Department of Epidemiology and Public Health, Division of Biostatistics and Bioinformatics, University of Maryland School of Medicine, Baltimore, Maryland.
Department of Oncology, Rigshospitalet, University of Copenhagen, Denmark.
Int J Radiat Oncol Biol Phys. 2024 Jun 1;119(2):338-353. doi: 10.1016/j.ijrobp.2023.11.028.
At its very core, radiation oncology involves a trade-off between the benefits and risks of exposing tumors and normal tissue to relatively high doses of ionizing radiation. This trade-off is particularly critical in childhood cancer survivors (CCS), in whom both benefits and risks can be hugely consequential due to the long life expectancy if the primary cancer is controlled. Estimating the normal tissue-related risks of a specific radiation therapy plan in an individual patient relies on predictive mathematical modeling of empirical data on adverse events. The Pediatric Normal-Tissue Effects in the Clinic (PENTEC) collaborative network was formed to summarize and, when possible, to synthesize dose-volume-response relationships for a range of adverse events incident in CCS based on the literature. Normal-tissue clinical radiation biology in children is particularly challenging for many reasons: (1) Childhood malignancies are relatively uncommon-constituting approximately 1% of new incident cancers in the United States-and biologically heterogeneous, leading to many small series in the literature and large variability within and between series. This creates challenges in synthesizing data across series. (2) CCS are at an elevated risk for a range of adverse health events that are not specific to radiation therapy. Thus, excess relative or absolute risk compared with a reference population becomes the appropriate metric. (3) Various study designs and quantities to express risk are found in the literature, and these are summarized. (4) Adverse effects in CCS often occur 30, 50, or more years after therapy. This limits the information content of series with even very extended follow-up, and lifetime risk estimates are typically extrapolations that become dependent on the mathematical model used. (5) The long latent period means that retrospective dosimetry is required, as individual computed tomography-based radiation therapy plans gradually became available after 1980. (6) Many individual patient-level factors affect outcomes, including age at exposure, attained age, lifestyle exposures, health behaviors, other treatment modalities, dose, fractionation, and dose distribution. (7) Prospective databases with individual patient-level data and radiation dosimetry are being built and will facilitate advances in dose-volume-response modeling. We discuss these challenges and attempts to overcome them in the setting of PENTEC.
放射肿瘤学的核心是在将肿瘤和正常组织暴露于相对高剂量电离辐射的获益与风险之间进行权衡。这种权衡在儿童癌症幸存者(CCS)中尤为关键,因为如果主要癌症得到控制,他们的预期寿命很长,因此获益和风险都可能产生巨大影响。在个体患者中估计特定放射治疗计划的正常组织相关风险依赖于对不良事件的经验数据的预测数学建模。成立儿科正常组织效应临床(PENTEC)合作网络,是为了根据文献总结和尽可能综合一系列 CCS 中发生的不良事件的剂量-体积-反应关系。由于多种原因,儿童正常组织临床放射生物学特别具有挑战性:(1)儿童恶性肿瘤相对罕见-在美国新发生的癌症中约占 1%-并且具有生物学异质性,导致文献中有许多小系列,并且系列内和系列之间存在很大的变异性。这给跨系列数据综合带来了挑战。(2)CCS 发生一系列与放射治疗无关的不良健康事件的风险增加。因此,与参考人群相比,超额相对或绝对风险成为适当的指标。(3)文献中发现了各种研究设计和表达风险的数量,对这些进行了总结。(4)CCS 的不良影响通常发生在治疗后 30、50 或更长时间。这限制了具有甚至非常长随访的系列的信息量,并且终生风险估计通常是依赖于所使用的数学模型的外推。(5)潜伏期长意味着需要进行回顾性剂量测定,因为基于个人计算机断层扫描的放射治疗计划在 1980 年后才逐渐可用。(6)许多个体患者水平的因素会影响结果,包括暴露年龄、达到年龄、生活方式暴露、健康行为、其他治疗方式、剂量、分割和剂量分布。(7)正在建立具有个体患者水平数据和放射剂量测定的前瞻性数据库,这将促进剂量-体积-反应建模的进展。我们讨论了这些挑战以及在 PENTEC 中克服这些挑战的尝试。