Emily Ho,Loris De Cecco,Steven A Eschrich,Stefano Cavalieri,Geoffrey Sedor,Frank Hoebers,Ruud H Brakenhoff,Kathrin Scheckenbach,Tito Poli,Kailin Yang,Jessica A Scarborough,Shivani Nellore,Shauna Campbell,Neil Woody,Tim Chan,Jacob Miller,Natalie Silver,Shlomo Koyfman,James Bates,Jimmy J Caudell,Michael W Kattan,Lisa Licitra,Javier F Torres-Roca,Jacob G Scott
{"title":"使用基因组调整辐射剂量对HPV+口咽癌进行个性化治疗。","authors":"Emily Ho,Loris De Cecco,Steven A Eschrich,Stefano Cavalieri,Geoffrey Sedor,Frank Hoebers,Ruud H Brakenhoff,Kathrin Scheckenbach,Tito Poli,Kailin Yang,Jessica A Scarborough,Shivani Nellore,Shauna Campbell,Neil Woody,Tim Chan,Jacob Miller,Natalie Silver,Shlomo Koyfman,James Bates,Jimmy J Caudell,Michael W Kattan,Lisa Licitra,Javier F Torres-Roca,Jacob G Scott","doi":"10.1172/jci194073","DOIUrl":null,"url":null,"abstract":"BACKGROUNDA key objective in managing HPV+ oropharyngeal squamous cell carcinoma (OPSCC) is reducing radiation therapy (RT) doses without compromising cure rates. A recent phase II/III HN005 trial revealed that clinical factors alone are insufficient to guide safe RT dose de-escalation. Our prior research demonstrated that the genomic adjusted radiation dose (GARD) predicts RT benefit and may inform dose selection. We hypothesize that GARD can guide personalized RT de-escalation in HPV+ OPSCC patients.METHODSGene expression profiles were analyzed in 191 HPV+ OPSCC patients enrolled in an international, multi-institutional observational study (AJCC Eighth Edition, stages I-III). Most patients received 70 Gy in 35 fractions or 69.96 Gy in 33 fractions (median dose: 70 Gy; range: 51.0-74.0 Gy). Overall survival (OS) was 94.1% at 36 months and 87.3% at 60 months. A Cox proportional hazards model assessed association between GARD and OS, and time-dependent receiver operating characteristic analyses compared GARD with traditional clinical predictors.RESULTSDespite uniform RT dosing, GARD showed wide heterogeneity, ranging from 15.4 to 71.7. Higher GARD values were significantly associated with improved OS in univariate (HR = 0.941, P = 0.041) and multivariable analyses (HR = 0.943, P = 0.046), while T and N stages were not. GARD demonstrated superior predictive performance at 36 months (AUC = 78.26) versus clinical variables (AUC = 71.20). Two GARD-based RT de-escalation strategies were identified, offering potential survival benefits while reducing radiation exposure.CONCLUSIONGARD predicts OS and outperforms clinical variables, supporting its integration into the diagnostic workflow for personalized RT in HPV+ OPSCC.FUNDINGThis work was supported by the National Cancer Institute through the Cleveland Clinic/Emory ROBIN center (U54-CA274513, project 2), the European Union Horizon 2020 Framework Programme (grant/award 689715), the Italian Association for Cancer Research (AIRC project ID 23573), and the European Research Area Network ERA PerMed JTC2019/Fondazione Regionale per la Ricerca Biomedica project SuPerTreat (Supporting Personalized Treatment Decisions in Head and Neck Cancer through Big Data).","PeriodicalId":520097,"journal":{"name":"The Journal of Clinical Investigation","volume":"4565 3 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Personalized treatment in HPV+ oropharynx cancer using genomic adjusted radiation dose.\",\"authors\":\"Emily Ho,Loris De Cecco,Steven A Eschrich,Stefano Cavalieri,Geoffrey Sedor,Frank Hoebers,Ruud H Brakenhoff,Kathrin Scheckenbach,Tito Poli,Kailin Yang,Jessica A Scarborough,Shivani Nellore,Shauna Campbell,Neil Woody,Tim Chan,Jacob Miller,Natalie Silver,Shlomo Koyfman,James Bates,Jimmy J Caudell,Michael W Kattan,Lisa Licitra,Javier F Torres-Roca,Jacob G Scott\",\"doi\":\"10.1172/jci194073\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"BACKGROUNDA key objective in managing HPV+ oropharyngeal squamous cell carcinoma (OPSCC) is reducing radiation therapy (RT) doses without compromising cure rates. A recent phase II/III HN005 trial revealed that clinical factors alone are insufficient to guide safe RT dose de-escalation. Our prior research demonstrated that the genomic adjusted radiation dose (GARD) predicts RT benefit and may inform dose selection. We hypothesize that GARD can guide personalized RT de-escalation in HPV+ OPSCC patients.METHODSGene expression profiles were analyzed in 191 HPV+ OPSCC patients enrolled in an international, multi-institutional observational study (AJCC Eighth Edition, stages I-III). Most patients received 70 Gy in 35 fractions or 69.96 Gy in 33 fractions (median dose: 70 Gy; range: 51.0-74.0 Gy). Overall survival (OS) was 94.1% at 36 months and 87.3% at 60 months. A Cox proportional hazards model assessed association between GARD and OS, and time-dependent receiver operating characteristic analyses compared GARD with traditional clinical