Comprehensive serial biobanking in advanced NSCLC: feasibility, challenges and perspectives.

Non-small cell lung cancer (NSCLC) biobanking cryoconserved biopsies serial blood sampling translational research

Journal

Translational lung cancer research
ISSN: 2218-6751
Titre abrégé: Transl Lung Cancer Res
Pays: China
ID NLM: 101646875

Informations de publication

Date de publication:
Aug 2020
Historique:
entrez: 21 9 2020
pubmed: 22 9 2020
medline: 22 9 2020
Statut: ppublish

Résumé

Availability of tumor material at baseline and disease progression is increasingly important for patient management in non-small-cell lung cancer (NSCLC), especially for the application of targeted therapies like tyrosine kinase inhibitors and for immune checkpoint inhibitor treatment. Here we report the experience of prospective biomaterial acquisition in advanced NSCLC from a pilot project. Main objective was the longitudinal collection of high-quality, cryoconserved biopsies in addition to formalin-fixed paraffin-embedded (FFPE) biopsies required for routine diagnostics, along with blood samples and detailed clinical annotation using standardized questionnaires. Over five years, 205 patients were enrolled for the project, yielding 387 cryoconserved biopsies and 1,098 serum, plasma and buffy-coat samples. The feasibility of obtaining the cryoconserved biopsies in addition to the FFPE biopsies was 89% for newly diagnosed cases, but dropped down to 56% and 47% at first and second disease progression, respectively. While forceps biopsy was the preferred procedure for tissue acquisition, the highest tissue amounts were received using the cryobiopsy method. Biopsies had a median tumor cellularity of 34% and yielded in median 13.6 µg DNA and 12 µg RNA (median RIN =8). During the five-year project, a maximum of 38 follow-up blood samples per patient were assembled in up to four therapy lines. Despite the poor condition and limited prognosis of most NSCLC patients, this serial biomaterial acquisition including routine collection of cryoconserved biopsies is feasible to support individualized management. The standardized collection of high-quality material has enabled and enriched several translational research studies that can advance therapeutic options.

Sections du résumé

BACKGROUND BACKGROUND
Availability of tumor material at baseline and disease progression is increasingly important for patient management in non-small-cell lung cancer (NSCLC), especially for the application of targeted therapies like tyrosine kinase inhibitors and for immune checkpoint inhibitor treatment. Here we report the experience of prospective biomaterial acquisition in advanced NSCLC from a pilot project.
METHODS METHODS
Main objective was the longitudinal collection of high-quality, cryoconserved biopsies in addition to formalin-fixed paraffin-embedded (FFPE) biopsies required for routine diagnostics, along with blood samples and detailed clinical annotation using standardized questionnaires.
RESULTS RESULTS
Over five years, 205 patients were enrolled for the project, yielding 387 cryoconserved biopsies and 1,098 serum, plasma and buffy-coat samples. The feasibility of obtaining the cryoconserved biopsies in addition to the FFPE biopsies was 89% for newly diagnosed cases, but dropped down to 56% and 47% at first and second disease progression, respectively. While forceps biopsy was the preferred procedure for tissue acquisition, the highest tissue amounts were received using the cryobiopsy method. Biopsies had a median tumor cellularity of 34% and yielded in median 13.6 µg DNA and 12 µg RNA (median RIN =8). During the five-year project, a maximum of 38 follow-up blood samples per patient were assembled in up to four therapy lines.
CONCLUSIONS CONCLUSIONS
Despite the poor condition and limited prognosis of most NSCLC patients, this serial biomaterial acquisition including routine collection of cryoconserved biopsies is feasible to support individualized management. The standardized collection of high-quality material has enabled and enriched several translational research studies that can advance therapeutic options.

Identifiants

pubmed: 32953480
doi: 10.21037/tlcr-20-137
pii: tlcr-09-04-1000
pmc: PMC7481602
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1000-1014

