Rice David, Kim Hyung-Woo, Sabichi Anita, Lippman Scott, Lee J Jack, Williams Brendell, Vaporciyan Ara, Smythe W Roy, Swisher Stephen, Walsh Garrett, Putnam Joe B, Hong Waun Ki, Roth Jack
Department of Thoracic and Cardiovascular Surgery, University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
Ann Thorac Surg. 2003 Oct;76(4):1001-7; discussion 1007-8. doi: 10.1016/s0003-4975(03)00821-x.
The incidence of second primary lung cancers (SPLC) after resection of nonsmall cell lung cancer (NSCLC) is estimated to be 1% to 4% per patient year. The overall effect of SPLC on survival after resection of stage I NSCLC is unknown. Here we report the incidence, management, and outcome of SPLC in a large prospective cohort of patients who underwent careful follow-up.
National Cancer Institute Intergroup Trial NCI #I91-0001 examined the effectiveness of isotretinoin A for chemoprevention of second primary tumors, the primary endpoint in that trial. Prospective data from patients randomly assigned to the placebo arm were analyzed.
Five hundred sixty-nine patients underwent complete resection of pathologic stage I NSCLC. The median follow-up was 5.9 years. Second primary tumors developed in 88 (15%) patients. Of these, 49 (56%) were SPLC (incidence = 1.99/100 patient-years), with a median interval from initial surgery of 4.2 years. Second primary lung cancer never developed in patients who had never smoked (n = 44, p = 0.046; never versus ever smokers). Current smokers had a higher incidence of SPLC than former smokers (hazard ratio = 1.91, p = 0.03). Age, sex, stage, histology, tumor location and initial surgery had no effect on SPLC development. Despite semiannual follow-up with chest radiographs, 12 (24%) patients had metastatic disease at the time of diagnosis of SPLC. Surgical resection was performed in 31 (63%) SPLC patients. Median survival was 4.1 years in those who underwent surgery and 1.4 years in those who did not (p = 0.003). Overall SPLC-related mortality in the original cohort was 3.7%.
Patients who undergo surgery for SPLC can achieve prolonged survival. Despite close follow-up however many patients with SPLC present with advanced disease. That indicates a need for continued lifelong postoperative surveillance.
非小细胞肺癌(NSCLC)切除术后第二原发性肺癌(SPLC)的发生率估计为每位患者每年1%至4%。SPLC对I期NSCLC切除术后生存的总体影响尚不清楚。在此,我们报告了一个接受仔细随访的大型前瞻性队列患者中SPLC的发生率、治疗及结局。
美国国立癌症研究所(National Cancer Institute)的肿瘤协作组试验NCI #I91 - 0001研究了异维甲酸A对第二原发性肿瘤化学预防的有效性,该试验的主要终点为此。对随机分配到安慰剂组的患者的前瞻性数据进行了分析。
569例患者接受了病理I期NSCLC的完全切除。中位随访时间为5.9年。88例(15%)患者发生了第二原发性肿瘤。其中,49例(56%)为SPLC(发生率 = 1.99/100患者年),从初次手术到发生SPLC的中位间隔时间为4.2年。从不吸烟者(n = 44)从未发生过第二原发性肺癌(p = 0.046;从不吸烟者与曾经吸烟者相比)。当前吸烟者的SPLC发生率高于既往吸烟者(风险比 = 1.91,p = 0.03)。年龄、性别、分期、组织学类型、肿瘤位置及初次手术对SPLC的发生无影响。尽管每半年进行胸部X线片随访,但12例(24%)患者在SPLC诊断时已有转移性疾病。31例(63%)SPLC患者接受了手术切除。接受手术的患者中位生存期为4.1年,未接受手术的患者中位生存期为1.4年(p = 0.003)。原始队列中与SPLC相关的总体死亡率为3.7%。
接受SPLC手术的患者可实现生存期延长。然而,尽管进行了密切随访,许多SPLC患者仍表现为晚期疾病。这表明需要进行持续的终身术后监测。