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      Children's Oncology Group's 2023 blueprint for research: Cancer control and supportive care

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          Abstract

          The objective of the Cancer Control and Supportive Care (CCL) Committee in the Children's Oncology Group (COG) is to reduce the overall morbidity and mortality of therapy‐related toxicities in children, adolescents, and young adults with cancer. We have targeted five major domains that cause clinically important toxicity: (i) infections and inflammation; (ii) malnutrition and metabolic dysfunction; (iii) chemotherapy‐induced nausea and vomiting; (iv) neuro‐ and oto‐toxicty; and (v) patient‐reported outcomes and health‐related quality of life. Subcommittees for each domain prioritize randomized controlled trials and biology aims to determine which strategies best mitigate the toxicities. The findings of these trials are impactful, informing clinical practice guidelines (CPGs) and directly leading to changes in the standard of care for oncology practice. With the development of new therapies, there will be new toxicities, and the COG CCL Committee is dedicated to developing interventions to minimize acute and delayed toxicities, lessen morbidity and mortality, and improve quality of life in pediatric and young adult patients with cancer.

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          Most cited references65

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          Letermovir Prophylaxis for Cytomegalovirus in Hematopoietic-Cell Transplantation

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            Metabolomics in cancer research and emerging applications in clinical oncology

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              The effect of guideline-consistent antiemetic therapy on chemotherapy-induced nausea and vomiting (CINV): the Pan European Emesis Registry (PEER).

              While guidelines for preventing chemotherapy-induced nausea and vomiting (CINV) are widely available, clinical uptake of guidelines remains low. Our objective was to evaluate the effect of guideline-consistent CINV prophylaxis (GCCP) on patient outcomes. This prospective, observational multicenter study enrolled chemotherapy-naive adults initiating single-day highly or moderately emetogenic chemotherapy (HEC or MEC) for cancer. Patients completed 6-day daily diaries beginning with cycle 1 for up to three chemotherapy cycles. The primary study end point, complete response (no emesis and no use of rescue therapy) during 120 h after cycle 1 chemotherapy, was compared between GCCP and guideline-inconsistent CINV prophylaxis (GICP) cohorts using multivariate logistic regression, adjusting for potential confounding factors. In cycle 1 (N=991), use of GCCP was 55% and 46% during acute and delayed phases, respectively, and 29 % for the overall study period (acute plus delayed phases). Complete response was recorded by 172/287 (59.9%) and 357/704 (50.7%) patients in GCCP and GICP cohorts, respectively (P=0.008). The adjusted odds ratio for complete response was 1.43 (95% confidence interval 1.04-1.97; P=0.027) for patients receiving GCCP versus GICP. GCCP reduces the incidence of CINV after single-day HEC and MEC.
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                Author and article information

                Contributors
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                Journal
                Pediatric Blood & Cancer
                Pediatric Blood & Cancer
                Wiley
                1545-5009
                1545-5017
                September 2023
                July 10 2023
                September 2023
                : 70
                : S6
                Affiliations
                [1 ]Department of Pediatrics Vanderbilt University Medical Center and the Vanderbilt Ingram Cancer Nashville Tennessee USA
                [2 ]Division of Haematology/Oncology The Hospital for Sick Children Toronto Ontario Canada
                [3 ]Department of Pediatrics Division of Pediatric Hematology‐Oncology Texas Children's Cancer and Hematology Center Baylor College of Medicine Houston Texas USA
                [4 ]Department of Pharmacy and Research Institute The Hospital for Sick Children and Leslie Dan Faculty of Pharmacy University of Toronto Toronto Canada
                [5 ]Department of Pediatrics Division of Infectious Diseases Children's Hospital of Philadelphia Philadelphia Pennsylvania USA
                [6 ]Department of Pediatrics University of Texas San Antonio San Antonio Texas USA
                [7 ]Department of Pediatrics Emory University School of Medicine/Children's Healthcare of Atlanta Atlanta Georgia USA
                [8 ]Department of Neurology Boston Children's Hospital, Pediatric Brain Tumor Program Dana‐Farber Cancer Institute Boston Massachusetts USA
                [9 ]Division of Pediatric Allergy Immunology & Bone Marrow Transplantation University of California San Francisco San Francisco California USA
                Article
                10.1002/pbc.30568
                10528808
                37430431
                654206c9-e0dc-42d6-98a7-45d3c89e25ec
                © 2023

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