TY - JOUR
T1 - Geriatric assessment for older adults receiving less-intensive therapy for acute myeloid leukemia
T2 - report of CALGB 361101
AU - Ritchie, Ellen K.
AU - Klepin, Heidi D.
AU - Storrick, Elizabeth
AU - Major, Brittny
AU - Le-Rademacher, Jennifer
AU - Wadleigh, Martha
AU - Walker, Alison
AU - Larson, Richard A.
AU - Roboz, Gail J.
N1 - Funding Information:
The following institutional networks participated in this study: Cancer Research Consortium of West Michigan NCORP, Grand Rapids, MI; Kathleen Yost, UG1CA189971, Dana-Farber/Partners Cancer Care LAPS, Boston, MA; Harold Burstein, UG1CA233180, Dartmouth College - Norris Cotton Cancer Center LAPS, Lebanon, NH; Konstantin Dragnev, UG1CA233323, Mount Sinai Hospital, New York, NY; Lewis Silverman, NYP/Weill Cornell Medical Center, New York, NY; Scott Tagawa, National Capital Area Minority Underserved NCORP, Washington, DC; Marcus Noel, UG1CA239758, North-Shore University Health System-Evanston Hospital, Evanston, IL; David Grinblatt, Northwell Health NCORP, Lake Success, NY; Jonathan Kolitz, The Ohio State University Comprehensive Cancer Center LAPS, Columbus, OH; Claire Verschraegen, UG1CA233331, Roswell Park Cancer Institute LAPS, Buffalo, NY; Ellis Levine UG1CA233191, Southeast Cancer Control Consortium CCOP, UNC Lineberger Comprehensive Cancer Center LAPS, Chapel Hill, NC; Matthew Milowsky, UG1CA233373, University of Chicago Comprehensive Cancer Center LAPS, Chicago, IL; Hedy Kindler, UG1CA233327, University of Iowa/Holden Comprehensive Cancer Center, Iowa City, IA; Umar Farooq, University of Missouri; Ellis Fischel, Columbia, MO; Puja Nistala, and Wake Forest University Health Sciences, Winston-Salem, NC, H.D.K. Research reported in this publication was supported by the National Cancer Institute, National Institutes of Health under Award Numbers U10CA180821 and U10CA180882 (to the Alliance for Clinical Trials in Oncology), UG1CA233180, UG1CA233327, UG1CA233331, UG1CA189823, U10CA180833, U10CA180836, U10CA180850, U10CA180857, U10CA180867, and U10CA-180888 and U10CA180819 (SWOG). Support to Alliance for Clinical Trials in Oncology and Alliance Foundation Trials programs is listed at https://acknowledgements.alliancefound.org. H.D.K. was funded by the American Society of Hematology (ASH); Association of Specialty Professors (ASP) Junior Faculty Scholar Award in Clinical and Translational Research (supported by ASH, Atlantic Philanthropies, John A. Hartford Foundation, Association of Specialty Professors); the Wake Forest University Claude D. Pepper Older Americans Independence Center (P30 AG-021332); Paul Beeson Career Development Award in Aging Research (K23AG038361, supported by National Institute on Aging, American Federation for Aging Research, John A. Hartford Foundation, and Atlantic Philanthropies); the Gabrielle's Angel Foundation for Cancer Research; and also supported in part by Millennium.
Publisher Copyright:
© 2022 by The American Society of Hematology.
PY - 2022/6/28
Y1 - 2022/6/28
N2 - Geriatric assessment (GA) predicts survival among older adults with acute myeloid leukemia (AML) treated intensively. We evaluated the predictive utility of GA among older adults treated with low-intensity therapy on a multisite trial. We conducted a companion study (CALGB 361101) to a randomized phase 2 trial (CALGB 11002) of adults ≥60 years and considered “unfit” for intensive therapy, testing the efficacy of adding bortezomib to decitabine therapy. On 361101, GA and quality of life (QOL) assessment was administered prior to treatment and every other subsequent cycle. Relationships between baseline GA and QOL measures with survival were evaluated using Kaplan-Meier estimation and Cox proportional hazards models. One-hundred sixty-five patients enrolled in CALGB 11002, and 96 (52%) of them also enrolled in 361101 (median age, 73.9 years). Among participants, 85.4% completed ≥1 baseline assessment. In multivariate analyses, greater comorbidity (hematopoietic cell transplantation-specific comorbidity index >3), worse cognition (Blessed Orientation-Memory-Concentration score >4), and lower European Organization for Research and Treatment of Cancer global QOL scores at baseline were significantly associated with shorter overall survival (P < .05 each) after adjustment for Karnofsky Performance Status, age, and treatment arm. Dependence in instrumental activities of daily living and cognitive impairment were associated with 6-month mortality (hazard ratio [HR], 3.5; confidence interval [CI], 1.2-10.4; and HR, 3.1; CI, 1.1-8.6, respectively). GA measures evaluating comorbidity, cognition, and self-reported function were associated with survival and represent candidate measures for screening older adults planned to receive lower-intensity AML therapies. This trial was registered at www.clinicaltrials.gov as #NCT01420926 (CALGB 11002).
AB - Geriatric assessment (GA) predicts survival among older adults with acute myeloid leukemia (AML) treated intensively. We evaluated the predictive utility of GA among older adults treated with low-intensity therapy on a multisite trial. We conducted a companion study (CALGB 361101) to a randomized phase 2 trial (CALGB 11002) of adults ≥60 years and considered “unfit” for intensive therapy, testing the efficacy of adding bortezomib to decitabine therapy. On 361101, GA and quality of life (QOL) assessment was administered prior to treatment and every other subsequent cycle. Relationships between baseline GA and QOL measures with survival were evaluated using Kaplan-Meier estimation and Cox proportional hazards models. One-hundred sixty-five patients enrolled in CALGB 11002, and 96 (52%) of them also enrolled in 361101 (median age, 73.9 years). Among participants, 85.4% completed ≥1 baseline assessment. In multivariate analyses, greater comorbidity (hematopoietic cell transplantation-specific comorbidity index >3), worse cognition (Blessed Orientation-Memory-Concentration score >4), and lower European Organization for Research and Treatment of Cancer global QOL scores at baseline were significantly associated with shorter overall survival (P < .05 each) after adjustment for Karnofsky Performance Status, age, and treatment arm. Dependence in instrumental activities of daily living and cognitive impairment were associated with 6-month mortality (hazard ratio [HR], 3.5; confidence interval [CI], 1.2-10.4; and HR, 3.1; CI, 1.1-8.6, respectively). GA measures evaluating comorbidity, cognition, and self-reported function were associated with survival and represent candidate measures for screening older adults planned to receive lower-intensity AML therapies. This trial was registered at www.clinicaltrials.gov as #NCT01420926 (CALGB 11002).
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U2 - 10.1182/bloodadvances.2021006872
DO - 10.1182/bloodadvances.2021006872
M3 - Article
C2 - 35420672
AN - SCOPUS:85133128235
SN - 2473-9529
VL - 6
SP - 3812
EP - 3820
JO - Blood advances
JF - Blood advances
IS - 12
ER -