Bang Sun-Hwi, Yoon Jeung-Won, Cho Chong-Kwan, Shin Ji-Eun, Lee Yeon-Weol, Yoo Hwa-Seung
East-West Cancer Center, Dunsan Oriental Hospital of Daejeon University, Daejeon, Korea.
Department of Statistics, Chungnam National University, Daejeon, Korea.
J Pharmacopuncture. 2012 Jun;15(2):31-5. doi: 10.3831/KPI.2012.15.2.031.
Non-small-cell lung cancer (NSCLC) represents approximately 80% of all lung cancers. Unfortunately, at their time of diagnosis, most patients have advanced to unresectable disease with a very poor prognosis. The oriental herbal medicine HangAm-Plus(HAP) has been developed for antitumor purposes, and several previous studies have reported its therapeutic effects. In this study, the efficacy of HAP was evaluated as a third-line treatment for advanced-stage IIIb/IV NSCLC.
The study involved six patients treated at the East- West Cancer Center (EWCC) from April 2010 to October 2011. Inoperable advanced-stage IIIb/IV NSCLC patients received 3,000 or 6,000 mg of HAP on a daily basis over a 12-week period. Computed tomography (CT) scans were obtained from the patients at the time of the initial administration and after 12 weeks of treatment. We observed and analyzed the patients overall survival (OS) and progression-free survival (PFS).
Of the six patients, three expired during the study, and the three remaining patients were alive as of October 31, 2011. The OS ranged from 234 to 512 days, with a median survival of 397 days and a one-year survival rate of 66.7%. In the 12-week-interval chest CT assessment, three patients showed stable disease (SD), and the other three showed progressive disease (PD). The PFS of patients ranged from 88 to 512 days, the median PFS being 96 days. Longer OS and PFS were correlated with SD. Although not directly comparable, the OS and the PFS of this study were greater than those of the docetaxel or the best supportive care group in other studies.
HAP may prolong the OS and the PFS of inoperable stage IIIb/IV NSCLC patients without significant adverse effects. In the future, more controlled clinical trials with larger samples from multi-centers should be conducted to evaluate the efficacy and the safety of HAP.
非小细胞肺癌(NSCLC)约占所有肺癌的80%。不幸的是,大多数患者在确诊时已发展为无法切除的疾病,预后很差。东方草药汉方加(HAP)已被开发用于抗肿瘤目的,先前的几项研究报道了其治疗效果。在本研究中,评估了HAP作为晚期IIIb/IV期NSCLC三线治疗的疗效。
该研究纳入了2010年4月至2011年10月在东西方癌症中心(EWCC)接受治疗的6例患者。无法手术的晚期IIIb/IV期NSCLC患者在12周内每天接受3000或6000毫克HAP治疗。在初次给药时和治疗12周后对患者进行计算机断层扫描(CT)。我们观察并分析了患者的总生存期(OS)和无进展生存期(PFS)。
6例患者中,3例在研究期间死亡,其余3例截至2011年10月31日仍存活。OS为234至512天,中位生存期为397天,一年生存率为66.7%。在12周间隔的胸部CT评估中,3例患者疾病稳定(SD),另外3例疾病进展(PD)。患者的PFS为88至512天,中位PFS为96天。较长的OS和PFS与SD相关。尽管无法直接比较,但本研究的OS和PFS高于其他研究中多西他赛或最佳支持治疗组的OS和PFS。
HAP可能延长无法手术的IIIb/IV期NSCLC患者OS和PFS,且无明显不良反应。未来,应进行更多来自多中心的大样本对照临床试验,以评估HAP的疗效和安全性。