Renfro Lindsay A, Ji Lingyun, Piao Jin, Onar-Thomas Arzu, Kairalla John A, Alonzo Todd A
University of Southern California, Los Angeles, CA.
St Jude Children's Research Hospital, Memphis, TN.
JCO Precis Oncol. 2019 Oct 24;3. doi: 10.1200/PO.19.00060. eCollection 2019.
In the United States, cancer remains the leading cause of disease-related death in children. Although survival from any pediatric cancer has improved dramatically during past decades, a number of cancers continue to yield dismal prognoses, which has motivated the continued study of novel therapeutic strategies. Furthermore, even patients cured of pediatric cancer often experience severe adverse effects of treatment and other long-term health implications, such as cardiotoxicity or loss of fertility. For these patients, improved risk stratification to identify those who could safely receive alternate or less-intensive therapy without affecting prognosis is a key objective. Fortunately, pediatric cancers are rare overall, but even among patients with the same narrow cancer type, there is often broad heterogeneity in terms of prognosis, molecular features or pathology, current treatment strategies, and scientific objectives. As a result, the design of clinical trials in the pediatric cancer setting is challenged by a number of practical issues that must be addressed to ensure trial feasibility for this vulnerable group of patients. In this review, we discuss some of the unique trial design considerations often encountered in any rare tumor setting through the lens of our experiences as faculty statisticians for the Children's Oncology Group, the largest organization in the world dedicated exclusively to pediatric cancer research and clinical trials. These topics include risk stratification within individual trials, relaxation of trial operating characteristics and parameters, use of historical controls, and address of noninferiority-type objectives in small cohorts. We review each in terms of practical motivation, present challenges, and potential solutions described in the literature and implemented in selected example trials from the Children's Oncology Group.
在美国,癌症仍是儿童疾病相关死亡的主要原因。尽管在过去几十年里,任何一种儿科癌症的生存率都有了显著提高,但仍有一些癌症的预后依然很差,这促使人们继续研究新的治疗策略。此外,即使是治愈了儿科癌症的患者,也常常会经历治疗的严重不良反应以及其他长期健康问题,如心脏毒性或生育能力丧失。对于这些患者来说,改进风险分层以识别那些能够在不影响预后的情况下安全接受替代疗法或强度较低疗法的患者是一个关键目标。幸运的是,儿科癌症总体上较为罕见,但即使在患有同一种狭义癌症类型的患者中,在预后、分子特征或病理、当前治疗策略以及科学目标方面往往也存在很大的异质性。因此,儿科癌症临床试验的设计面临着一些实际问题的挑战,必须解决这些问题以确保该弱势群体患者的试验可行性。在本综述中,我们将通过作为儿童肿瘤学组(世界上最大的专门致力于儿科癌症研究和临床试验的组织)教员统计学家的经验,讨论在任何罕见肿瘤背景下经常遇到的一些独特的试验设计考虑因素。这些主题包括单个试验中的风险分层、试验操作特征和参数的放宽、历史对照的使用以及小队列中非劣效性类型目标的处理。我们将从实际动机、当前挑战以及文献中描述并在儿童肿瘤学组的选定示例试验中实施的潜在解决方案等方面对每个主题进行综述。