Background:Conditional survival(CS)provides dynamic prognostic estimates by considering the patients existing survival time.Since CS for endemic nasopharyngeal carcinoma(NPC)is lacking,we aimed to assess the CS of end...Background:Conditional survival(CS)provides dynamic prognostic estimates by considering the patients existing survival time.Since CS for endemic nasopharyngeal carcinoma(NPC)is lacking,we aimed to assess the CS of endemic NPC and establish a web-based calculator to predict individualized,conditional sitespecific recurrence risk.Methods:Using an NPC-specific database with a big-data intelligence platform,10,058 endemic patients with non-metastatic stage I–IVA NPC receiving intensity-modulated radiotherapy with or without chemotherapy between April 2009 and December 2015 were investigated.Crude CS estimates of conditional overall survival(COS),conditional disease-free survival(CDFS),conditional locoregional relapse-free survival(CLRRFS),conditional distant metastasis-free survival(CDMFS),and conditional NPC-specific survival(CNPC-SS)were calculated.Covariate-adjusted CS estimates were generated using inverse probability weighting.A prediction model was established using competing risk models and was externally validated with an independent,non-metastatic stage I–IVA NPC cohort undergoing intensity-modulated radiotherapy with or without chemotherapy(n=601)at another institution.Results:The median follow-up of the primary cohort was 67.2 months.The 5-year COS,CDFS,CLRRFS,CDMFS,and CNPC-SS increased from 86.2%,78.1%,89.8%,87.3%,and 87.6%at diagnosis to 87.3%,87.7%,94.4%,96.0%,and 90.1%,respectively,for an existing survival time of 3 years since diagnosis.Differences in CS estimates between prognostic factor subgroups of each endpoint were noticeable at diagnosis but diminished with time,whereas an ever-increasing disparity in CS between different age subgroups was observed over time.Notably,the prognoses of patients that were poor at diagnosis improved greatly as patients survived longer.For individualized CS predictions,we developed a web-based model to estimate the conditional risk of local(C-index,0.656),regional(0.667),bone(0.742),lung(0.681),and liver(0.711)recurrence,which significantly outperformed the current staging system(P<0.001).The performance of this webbased model was further validated using an external validation cohort(median follow-up,61.3 months),with C-indices of 0.672,0.736,0.754,0.663,and 0.721,respectively.Conclusions:We characterized the CS of endemic NPC in the largest cohort to date.Moreover,we established a web-based calculator to predict the CS of sitespecific recurrence,which may help to tailor individualized,risk-based,timeadapted follow-up strategies.展开更多
基金This work was supported by the National Natural Science Foundation of China(81872463 and 81930072)Special Support Program of Sun Yat-sen University(16zxtzlc06)+4 种基金Key-Area Research and Development Program of Guangdong Province(2019A1515012045 and 2019B020230002)Natural Science Foundation of Guangdong Province(2017A030312003)Health&Medical Collaborative Innovation Project of Guangzhou City,China(201803040003)Innovation Team Development Plan of the Ministry of Education(No.IRT_17R110)Overseas Expertise Introduction Project for Discipline Innovation(111 Project,B14035).
文摘Background:Conditional survival(CS)provides dynamic prognostic estimates by considering the patients existing survival time.Since CS for endemic nasopharyngeal carcinoma(NPC)is lacking,we aimed to assess the CS of endemic NPC and establish a web-based calculator to predict individualized,conditional sitespecific recurrence risk.Methods:Using an NPC-specific database with a big-data intelligence platform,10,058 endemic patients with non-metastatic stage I–IVA NPC receiving intensity-modulated radiotherapy with or without chemotherapy between April 2009 and December 2015 were investigated.Crude CS estimates of conditional overall survival(COS),conditional disease-free survival(CDFS),conditional locoregional relapse-free survival(CLRRFS),conditional distant metastasis-free survival(CDMFS),and conditional NPC-specific survival(CNPC-SS)were calculated.Covariate-adjusted CS estimates were generated using inverse probability weighting.A prediction model was established using competing risk models and was externally validated with an independent,non-metastatic stage I–IVA NPC cohort undergoing intensity-modulated radiotherapy with or without chemotherapy(n=601)at another institution.Results:The median follow-up of the primary cohort was 67.2 months.The 5-year COS,CDFS,CLRRFS,CDMFS,and CNPC-SS increased from 86.2%,78.1%,89.8%,87.3%,and 87.6%at diagnosis to 87.3%,87.7%,94.4%,96.0%,and 90.1%,respectively,for an existing survival time of 3 years since diagnosis.Differences in CS estimates between prognostic factor subgroups of each endpoint were noticeable at diagnosis but diminished with time,whereas an ever-increasing disparity in CS between different age subgroups was observed over time.Notably,the prognoses of patients that were poor at diagnosis improved greatly as patients survived longer.For individualized CS predictions,we developed a web-based model to estimate the conditional risk of local(C-index,0.656),regional(0.667),bone(0.742),lung(0.681),and liver(0.711)recurrence,which significantly outperformed the current staging system(P<0.001).The performance of this webbased model was further validated using an external validation cohort(median follow-up,61.3 months),with C-indices of 0.672,0.736,0.754,0.663,and 0.721,respectively.Conclusions:We characterized the CS of endemic NPC in the largest cohort to date.Moreover,we established a web-based calculator to predict the CS of sitespecific recurrence,which may help to tailor individualized,risk-based,timeadapted follow-up strategies.