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1000 Titel
  • Clinical responses to PD-1 inhibition and their molecular characterization in six patients with mismatch repair-deficient metastatic cancer of the digestive system
1000 Autor/in
  1. Hirsch, Daniela |
  2. Gaiser, Timo |
  3. Merx, Kirsten |
  4. Weingaertner, Simone |
  5. Forster, Michael |
  6. Hendricks, Alexander |
  7. Woenckhaus, Matthias |
  8. Schubert, Thomas |
  9. Hofheinz, Ralf-Dieter |
  10. Gencer, Deniz |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-08-09
1000 Erschienen in
1000 Quellenangabe
  • 147(1):263-273
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00432-020-03335-2 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7810640/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Purpose!#!Immune checkpoint inhibitors have shown efficacy in patients with microsatellite instability-high/mismatch repair-deficient (MSI-H/dMMR) gastrointestinal (GI) cancers. However, depth and duration of clinical response is not uniform. We assessed tumor mutation burden (TMB) as a response marker in patients with GI cancers treated with immune checkpoint inhibitors.!##!Methods!#!Detailed clinical and response data were collected from six patients with metastatic MSI-H/dMMR GI cancers treated with immune checkpoint inhibitors. Efficacy was assessed by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1. Tumors and matched normal tissue were profiled by targeted next generation sequencing (127 gene panel, size 0.8 Mb). Impact of included mutation types, germline filtering methodology and different variant allele frequency thresholds on TMB estimation was assessed.!##!Results!#!Objective radiographic responses were observed in all six patients, and complete response was achieved in two of the six patients. Responses were durable (minimum 25 months). TMB estimates were clearly above the two recently reported cut-offs for metastatic colorectal cancer of 12 or 37 mutations per megabase for five of six patients, respectively, while one patient had borderline TMB elevation. TMB did not show an association with extent and duration of response but was influenced by included mutation types, germline filtering method and variant allele frequency threshold.!##!Conclusion!#!Our case series confirms the clinical benefit of immune checkpoint blockade in patients with metastatic MSI-H/dMMR GI cancers and illustrates the vulnerability of TMB as predictive marker in a subset of patients.
1000 Sacherschließung
lokal Original Article – Clinical Oncology
lokal Colorectal cancer
lokal Microsatellite instability
lokal Programmed Cell Death 1 Receptor/antagonists
lokal Male [MeSH]
lokal Female [MeSH]
lokal Follow-Up Studies [MeSH]
lokal Adult [MeSH]
lokal Humans [MeSH]
lokal Neoplasm Metastasis [MeSH]
lokal DNA Repair Enzymes/genetics [MeSH]
lokal Gastrointestinal Neoplasms/drug therapy [MeSH]
lokal Middle Aged [MeSH]
lokal Gastrointestinal Neoplasms/metabolism [MeSH]
lokal Microsatellite Instability [MeSH]
lokal Gastrointestinal Neoplasms/genetics [MeSH]
lokal Nivolumab
lokal Survival Rate [MeSH]
lokal Tumor mutation burden
lokal Antineoplastic Agents, Immunological/therapeutic use [MeSH]
lokal DNA Mismatch Repair [MeSH]
lokal Immunotherapy
lokal Prognosis [MeSH]
lokal Gastrointestinal Neoplasms/pathology [MeSH]
lokal Pembrolizumab
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0001-8883-922X|https://frl.publisso.de/adhoc/uri/R2Fpc2VyLCBUaW1v|https://frl.publisso.de/adhoc/uri/TWVyeCwgS2lyc3Rlbg==|https://frl.publisso.de/adhoc/uri/V2VpbmdhZXJ0bmVyLCBTaW1vbmU=|https://frl.publisso.de/adhoc/uri/Rm9yc3RlciwgTWljaGFlbA==|https://frl.publisso.de/adhoc/uri/SGVuZHJpY2tzLCBBbGV4YW5kZXI=|https://frl.publisso.de/adhoc/uri/V29lbmNraGF1cywgTWF0dGhpYXM=|https://frl.publisso.de/adhoc/uri/U2NodWJlcnQsIFRob21hcw==|https://frl.publisso.de/adhoc/uri/SG9maGVpbnosIFJhbGYtRGlldGVy|https://frl.publisso.de/adhoc/uri/R2VuY2VyLCBEZW5peg==
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1000 Erstellt am 2023-11-17T22:16:46.936+0100
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