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BIOMARKER:

DDR signature score

1year
Exploring Genomic Biomarkers for Pembrolizumab Response: A Real-World Approach and Patient Similarity Network Analysis Reveal DNA Response and Repair Gene Mutations as a Signature. (PubMed, Cancers (Basel))
This subgroup of IO-responsive NS-pts may have better prognosis. Our findings suggest that DDR-based mutational profiling may help identify NS-pts who could benefit from IO therapy.
Journal • Real-world evidence • Tumor mutational burden • PD(L)-1 Biomarker • IO biomarker • Real-world
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TMB (Tumor Mutational Burden)
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TMB-H • TMB-L • DDR signature score
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FoundationOne® CDx
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Keytruda (pembrolizumab)
1year
SNMF: Integrated Learning of Mutational Signatures and Prediction of DNA Repair Deficiencies. (PubMed, bioRxiv)
Cell line SNMF signatures recapitulated tumour-derived COSMIC signatures and predicted DDR pathway deficiency of TCGA tumours with high recall, suggesting that SNMF-like models can leverage libraries of induced DDR deficiencies to decipher intricate DDR signatures underlying patient tumours. https://github.com/joanagoncalveslab/SNMF .
Journal
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DRD (DNA Repair Deficiency)
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DDR • DDR signature score
2years
MGMT function determines the differential response of ATR inhibitors with DNA-damaging agents in glioma stem cells for GBM therapy. (PubMed, Neurooncol Adv)
We found a subpopulation of glioma sphere-forming cells (GSCs) with substantial synergism with temozolomide (TMZ) using a panel of 3 clinical-grade ataxia-telangiectasia- and Rad3-related kinase inhibitors (ATRis), (elimusertib, berzosertib, and ceralasertib). This research provides a rationale for selectively targeting MGMT-methylated cells using ATRis and TMZ combination. Overall, we believe that MGMT methylation status in GBM could serve as a robust biomarker for patient selection for ATRi combined with TMZ.
Journal
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MGMT (6-O-methylguanine-DNA methyltransferase) • CHEK1 (Checkpoint kinase 1)
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DDR signature score
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temozolomide • berzosertib (M6620) • ceralasertib (AZD6738) • elimusertib (BAY 1895344)
2years
Attenuated cell cycle and DNA damage response transcriptome signatures and overrepresented cell adhesion processes imply accelerated progression in patients with lower-risk myelodysplastic neoplasms. (PubMed, Int J Cancer)
Collectively, accelerated progression of LR-MDS appears to be associated with transcriptome patterns of a quiescent-like cell state, reduced lineage differentiation and suppressed DDR, inherent to CD34+ cells. The attenuation of DDR-related gene-expression signature may refine risk assessment in LR-MDS patients.
Journal
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CD34 (CD34 molecule) • ZEB1 (Zinc Finger E-box Binding Homeobox 1)
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DDR signature score • ZEB1 expression
over2years
Integrated Multimodal Analyses of DNA Damage Response and Immune Markers as Predictors of Response in Metastatic Triple-Negative Breast Cancer in the TNT Trial (NCT00532727). (PubMed, Clin Cancer Res)
The TNT trial (NCT00532727) showed no evidence of carboplatin superiority over docetaxel in metastatic triple-negative breast cancer (mTNBC), but carboplatin benefit was observed in the germline BRCA1/2 mutation subgroup. Treatment options for patients with immune-low and DDR-proficient tumors remains an outstanding need. Caution is needed using PT-derived transcriptional signatures to direct treatment in mTNBC, particularly DDR-related markers following prior chemotherapy.
Journal • BRCA Biomarker • Metastases
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BRCA1 (Breast cancer 1, early onset) • BRCA2 (Breast cancer 2, early onset)
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BRCA2 mutation • BRCA1 mutation • DDR signature score
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carboplatin • docetaxel
over2years
RNASEH2B loss and PARP inhibition (parpi) in metastatic castration resistant prostate cancer (mCRPC) (ESMO 2023)
Conclusions RNASEH2B protein is frequently lost in mCRPC subclones, with RB1 loss being less common, and may be of critical importance as this discordant loss is most likely to sensitise to PARPi. This needs further exploration in clinical trials of PARPi.
PARP Biomarker • Metastases
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RB1 (RB Transcriptional Corepressor 1)
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RB1 deletion • DDR signature score