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Society for immunotherapy of cancer (SITC) statement on the proposed changes to the common rule

机译:癌症免疫疗法学会(SITC)关于共同规则拟议变更的声明

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摘要

The Common Rule is a set of ethical principles that provide guidance on the management of human subjects taking part in biomedical and behavioral research in the United States. The elements of the Common Rule were initially developed in 1981 following a revision of the Declaration of Helsinki in 1975. Most academic facilities follow the Common Rule in the regulation of clinical trials research. Recently, the government has suggested a revision of the Common Rule to include more contemporary and streamlined oversight of clinical research. In this commentary, the leadership of the Society for Immunotherapy of Cancer (SITC) provides their opinion on this plan. While the Society recognizes the considerable contribution of clinical research in supporting progress in tumor immunotherapy and supports the need for revisions to the Common Rule, there is also some concern over certain elements which may restrict access to biospecimens and clinical data at a time when high throughput technologies, computational biology and assay standardization is allowing major advances in understanding cancer biology and providing potential predictive biomarkers of immunotherapy response. The Society values its professional commitment to patients for improving clinical outcomes with tumor immunotherapy and supports continued discussion with all stakeholders before implementing changes to the Common Rule in order to ensure maximal patient protections while promoting continued clinical research at this historic time in cancer research.
机译:通用规则是一套道德原则,可为在美国从事生物医学和行为研究的人类受试者的管理提供指导。在1975年修订《赫尔辛基宣言》之后,《通用规则》的要素最初于1981年制定。大多数学术机构在临床试验研究的监管中都遵循《通用规则》。最近,政府建议对《通用规则》进行修订,以包括更现代,更简化的临床研究监督。在此评论中,癌症免疫疗法协会(SITC)的领导者对此计划发表了意见。尽管学会认识到临床研究在支持肿瘤免疫治疗方面的巨大贡献,并支持对《通用规则》进行修订的必要性,但对于某些因素也存在一些担忧,这些因素可能会限制在高通量的情况下获取生物标本和临床数据技术,计算生物学和测定法的标准化在了解癌症生物学和提供免疫疗法反应的潜在预测生物标志物方面取得了重大进展。协会重视其对患者改善肿瘤免疫疗法临床效果的专业承诺,并支持在实施《通用规则》变更之前与所有利益相关者进行持续讨论,以确保最大程度地保护患者,同时促进癌症研究这个历史性时期的持续临床研究。

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