Protocol for the Veterans Affairs Cooperative Studies Program Study Number 2005

Drew Moghanaki MD, MPH , Tomer Karas MD , Robert D. Timmerman MD , Robert B. Cameron MD , Timothy A. Ritter PhD , Hairong Shi PhD , Matthew K. Leiner MS , Hua Feng PhD , Vicki L. Skinner RN, MSN , Lisa Robin MA , Cheryl Odle MBA , Tom Sindowski BS , Amanda J. Snodgrass PharmD , Grant D. Huang MPH, PhD , Domenic J. Reda PhD , David H. Harpole MD , Veterans Affairs Lung Cancer Surgery or Stereotactic Radiotherapy Study Team
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Abstract

Background

Standard-of-care treatment options for stage I non-small cell lung cancer (NSCLC) include surgery and stereotactic body radiation therapy (SBRT). Notwithstanding a lack of prospective evidence demonstrating superior long-term survival with either of these treatments, evidence-based guidelines currently recommend only surgery for patients with operable disease and to limit SBRT for patients with inoperable disease.

Research Question

Do surgery or SBRT lead to superior survival rates for operable stage I NSCLC?

Study Design and Methods

A phase 3 randomized clinical trial was designed to compare the overall survival (OS) rates after surgery or SBRT for stage I NSCLC. Eligible participants must have biopsy-confirmed NSCLC measuring ≤ 5 cm in maximum diameter located > 1 cm from the trachea, proximal bronchial tree, esophagus, and spinal cord. Participants must be staged with fluorodeoxyglucose PET scans with mandatory biopsies of all radiographic areas concerning for regional or distant metastatic disease. The planned accrual is 670 patients to detect a 10% absolute benefit in 5-year OS with surgery or SBRT. Secondary outcome measures include patient-reported quality of life, respiratory function, health state utilities, patterns of lung cancer relapse, and causes of mortality by independent adjudication.

Results

The study was initiated in April 2017 with a planned ramp-up phase at six Veterans Affairs medical centers. Adapted recruitment interventions contributed to overcoming historical barriers to randomizing eligible participants between surgery and SBRT, and the study was expanded to 16 sites in May 2019. As of July 5, 2023, 280 of 670 planned participants have been enrolled.

Interpretation

The final results are expected to clarify the role of SBRT in lieu of surgery for patients with operable stage I NSCLC and to facilitate more informed discussions about these treatment options.

Trial Registry

ClinicalTrials.gov; No.: NCT02984761; URL: www.clinicaltrials.gov

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退伍军人事务合作研究计划 2005 年研究号议定书
背景I期非小细胞肺癌(NSCLC)的常规治疗方案包括手术和立体定向体放射治疗(SBRT)。尽管缺乏前瞻性证据证明这两种治疗方法的长期生存率更高,但循证指南目前只建议对可手术的患者进行手术治疗,并限制对不可手术的患者进行SBRT治疗。研究问题对于可手术的I期NSCLC,手术或SBRT是否能带来更高的生存率? 研究设计与方法一项3期随机临床试验旨在比较I期NSCLC手术或SBRT治疗后的总生存率(OS)。符合条件的参与者必须是经活检证实的NSCLC,最大直径不超过5厘米,距离气管、近端支气管、食管和脊髓1厘米。参与者必须通过氟脱氧葡萄糖 PET 扫描进行分期,并对所有涉及区域或远处转移性疾病的放射区域进行强制性活检。计划招募 670 名患者,以检测手术或 SBRT 对患者 5 年生存率是否有 10% 的绝对益处。次要结局指标包括患者报告的生活质量、呼吸功能、健康状态效用、肺癌复发模式以及独立裁定的死亡原因。经过调整的招募干预措施有助于克服在手术和SBRT之间对符合条件的参与者进行随机分配的历史障碍,该研究于2019年5月扩展到16个地点。截至2023年7月5日,计划招募的670名参与者中已有280名被招募。解读最终结果有望明确SBRT在可手术的I期NSCLC患者中替代手术的作用,并促进关于这些治疗方案的讨论。
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