Paolo Marchetti, Simone Scagnoli, Edoardo Crimini, Simona Pisegna, Sofia Verkhovskaia, Giuseppe Curigliano, Sara Lonardi, Valentina Guarneri, Chiara Cremolini, Umberto Malapelle, Ettore D. Capoluongo, Paolo A. Ascierto, Fabio Puglisi, Giancarlo Pruneri, Giulia D'Amati, Bruna Cerbelli, Mauro Biffoni, Giuseppe Tonini, Lucia Del Mastro, Andrea Botticelli
{"title":"组织和液体联合活检改善晚期实体瘤的预后:对ROME试验的探索性分析","authors":"Paolo Marchetti, Simone Scagnoli, Edoardo Crimini, Simona Pisegna, Sofia Verkhovskaia, Giuseppe Curigliano, Sara Lonardi, Valentina Guarneri, Chiara Cremolini, Umberto Malapelle, Ettore D. Capoluongo, Paolo A. Ascierto, Fabio Puglisi, Giancarlo Pruneri, Giulia D'Amati, Bruna Cerbelli, Mauro Biffoni, Giuseppe Tonini, Lucia Del Mastro, Andrea Botticelli","doi":"10.1158/1538-7445.am2025-6372","DOIUrl":null,"url":null,"abstract":"Background: The ROME trial, a phase II multicenter study, enrolled 1,794 patients with advanced solid tumors. Centralized next-generation sequencing (NGS) was performed on both tissue and liquid biopsies using FoundationOne CDx and FoundationOne Liquid CDx. A centralized Molecular Tumor Board (MTB) reviewed results to identify actionable alterations, with 400 patients subsequently randomized to tailored therapy (TT) or standard-of-care (SoC). In this trial, TT improved objective response rate (ORR) and progression-free survival (PFS) in the Intention to Treat population (ITT) Methods: This exploratory analysis evaluated the concordance between tissue (T) and liquid (L) biopsy results in detecting actionable alterations in ITT population. Concordance was defined as the detection of the same significant alterations in both biopsy types; discordance indicated detection in only one. Survival outcomes (OS and PFS) were analyzed across concordance groups. Due to the exploratory nature of the analysis, statistical significance was not determined Results: Concordance between tissue (T) and liquid (L) biopsies was 49%, with actionable alterations detected exclusively in tissue biopsies in 35% of patients and exclusively in liquid biopsies in 16%. Of the 203 discordant cases, 21% were attributed to test failures, 35% to discordant high tumor mutational burden (hTMB) detection, 1% to microsatellite instability (MSI) discrepancies, and 43.3% to differences in the detection of molecular alterations. The PI3K/PTEN/AKT/mTOR and ERBB2 pathways showed the highest discordance rates. Test results guided therapeutic choices in 84% and 65% of cases for tissue biopsy and liquid biopsy, respectively. Patients in the concordant T+L group receiving tailored therapy (TT) experienced significantly improved survival outcomes. Median overall survival (OS) was 11.05 vs. 7.70 months in the standard-of-care (SoC) group (HR 0.74; 95% CI: 0.51-1.07), and median progression-free survival (PFS) was 4.93 vs. 2.80 months (HR 0.55; 95% CI: 0.40-0.76). In contrast, the survival benefit of TT was less pronounced or absent in patients with discordant results. Overall, OS was higher in the T+L group (11.05 months), followed by the tissue-only group (9.93 months), and the liquid-only group (4.05 months). PFS followed a similar pattern, with the longest PFS observed in the T+L group (4.93 months) compared to 3.06 months in the tissue-only group and 2.07 months in the liquid-only group. Conclusions: Although the concordance rate between tissue and liquid biopsies was only 49%, the substantial increase in detection of