ASH Clinical News March 2015 | Page 23

CLINICAL NEWS benchmarks,” Ms. Saret explained to ASH Clinical News. “Cost-effectiveness is one important input that decision-makers can use alongside other factors such as side effects, affordability, overall budget impact, and ethical and social considerations.” However, she pointed out that her group’s analysis did not examine “the question of affordability at the patient level which is a related, but different, issue.” Across the four cancer types, the median ratio reported by industry-funded studies ($26,000/QALY) was lower (more favorable) than the median reported by non-industry-funded studies ($33,000/QALY), but these differences were not statistically significant. Median ratios fluctu- ated across the time examined in their research: • $35,000/QALY (1996-2002) • $52,000/QALY (2003-2006) • $22,000/QALY (2007-2012) The number of years a treatment has been on the market, differences in therapy dose administration, and manufacturers’ pricing strategies were cited as possible actors on median ratio variability across time. “Given the increased discussion about the high cost of these treatments, we were somewhat surprised to discover that their cost-effectiveness ratios were lower than expected,” senior study author Peter S. Neumann, ScD, Director of the Center for Evaluation of Value and Risk in Health at Tufts, told ASH Clinical News. Although he noted that the current study had a small sample size and cost-effectiveness ratios may have changed over time (as associated costs or benefits have also changed), “the study underscores that debates in health care should consider the value of breakthrough drugs, and not just costs.” Cost-effectiveness studies may help payers create more knowledgeable coverage policies, Ms. Saret added. “These data may be used as a component of the decision-making process when health insurance MDS/MPN Overlap: The Time is Now for Uniform Response Criteria Myelodysplastic syndromes (MDS)/myeloproliferative neoplasms (MPNs) are clonal myeloid disorders possessing both dysplastic and proliferative features that cannot be classified as one or the other – and for which there are no standard adult treatment recommendations. In an effort to identify meaningful clinical and biologic endpoints to improve management and disease outcomes, an international consortium has developed a standardized response criteria for clinical trials, according to a report in Blood. “We propose response assessment guidelines to harmonize future clinical trials with the principal objective of establishing suitable treatment algorithms,” wrote Michael Savona, MD, from Vanderbilt University Medical Center in Nashville, Tennessee, and colleagues. MDS/MPN, as characterized by the World Health Organization, include