ASH Clinical News October 2016 | Page 26

On Location American Society of Hematology’s MEETING ON HEMATOLOGIC MALIGNANCIES t this year’s ASH Meeting on Hematologic Malignancies, which took place September 16-17 in Chicago, speakers and attendees gathered to discuss important research and clinical updates in malignant hematology. Here, we share some of the highlights of the meeting, including the under-representation of youger patients in clinical trials and the prognostic significance of TP53 mutations in myelodysplastic syndromes. ASH Clinical News was on site in Chicago to speak with presenters at the meeting. See all of our video interviews at ashclinicalnews.org/mhmvideos. Improving Risk Stratification in Standar d-Risk Myeloma Patients: Age, Bone Marrow Involvement Independently Predict Survival Though the field of multiple myeloma TABLE 1. Factors Associated With Poor Overall Survival at Three Years (MM) has seen many advances in treatParameter Value Odds Ratio p Value ment in the past two years – including ISS stage I, II, III 1.85 0.001 three new drug approvals – patients who (95% CI 1.29-2.66) have so-called standard-risk cytogenetAge <65 years, 65-75 years, >75 years 1.81 0.001 ics often have poor survival outcomes. (95% CI 1.28-2.56) These poor outcomes indicate that there Plasma cells <20% in bone marrow 2.64 0.010 is still a need for better risk-stratification (95% CI 1.26-5.54) methods, according to Moritz Binder, Karyotype Normal, hyperdiploid, other 2.8 <0.001 MD, MPH, of the Department of Internal (95% CI 2.09-3.74) Medicine at the Mayo Clinic in Rochester, Thrombocytopenia <150x109/L 2.74 0.001 Minnesota, who presented results of a (95% CI 1.47-5.09) new risk prediction model using fluoISS = International Staging System rescence in situ hybridization (FISH) at the 2016 ASH Meeting on Hematologic Bone marrow aspirates were evaluated for dele- with lower rates of three-year OS included Malignancies. tions, monosomies, trisomies, and tetrasomies With this study, Dr. Binder and colleagues disease stage, older age, greater extent of bone using chromosome- or centromere-specific sought to identify demographic, clinical, and marrow involvement, karyotype, and lower FISH probes. cytogenetic characteristics that would predisplatelet count at the time of diagnosis (TABLE 1). The median patient age was 65 years (range pose MM patients with standard-risk cytoge“The model had excellent discrimination,” Dr. = 31-95 years), and 60 percent were male netics to poor three-year overall survival (OS). Binder and colleagues noted, “and correctly clas(n=270). Median OS was longest in the group The study included 449 patients diagnosed sified 83 percent of the patients, with 56 percent of patients who survived at least three years with MM between July 2004 and July 2014 at sensitivity and 92 percent specificity.” This trans(n=332; 74%), compared with the entire patient lated to a positive predictive value of 71 percent, the Mayo Clinic. Patients were included if they cohort (n=449) and those who did not achieve underwent FISH evaluation within six months and a negative predictive value of 86 percent. three-year OS (n=117; 26%): of diagnosis and received treatment with an “One-fourth of the patients are experiencimmunomodulator, proteasome inhibitor, or a ing less than three years of overall survival after • 8.0 years for the entire patient cohort combination of both. diagnosis,” Dr. Binder and colleagues conclud(range = 6.4-8.6 years) Patients were excluded from the study if they: ed. “These findings emphasize the importance of further risk stratification and the need for • 10.5 years for those who survived at least 3 reliable predictors of poor clinical outcomes in • had high-risk cytogenetics, which was years (range = 8.3 years - not reached) defined as del(17p), t(14;16), and t(14;20) this patient population.” • had intermediate-risk cytogenetics, which was defined as t(4;14) and gain(1q) • were lost to follow-up within three years 24 ASH Clinical News • 1.4 years for those who did not survive at least 3 years (range = 1.1-1.6 years) Other risk factors independently associated REFERENCE Binder M, Rajkumar SV, Ketterling RP, et al. Predicting poor overall survival in patients with newly diagnosed multiple myeloma and standard-risk cytogenetics treated with novel agents. Abstract #89267. Presented at the ASH Meeting on Hematologic Malignancies, September 16-17, 2016; Chicago, IL. October 2016