actionable alterations (over 60% with the addition of liquid biopsy) and significative improvement of survival outcomes observed with combined T+L concordance strongly emphasize the importance of integrating both biopsy modalities to enhance precision oncology approaches. Citation Format: Paolo Marchetti, Simone Scagnoli, Edoardo Crimini, Simona Pisegna, Sofia Verkhovskaia, Giuseppe Curigliano, Sara Lonardi, Valentina Guarneri, Chiara Cremolini, Umberto Malapelle, Ettore D. Capoluongo, Paolo A. Ascierto, Fabio Puglisi, Giancarlo Pruneri, Giulia D'Amati, Bruna Cerbelli, Mauro Biffoni, Giuseppe Tonini, Lucia Del Mastro, Andrea Botticelli. Combined tissue and liquid biopsy improves outcomes in advanced solid tumors: an exploratory analysis of the ROME trial [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular s); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1): nr 6372.","PeriodicalId":9441,"journal":{"name":"Cancer research","volume":"21 1","pages":""},"PeriodicalIF":16.6000,"publicationDate":"2025-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Abstract 6372: Combined tissue and liquid biopsy improves outcomes in advanced solid tumors: an exploratory analysis of the ROME trial\",\"authors\":\"Paolo Marchetti, Simone Scagnoli, Edoardo Crimini, Simona Pisegna, Sofia Verkhovskaia, Giuseppe Curigliano, Sara Lonardi, Valentina Guarneri, Chiara Cremolini, Umberto Malapelle, Ettore D. Capoluongo, Paolo A. Ascierto, Fabio Puglisi, Giancarlo Pruneri, Giulia D'Amati, Bruna Cerbelli, Mauro Biffoni, Giuseppe Tonini, Lucia Del Mastro, Andrea Botticelli\",\"doi\":\"10.1158/1538-7445.am2025-6372\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: The ROME trial, a phase II multicenter study, enrolled 1,794 patients with advanced solid tumors. Centralized next-generation sequencing (NGS) was performed on both tissue and liquid biopsies using FoundationOne CDx and FoundationOne Liquid CDx. A centralized Molecular Tumor Board (MTB) reviewed results to identify actionable alterations, with 400 patients subsequently randomized to tailored therapy (TT) or standard-of-care (SoC). In this trial, TT improved objective response rate (ORR) and progression-free survival (PFS) in the Intention to Treat population (ITT) Methods: This exploratory analysis evaluated the concordance between tissue (T) and liquid (L) biopsy results in detecting actionable alterations in ITT population. Concordance was defined as the detection of the same significant alterations in both biopsy types; discordance indicated detection in only one. Survival outcomes (OS and PFS) were analyzed across concordance groups. Due to the exploratory nature of the analysis, statistical significance was not determined Results: Concordance between tissue (T) and liquid (L) biopsies was 49%, with actionable alterations detected exclusively in tissue biopsies in 35% of patients and exclusively in liquid biopsies in 16%. Of the 203 discordant cases, 21% were attributed to test failures, 35% to discordant high tumor mutational burden (hTMB) detection, 1% to microsatellite instability (MSI) discrepancies, and 43.3% to differences in the detection of molecular alterations. The PI3K/PTEN/AKT/mTOR and ERBB2 pathways showed the highest discordance rates. Test results guided therapeutic choices in 84% and 65% of cases for tissue biopsy and liquid biopsy, respectively. Patients in the concordant T+L group receiving tailored therapy (TT) experienced significantly