Children's Oncology Group's 2023 blueprint for research: Germ cell tumors

Author:

Bhuta Roma1ORCID,Shah Rachana2ORCID,Gell Joanna J.345ORCID,Poynter Jenny N.67,Bagrodia Aditya8,Dicken Bryan J.9ORCID,Pashankar Farzana10ORCID,Frazier A Lindsay11ORCID,Shaikh Furqan12ORCID

Affiliation:

1. Division of Pediatric Hematology‐Oncology Hasbro Children's Hospital The Warren Alpert Medical School of Brown University Providence Rhode Island USA

2. Division of Hematology‐Oncology Cancer and Blood Disease Institute Children's Hospital Los Angeles Keck School of Medicine University of Southern California Los Angeles California USA

3. The Center for Cancer and Blood Disorders Connecticut Children's Medical Center Hartford Connecticut USA

4. Department of Pediatrics University of Connecticut Medical School Farmington Connecticut USA

5. The Jackson Laboratory for Genomic Medicine Farmington Connecticut USA

6. Division of Epidemiology and Clinical Research Department of Pediatrics University of Minnesota Minneapolis Minnesota USA

7. Masonic Cancer Center University of Minnesota Minneapolis Minnesota USA

8. Department of Urology University of California San Diego San Diego California USA

9. Department of Surgery University of Alberta Stollery Children's Hospital Edmonton Alberta Canada

10. Department of Pediatrics Yale University School of Medicine New Haven Connecticut USA

11. Dana‐Farber/Boston Children's Cancer and Blood Disorders Center Boston Massachusetts USA

12. Department of Pediatrics Division of Hematology/Oncology The Hospital for Sick Children University of Toronto Toronto Ontario Canada

Abstract

AbstractExtracranial germ cell tumors (GCT) are a biologically diverse group of tumors occurring in children, adolescents, and young adults. The majority of patients have excellent outcomes, but treatment‐related toxicities impact their quality of survivorship. A subset of patients succumbs to the disease. Current unmet needs include clarifying which patients can be safely observed after initial surgical resection, refinement of risk stratification to reduce chemotherapy burden in patients with standard‐risk disease, and intensify therapy for patients with poor‐risk disease. Furthermore, enhancing strategies for detection of minimal residual disease and early detection of relapse, particularly in serum tumor marker‐negative histologies, is critical. Improving the understanding of the developmental and molecular origins of GCTs may facilitate discovery of novel targets. Future efforts should be directed toward assessing novel therapies in a biology‐driven, biomarker‐defined, histology‐specific, risk‐stratified patient population. Fragmentation of care between subspecialists restricts the unified study of these rare tumors. It is imperative that trials be conducted in collaboration with national and international cooperative groups, with harmonized data and biospecimen collection. Key priorities for the Children's Oncology Group (COG) GCT Committee include (a) better understanding the biology of GCTs, with a focus on molecular targets and mechanisms of treatment resistance; (b) strategic development of pediatric and young adult clinical trials; (c) understanding late effects of therapy and identifying individuals most at risk; and (d) prioritizing diversity, equity, and inclusion to reduce cancer health disparities and studying the impacts of social determinants of health on outcomes.

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference74 articles.

1. Pediatric Germ Cell Tumors: A Developmental Perspective

2. Surveillance Epidemiology and End Results (SEER) Program. SEER*Stat database: incidence ‐ SEER research data 8 registries Nov 2021 sub (1975–2020) ‐ linked to county attributes ‐ time dependent (1990–2020) income/rurality 1969–2020 counties based on the November 2022 submission.National Cancer Institute DCCPS Surveillance Research Program; Released April2023. Accessed May 19 2023.http://seer.cancer.gov/

3. Trends in incidence and survival of pediatric and adolescent patients with germ cell tumors in the United States, 1975 to 2006

4. Randomized Comparison of Combination Chemotherapy With Etoposide, Bleomycin, and Either High-Dose or Standard-Dose Cisplatin in Children and Adolescents With High-Risk Malignant Germ Cell Tumors: A Pediatric Intergroup Study—Pediatric Oncology Group 9049 and Children's Cancer Group 8882

5. The American Joint Committee on Cancer: the 7th Edition of the AJCC Cancer Staging Manual and the Future of TNM

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3