Genomic profiling in pancreatic ductal adenocarcinoma and a pathway towards therapy individualization: A scoping review

•Genomic alterations in PDAC represent potential targeting opportunities to individualize therapy.•Attempts to target key somatic driver mutations in PDAC have been unsuccessful.•DNA-damage repair gene mutations confer vulnerability to platinum agents and PARP-inhibitors.•Microsatellite unstable PDA...

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Veröffentlicht in:Cancer treatment reviews Jg. 75; S. 27 - 38
Hauptverfasser: Singh, Ritu R., Goldberg, Johanna, Varghese, Anna M., Yu, Kenneth H., Park, Wungki, O'Reilly, Eileen M.
Format: Journal Article
Sprache:Englisch
Veröffentlicht: Netherlands Elsevier Ltd 01.05.2019
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ISSN:0305-7372, 1532-1967, 1532-1967
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Abstract •Genomic alterations in PDAC represent potential targeting opportunities to individualize therapy.•Attempts to target key somatic driver mutations in PDAC have been unsuccessful.•DNA-damage repair gene mutations confer vulnerability to platinum agents and PARP-inhibitors.•Microsatellite unstable PDAC (1%) can benefit from checkpoint point inhibitor therapy.•The KRAS wild-type subset of PDAC (5%) is enriched for actionability, e.g., ALK, NTRK, NRG-1 fusions and others. Pancreatic cancer (PDAC) is one of the most challenging cancers to treat with modest recent improvements in survival from new systemic therapies. There is growing interest in individualized therapy underpinned by somatic and germline genomic alterations. A systematic review of data on therapies targeting somatic and germline alterations, and their downstream pathways in PDAC. A systematic literature search was conducted using PRISMA guidelines to include relevant results published after January 1, 2008. A total of 71 relevant studies were included. We identified 36 studies targeting the KRAS-pathway, the most common being with MEK-inhibitor therapy. Twenty-two studies were identified that evaluated platinum-based chemotherapy and PARP inhibitors in patients with deleterious mutations in DNA damage repair genes and have shown encouraging results. Immunotherapy has demonstrated activity in patients with mismatch repair deficiency/microsatellite instability. Evidence from translational and clinical research presents an exciting platform for genomic targeted therapy in PDAC. Validity for targeting BRCA with platinum and PARP inhibitors and microsatellite instability with immune therapy has been established, nonetheless, evidence for targeting the common driver oncogenes is lacking and much work is needed. Of importance is identifying the subgroup of KRAS -wild type PDAC (approximately 5%) where there is enrichment for targetable opportunities.
AbstractList Pancreatic cancer (PDAC) is one of the most challenging cancers to treat with modest recent improvements in survival from new systemic therapies. There is growing interest in individualized therapy underpinned by somatic and germline genomic alterations.CONTEXTPancreatic cancer (PDAC) is one of the most challenging cancers to treat with modest recent improvements in survival from new systemic therapies. There is growing interest in individualized therapy underpinned by somatic and germline genomic alterations.A systematic review of data on therapies targeting somatic and germline alterations, and their downstream pathways in PDAC.OBJECTIVEA systematic review of data on therapies targeting somatic and germline alterations, and their downstream pathways in PDAC.A systematic literature search was conducted using PRISMA guidelines to include relevant results published after January 1, 2008.METHODA systematic literature search was conducted using PRISMA guidelines to include relevant results published after January 1, 2008.A total of 71 relevant studies were included. We identified 36 studies targeting the KRAS-pathway, the most common being with MEK-inhibitor therapy. Twenty-two studies were identified that evaluated platinum-based chemotherapy and PARP inhibitors in patients with deleterious mutations in DNA damage repair genes and have shown encouraging results. Immunotherapy has demonstrated activity in patients with mismatch repair deficiency/microsatellite instability.RESULTSA total of 71 relevant studies were included. We identified 36 studies targeting the KRAS-pathway, the most common being with MEK-inhibitor therapy. Twenty-two studies were identified that evaluated platinum-based chemotherapy and PARP inhibitors in patients with deleterious mutations in DNA damage repair genes and have shown encouraging results. Immunotherapy has demonstrated activity in patients with mismatch repair deficiency/microsatellite instability.Evidence from translational and clinical research presents an exciting platform for genomic targeted therapy in PDAC. Validity for targeting BRCA with platinum and PARP inhibitors and microsatellite instability with immune therapy has been established, nonetheless, evidence for targeting the common driver oncogenes is lacking and much work is needed. Of importance is identifying the subgroup of KRAS -wild type PDAC (approximately 5%) where there is enrichment for targetable opportunities.CONCLUSIONEvidence from translational and clinical research presents an exciting platform for genomic targeted therapy in PDAC. Validity for targeting BRCA with platinum and PARP inhibitors and microsatellite instability with immune therapy has been established, nonetheless, evidence for targeting the common driver oncogenes is lacking and much work is needed. Of importance is identifying the subgroup of KRAS -wild type PDAC (approximately 5%) where there is enrichment for targetable opportunities.
