Yoh Kiyotaka, Takamochi Kazuya, Shukuya Takehito, Hishida Tomoyuki, Tsuboi Masahiro, Sakurai Hiroyuki, Goto Yasushi, Yoshida Koichi, Ohde Yasuhisa, Okumura Sakae, Ohashi Yasuo, Kunitoh Hideo
Department of Thoracic Oncology, National Cancer Center Hospital East.
Department of General Thoracic Surgery, Juntendo University, Graduate School of Medicine.
Jpn J Clin Oncol. 2019 Jan 1;49(1):63-68. doi: 10.1093/jjco/hyy165.
Adjuvant tegafur/uracil (UFT) chemotherapy is recommended for patients with completely resected Stage I non-small cell lung cancer (NSCLC) in Japan. A Phase III trial, the Japan Clinical Oncology Group (JCOG) 0707, comparing the survival benefit of UFT and S-1 (tegafur/gimeracil/oteracil) for this population is being conducted. However, the selection of patients in the randomized clinical trial (RCT) may not represent the real-world population. The present study aimed to investigate the pattern of care for patients receiving adjuvant chemotherapy for completely resected NSCLC.
Patients with completely resected pathological Stage I (T1 > 2 cm and T2 in 6th TNM edition) NSCLC eligible for the JCOG0707 trial but excluded from it during the enrollment period (2008-13) were eligible for this study. Physicians from institutions that participated in the JCOG0707 retrospectively assessed the medical records of each patient.
This study enrolled 5006 patients, 85% of those initially considered for participation in the JCOG0707 trial (5006 of 5923 patients). Among them, 2389 were ineligible for the trial and 2617 had not been enrolled despite being eligible. The most frequent reason for non-enrollment despite eligibility was the decline in patients' participation, and the major reasons for trial ineligibility were concomitant malignancy and comorbidities. Of all the patients enrolled in our study, 1659 received adjuvant chemotherapy, mainly UFT.
Our study indicates that only 15% of the real-world patients with completely resected NSCLC were enrolled into the adjuvant chemotherapy RCT, and among those not participating in the trial, one-third received adjuvant chemotherapy.
在日本,对于完全切除的Ⅰ期非小细胞肺癌(NSCLC)患者,推荐使用替加氟/尿嘧啶(UFT)辅助化疗。一项比较UFT和S-1(替加氟/吉美嘧啶/奥替拉西)对该人群生存获益的Ⅲ期试验——日本临床肿瘤学会(JCOG)0707正在进行。然而,随机临床试验(RCT)中患者的选择可能无法代表真实世界的人群。本研究旨在调查完全切除的NSCLC患者接受辅助化疗的治疗模式。
符合JCOG0707试验标准但在入组期间(2008 - 13年)被排除的完全切除的病理Ⅰ期(第6版TNM分期中T1>2 cm和T2)NSCLC患者符合本研究标准。参与JCOG0707的机构的医生对每位患者的病历进行回顾性评估。
本研究纳入了5006例患者,占最初考虑参与JCOG0707试验患者的85%(5923例患者中的5006例)。其中,2389例不符合试验标准,2617例尽管符合标准但未入组。尽管符合标准但未入组的最常见原因是患者拒绝参与,而不符合试验标准的主要原因是合并恶性肿瘤和合并症。在我们研究纳入的所有患者中,1659例接受了辅助化疗,主要是UFT。
我们的研究表明,在真实世界中,只有15%的完全切除的NSCLC患者被纳入辅助化疗RCT,在未参与试验的患者中,三分之一接受了辅助化疗。