improved survival outcomes. Median overall survival (OS) was 11.05 vs. 7.70 months in the standard-of-care (SoC) group (HR 0.74; 95% CI: 0.51-1.07), and median progression-free survival (PFS) was 4.93 vs. 2.80 months (HR 0.55; 95% CI: 0.40-0.76). In contrast, the survival benefit of TT was less pronounced or absent in patients with discordant results. Overall, OS was higher in the T+L group (11.05 months), followed by the tissue-only group (9.93 months), and the liquid-only group (4.05 months). PFS followed a similar pattern, with the longest PFS observed in the T+L group (4.93 months) compared to 3.06 months in the tissue-only group and 2.07 months in the liquid-only group. 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引用次数: 0
摘要
背景:ROME试验是一项II期多中心研究,纳入了1794例晚期实体瘤患者。使用FoundationOne CDx和FoundationOne liquid CDx对组织和液体活检进行集中式下一代测序(NGS)。集中的分子肿瘤委员会(MTB)审查了结果以确定可操作的改变,随后将400名患者随机分配到定制治疗(TT)或标准治疗(SoC)。在本试验中,TT提高了意向治疗人群(ITT)的客观缓解率(ORR)和无进展生存期(PFS)。方法:本探索性分析评估了组织(T)和液体(L)活检结果在检测ITT人群可操作改变方面的一致性。一致性定义为在两种活检类型中检测到相同的显著改变;不一致表明只有一个检测。生存结果(OS和PFS)在不同的一致性组中进行分析。结果:组织(T)和液体(L)活检之间的一致性为49%,35%的患者仅在组织活检中检测到可操作的改变,16%的患者仅在液体活检中检测到可操作的改变。203例不一致病例中,21%归因于检测失败,35%归因于高肿瘤突变负担(hTMB)检测不一致,1%归因于微卫星不稳定性(MSI)差异,43.3%归因于分子改变检测差异。PI3K/PTEN/AKT/mTOR和ERBB2通路的不一致率最高。检测结果分别指导了84%和65%的组织活检和液体活检病例的治疗选择。接受量身定制治疗(TT)的和谐T+L组患者的生存结果显着改善。标准治疗组的中位总生存期(OS)为11.05个月,而标准治疗组为7.70个月(HR 0.74;95% CI: 0.51-1.07),中位无进展生存期(PFS)为4.93个月vs 2.80个月(HR 0.55;95% ci: 0.40-0.76)。相比之下,在结果不一致的患者中,TT的生存获益不太明显或不存在。总体而言,T+L组的OS最高(11.05个月),其次是纯组织组(9.93个月)和纯液体组(4.05个月)。PFS遵循类似的模式,T+L组观察到的PFS最长(4.93个月),而纯组织组为3.06个月,纯液体组为2.07个月。结论:尽管组织活检和液体活检之间的一致性率仅为49%,但T+L联合一致性观察到的可操作改变的检出率大幅增加(增加液体活检后超过60%)和生存结果的显着改善,强烈强调了整合两种活检方式以增强精确肿瘤学方法的重要性。引文格式:Paolo Marchetti, Simone Scagnoli, Edoardo Crimini, Simona Pisegna, Sofia Verkhovskaia, Giuseppe Curigliano, Sara Lonardi, Valentina Guarneri, Chiara Cremolini, Umberto Malapelle, Ettore D. Capoluongo, Paolo A. Ascierto, Fabio Puglisi, Giancarlo Pruneri, Giulia D'Amati, Bruna Cerbelli, Mauro Biffoni, Giuseppe Tonini, Lucia Del Mastro, Andrea Botticelli。组织和液体联合活检改善晚期实体瘤的预后:对ROME试验的探索性分析[摘要]。摘自:《2025年美国癌症研究协会年会论文集》;第1部分(常规);2025年4月25日至30日;费城(PA): AACR;中国生物医学工程学报,2015;31(5):563 - 567。
Abstract 6372: Combined tissue and liquid biopsy improves outcomes in advanced solid tumors: an exploratory analysis of the ROME trial
Background: The ROME trial, a phase II multicenter study, enrolled 1,794 patients with advanced solid tumors. Centralized next-generation sequencing (NGS) was performed on both tissue and liquid biopsies using FoundationOne CDx and FoundationOne Liquid CDx. A centralized Molecular Tumor Board (MTB) reviewed results to identify actionable alterations, with 400 patients subsequently randomized to tailored therapy (TT) or standard-of-care (SoC). In this trial, TT improved objective response rate (ORR) and progression-free survival (PFS) in the Intention to Treat population (ITT) Methods: This exploratory analysis evaluated the concordance between tissue (T) and liquid (L) biopsy results in detecting actionable alterations in ITT population. Concordance was defined as the detection of the same significant alterations in both biopsy types; discordance indicated detection in only one. Survival outcomes (OS and PFS) were analyzed across concordance groups. Due to the exploratory nature of the analysis, statistical significance was not determined Results: Concordance between tissue (T) and liquid (L) biopsies was 49%, with