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下一代快速尸检可实现肿瘤演变追踪并生成临床前模型。

Next-Generation Rapid Autopsies Enable Tumor Evolution Tracking and Generation of Preclinical Models.

作者信息

Pisapia David J, Salvatore Steven, Pauli Chantal, Hissong Erika, Eng Ken, Prandi Davide, Sailer Verena-Wilbeth, Robinson Brian D, Park Kyung, Cyrta Joanna, Tagawa Scott T, Kossai Myriam, Fontugne Jacqueline, Kim Robert, Sigaras Alexandros, Rao Rema, Pancirer Danielle, Faltas Bishoy, Bareja Rohan, Molina Ana M, Nanus David M, Rajappa Prajwal, Souweidane Mark M, Greenfield Jeffrey, Emde Anne-Katrin, Robine Nicolas, Elemento Olivier, Sboner Andrea, Demichelis Francesca, Beltran Himisha, Rubin Mark A, Mosquera Juan Miguel

机构信息

Weill Cornell Medicine. The Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine and NewYork-Presbyterian Hospital.

Weill Cornell Medicine.

出版信息

JCO Precis Oncol. 2017;2017. doi: 10.1200/PO.16.00038. Epub 2017 Jun 14.

Abstract

PURPOSE

Patients with cancer who graciously consent for autopsy represent an invaluable resource for the study of cancer biology. To advance the study of tumor evolution, metastases, and resistance to treatment, we developed a next-generation rapid autopsy program integrated within a broader precision medicine clinical trial that interrogates pre- and postmortem tissue samples for patients of all ages and cancer types.

MATERIALS AND METHODS

One hundred twenty-three (22%) of 554 patients who consented to the clinical trial also consented for rapid autopsy. This report comprises the first 15 autopsies, including patients with metastatic carcinoma (n = 10), melanoma (n = 1), and glioma (n = 4). Whole-exome sequencing (WES) was performed on frozen autopsy tumor samples from multiple anatomic sites and on non-neoplastic tissue. RNA sequencing (RNA-Seq) was performed on a subset of frozen samples. Tissue was also used for the development of preclinical models, including tumor organoids and patient-derived xenografts.

RESULTS

Three hundred forty-six frozen samples were procured in total. WES was performed on 113 samples and RNA-Seq on 72 samples. Successful cell strain, tumor organoid, and/or patient-derived xenograft development was achieved in four samples, including an inoperable pediatric glioma. WES data were used to assess clonal evolution and molecular heterogeneity of tumors in individual patients. Mutational profiles of primary tumors and metastases yielded candidate mediators of metastatic spread and organotropism including and in metastatic ependymoma and in metastatic melanoma to the lung. RNA-Seq data identified novel gene fusion candidates.

CONCLUSION

A next-generation sequencing-based autopsy program in conjunction with a pre-mortem precision medicine pipeline for diverse tumors affords a valuable window into clonal evolution, metastasis, and alterations underlying treatment. Moreover, such an autopsy program yields robust preclinical models of disease.

摘要

目的

那些欣然同意进行尸检的癌症患者是癌症生物学研究的宝贵资源。为了推进肿瘤进化、转移及治疗耐药性的研究,我们开展了一项新一代快速尸检计划,该计划整合于一个更广泛的精准医学临床试验中,对所有年龄和癌症类型的患者的生前和死后组织样本进行检测。

材料与方法

554名同意参加该临床试验的患者中,有123名(22%)也同意进行快速尸检。本报告涵盖了首批15例尸检,包括转移性癌患者(n = 10)、黑色素瘤患者(n = 1)和神经胶质瘤患者(n = 4)。对来自多个解剖部位的冷冻尸检肿瘤样本以及非肿瘤组织进行了全外显子组测序(WES)。对一部分冷冻样本进行了RNA测序(RNA-Seq)。组织还被用于临床前模型的构建,包括肿瘤类器官和患者来源的异种移植。

结果

共采集了346份冷冻样本。对113份样本进行了WES,对72份样本进行了RNA-Seq。在4份样本中成功培养出了细胞株、肿瘤类器官和/或患者来源的异种移植,其中包括一例无法手术的儿童神经胶质瘤。WES数据用于评估个体患者肿瘤的克隆进化和分子异质性。原发性肿瘤和转移灶的突变谱产生了转移扩散和器官嗜性的候选介质,包括转移性室管膜瘤中的 和 ,以及肺转移性黑色素瘤中的 。RNA-Seq数据鉴定出了新的基因融合候选物。

结论

基于新一代测序的尸检计划与针对多种肿瘤的生前精准医学流程相结合,为克隆进化、转移及治疗相关改变提供了一个宝贵的窗口。此外,这样的尸检计划还能产生强大的疾病临床前模型。

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