Details

Autor(en) / Beteiligte

• Vandekerkhove, Gillian
• Lavoie, Jean-Michel
• Annala, Matti
• Murtha, Andrew J.
• Sundahl, Nora
• Walz, Simon
• Sano, Takeshi
• Taavitsainen, Sinja
• Ritch, Elie
• Fazli, Ladan
• Hurtado-Coll, Antonio
• Wang, Gang
• Nykter, Matti
• Black, Peter C.
• Todenhöfer, Tilman
• Ost, Piet
• Gibb, Ewan A.
• Chi, Kim N.
• Eigl, Bernhard J.
• Wyatt, Alexander W.

Titel

Plasma ctDNA is a tumor tissue surrogate and enables clinical-genomic stratification of metastatic bladder cancer

Ist Teil von

• Nature communications, 2021-01, Vol.12 (1), p.184-12, Article 184

Ort / Verlag

London: Nature Publishing Group UK

Erscheinungsjahr

2021

Quelle

MEDLINE

Beschreibungen/Notizen

• Molecular stratification can improve the management of advanced cancers, but requires relevant tumor samples. Metastatic urothelial carcinoma (mUC) is poised to benefit given a recent expansion of treatment options and its high genomic heterogeneity. We profile minimally-invasive plasma circulating tumor DNA (ctDNA) samples from 104 mUC patients, and compare to same-patient tumor tissue obtained during invasive surgery. Patient ctDNA abundance is independently prognostic for overall survival in patients initiating first-line systemic therapy. Importantly, ctDNA analysis reproduces the somatic driver genome as described from tissue-based cohorts. Furthermore, mutation concordance between ctDNA and matched tumor tissue is 83.4%, enabling benchmarking of proposed clinical biomarkers. While 90% of mutations are identified across serial ctDNA samples, concordance for serial tumor tissue is significantly lower. Overall, our exploratory analysis demonstrates that genomic profiling of ctDNA in mUC is reliable and practical, and mitigates against disease undersampling inherent to studying archival primary tumor foci. We urge the incorporation of cell-free DNA profiling into molecularly-guided clinical trials for mUC. In metastatic urothelial carcinoma, it has not been established whether circulating tumor DNA (ctDNA) can replace archival primary tissue to assess mutations and biomarkers. Here, the authors show high mutation concordance between ctDNA and tumour tissue, with high consistency in serial samples.