Paired Tissue and Plasma Comprehensive Genomic Profiling in Advanced Solid Tumors: A Retrospective Study from India.

IF 3.6 4区 医学 Q2 ONCOLOGY
Ankur Bahl, Nitesh Rohatgi, Suman S Karanth, Aakriti Aggarwal, Rohit Bharat, Nippun Sandhir
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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.

晚期实体瘤的配对组织和血浆综合基因组分析:来自印度的回顾性研究。
背景:组织和血浆综合基因组分析(CGP)取样不同的区室,可能产生不重叠的临床相关发现。我们在印度的一个泛癌症队列中评估了配对检测增加的患者水平的产量。方法:这项回顾性的单机构研究纳入了2022年11月至2024年10月期间接受配对组织和血浆CGP的IV期实体瘤患者。主要终点是在患者中检测到OncoKB 1级或2级或R1改变,高肿瘤突变负担或微卫星不稳定性。描述性地评估分子知情治疗和实验室周转时间。结果:158例患者中,分析了123对匹配的可评价对。123例患者中有46例(37.4%,95%可信区间为29.4-46.2%)检测到临床相关发现:组织CGP 33例(26.8%),血浆CGP 35例(28.5%),两者均有22例(17.9%),仅组织CGP 11例(8.9%),仅血浆CGP 13例(10.6%)。在探索性分析中,这种互补性仍然是双向的,包括排除非小细胞肺癌的亚组(33.0%),所有139对技术上成功的样本组(33.8%),所有158对样本组(32.3%),甚至当终点仅限于OncoKB改变时(22.0%)。在91例具有治疗一致性数据的患者中,25例(27.5%)接受了分子知情治疗。血浆CGP的平均实验室周转时间为7天,组织CGP为13天。结论:在这个选定的队列中,组织和血浆CGP是互补的,而不是可互换的:单独的任何一种方式都可能错过临床相关的发现。这是否能改善结果还未经检验;需要将检测策略与治疗交付和生存联系起来的前瞻性研究。
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来源期刊
Current oncology
Current oncology ONCOLOGY-
CiteScore
3.30
自引率
7.70%
发文量
664
审稿时长
1 months
期刊介绍: Current Oncology is a peer-reviewed, Canadian-based and internationally respected journal. Current Oncology represents a multidisciplinary medium encompassing health care workers in the field of cancer therapy in Canada to report upon and to review progress in the management of this disease. We encourage submissions from all fields of cancer medicine, including radiation oncology, surgical oncology, medical oncology, pediatric oncology, pathology, and cancer rehabilitation and survivorship. Articles published in the journal typically contain information that is relevant directly to clinical oncology practice, and have clear potential for application to the current or future practice of cancer medicine.
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