Pancreatic cancer (PDAC) is one of the most challenging cancers to treat with modest recent improvements in survival from new systemic therapies. There is growing interest in individualized therapy underpinned by somatic and germline genomic alterations. A systematic review of data on therapies targeting somatic and germline alterations, and their downstream pathways in PDAC. A systematic literature search was conducted using PRISMA guidelines to include relevant results published after January 1, 2008. A total of 71 relevant studies were included. We identified 36 studies targeting the KRAS-pathway, the most common being with MEK-inhibitor therapy. Twenty-two studies were identified that evaluated platinum-based chemotherapy and PARP inhibitors in patients with deleterious mutations in DNA damage repair genes and have shown encouraging results. Immunotherapy has demonstrated activity in patients with mismatch repair deficiency/microsatellite instability. Evidence from translational and clinical research presents an exciting platform for genomic targeted therapy in PDAC. Validity for targeting BRCA with platinum and PARP inhibitors and microsatellite instability with immune therapy has been established, nonetheless, evidence for targeting the common driver oncogenes is lacking and much work is needed. Of importance is identifying the subgroup of KRAS -wild type PDAC (approximately 5%) where there is enrichment for targetable opportunities.
•Genomic alterations in PDAC represent potential targeting opportunities to individualize therapy.•Attempts to target key somatic driver mutations in PDAC have been unsuccessful.•DNA-damage repair gene mutations confer vulnerability to platinum agents and PARP-inhibitors.•Microsatellite unstable PDAC (1%) can benefit from checkpoint point inhibitor therapy.•The KRAS wild-type subset of PDAC (5%) is enriched for actionability, e.g., ALK, NTRK, NRG-1 fusions and others. Pancreatic cancer (PDAC) is one of the most challenging cancers to treat with modest recent improvements in survival from new systemic therapies. There is growing interest in individualized therapy underpinned by somatic and germline genomic alterations. A systematic review of data on therapies targeting somatic and germline alterations, and their downstream pathways in PDAC. A systematic literature search was conducted using PRISMA guidelines to include relevant results published after January 1, 2008. A total of 71 relevant studies were included. We identified 36 studies targeting the KRAS-pathway, the most common being with MEK-inhibitor therapy. Twenty-two studies were identified that evaluated platinum-based chemotherapy and PARP inhibitors in patients with deleterious mutations in DNA damage repair genes and have shown encouraging results. Immunotherapy has demonstrated activity in patients with mismatch repair deficiency/microsatellite instability. Evidence from translational and clinical research presents an exciting platform for genomic targeted therapy in PDAC. Validity for targeting BRCA with platinum and PARP inhibitors and microsatellite instability with immune therapy has been established, nonetheless, evidence for targeting the common driver oncogenes is lacking and much work is needed. Of importance is identifying the subgroup of KRAS -wild type PDAC (approximately 5%) where there is enrichment for targetable opportunities.
Author O'Reilly, Eileen M.
Park, Wungki
Varghese, Anna M.
Yu, Kenneth H.
Singh, Ritu R.
Goldberg, Johanna
AuthorAffiliation 5. David M. Rubenstein Center for Pancreatic Research, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA
4. Weill Cornell Department of Medicine, Weill Cornell Medicine, New York, New York 10065, USA
2. MSK library, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA
3. Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA
1. Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai St. Luke’s and Mount Sinai West, New York, New York 10019, USA
AuthorAffiliation_xml – name: 5. David M. Rubenstein Center for Pancreatic Research, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA
– name: 1. Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai St. Luke’s and Mount Sinai West, New York, New York 10019, USA
– name: 3. Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA
– name: 4. Weill Cornell Department of Medicine, Weill Cornell Medicine, New York, New York 10065, USA
– name: 2. MSK library, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA
Author_xml – sequence: 1
  givenname: Ritu R.
  surname: Singh
  fullname: Singh, Ritu R.
  email: ritu.singh@mountsinai.org
  organization: Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai St. Luke’s and Mount Sinai West, New York, NY 10019, USA
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  givenname: Johanna
  surname: Goldberg
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  surname: Varghese
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  organization: Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA
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  surname: O'Reilly
  fullname: O'Reilly, Eileen M.
  email: oreillye@mskcc.org
  organization: Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30927677$$D View this record in MEDLINE/PubMed
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Keywords Somatic mutation
Mismatch repair (MMR)
DNA damage repair
Pancreatic ductal adenocarcinoma (PDAC)
Genomic alteration (GA)
Germline mutation
Microsatellite instability
Language English
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Snippet •Genomic alterations in PDAC represent potential targeting opportunities to individualize therapy.•Attempts to target key somatic driver mutations in PDAC have...
Pancreatic cancer (PDAC) is one of the most challenging cancers to treat with modest recent improvements in survival from new systemic therapies. There is...
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SubjectTerms Animals
Carcinoma, Pancreatic Ductal - drug therapy
Carcinoma, Pancreatic Ductal - genetics
DNA damage repair
DNA Repair - drug effects
DNA Repair - genetics
Genomic alteration (GA)
Genomics - methods
Germline mutation
Humans
Microsatellite instability
Mismatch repair (MMR)
Pancreatic ductal adenocarcinoma (PDAC)
Pancreatic Neoplasms - drug therapy
Pancreatic Neoplasms - genetics
Poly(ADP-ribose) Polymerase Inhibitors - pharmacology
Poly(ADP-ribose) Polymerase Inhibitors - therapeutic use
Somatic mutation
Title Genomic profiling in pancreatic ductal adenocarcinoma and a pathway towards therapy individualization: A scoping review
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0305737219300519
https://dx.doi.org/10.1016/j.ctrv.2019.03.003
https://www.ncbi.nlm.nih.gov/pubmed/30927677
https://www.proquest.com/docview/2200768804
https://pubmed.ncbi.nlm.nih.gov/PMC6504563
Volume 75
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