Informations de copyright

2020 Translational Lung Cancer Research. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tlcr-20-137). SW reports grants and personal fees from German Center for Lung Research (DZL), during the conduct of the study. TM reports grants and personal fees from BMBF, German Center for Lung Research (DZL), during the conduct of the study; grants and personal fees from Roche, outside the submitted work. PC reports grants and personal fees from Novartis, grants and personal fees from Roche, grants from AstraZeneca, grants from Takeda, personal fees from Chugai, personal fees from Boehringer, outside the submitted work. MM reports grants from German Center for Lung Research, during the conduct of the study. CPH’s disclosure see the COI statement enclosed. AS reports personal fees from Astra Zeneca, personal fees from Novartis, grants and personal fees from BMS, personal fees from MSD, grants and personal fees from Bayer, personal fees from Seattle Genetics, personal fees from Takeda, personal fees from Eli Lilly, personal fees from Illumina, personal fees from Thermo Fisher, grants from Chugai, personal fees from Roche, personal fees from Pfizer, personal fees from Janssen, during the conduct of the study; serves as an unpaid editorial board member of Translational Lung Cancer Research from Sep 2019 to Sep 2021. RMH reports grants from German Center for Lung Research (DZL), during the conduct of the study. MT reports grants, personal fees and non-financial support from AstraZeneca, grants, personal fees and non- financial support from Bristol-Myers Squibb, personal fees and non-financial support from Boehringer Ingelheim, personal fees and non-financial support from Celgene, personal fees and non-financial support from Chugai, personal fees and non-financial support from Lilly, personal fees and non-financial support from MSD, personal fees and non-financial support from Novartis, personal fees and non-financial support from Pfizer, grants, personal fees and non-financial support from Roche, grants, personal fees and non-financial support from Takeda, outside the submitted work. MAS reports grants and personal fees from German Center for Lung Research (DZL), during the conduct of the study. The other authors have no conflicts of interest to declare.

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Auteurs

Sabine Wessels (S)

Department of Thoracic Oncology, Thoraxklinik at University Hospital Heidelberg, D-69126 Heidelberg, Germany.
Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.

Thomas Muley (T)

Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.
Translational Research Unit, Thoraxklinik at University Hospital Heidelberg, D-69126 Heidelberg, Germany.

Petros Christopoulos (P)

Department of Thoracic Oncology, Thoraxklinik at University Hospital Heidelberg, D-69126 Heidelberg, Germany.
Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.

Michael Meister (M)

Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.
Translational Research Unit, Thoraxklinik at University Hospital Heidelberg, D-69126 Heidelberg, Germany.

Ingrid Heinzmann-Groth (I)

Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.
Translational Research Unit, Thoraxklinik at University Hospital Heidelberg, D-69126 Heidelberg, Germany.

Arne Warth (A)

Institute of Pathology, University Hospital Heidelberg, D-69120 Heidelberg, Germany.

Esther Herpel (E)

Institute of Pathology, University Hospital Heidelberg, D-69120 Heidelberg, Germany.
NCT Tissue Bank, National Center for Tumor Diseases (NCT), Heidelberg, Germany.

Simone Hummler (S)

Department of Pneumology and Critical Care Medicine, Thoraxklinik at University Hospital Heidelberg, D-69126 Heidelberg, Germany.

Ursula Klingmüller (U)

Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.
Division Systems Biology of Signal Transduction, German Cancer Research Centre (DKFZ), INF 280, Heidelberg, Germany.

Jonas Kuon (J)

Department of Thoracic Oncology, Thoraxklinik at University Hospital Heidelberg, D-69126 Heidelberg, Germany.

Claus-Peter Heussel (CP)

Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.
Department of Diagnostic and Interventional Radiology with Nuclear Medicine, Thoraxklinik at University Hospital Heidelberg, D-69126 Heidelberg, Germany.
Department of Diagnostic and Interventional Radiology, University Hospital, D-69120 Heidelberg, Germany.

Ralf Eberhardt (R)

Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.
Department of Diagnostic and Interventional Radiology with Nuclear Medicine, Thoraxklinik at University Hospital Heidelberg, D-69126 Heidelberg, Germany.

Felix J F Herth (FJF)

Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.
Department of Pneumology and Critical Care Medicine, Thoraxklinik at University Hospital Heidelberg, D-69126 Heidelberg, Germany.

Hauke Winter (H)

Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.
Department of Surgery, Thoraxklinik at University Hospital Heidelberg, D-69126 Heidelberg, Germany.

Helge Bischoff (H)

Department of Thoracic Oncology, Thoraxklinik at University Hospital Heidelberg, D-69126 Heidelberg, Germany.

Albrecht Stenzinger (A)

Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.
Institute of Pathology, University Hospital Heidelberg, D-69120 Heidelberg, Germany.
German Cancer Consortium (DKTK), Heidelberg Site, Germany.

Martin Reck (M)

Department of Thoracic Oncology, Lung Clinic Grosshansdorf, D-22927 Grosshansdorf, Germany.
Airway Research Centre North (ARCN), German Centre for Lung Research (DZL), Grosshansdorf, Germany.

Rudolf Maria Huber (RM)

University Hospital Munich and Thoracic Oncology Centre Munich, D-80337 Munich, Germany.
Comprehensive Pneumology Centre Munich (CPC-M), German Centre for Lung Research (DZL), Munich, Germany.

Michael Thomas (M)

Department of Thoracic Oncology, Thoraxklinik at University Hospital Heidelberg, D-69126 Heidelberg, Germany.
Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.

Marc A Schneider (MA)

Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.
Translational Research Unit, Thoraxklinik at University Hospital Heidelberg, D-69126 Heidelberg, Germany.

Classifications MeSH