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基于三人体外全基因组测序的儿科和青少年新发癌症患者潜在癌症易感性的综合前瞻性队列研究方案:PREDICT 研究。

Protocol for a comprehensive prospective cohort study of trio-based whole-genome sequencing for underlying cancer predisposition in paediatric and adolescent patients newly diagnosed with cancer: the PREDICT study.

机构信息

Kids Cancer Centre, Sydney Children's Hospitals Network Randwick, Randwick, New South Wales, Australia.

Children's Cancer Institute, Lowy Cancer Centre, UNSW, Randwick, New South Wales, Australia.

出版信息

BMJ Open. 2023 May 30;13(5):e070082. doi: 10.1136/bmjopen-2022-070082.

Abstract

INTRODUCTION

Identifying an underlying germline cancer predisposition (CP) in a child with cancer has potentially significant implications for both the child and biological relatives. Cohort studies indicate that 10%-15% of paediatric cancer patients carry germline pathogenic or likely pathogenic variants in cancer predisposition genes, but many of these patients do not meet current clinical criteria for genetic testing. This suggests broad tumour agnostic germline testing may benefit paediatric cancer patients. However, the utility and psychosocial impact of this approach remain unknown. We hypothesise that an approach involving trio whole-genome germline sequencing (trio WGS) will identify children and families with an underlying CP in a timely fashion, that the trio design will streamline cancer risk counselling to at-risk relatives if CP was inherited, and that trio testing will not have a negative psychosocial impact on families.

METHOD AND ANALYSIS

To test this, we present the Cancer PREDisposition In Childhood by Trio sequencing study (PREDICT). This study will assess the clinical utility of trio WGS to identify CP in unselected patients with cancer 21 years or younger in New South Wales, Australia. PREDICT will perform analysis of biological parents to determine heritability and will examine the psychosocial impact of this trio sequencing approach. PREDICT also includes a broad genomics research programme to identify new candidate genes associated with childhood cancer risk.

ETHICS AND DISSEMINATION

By evaluating the feasibility, utility and psychosocial impact of trio WGS to identify CP in paediatric cancer, PREDICT will inform how such comprehensive testing can be incorporated into a standard of care at diagnosis for all childhood cancer patients.

TRIAL REGISTRATION NUMBER

NCT04903782.

摘要

简介

在癌症患儿中发现潜在的种系癌症易感性(CP)具有重要意义,不仅对患儿,对其生物学亲属也同样如此。队列研究表明,10%-15%的儿科癌症患者携带癌症易感性基因中的种系致病性或可能致病性变异,但这些患者中的许多不符合当前的遗传检测临床标准。这表明广泛的肿瘤未知种系检测可能使儿科癌症患者受益。然而,这种方法的实用性和心理社会影响仍不清楚。我们假设,涉及三系全基因组种系测序(trio WGS)的方法将及时发现具有潜在 CP 的儿童和家庭,如果 CP 是遗传的,则三系设计将简化对高危亲属的癌症风险咨询,并且三系检测不会对家庭产生负面影响。

方法和分析

为了验证这一点,我们提出了通过三系测序研究(PREDICT)来评估癌症 PREDisposition In Childhood 的方法。该研究将评估 trio WGS 在澳大利亚新南威尔士州 21 岁或以下的未选择癌症患者中识别 CP 的临床实用性。PREDICT 将对生物父母进行分析,以确定遗传率,并研究这种三系测序方法的心理社会影响。PREDICT 还包括一个广泛的基因组学研究计划,以确定与儿童癌症风险相关的新候选基因。

伦理和传播

通过评估 trio WGS 识别儿科癌症 CP 的可行性、实用性和心理社会影响,PREDICT 将为如何将这种全面的检测纳入所有儿童癌症患者的诊断标准提供信息。

试验注册号

NCT04903782。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dbb/10254808/cd6866c8a56e/bmjopen-2022-070082f01.jpg

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