In vivo optical imaging-guided targeted sampling for precise diagnosis and molecular pathology

Abstract Conventional tissue sampling can lead to misdiagnoses and repeated biopsies. Additionally, tissue processed for histopathology suffers from poor nucleic acid quality and/or quantity for downstream molecular profiling. Targeted micro-sampling of tissue can ensure accurate diagnosis and molec...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Aditi Sahu, Yuna Oh, Gary Peterson, Miguel Cordova, Cristian Navarrete-Dechent, Melissa Gill, Christi Alessi-Fox, Salvador Gonzalez, William Phillips, Steven Wilson, Reza Afzalneia, Raven Rose, Abu-Akeel Mohsen, Danielle Bello, Ashfaq Marghoob, Anthony Rossi, Jedd D. Wolchok, Taha Merghoub, Veronica Rotemberg, Chih-Shan Jason Chen, Milind Rajadhyaksha
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
R
Q
Acceso en línea:https://doaj.org/article/9734a66b39b6499fa4d1a1a17f6f228b
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:9734a66b39b6499fa4d1a1a17f6f228b
record_format dspace
spelling oai:doaj.org-article:9734a66b39b6499fa4d1a1a17f6f228b2021-12-05T12:12:36ZIn vivo optical imaging-guided targeted sampling for precise diagnosis and molecular pathology10.1038/s41598-021-01447-42045-2322https://doaj.org/article/9734a66b39b6499fa4d1a1a17f6f228b2021-11-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-01447-4https://doaj.org/toc/2045-2322Abstract Conventional tissue sampling can lead to misdiagnoses and repeated biopsies. Additionally, tissue processed for histopathology suffers from poor nucleic acid quality and/or quantity for downstream molecular profiling. Targeted micro-sampling of tissue can ensure accurate diagnosis and molecular profiling in the presence of spatial heterogeneity, especially in tumors, and facilitate acquisition of fresh tissue for molecular analysis. In this study, we explored the feasibility of performing 1–2 mm precision biopsies guided by high-resolution reflectance confocal microscopy (RCM) and optical coherence tomography (OCT), and reflective metallic grids for accurate spatial targeting. Accurate sampling was confirmed with either histopathology or molecular profiling through next generation sequencing (NGS) in 9 skin cancers in 7 patients. Imaging-guided 1–2 mm biopsies enabled spatial targeting for in vivo diagnosis, feature correlation and depth assessment, which were confirmed with histopathology. In vivo 1-mm targeted biopsies achieved adequate quantity and high quality of DNA for next-generation sequencing. Subsequent mutational profiling was confirmed on 1 melanoma in situ and 2 invasive melanomas, using a 505-gene mutational panel called Memorial Sloan Kettering-Integrated mutational profiling of actionable cancer targets (MSK-IMPACT). Differential mutational landscapes, in terms of number and types of mutations, were found between invasive and in situ melanomas in a single patient. Our findings demonstrate feasibility of accurate sampling of regions of interest for downstream histopathological diagnoses and molecular pathology in both in vivo and ex vivo settings with broad diagnostic, therapeutic and research potential in cutaneous diseases accessible by RCM-OCT imaging.Aditi SahuYuna OhGary PetersonMiguel CordovaCristian Navarrete-DechentMelissa GillChristi Alessi-FoxSalvador GonzalezWilliam PhillipsSteven WilsonReza AfzalneiaRaven RoseAbu-Akeel MohsenDanielle BelloAshfaq MarghoobAnthony RossiJedd D. WolchokTaha MerghoubVeronica RotembergChih-Shan Jason ChenMilind RajadhyakshaNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Aditi Sahu
Yuna Oh
Gary Peterson
Miguel Cordova
Cristian Navarrete-Dechent
Melissa Gill
Christi Alessi-Fox
Salvador Gonzalez
William Phillips
Steven Wilson
Reza Afzalneia
Raven Rose
Abu-Akeel Mohsen
Danielle Bello
Ashfaq Marghoob
Anthony Rossi
Jedd D. Wolchok
Taha Merghoub
Veronica Rotemberg
Chih-Shan Jason Chen
Milind Rajadhyaksha
In vivo optical imaging-guided targeted sampling for precise diagnosis and molecular pathology
