Absolute increase in tumour size can improve the metric evaluating disease progression in metastatic colorectal cancer

Author:

Robinson Ari1,Agur Zvia1,Kogan Yuri1

Affiliation:

1. Institute for Medical BioMathematics

Abstract

Abstract

Background The assessment of response to therapy in advanced solid cancer diseases is predicated on the Response Evaluation Criteria In Solid Tumours for the evaluation of disease state by the relative changes in lesion size. The underlying assumption is that a larger relative increase in lesion size implicates less efficacious therapy, worse prognosis and shorter survival. Methods We analyzed retrospective data of metastatic colorectal cancer patients from three clinical datasets, stratified into three cohorts by the treatment protocol. We evaluated the first relative and absolute increase in target lesion size for their association with overall survival. Results About fifty four percent of the patient population increased in target lesion size during the first-line treatment. A multivariate analysis showed that patients with larger relative increase in lesion size had slightly longer survival in all three cohorts (\(HR = 0.85, HR=0.95 ,HR = 0.75\) for Cohorts 1–3, respectively); p-values showed no significance. In contrast, patients with larger absolute increase in total lesion size had significantly shorter survival (\(HR = 1.1 \left(p=0.05\right), HR=1.2 \left(p=0.04\right), HR = 1.25(p=0.02)\) for Cohorts 1–3, respectively). We also found a negative correlation between the SLD at nadir and relative increase. Conclusions The different impact of the absolute and the relative increase in SLD at relapse reflects the different growth patterns of small and big tumours. Further validation of our results is required. We believe that the first absolute increase in total lesion size may become a useful metric, upon which a more precise categorization of survival-related disease progression can be based.

Publisher

Research Square Platform LLC

Reference31 articles.

1. Amir E et al. Poor correlation between progression-free and overall survival in modern clinical trials: are composite endpoints the answer? European Journal of Cancer, 2012. 48(3): p. 385–388.

2. Poad H et al. The Validity of Surrogate Endpoints in Sub Groups of Metastatic Colorectal Cancer Patients Defined by Treatment Class and KRAS Status. Cancers, 2022. 14(21): p. 5391.

3. Korn RL, Crowley JJ. Overview: progression-free survival as an endpoint in clinical trials with solid tumors. Clinical cancer research, 2013. 19(10): p. 2607–2612.

4. Aprile G et al. Timing and extent of response in colorectal cancer: critical review of current data and implication for future trials. Oncotarget, 2015. 6(30): p. 28716.

5. Buyse M et al. Progression-free survival is a surrogate for survival in advanced colorectal cancer. Journal of clinical oncology, 2007. 25(33): p. 5218–5224.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3