Lee Bo-Ram, Yu Jin-Yeong, Yoon Seong-Hoon, Ban Hee-Jung, Kwon Yong-Soo, Oh In-Jae, Kim Kyu-Sik, Kim Yu-Il, Lim Sung-Chul, Kim Young-Chul
Department of Internal Medicine, Chonnam National University, Gwangju, Republic of Korea.
J Thorac Dis. 2015 Mar;7(3):433-8. doi: 10.3978/j.issn.2072-1439.2015.01.22.
Tegafur-uracil (UFT) is an anticancer agent that inhibits thymidylate synthase (TS). The degree of TS expression in primary lung cancer (LC) is different according to histologic cell type. In this study, we examined the variability of the anti-tumor efficacy of UFT monotherapy depending on histological subtypes of LC.
In the current single-institution, retrospective study, we assigned the patients with LC to three histologic groups [the squamous (Sq) non-small cell lung cancer (NSCLC)] group, the non-Sq NSCLC group and the SCLC group] and then compared the clinical response to UFT monotherapy between the three groups.
Our clinical series of 149 patients include 54 cases of Sq NSCLC, 67 cases of non-Sq NSCLC and 28 cases of SCLC. For Sq NSCLC, non-Sq NSCLC and SCLC group, the overall response rates (ORRs) were 1%, 1% and 0% (P=0.522), respectively. The disease control rates (DCRs) were 38.9%, 31.3% and 10.7% (P=0.012), respectively. The median progression-free survivals (PFSs) were 2.68, 2.25 and 1.46 months (P=0.004 for three groups and P=0.773 for two groups except for the SCLC group at the log-rank test), respectively. There was no significant difference between the groups in median overall survival (OS).
Our results indicate that the degree of the anti-tumor effect of UFT was higher in patients with NSCLC as compared with SCLC. But it showed no significant difference between the patients with Sq NSCLC and those with non-Sq NSCLC.
替加氟尿嘧啶(UFT)是一种抑制胸苷酸合成酶(TS)的抗癌药物。原发性肺癌(LC)中TS的表达程度因组织学细胞类型而异。在本研究中,我们研究了UFT单药治疗的抗肿瘤疗效因LC组织学亚型的不同而产生的差异。
在本次单机构回顾性研究中,我们将LC患者分为三个组织学组[鳞状(Sq)非小细胞肺癌(NSCLC)组、非Sq NSCLC组和小细胞肺癌(SCLC)组],然后比较三组对UFT单药治疗的临床反应。
我们的149例临床系列患者包括54例Sq NSCLC、67例非Sq NSCLC和28例SCLC。对于Sq NSCLC、非Sq NSCLC和SCLC组,总缓解率(ORR)分别为1%、1%和0%(P = 0.522)。疾病控制率(DCR)分别为38.9%、31.3%和10.7%(P = 0.012)。中位无进展生存期(PFS)分别为2.68、2.25和1.46个月(三组比较P = 0.004,除SCLC组外两组比较P = 0.773,对数秩检验)。三组的中位总生存期(OS)无显著差异。
我们的结果表明,与SCLC患者相比,UFT对NSCLC患者的抗肿瘤作用程度更高。但Sq NSCLC患者和非Sq NSCLC患者之间没有显著差异。