Risk and Benefit for Targeted Therapy Agents in Pediatric Phase II Trials in Oncology: A Systematic Review with a Meta-Analysis
Autor: | Jakub Stras, Marcin Waligóra, Maciej Polak, Mateusz T. Wasylewski, Bishal Gyawali, Lucja Zaborowska, Karolina Strzebonska, Emilia Slugocka, Mateusz Blukacz |
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Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Cancer Research medicine.medical_specialty medicine.medical_treatment MEDLINE Antineoplastic Agents Medical Oncology Targeted therapy 03 medical and health sciences 0302 clinical medicine Neoplasms Internal medicine medicine Pharmacology (medical) Adverse effect business.industry Cancer targeted therapy medicine.disease Pediatric cancer Confidence interval pediatric cancer Clinical trial 030104 developmental biology Oncology 030220 oncology & carcinogenesis Meta-analysis Systematic Review business |
Zdroj: | Targeted Oncology |
ISSN: | 1776-260X 1776-2596 |
DOI: | 10.1007/s11523-021-00822-5 |
Popis: | Background For research with human participants to be ethical, risk must be in a favorable balance with potential benefits. Little is known about the risk/benefit ratio for pediatric cancer phase II trials testing targeted therapies. Objective Our aim was to conduct a systematic review of preliminary efficacy and safety profiles of phase II targeted therapy clinical trials in pediatric oncology. Methods Our protocol was prospectively registered in PROSPERO (CRD42020146491). We searched EMBASE and PubMed for phase II pediatric cancer trials testing targeted agents. We included solid and hematological malignancy studies published between 1 January, 2015 and 27 February, 2020. We measured risk using drug-related grade 3 or higher adverse events, and benefit by response rates. When possible, data were meta-analyzed. All statistical tests were two-sided. Results We identified 34 clinical trials (1202 patients) that met our eligibility criteria. The pooled overall response rate was 24.4% (95% confidence interval [CI] 14.5–34.2) and was lower in solid tumors, 6.4% (95% CI 3.2–9.6), compared with hematological malignancies, 55.1% (95% CI 35.9–74.3); p < 0.001. The overall fatal drug-related (grade 5) adverse event rate was 1.6% (95% CI 0.6–2.5), and the average drug-related grade 3/4 adverse event rate per person was 0.66 (95% CI 0.55–0.78). Conclusions We provide an estimate for the risks and benefits of participation in pediatric phase II cancer trials. These data may be used as an empirical basis for informed communication about benefits and burdens in pediatric oncology research. Supplementary Information The online version contains supplementary material available at 10.1007/s11523-021-00822-5. |
Databáze: | OpenAIRE |
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