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      Cost comparison by treatment arm and center‐level variations in cost and inpatient days on the phase III high‐risk B acute lymphoblastic leukemia trial AALL0232

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          Abstract

          The Children's Oncology Group ( COG) develops and implements multi‐institutional clinical trials with the primary goal of assessing the efficacy and safety profile of treatment regimens for various pediatric cancers. However, the monetary costs of treatment regimens are not measured. AALL0232 was a COG randomized phase III trial for children with acute lymphoblastic leukemia that found that dexamethasone ( DEX) was a more effective glucocorticoid than prednisone ( PRED) in patients younger than 10 years, but PRED was equally effective and less toxic in older patients. In addition, high‐dose methotrexate ( HDMTX) led to better survival than escalating doses of methotrexate (C‐ MTX). Cost data from the Pediatric Health Information System database were merged with clinical data from the COG AALL0232 trial. Total and component costs were compared between treatment arms and across hospitals. Inpatient costs were higher in the HDMTX and DEX arms when compared to the C‐ MTX and PRED arms at the end of therapy. There was no difference in cost between these arms at last follow‐up. Considerable variation in total costs existed across centers to deliver the same therapy that was driven by differences in inpatient days and pharmacy costs. The more effective regimens were found to be more expensive during therapy but were ultimately cost‐neutral in longer term follow‐up. The variations in cost across centers suggest an opportunity to standardize resource utilization for patients receiving similar therapies, which could translate into reduced healthcare expenditures.

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          Dexamethasone and High-Dose Methotrexate Improve Outcome for Children and Young Adults With High-Risk B-Acute Lymphoblastic Leukemia: A Report From Children’s Oncology Group Study AALL0232

          Survival for children and young adults with high-risk B-acute lymphoblastic leukemia has improved significantly, but 20% to 25% of patients are not cured. Children's Oncology Group study AALL0232 tested two interventions to improve survival.
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            The natural history of asymptomatic osteonecrosis of the femoral head.

            To observe the natural history of asymptomatic osteonecrosis of the femoral head, and to analyse the associations between the subsequent development of symptoms, epidemiological risk factors and the character of the lesions. Sixty-eight patients were diagnosed with asymptomatic osteonecrosis of the femoral head. The patients were classified based on the development of symptoms. Relations were sought between symptom development and epidemiological risk factors, and the size and location of the necrotic lesions. Thirty-eight patients developed symptoms (55.9%) at a mean 2.27 years after diagnosis. Symptoms developed in 18 of 28 patients with alcohol-related necrosis (64.3%), in eight of 14 patients with steroid-related necrosis (57.1%), and in 12 of 26 patients with idiopathic necrosis (46.2%). None of the following: gender, age, body mass index (BMI), smoking status, or cholesterol level, was found to be significantly associated with the development of symtoms in asymptomatic osteonecrosis of femoral head (ONFH). Duration and amount of exposure to steroid were not significantly associated with symptom development. In the groups of heavy alcohol drinkers, large necrotic lesions and laterally located lesions showed a higher prevalence of symptom development. Symptoms developed in 55.9% of asymptomatic osteonecrosis of the femoral head. Prevalence of symptom development was significantly higher in heavy alcohol drinkers and large-sized lateral lesions.
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              Economic evaluation of pediatric cancer treatment: a systematic literature review.

              Although there is a growing national focus on health care cost containment and accountability in resource utilization, childhood cancer therapy costs continue to increase without proportionate survival improvements. Economic evaluations (EEs) such as cost and/or cost effectiveness analysis may identify areas to improve resource efficiency. This review aims to identify and characterize the EE studies performed in this field. We performed a structured literature search of the Medline, PubMed, and the National Health Service EE databases from 2000 to 2011. Concepts for the search included "cost analyses," "child," and "cancer." Studies were limited to original research, comparison of 2 or more treatments using monetary units, English language, and originating from economically developed countries. Identified studies were assessed by the Drummond checklist and characterized by the therapy studied, data sources, and research perspectives. Forty studies met inclusion criteria. Eleven studied chemotherapy, surgery, or radiation. Twenty-nine studied supportive measures such as growth factor support or treatment of infection. The median Drummond score was 6 of 10 (range, 2-9). Only 15 (36%) included treatment outcomes when comparing costs. Methodological limitations were common. A wide variety of topics and methodological limitations made comparisons between studies difficult. Strategies for increasing the generalizability of future EE studies are presented. Substantial opportunity exists for EE research in childhood cancer.
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                Author and article information

                Contributors
                dinofiaa@email.chop.edu
                Journal
                Cancer Med
                Cancer Med
                10.1002/(ISSN)2045-7634
                CAM4
                Cancer Medicine
                John Wiley and Sons Inc. (Hoboken )
                2045-7634
                23 December 2017
                January 2018
                : 7
                : 1 ( doiID: 10.1002/cam4.2018.7.issue-1 )
                : 3-12
                Affiliations
                [ 1 ] Division of Oncology The Children's Hospital of Philadelphia Philadelphia Pennsylvania
                [ 2 ] Department of Pediatrics University of Pennsylvania Perelman School of Medicine Philadelphia Pennsylvania
                [ 3 ] Division of Biostatistics University of Florida Gainesville Florida
                [ 4 ] The Center for Clinical Epidemiology and Biostatistics University of Pennsylvania Perelman School of Medicine Philadelphia Pennsylvania
                [ 5 ] Children's Hospital Association Lenexa Kansas
                [ 6 ] Center for Pediatric Clinical Effectiveness The Children's Hospital of Philadelphia Philadelphia Pennsylvania
                [ 7 ] Division of Hematology‐Oncology Department of Pediatrics Center for Cancer and Blood Disorders University of Texas at Southwestern Medical Center Dallas Texas
                [ 8 ] Perlmutter Cancer Center Departments of Pediatrics and Pathology NYU Langone Medical Center New York New York
                [ 9 ] Division of Infectious Diseases The Children's Hospital of Philadelphia Philadelphia Pennsylvania
                [ 10 ] Division of Pediatric Hematology/Oncology Maine Medical Center Scarborough Maine
                Author notes
                [*] [* ] Correspondence

                Amanda DiNofia, Children's Hospital of Philadelphia, Division of Oncology, 3501 Civic Center Blvd, CTRB, Room 3016, Philadelphia, PA 19104. Tel: 267 250 9926; Fax: 215 590 3296; E‐mail: dinofiaa@ 123456email.chop.edu

                Author information
                http://orcid.org/0000-0002-8321-0403
                Article
                CAM41206
                10.1002/cam4.1206
                5773964
                29274118
                6bb119cc-7806-40eb-bb28-2e91206571eb
                © 2017 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 01 May 2017
                : 26 August 2017
                : 28 August 2017
                Page count
                Figures: 2, Tables: 4, Pages: 10, Words: 6436
                Funding
                Funded by: National Institutes of Health
                Award ID: 5T32HD064567‐05
                Award ID: 5T32CA009679‐24
                Award ID: U10 CA180886
                Award ID: U10 CA180899
                Funded by: Alex's Lemonade Stand Foundation Young Investigator Award
                Categories
                Original Research
                Clinical Cancer Research
                Original Research
                Custom metadata
                2.0
                cam41206
                January 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.3.1 mode:remove_FC converted:19.01.2018

                Oncology & Radiotherapy
                child,clinical trial,costs,leukemia,variation
                Oncology & Radiotherapy
                child, clinical trial, costs, leukemia, variation

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