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A simple blood test has been created that can detect the beginning stages of cancer, before symptoms like coughing and weight loss start. Read More ›

The success rate of clinical trials for breast cancer drugs can increase by almost 50% when biological markers are used, according to new research from the University of Toronto Mississauga. Read More ›

Cancer treatment protocols is one reason a virtual monopoly is held by some cancer drug manufacturers, which in turn helps to create the high cost of cancer drugs in the United States, according to a commentary by 2 Mayo Clinic physicians in a recent issue of the journal Mayo Clinic Proceedings. Read More ›

By determining how water moves through tissue, water diffusion measurements with MRI could decrease false-positive breast cancer results and reduce preventable biopsies, according to recent study findings. Read More ›

What are some treatment options for elderly patients with chronic lymphocytic leukemia? Read More ›


A study by the National Cancer Institute reports that approximately 1 in 5 patients with lung cancer continue to smoke after diagnosis.

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Novartis has discontinued a phase 3 trial assessing whether its TKI nilotinib (Tasigna) might be a more effective first-line therapy than imatinib (Gleevec) in patients with unresectable or metastatic gastrointestinal stromal tumors (GISTs).

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Isoflavones from soy foods do not increase breast cancer recurrence risks said researchers at the American Association for Cancer Research annual meeting. Isoflavones have estrogen-like properties, prompting some survivors to avoid soy foods.

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On July 20, 2012, the FDA granted accelerated approval to carfilzomib injection (Kyprolis; Onyx Pharmaceuticals) for the treatment of patients with multiple myeloma who have received at least 2 prior therapies, including bortez­omib and an immunomodulatory agent, and who have demonstrated disease progression on or within 60 days of the completion of their last therapy.

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Two studies presented at the 2012 American Society of Clinical Oncology (ASCO) Annual Meet­ing suggested that abiraterone acetate (AA; Zytiga), an androgen biosynthesis inhibitor,1 has the potential to be used earlier in the course of prostate cancer than its current US Food and Drug Administration (FDA) indication (ie, after failure of chemotherapy in men with metastatic castration-resistant prostate cancer [CRPC]). A second interim analysis of a phase 3 trial had positive outcomes with AA in men with metastatic CRPC who had not yet received chemotherapy,1 and a preliminary phase 2 study suggested AA may have a role in the neoadjuvant setting before radical prostatectomy is performed in men with early-stage localized high-risk prostate cancer.2 In addition, secondary results from the AFFIRM trial confirmed the superiority of enzalutamide to placebo in men with CRPC following treatment with docetaxel.3

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