actionable alterations detected exclusively in tissue biopsies in 35% of patients and exclusively in liquid biopsies in 16%. Of the 203 discordant cases, 21% were attributed to test failures, 35% to discordant high tumor mutational burden (hTMB) detection, 1% to microsatellite instability (MSI) discrepancies, and 43.3% to differences in the detection of molecular alterations. The PI3K/PTEN/AKT/mTOR and ERBB2 pathways showed the highest discordance rates. Test results guided therapeutic choices in 84% and 65% of cases for tissue biopsy and liquid biopsy, respectively. Patients in the concordant T+L group receiving tailored therapy (TT) experienced significantly improved survival outcomes. Median overall survival (OS) was 11.05 vs. 7.70 months in the standard-of-care (SoC) group (HR 0.74; 95% CI: 0.51-1.07), and median progression-free survival (PFS) was 4.93 vs. 2.80 months (HR 0.55; 95% CI: 0.40-0.76). In contrast, the survival benefit of TT was less pronounced or absent in patients with discordant results. Overall, OS was higher in the T+L group (11.05 months), followed by the tissue-only group (9.93 months), and the liquid-only group (4.05 months). PFS followed a similar pattern, with the longest PFS observed in the T+L group (4.93 months) compared to 3.06 months in the tissue-only group and 2.07 months in the liquid-only group. Conclusions: Although the concordance rate between tissue and liquid biopsies was only 49%, the substantial increase in detection of actionable alterations (over 60% with the addition of liquid biopsy) and significative improvement of survival outcomes observed with combined T+L concordance strongly emphasize the importance of integrating both biopsy modalities to enhance precision oncology approaches. Citation Format: Paolo Marchetti, Simone Scagnoli, Edoardo Crimini, Simona Pisegna, Sofia Verkhovskaia, Giuseppe Curigliano, Sara Lonardi, Valentina Guarneri, Chiara Cremolini, Umberto Malapelle, Ettore D. Capoluongo, Paolo A. Ascierto, Fabio Puglisi, Giancarlo Pruneri, Giulia D'Amati, Bruna Cerbelli, Mauro Biffoni, Giuseppe Tonini, Lucia Del Mastro, Andrea Botticelli. Combined tissue and liquid biopsy improves outcomes in advanced solid tumors: an exploratory analysis of the ROME trial [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular s); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1): nr 6372.
期刊介绍:
Cancer Research, published by the American Association for Cancer Research (AACR), is a journal that focuses on impactful original studies, reviews, and opinion pieces relevant to the broad cancer research community. Manuscripts that present conceptual or technological advances leading to insights into cancer biology are particularly sought after. The journal also places emphasis on convergence science, which involves bridging multiple distinct areas of cancer research.
With primary subsections including Cancer Biology, Cancer Immunology, Cancer Metabolism and Molecular Mechanisms, Translational Cancer Biology, Cancer Landscapes, and Convergence Science, Cancer Research has a comprehensive scope. It is published twice a month and has one volume per year, with a print ISSN of 0008-5472 and an online ISSN of 1538-7445.
Cancer Research is abstracted and/or indexed in various databases and platforms, including BIOSIS Previews (R) Database, MEDLINE, Current Contents/Life Sciences, Current Contents/Clinical Medicine, Science Citation Index, Scopus, and Web of Science.