Department of Surgery, State University of New York Upstate Medical University, Syracuse, NY.
Alliance Statistics and Data Center, Duke University Medical Center, Durham, NC.
J Thorac Cardiovasc Surg. 2017 Jun;153(6):1592-1597. doi: 10.1016/j.jtcvs.2016.12.045. Epub 2017 Feb 7.
Cancer and Leukemia Group B 140503 is an ongoing, multicenter randomized trial assessing whether sublobar resection is equivalent to lobectomy for the treatment of stage I A non-small cell lung cancer (NSCLC) ≤2 cm in diameter. The objective of this report is to determine the reasons precluding intraoperative randomization.
From June 15, 2007, to March 22, 2013, 637 patients were preregistered to the trial. Three hundred eighty-nine were randomized successfully (61%), and 248 patients were not randomized (39%). We analyzed the reasons for nonrandomization among a subset of the nonrandomized patients (208) for whom additional data were available.
Of these 208 patients, undiagnosed benign nodules (n =104, 16% of all registered patients) and understaging of NSCLC (n =45, 7% of all registered patients) were the dominant reasons precluding randomization. Granulomas represent one-quarter of the benign nodules. The understaged patients had unsuspected nodal metastases (n =28) or other more advanced NSCLC. The rate of randomization was significantly greater in those patients who had a preoperative biopsy (P <.001).
In a carefully monitored cohort of patients with suspected small NSCLC ≤2 cm, a substantial number are misdiagnosed (benign nodules) or understaged. These patients may not have benefited from a thoracic surgical procedure. Preoperative biopsy significantly increased the rate of correct diagnosis. Preoperative biopsy of small suspected NSCLC will reduce the number of nontherapeutic or unnecessary thoracic procedures. Accuracy in preoperative diagnosis is increasingly important as more such small nodules are discovered through lung cancer screening.
癌症和白血病组 B140503 是一项正在进行的多中心随机试验,旨在评估亚肺叶切除术是否与肺叶切除术等效,用于治疗直径≤2cm 的 I 期 A 型非小细胞肺癌(NSCLC)。本报告的目的是确定妨碍术中随机分组的原因。
从 2007 年 6 月 15 日至 2013 年 3 月 22 日,有 637 名患者预先登记参加该试验。其中 389 名患者成功随机分组(61%),248 名患者未随机分组(39%)。我们分析了其中 208 名未随机分组患者(所有登记患者的 16%)无法随机分组的原因,这些患者有额外的数据。
在这 208 名患者中,未确诊的良性结节(n=104,所有登记患者的 16%)和 NSCLC 分期过低(n=45,所有登记患者的 7%)是妨碍随机分组的主要原因。肉芽肿占良性结节的四分之一。分期过低的患者存在未被怀疑的淋巴结转移(n=28)或其他更晚期的 NSCLC。术前活检的患者随机分组率显著更高(P<.001)。
在一组精心监测的疑似≤2cm 的小 NSCLC 患者中,相当一部分被误诊(良性结节)或分期过低。这些患者可能没有从胸部外科手术中获益。术前活检显著提高了正确诊断的比例。术前对疑似小 NSCLC 的活检将减少非治疗性或不必要的胸部手术数量。随着通过肺癌筛查发现更多的此类小结节,术前诊断的准确性变得越来越重要。