Nakamura Yoshiaki, Ozaki Hiroshi, Ueno Makoto, Komatsu Yoshito, Yuki Satoshi, Esaki Taito, Taniguchi Hiroya, Sunakawa Yu, Yamaguchi Kensei, Kato Ken, Denda Tadamichi, Nishina Tomohiro, Takahashi Naoki, Satoh Taroh, Yasui Hisateru, Satake Hironaga, Oki Eiji, Kato Takeshi, Ohta Takashi, Matsuhashi Nobuhisa, Goto Masahiro, Okano Naohiro, Ohtsubo Koushiro, Yamazaki Kentaro, Yamashita Riu, Iida Naoko, Yuasa Mihoko, Bando Hideaki, Yoshino Takayuki
International Research Promotion Office, National Cancer Center Hospital East, Kashiwa, Japan.
Translational Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan.
Nat Med. 2025 Jan;31(1):165-175. doi: 10.1038/s41591-024-03244-8. Epub 2024 Sep 16.
Although comprehensive genomic profiling has become standard in oncology for advanced solid tumors, the full potential of circulating tumor DNA (ctDNA)-based profiling in capturing tumor heterogeneity and guiding therapy selection remains underexploited, marked by a scarcity of evidence on its clinical impact and the assessment of intratumoral heterogeneity. The GOZILA study, a nationwide, prospective observational ctDNA profiling study, previously demonstrated higher clinical trial enrollment rates using liquid biopsy compared with tissue screening. This updated analysis of 4,037 patients further delineates the clinical utility of ctDNA profiling in advanced solid tumors, showcasing a significant enhancement in patient outcomes with a 24% match rate for targeted therapy. Patients treated with matched targeted therapy based on ctDNA profiling demonstrated significantly improved overall survival compared with those receiving unmatched therapy (hazard ratio, 0.54). Notably, biomarker clonality and adjusted plasma copy number were identified as predictors of therapeutic efficacy, reinforcing the value of ctDNA in reflecting tumor heterogeneity for precise treatment decisions. These new insights into the relationship between ctDNA characteristics and treatment outcomes advance our understanding beyond the initial enrollment benefits. Our findings advocate for the broader adoption of ctDNA-guided treatment, signifying an advancement in precision oncology and improving survival outcomes in advanced solid tumors.
尽管全面基因组分析已成为晚期实体瘤肿瘤学的标准,但基于循环肿瘤DNA(ctDNA)的分析在捕捉肿瘤异质性和指导治疗选择方面的全部潜力仍未得到充分利用,其临床影响和肿瘤内异质性评估的证据匮乏便是明证。GOZILA研究是一项全国性的前瞻性观察性ctDNA分析研究,此前已证明,与组织筛查相比,使用液体活检进行临床试验的入组率更高。这项对4037名患者的更新分析进一步阐述了ctDNA分析在晚期实体瘤中的临床效用,显示出靶向治疗匹配率达24%,患者预后有显著改善。与接受不匹配治疗的患者相比,基于ctDNA分析接受匹配靶向治疗的患者总生存期显著改善(风险比,0.54)。值得注意的是,生物标志物克隆性和调整后的血浆拷贝数被确定为治疗疗效的预测指标,强化了ctDNA在反映肿瘤异质性以做出精确治疗决策方面的价值。这些关于ctDNA特征与治疗结果之间关系的新见解,使我们的理解超越了最初的入组益处。我们的研究结果倡导更广泛地采用ctDNA指导的治疗,这标志着精准肿瘤学的进步,并改善晚期实体瘤的生存结果。