predictors.RESULTSDespite uniform RT dosing, GARD showed wide heterogeneity, ranging from 15.4 to 71.7. Higher GARD values were significantly associated with improved OS in univariate (HR = 0.941, P = 0.041) and multivariable analyses (HR = 0.943, P = 0.046), while T and N stages were not. GARD demonstrated superior predictive performance at 36 months (AUC = 78.26) versus clinical variables (AUC = 71.20). Two GARD-based RT de-escalation strategies were identified, offering potential survival benefits while reducing radiation exposure.CONCLUSIONGARD predicts OS and outperforms clinical variables, supporting its integration into the diagnostic workflow for personalized RT in HPV+ OPSCC.FUNDINGThis work was supported by the National Cancer Institute through the Cleveland Clinic/Emory ROBIN center (U54-CA274513, project 2), the European Union Horizon 2020 Framework Programme (grant/award 689715), the Italian Association for Cancer Research (AIRC project ID 23573), and the European Research Area Network ERA PerMed JTC2019/Fondazione Regionale per la Ricerca Biomedica project SuPerTreat (Supporting Personalized Treatment Decisions in Head and Neck Cancer through Big Data).\",\"PeriodicalId\":520097,\"journal\":{\"name\":\"The Journal of Clinical Investigation\",\"volume\":\"4565 3 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Clinical Investigation\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1172/jci194073\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Clinical Investigation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1172/jci194073","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景:控制HPV+口咽鳞状细胞癌(OPSCC)的关键目标是在不影响治愈率的情况下减少放射治疗(RT)剂量。最近的一项II/III期HN005试验显示,仅凭临床因素不足以指导安全的放疗剂量递减。我们之前的研究表明,基因组调整辐射剂量(GARD)可以预测放射治疗的益处,并可能为剂量选择提供信息。我们假设GARD可以指导HPV+ OPSCC患者的个体化RT降级。方法对一项国际多机构观察性研究(AJCC第八版,I-III期)中191例HPV+ OPSCC患者的基因表达谱进行分析。大多数患者接受35次70 Gy或33次69.96 Gy(中位剂量:70 Gy,范围:51.0-74.0 Gy)。总生存率(OS) 36个月为94.1%,60个月为87.3%。Cox比例风险模型评估GARD与OS之间的关联,并通过时间相关的受试者操作特征分析将GARD与传统临床预测指标进行比较。结果尽管给予统一的放疗剂量,但GARD表现出广泛的异质性,范围从15.4到71.7。在单变量分析(HR = 0.941, P = 0.041)和多变量分析(HR = 0.943, P = 0.046)中,较高的GARD值与改善的OS有显著相关性,而T期和N期则无显著相关性。与临床变量(AUC = 71.20)相比,GARD在36个月时显示出更好的预测性能(AUC = 78.26)。确定了两种基于gard的放疗降级策略,在减少辐射暴露的同时提供潜在的生存益处。结论:ard预测OS并优于临床变量,支持其整合到HPV+ OPSCC个性化RT的诊断工作流程中。本研究由美国国家癌症研究所通过克利夫兰诊所/埃莫里·罗宾中心(U54-CA274513,项目2)、欧盟地平线2020框架计划(资助/奖励689715)、意大利癌症研究协会(AIRC项目ID 23573)和欧洲研究区域网络ERA PerMed JTC2019/Fondazione Regionale per la Ricerca生物医学项目SuPerTreat(通过大数据支持头颈癌的个性化治疗决策)提供支持。
Personalized treatment in HPV+ oropharynx cancer using genomic adjusted radiation dose.
BACKGROUNDA key objective in managing HPV+ oropharyngeal squamous cell carcinoma (OPSCC) is reducing radiation therapy (RT) doses without compromising cure rates. A recent phase II/III HN005 trial revealed that clinical factors alone are insufficient to guide safe RT dose de-escalation. Our prior research demonstrated that the genomic adjusted radiation dose (GARD) predicts RT benefit and may inform dose selection. We hypothesize that GARD can guide personalized RT de-escalation in HPV+ OPSCC patients.METHODSGene expression profiles were analyzed in 191 HPV+ OPSCC patients enrolled in an international, multi-institutional observational study (AJCC Eighth Edition, stages I-III). Most patients received 70 Gy in 35 fractions or 69.96 Gy in 33 fractions (median dose: 70 Gy; range: 51.0-74.0 Gy). Overall survival (OS) was 94.1% at 36 months and 87.3% at 60 months. A Cox proportional hazards model assessed association between GARD and OS, and time-dependent receiver operating characteristic analyses compared GARD with traditional clinical predictors.RESULTSDespite uniform RT dosing, GARD showed wide heterogeneity, ranging from 15.4 to 71.7. Higher GARD values were significantly associated with improved OS in univariate (HR = 0.941, P = 0.041) and multivariable analyses (HR = 0.943, P = 0.046), while T and N stages were not. GARD demonstrated superior predictive performance at 36 months (AUC = 78.26) versus clinical variables (AUC = 71.20). Two GARD-based RT de-escalation strategies were identified, offering potential survival benefits while reducing radiation exposure.CONCLUSIONGARD predicts OS and outperforms clinical variables, supporting its integration into the diagnostic workflow for personalized RT in HPV+ OPSCC.FUNDINGThis work was supported by the National Cancer Institute through the Cleveland Clinic/Emory ROBIN center (U54-CA274513, project 2), the European Union Horizon 2020 Framework Programme (grant/award 689715), the Italian Association for Cancer Research (AIRC project ID 23573), and the European Research Area Network ERA PerMed JTC2019/Fondazione Regionale per la Ricerca Biomedica project SuPerTreat (Supporting Personalized Treatment Decisions in Head and Neck Cancer through Big Data).