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Uridine Triacetate Approved by FDA to Deter Chemo Overdose and Toxicities
December 12th 2015Uridine triacetate (Vistogard) has been given a green light by the FDA to treat adult and pediatric patients who have severe or life-threatening toxicities within 4 days of treatment following an overdose of 5-fluorouracil (5-FU) or capecitabine.
FDA Gives Palbociclib Priority Review for Pretreated HR-Positive/HER2-Negative Breast Cancer
December 10th 2015Palbociclib (Ibrance) has been given a priority review by the FDA. The treatment will be looked at as a combination with fulvestrant in pretreated patients with HR-positive, HER2-negative metastatic breast cancer, said Pfizer, the manufacturer of the CDK 4/6 inhibitor.
FDA Approves Rapid Infusion Bendamustine for CLL and NHL
December 10th 2015A rapid infusion formulation of bendamustine (Bendeka) has received FDA approval for the treatment of patients with CLL or indolent B-cell NHL that has progressed during or within 6 months of treatment with rituximab or a rituximab-containing regimen.
Healthy Living May Reduce Risk of Severe Prostate Cancer By Over Half
December 4th 2015Living a healthier lifestyle could be a robust preventative measure against metastatic prostate cancer. One new study suggests that leading a healthy lifestyle could reduce a man's chances of developing the cancer by up to 68%.
Studies Suggest Radical Prostatectomy May Be Optimal in Men With High-Risk Prostate Cancer
December 3rd 2015Recent studies suggest that RP may be a better initial treatment given many of these patients require multimodal therapy to manage their disease. The question about radiation versus surgery lies in the details, with treatment tailored to each patient.
Roll-Your-Own-Tumor Technology for Cancer Research May Boost Personalized Treatments
December 1st 2015Details of a new technology for studying tumor metabolism have been published in Nature Materials, whereby a cellulose strip containing tumor cells was wrapped around a metal core and incubated, mimicking conditions consistent with in vivo tumors.
FDA Hands Down Complete Response Letter for Use of Nivolumab in BRAF-Mutated Melanoma
November 30th 2015The FDA has issued a complete response letter to Bristol-Myers Squibb regarding its supplemental biologics license application for the use of single-agent nivolumab in previously untreated patients with BRAF V600 mutation-positive advanced melanoma.
Advanced Melanoma Responds Well to Pembrolizumab/Ipilimumab Combination
November 25th 2015A regimen of pembrolizumab (Keytruda) and low-dose ipilimumab (Yervoy) was effective, and tolerable, for patients with advanced melanoma, according to results from the phase Ib KEYNOTE-029 clinical trial presented by lead investigator Georgina Long, BSc, PhD, MBBS.
Next-Generation Sequencing in Contralateral Breast Cancer Could Affect Treatment Decisions
November 23rd 2015A new method to elucidate the clonal relationship between tumors used tissues and clinical details from patients with contralateral breast cancer, and for the first time, next-generation sequencing.
Dabrafenib/Trametinib Fully Approved by FDA for BRAF-Mutant Melanoma
November 21st 2015A combination of dabrafenib and trametinib has been approved by the FDA for patients with unresectable or metastatic BRAF-mutated melanoma, based on an extension in overall survival (OS) from two phase III studies.
Ixazomib Approved for Relapsed Multiple Myeloma by FDA
November 20th 2015A combination of the oral proteasome inhibitor ixazomib (Ninlaro), lenalidomide (Revlimid) and dexamethasone has been approved by the FDA a full 4 months ahead of schedule for patients with multiple myeloma with at least 1 prior surgery.