Sep 2026· Current Oncology· Vol 33, pp. 575· 0 citations· 41 references
TL;DR
Tissue and plasma CGP were complementary rather than interchangeable in this selected cohort: either modality alone would have missed clinically relevant findings.
Abstract
Background: Tissue and plasma comprehensive genomic profiling (CGP) sample different compartments and may yield nonoverlapping clinically relevant findings. We assessed the added patient-level yield of paired testing in a pan-cancer cohort from India. Methods: This retrospective, single-institution study included patients with stage IV solid tumors who underwent paired tissue and plasma CGP between November 2022 and October 2024. The primary endpoint was detection in a patient of an OncoKB Level 1 or Level 2 or R1 alteration, high tumor mutational burden, or microsatellite instability. Molecularly informed therapy and laboratory turnaround time were assessed descriptively. Results: Of 158 patients, 123 matched evaluable pairs were analyzed. Either modality detected a clinically relevant finding in 46 of 123 patients (37.4%; 95% confidence interval, 29.4–46.2%): tissue CGP in 33 (26.8%), plasma CGP in 35 (28.5%), both in 22 (17.9%), tissue only in 11 (8.9%) and plasma only in 13 (10.6%). This complementarity remained bidirectional across exploratory analyses, including a subgroup that excluded non-small cell lung cancer (33.0%), all 139 technically successful pairs (33.8%), all 158 paired sample sets (32.3%), and even when the endpoint was restricted to OncoKB alterations (22.0%). Among 91 patients with therapy-alignment data, 25 (27.5%) received molecularly informed therapy. Median laboratory turnaround time was 7 days for plasma and 13 days for tissue CGP. Conclusions: Tissue and plasma CGP were complementary rather than interchangeable in this selected cohort: either modality alone would have missed clinically relevant findings. Whether this improves outcomes is untested; prospective studies linking testing strategy to treatment delivery and survival are needed.
Targeted cfDNA sequencing is feasible in preoperative CRC patients undergoing CME and provides a molecular baseline for future perioperative studies, support its potential for minimally invasive molecular characterization and define its prognostic and clinical utility.
Mária Škereňová, E. Halašová, M. Šarlinová et al.· Current molecular medicine· 0 citations
BACKGROUND
The clinical characteristics of BRCA1 and BRCA2 (BRCA) deleterious alterations in advanced prostate cancer-considering age, family history, co-occurring gene alterations, and variant type-remain incompletely understood in patients undergoing tumor-only panel testing.
MATERIALS AND METHODS
We analyzed 2,815...
H. Tsumura, Dai Koguchi, K. Tabata et al.· The Prostate· 0 citations
Early implementation of CGP testing could reduce redundant testing and associated delays in treatment, thereby contributing to lower overall healthcare costs and more efficient treatment selection amid rapid advances in targeted therapies.
K. Sunami, Sona-Sanae Aoyagi, Masashi Mikami et al.· Oncology and Therapy· 0 citations
Routine genomic profiling in NSCLC provides clinically relevant information beyond actionable driver detection when interpreted together with stage, smoking history, age, sex, and regional molecular context, and support a more context-aware interpretation of routine molecular diagnostics in thoracic oncology.
N. Karlowatz, L. Kohn, C. Patthey et al.· Frontiers in Oncology· 0 citations
Background/Objectives: Tumor-agnostic plasma ctDNA profiling is used when tumor tissue is unavailable, insufficient, or unrepresentative. We investigated analytical and biological factors associated with oncogenic variant yield. Methods: In the prospective EXMASTER study, plasma cfDNA was analyzed using a 265-gene targ...
Stephen George, L. Ranganathan, Yi-Zhen Xiang et al.· Diagnostics· 0 citations
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