description Abstract Conventional tissue sampling can lead to misdiagnoses and repeated biopsies. Additionally, tissue processed for histopathology suffers from poor nucleic acid quality and/or quantity for downstream molecular profiling. Targeted micro-sampling of tissue can ensure accurate diagnosis and molecular profiling in the presence of spatial heterogeneity, especially in tumors, and facilitate acquisition of fresh tissue for molecular analysis. In this study, we explored the feasibility of performing 1–2 mm precision biopsies guided by high-resolution reflectance confocal microscopy (RCM) and optical coherence tomography (OCT), and reflective metallic grids for accurate spatial targeting. Accurate sampling was confirmed with either histopathology or molecular profiling through next generation sequencing (NGS) in 9 skin cancers in 7 patients. Imaging-guided 1–2 mm biopsies enabled spatial targeting for in vivo diagnosis, feature correlation and depth assessment, which were confirmed with histopathology. In vivo 1-mm targeted biopsies achieved adequate quantity and high quality of DNA for next-generation sequencing. Subsequent mutational profiling was confirmed on 1 melanoma in situ and 2 invasive melanomas, using a 505-gene mutational panel called Memorial Sloan Kettering-Integrated mutational profiling of actionable cancer targets (MSK-IMPACT). Differential mutational landscapes, in terms of number and types of mutations, were found between invasive and in situ melanomas in a single patient. Our findings demonstrate feasibility of accurate sampling of regions of interest for downstream histopathological diagnoses and molecular pathology in both in vivo and ex vivo settings with broad diagnostic, therapeutic and research potential in cutaneous diseases accessible by RCM-OCT imaging.
format article
author Aditi Sahu
Yuna Oh
Gary Peterson
Miguel Cordova
Cristian Navarrete-Dechent
Melissa Gill
Christi Alessi-Fox
Salvador Gonzalez
William Phillips
Steven Wilson
Reza Afzalneia
Raven Rose
Abu-Akeel Mohsen
Danielle Bello
Ashfaq Marghoob
Anthony Rossi
Jedd D. Wolchok
Taha Merghoub
Veronica Rotemberg
Chih-Shan Jason Chen
Milind Rajadhyaksha
author_facet Aditi Sahu
Yuna Oh
Gary Peterson
Miguel Cordova
Cristian Navarrete-Dechent
Melissa Gill
Christi Alessi-Fox
Salvador Gonzalez
William Phillips
Steven Wilson
Reza Afzalneia
Raven Rose
Abu-Akeel Mohsen
Danielle Bello
Ashfaq Marghoob
Anthony Rossi
Jedd D. Wolchok
Taha Merghoub
Veronica Rotemberg
Chih-Shan Jason Chen
Milind Rajadhyaksha
author_sort Aditi Sahu
title In vivo optical imaging-guided targeted sampling for precise diagnosis and molecular pathology
title_short In vivo optical imaging-guided targeted sampling for precise diagnosis and molecular pathology
title_full In vivo optical imaging-guided targeted sampling for precise diagnosis and molecular pathology
title_fullStr In vivo optical imaging-guided targeted sampling for precise diagnosis and molecular pathology
title_full_unstemmed In vivo optical imaging-guided targeted sampling for precise diagnosis and molecular pathology
title_sort in vivo optical imaging-guided targeted sampling for precise diagnosis and molecular pathology
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/9734a66b39b6499fa4d1a1a17f6f228b
work_keys_str_mv AT aditisahu invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT yunaoh invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT garypeterson invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT miguelcordova invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT cristiannavarretedechent invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT melissagill invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT christialessifox invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT salvadorgonzalez invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT williamphillips invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT stevenwilson invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT rezaafzalneia invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT ravenrose invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT abuakeelmohsen invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT daniellebello invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT ashfaqmarghoob invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT anthonyrossi invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT jedddwolchok invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT tahamerghoub invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT veronicarotemberg invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT chihshanjasonchen invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
AT milindrajadhyaksha invivoopticalimagingguidedtargetedsamplingforprecisediagnosisandmolecularpathology
_version_ 1718372145777606656