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R.A. Stahel

Moderator of

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    Mesothelioma: New roads through understanding biology (ID 24)

    • Event: ELCC 2018
    • Type: Educational session
    • Track:
    • Presentations: 4
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      Immunotherapy: Clinical results (ID 101)

      09:00 - 10:30  |  Presenting Author(s): A. Scherpereel

      • Abstract
      • Presentation
      • Slides

      Abstract not provided

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      Immunotherapy: The basics (ID 100)

      09:00 - 10:30  |  Presenting Author(s): J. Aerts

      • Abstract
      • Presentation
      • Slides

      Abstract not provided

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      Molecular targets: Clinical results (ID 99)

      09:00 - 10:30  |  Presenting Author(s): R. Hassan

      • Abstract
      • Presentation
      • Slides

      Abstract not provided

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      Molecular targets: The basics (ID 98)

      09:00 - 10:30  |  Presenting Author(s): D. Fennell

      • Abstract
      • Presentation
      • Slides

      Abstract not provided

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Author of

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    First line for non-oncogene addicted lung cancer (ID 4)

    • Event: ELCC 2018
    • Type: Educational session
    • Track:
    • Presentations: 1
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      First-line chemotherapy in NSCLC: Where do we stand? (ID 12)

      16:30 - 18:00  |  Presenting Author(s): R.A. Stahel

      • Abstract
      • Presentation
      • Slides

      Abstract not provided

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    New approaches in rare thoracic tumors (ID 60)

    • Event: ELCC 2018
    • Type: Proffered Paper session
    • Track:
    • Presentations: 1
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      214O - Multiplexed proteomics biomarkers for malignant pleural mesothelioma detection in blood (ID 385)

      11:00 - 12:30  |  Author(s): R.A. Stahel

      • Abstract
      • Slides

      Background:
      Blood biomarkers are not routinely applied for the diagnosis of malignant pleural mesothelioma (MPM). We investigated a multiplexed biomarkers signature composed of 6 glycopeptides for the diagnosis of MPM in blood using mass spectrometry based targeted proteomics.

      Methods:
      We applied the targeted proteomics technology selected reaction monitoring (SRM, also known as multiple reaction monitoring – MRM) to investigate more than 400 serum samples from early and advanced stages MPM patients and asbestos exposed donors. Samples were from biobanks in the USA, Australia and Europe. Samples were enriched for N-linked glycoproteins using hydrazide chemistry. After tryptic digestion, N-linked glycopeptides were separated by liquid chromatography before analysis on a triple quadrupole mass spectrometer (LC-MS/MS). Logistic regression was fitted on a training set of 212 samples followed by evaluation of predictive accuracy of the signature in a validation set of 193 samples.

      Results:
      The proteomics platform for serum processing on 96-well plates and LC-MS/MS analysis had coefficient of variation between 2.0 and 11.4% for peptide quantification over more than 700 measurements, and standard deviation of 0.42 for processing more than 400 replicates. The predictive accuracy for MPM discrimination was significantly higher using multiplexed biomarkers by mass spectrometry compared to using single biomarkers alone. The multiplexed proteomics signature separated MPM patients and asbestos exposed donors with an area under the receiver operating characteristic curve (AUC) of 0.72 in the validation set, and AUC for discriminating early stage MPM from asbestos exposed donors was 0.74. Predictive accuracy of the proteomics signature was not inferior to the currently best available MPM blood biomarker soluble-mesothelin related peptides (SMRP) measured in the samples of the validation set using an enzyme-linked immunosorbent assay (ELISA) approved by the US food and drug administration (FDA). Furthermore, signature was significantly associated with survival of MPM patients after treatment.

      Conclusions:
      Mass spectrometry based proteomics biomarkers have potential for MPM diagnosis in blood.

      Clinical trial identification:


      Legal entity responsible for the study:
      The Ohio State University Medical Center

      Funding:
      Kathy and Jay Worly Lung Cancer Early Detection Fund Don Ward, President, Special Claims Services, Inc. at The Ohio State University Comprehensive Cancer Center (OSUCCC) The Swiss National Science Foundation (postdoc mobility fellowship)

      Disclosure:
      All authors have declared no conflicts of interest.

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    Poster Display session (Friday) (ID 65)

    • Event: ELCC 2018
    • Type: Poster Display session
    • Track:
    • Presentations: 1
    • Moderators:
    • Coordinates: 4/13/2018, 12:30 - 13:00, Hall 1
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      21P - Influence of delayed and prolonged fixation on the evaluation of immunohistochemical staining on pulmonary resection specimen (ID 539)

      12:30 - 13:00  |  Author(s): R.A. Stahel

      • Abstract
      • Slides

      Background:
      Pre-analytical factors as fixation time has influence on morphology of diagnostic and predictive immunohistochemical staining and are increasingly used in the evaluation of lung cancer. Our aim was to investigate if variations in fixation time influence the outcome of immunohistochemical staining in lung cancer.

      Methods:
      From lung cancer resections specimen with tumor size >4 cm, 10 fragments were sampled: 2 received standard fixation, 5 delayed, and 3 prolonged fixation. After paraffin embedding, tissue microarrays (TMA) were made. Immunohistochemistry (IHC) of 20 antibodies were applied and scored for quality and intensity of staining. TMA slides were scored by core/case: quality of cores and IHC intensity in cores of sufficient quality.

      Results:
      Tissue with delay in start of fixation showed deterioration of tissue quality leading to reduction in the evaluation of staining for CK-7, Keratin MNF116, Cam5.2, CK5/6, TTF-1, CMET, Napsin-A, D2-40, PD-L1 antibodies. Prolonged fixation had no influence on the performance of immunohistochemical stains.

      Conclusions:
      Delay of fixation negatively effects the evaluation of IHC staining. Therefore, tissue should be fixated soon after surgery.

      Clinical trial identification:


      Legal entity responsible for the study:
      European Thoracic Oncology Platform (ETOP)

      Funding:
      VU University Medical Center

      Disclosure:
      All authors have declared no conflicts of interest.

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    Young Oncologist session (ID 9)

    • Event: ELCC 2018
    • Type: Young Oncologist session
    • Track:
    • Presentations: 1
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      The importance of mentorship in the European environment (ID 37)

      09:00 - 10:30  |  Presenting Author(s): R.A. Stahel

      • Abstract
      • Presentation
      • Slides

      Abstract not provided

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