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Evidence-Based Guidelines/Pathways Critical for Value-Based Benefit Design in Oncology
By
Caroline Helwick
July 2012, Vol 3, No 5
Houston, TX—There is no question that evidence-based guidelines and pathways are critical to the success of value-based oncology, but not all stakeholders have an equal voice, said Craig Deligdish, MD, Chief Medical Officer at Oncology Resource Networks of America at the Second Annual Meeting of the Association for Value-Based Cancer Care.
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Chemotherapy-Related Toxicity Adds to Economic Burden in Metastatic Breast Cancer
By
Caroline Helwick
ASCO Annual Meeting
,
ASCO
July 2012, Vol 3, No 5
Chicago, IL—Adverse events (AEs) related to chemotherapy for metastatic breast cancer create a substantial economic burden that is primarily explained by increased inpatient, outpatient, and pharmacy costs, said lead investigator Sara A. Hurvitz, MD, Director of the Oncology Breast Can cer Program at University of California, Los Angeles (UCLA) Jonsson Comprehensive Cancer Center and Assistant Clinical Professor at UCLA School of Medicine, who presented an economic analysis at the 2012 Ameri can Society of Clinical Oncology meeting.
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Tivozanib Outperforms Sorafenib as First-Line Treatment in Advanced Renal-Cell Carcinoma
By
Wayne Kuznar
ASCO Annual Meeting
,
ASCO
July 2012, Vol 3, No 5
Tivozanib, a potent investigational tyrosine kinase inhibitor with a long half-life, demonstrated significant improvement in progression-free survival (PFS) as first-line targeted therapy for metastatic renal-cell carcinoma (RCC), according to results from a phase 3 randomized, open-label trial.
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Endocrine Therapy Substantially Underutilized Among Low-Income Patients with Breast Cancer
By
Caroline Helwick
ASCO Annual Meeting
,
ASCO
July 2012, Vol 3, No 5
Chicago, IL—Researchers from the University of North Carolina in Chapel Hill reported at the 2012 American Society of Clinical Oncology meeting that endocrine therapy is substantially underutilized among the low-income breast cancer population.
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Cancer Screening Saves Lives, Is Cost-Effective
By
Wayne Kuznar
ASCO Annual Meeting
,
ASCO
July 2012, Vol 3, No 5
Chicago, IL—Improved cancer screening can save lives, and despite the high cost of implementing such a measure, it was found cost-effective and therefore valuable in a recent analysis using quality-adjusted life-years (QALYs), said Michael S. Broder, MD, President of Partnership for Health Analytic Research, LLC (PHAR), CA, and colleagues, at the 2012 American Society of Clinical Oncology meeting.
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Patients Willing to Pay Out of Pocket for Genetic Testing to Assess Colorectal Cancer Risk
By
Audrey Andrews
ASCO Annual Meeting
,
ASCO
July 2012, Vol 3, No 5
Chicago, IL—In a cohort of patients at risk for colorectal cancer (CRC), the majority were willing to pay some out-of-pocket (OOP) expenses for genetic testing, Fox Chase Cancer Center researchers reported in a poster that was presented at the 2012 American Society of Clinical Oncology (ASCO) meeting and earned an ASCO Merit Award.
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High OOP Costs for Medicare Patients with Cancer
By
Mark Knight
ASCO Annual Meeting
,
ASCO
July 2012, Vol 3, No 5
Chicago, IL—Older patients with cancer and Medicare coverage often incur greater out-of-pocket (OOP) expenses compared with their counterparts without cancer.
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Unforeseen Hospital Admissions Are Frequent for Patients Receiving Radiotherapy
By
Wayne Kuznar
ASCO Annual Meeting
,
ASCO
July 2012, Vol 3, No 5
Approximately 1 in 5 patients with cancer who are undergoing radiotherapy as part of their treatment can count on unexpected hospital stays—adding an economic and clinical burden on the patient and on the healthcare system, according to an analysis by Nabeel H. Arastu, BS, and colleagues at the Brody School of Medicine at East Carolina University, Greenville, NC, which was presented at the 2012 ASCO meeting.
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ODAC Recommends Carfilzomib for Myeloma
FDA Approvals, News & Updates
July 2012, Vol 3, No 5
The FDA’s Oncologic Drugs Advisory Committee (ODAC) recommended in an 11 to 0 vote (and 1 absentee) to approve carfilzomib (Kyprolis; Onyx), a new-generation proteasome inhibitor, for the treatment of patients with refractory and relapsed multiple myeloma who have failed at least 2 other myeloma therapies—the proteasome inhibitor bortezomib (Velcade) and the immunomodulatory drug lenalidomide (Revlimid).
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New Test for Aiding Biopsy Decision after PSA Test
FDA Approvals, News & Updates
July 2012, Vol 3, No 5
The US Food and Drug Administration (FDA) has approved the Access Hybritech p2PSA (Beckman Coulter) test, which measures a form of prostate-specific antigen (PSA) called [-2]proPSA in the blood and can help men whose PSA test scores are elevated decide whether they should have a biopsy to rule out prostate cancer.
Read More
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Home
Issues
Online First
Latest Issue
Issue Archive
Special Issues
Browse By Topic
Personalized Medicine
Economics & Value
FDA Approvals, News & Updates
COVID-19
Cholangiocarcinoma
View All Topics ›
Conference Correspondent
ESMO 2025 - Wrap-Up: Triple-Negative Breast Cancer
ASCO 2025 - Wrap-Up: Triple-Negative Breast Cancer
Web Exclusives
Web Exclusive Articles
Videos
Interview with the Innovators
Prostate Cancer Diagnostics Monthly Minutes
Webinars
Quick Quiz
Press Releases
Association for Value-Based Cancer Care
VBCM
Value-Based Care in Myeloma