Division of Pulmonary Medicine, Infectious Disease, and Oncology, Department of Internal Medicine, Nippon Medical School, 1-1-5, Sendagi, Bunkyo-ku, Tokyo 113-8602, Japan.
Lung Cancer. 2011 Jan;71(1):70-4. doi: 10.1016/j.lungcan.2010.04.014. Epub 2010 May 20.
Idiopathic interstitial pneumonias (IIPs) are one of the most common complications in patients with lung cancer. In lung cancer patients with IIP, the most serious toxicity is acute exacerbation of IIP caused by anticancer treatment in Japan. However, there has been no consensus and no evidence presented, regarding optimal treatment for advanced lung cancer with IIP.
Chemotherapy-naïve patients of inoperable stage, or post-operative recurrent non-small cell lung cancer (NSCLC) with IIPs were enrolled. Patients received paclitaxel at a dose of 100mg/m(2) on Days 1, 8, 15, and carboplatin every 28 days at a target dose of area under the curve (AUC) 5.0 on Day 1.
Between May 2004 and October 2008, 18 patients, including 6 with idiopathic pulmonary fibrosis (IPF), were enrolled and treated for a median of four cycles (range, 1-6). One patient (5.6%; 95% confidence interval (CI), 0-17%) with histologically confirmed IPF had acute exacerbation of IIPs associated with the treatment. The overall response rate was 61% (95% CI, 36-86%). The median progression-free survival, median survival time, and 1-year survival rate were 5.3 months, 10.6 months, and 22%, respectively.
This is the first report indicating that advanced NSCLC patients with IIP may benefit from chemotherapy. Weekly paclitaxel and carboplatin combination chemotherapy was as effective as conventional regimens in advanced NSCLC patients without IIP and was safer than previously reported for NSCLC patients with IIP. The results from this study would support, on ethical grounds, the conduct of a large-scale study to confirm the feasibility of this regimen.
特发性间质性肺炎(IIPs)是肺癌患者最常见的并发症之一。在日本,肺癌合并 IIP 患者最严重的毒性是抗癌治疗引起的 IIP 急性加重。然而,对于合并 IIP 的晚期肺癌,尚无最佳治疗方法达成共识,也缺乏相关证据。
纳入未经化疗的不可手术或术后复发的合并 IIP 的非小细胞肺癌(NSCLC)患者。患者接受紫杉醇 100mg/m²,第 1、8、15 天用药,卡铂 28 天一次,目标 AUC 为 5.0,第 1 天用药。
2004 年 5 月至 2008 年 10 月,18 例患者(其中 6 例为特发性肺纤维化)接受了治疗,中位治疗周期为 4 个(1-6 个)。1 例(5.6%;95%可信区间,0-17%)组织学证实为特发性肺纤维化的患者在治疗后发生 IIP 急性加重。总缓解率为 61%(95%可信区间,36-86%)。中位无进展生存期、中位总生存期和 1 年生存率分别为 5.3 个月、10.6 个月和 22%。
这是第一个表明合并 IIP 的晚期 NSCLC 患者可能从化疗中获益的报告。与不含 IIP 的晚期 NSCLC 患者相比,每周紫杉醇和卡铂联合化疗与常规方案一样有效,且比先前报道的 NSCLC 合并 IIP 患者的方案更安全。基于伦理学考虑,本研究结果支持开展更大规模的研究来确认该方案的可行性。