic melanoma, regardless of BRAF mutation status, the checkpoint blockade has not automatically become the standard of care in this setting.
No New Safety Concerns Shown with Radium-223 Retreatment in mCRPC
June 21st 2016While the ALSYMPCA trial led to the FDA approval of radium-223 dichloride (Xofigo), the phase III study left several questions to be answered regarding its use in metastatic castration-resistant prostate cancer (mCRPC), says Luke Nordquist, MD.
Suggestion of Survival Benefit Persists with mTOR Inhibitor in Subset of NETs
June 18th 2016Patients with nonfunctioning neuroendocrine tumors of gastrointestinal or lung origin continued to live longer when treated with the mammalian target of rapamycin (mTOR) inhibitor everolimus than with placebo, ongoing follow-up in a randomized trial showed.
Tandem Transplant in Neuroblastoma Leads to Significant Survival Advantage
June 18th 2016Dual autologous stem-cell transplant (ASCT) led to a 13% absolute increase in 3-year event-free survival (EFS) for children with high-risk neuroblastoma as compared with a single transplant, a large randomized trial showed.
Apalutamide Investigated in High-Risk Prostate Cancer
June 18th 2016Researchers are hoping the results of a latestage efficacy and safety study of apalutamide (ARN-509) in patients with high-risk, localized, or locally advanced prostate cancer who are receiving primary radiation therapy will demonstrate an improvement in metastasis-free survival, according to global principal investigator, Howard M. Sandler, MD.
Two Immunotherapy Combinations Show Promise in Glioblastoma
June 15th 2016The combinations of nivolumab (Opdivo) plus ipilimumab (Yervoy) and pembrolizumab (Keytruda) plus bevacizumab (Avastin ), both show promising efficacy in recent trials, possibly paving the way toward a new era of treatment for patients with glioblastoma.
INO-VATE Updated Results Confirm PFS Benefit in Relapsed/Refractory ALL
June 14th 2016The anti-CD22 antibody-drug conjugate inotuzumab ozogamicin demonstrated significantly improved progression-free survival (PFS) and complete remission (CR) rates compared with chemotherapy for patients with relapsed or refractory acute lymphoblastic leukemia (ALL).
Ruxolitinib Improves Overall Survival in Myelofibrosis
June 14th 2016Final 5-year efficacy and safety data from the phase III COMFORT-I trial confirm previous findings that ruxolitinib (Jakafi) confers a significant benefit in patients with intermediate-2 and high-risk myelofibrosis. The JAK-2 inhibitor resulted in durable reductions in splenomegaly and improved overall survival, with patients experiencing no new or unexpected adverse events as a result of the long-term treatment.
Daratumumab Shown to Double Response in Refractory Multiple Myeloma
June 7th 2016Daratumumab (Darzalex), when added to the standard two-drug regimen of bortezomib and dexamethasone, reduced the risk of progression or death by 61% compared with the standard regimen alone for patients with recurrent or refractory multiple myeloma.
KPd Triple-Combination Shows Potential in Refractory Multiple Myeloma
June 7th 2016A regimen consisting of carfilzomib (Kyprolis), pomalidomide (Pomalyst), and dexamethasone (KPd) merits further investigation for the treatment of patients with multiple myeloma whose disease progresses while on lenalidomide (Revlimid) in the earlier stages of disease.
Isatuximab Demonstrates Activity as Single-Agent in Multiple Myeloma
June 7th 2016The anti-CD38 monoclonal antibody isatuximab (SAR650984) showed promising signs of activity as a single-agent for patients with heavily pretreated relapsed/refractory multiple myeloma, according to updated findings from a phase II study presented at the 2016 ASCO Annual Meeting.
Selective FGFR Inhibitor Shows Promise in Gastric and Breast Cancers
June 4th 2016Gastric cancers with high-level clonal FGFR2 gene amplification responded to AZD4547, a selective FGFR inhibitor, in a phase II open label trial of previously treated, advanced FGFR amplified cancer. Yet tumors with multiple FGFR1 genes, low level or subclonal amplification of FGFR2 did not respond similarly to the drug.