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完全切除的病理分期 IB-IIIA 期非小细胞肺癌患者术后辅助吉西他滨对比辅助尿嘧啶替加氟的 III 期研究(WJTOG0101)。

Phase III study of adjuvant gemcitabine compared with adjuvant uracil-tegafur in patients with completely resected pathological stage IB-IIIA non-small cell lung cancer (WJTOG0101).

机构信息

Department of Thoracic Oncology, National Hospital Organization Kyushu Cancer Center, Fukuoka City, Fukuoka, Japan.

Department of Thoracic Surgery, Osaka City General Hospital, Osaka City, Osaka, Japan.

出版信息

Int J Clin Oncol. 2021 Dec;26(12):2216-2223. doi: 10.1007/s10147-021-02012-9. Epub 2021 Aug 31.

Abstract

BACKGROUND

Adjuvant oral uracil-tegafur (UFT) has led to significantly longer postoperative survival among patients with non-small-cell lung cancer (NSCLC). Gemcitabine (GEM) monotherapy is also reportedly effective for NSCLC and has minor adverse events (AEs). This study compared the efficacy of GEM- versus UFT-based adjuvant regimens in patients with completely resected pathological stage (p-stage) IB-IIIA NSCLC.

PATIENTS AND METHODS

Patients with completely resected p-stage IB-IIIA NSCLC were randomly assigned to GEM or UFT. The primary endpoint was overall survival (OS); secondary endpoints were disease-free survival (DFS), and AEs.

RESULTS

We assigned 305 patients to the GEM group and 303 to the UFT group. Baseline factors were balanced between the arms. Of the 608 patients, 293 (48.1%) had p-stage IB disease, 195 (32.0%) had p-stage II disease and 121 (19.9%) had p-stage IIIA disease. AEs were generally mild in both groups, and only one death occurred, in the GEM group. After a median follow-up of 6.8 years, the two groups did not significantly differ in survival: 5 year OS rates were GEM: 70.0%, UFT: 68.8% (hazard ratio 0.948; 95% confidence interval 0.73-1.23; P = 0.69).

CONCLUSION

Although GEM-based adjuvant therapy for patients with completely resected stage IB-IIIA NSCLC was associated with acceptable toxicity, it did not provide longer OS than did UFT.

摘要

背景

辅助口服替加氟尿嘧啶(UFT)可显著延长非小细胞肺癌(NSCLC)患者的术后生存时间。吉西他滨(GEM)单药治疗也被报道对 NSCLC 有效,且不良反应(AE)较少。本研究比较了完全切除病理分期(p 分期)IB-IIIA NSCLC 患者以 GEM 或 UFT 为基础的辅助治疗方案的疗效。

患者和方法

完全切除 p 分期 IB-IIIA NSCLC 的患者被随机分配到 GEM 或 UFT 组。主要终点是总生存期(OS);次要终点是无病生存期(DFS)和 AE。

结果

我们将 305 例患者分配到 GEM 组,303 例患者分配到 UFT 组。两组间基线因素平衡。在 608 例患者中,293 例(48.1%)为 p 分期 IB 期疾病,195 例(32.0%)为 p 分期 II 期疾病,121 例(19.9%)为 p 分期 IIIA 期疾病。两组的 AE 均较轻,仅 GEM 组有 1 例死亡。中位随访 6.8 年后,两组的生存情况无显著差异:5 年 OS 率分别为 GEM:70.0%,UFT:68.8%(风险比 0.948;95%置信区间 0.73-1.23;P=0.69)。

结论

尽管完全切除 p 分期 IB-IIIA NSCLC 患者的 GEM 辅助治疗具有可接受的毒性,但与 UFT 相比,它并未提供更长的 OS。

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