26P Liquid biopsy-based percision immunotherapy: CCAT1 and HEIH lncRNAs identify young breast cancer patients likely to respond to PD-L1 blockade

enables the quantification of ctDNA for GNAQ Q209L, GNAQ Q209P and GNA11 Q209L mutations.Patients with at least 2 available samples and clinical data were included.Results: 576 samples from 72 patients with rare MUM were analyzed.37 patients had GNA11 Q209L, 19 e GNAQ Q209P, and 16 e GNAQ Q209L mutation.37 patients had baseline samples prior to first-line treatment, 27 of which had detectable levels of ctDNA.Out of 52 patients with baseline samples prior to any line of therapy, 40 had detectable levels.In the first line cohort, non-detectable baseline ctDNA was predictive of better PFS (p 0.02, and a hazard ratio of 0.28 with p 0.025) and OS (p 0.03, and a hazard ratio of 0.14 with p 0.058).Baseline ctDNA was also predictive for PFS and OS of non first-line therapies (p 0.03 and p 0.01).Conclusions: ctDNA levels have a significant predictive value for PFS and OS in metastatic uveal melanoma, treated with first or subsequent lines of therapy.It provides a non-invasive method to predict outcome.

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Publication Details

Journal
Immuno-Oncology Technology
Published
2024-12-01
DOI
https://doi.org/10.1016/j.iotech.2024.100908
Citations
1
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
0.28
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article

26P Liquid biopsy-based percision immunotherapy: CCAT1 and HEIH lncRNAs identify young breast cancer patients likely to respond to PD-L1 blockade

R.A. Youness, Mohamed A. Ragheb, Farhana Rashid, Menatallah Yasser et al.
1 citations
Immuno-Oncology Technology
Cancer Immunotherapy and Biomarkers
0.28
article

26P Liquid biopsy-based percision immunotherapy: CCAT1 and HEIH lncRNAs identify young breast cancer patients likely to respond to PD-L1 blockade

R.A. Youness, Mohamed A. Ragheb, Farhana Rashid, Menatallah Yasser, Asmaa M. Mohamed, Heba Nafea, Tamer Manie
article en
1 citations

Abstract

enables the quantification of ctDNA for GNAQ Q209L, GNAQ Q209P and GNA11 Q209L mutations.Patients with at least 2 available samples and clinical data were included.Results: 576 samples from 72 patients with rare MUM were analyzed.37 patients had GNA11 Q209L, 19 e GNAQ Q209P, and 16 e GNAQ Q209L mutation.37 patients had baseline samples prior to first-line treatment, 27 of which had detectable levels of ctDNA.Out of 52 patients with baseline samples prior to any line of therapy, 40 had detectable levels.In the first line cohort, non-detectable baseline ctDNA was predictive of better PFS (p 0.02, and a hazard ratio of 0.28 with p 0.025) and OS (p 0.03, and a hazard ratio of 0.14 with p 0.058).Baseline ctDNA was also predictive for PFS and OS of non first-line therapies (p 0.03 and p 0.01).Conclusions: ctDNA levels have a significant predictive value for PFS and OS in metastatic uveal melanoma, treated with first or subsequent lines of therapy.It provides a non-invasive method to predict outcome.

Immuno-Oncology TechnologyVol. 24
Cairo University (EG), Nile University (EG), German University in Cairo (EG)
Good health and well-being
Openalex Percentile: Top 33%
Cancer Immunotherapy and Biomarkers
0.28
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