Department of Internal Medicine/Infectious and Respiratory Diseases, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Cancer Chemother Pharmacol. 2011 Dec;68(6):1575-83. doi: 10.1007/s00280-011-1648-2. Epub 2011 May 6.
The combination of docetaxel and gemcitabine was tested in several studies in patients with lung, breast, and pancreatic cancers and other tumor entities. Some studies reported cases of severe or even fatal pulmonary toxicity that led to early termination of some trials. We created a meta-analysis model of published studies to identify explanatory factors for docetaxel-gemcitabine-dependent pulmonary toxicity.
We searched MEDLINE/Pubmed, EMBASE, and Cochrane Clinical Trials database for prospective full-text studies that used a schedule of docetaxel and gemcitabine to treat a malignant disease. We performed a meta-analysis for proportions using the arcsine transformation and a meta-regression using a generalized linear mixed model based on a binomial distribution and a logit link.
We included 103 trials with 113 treatment arms comprising 5,065 patients (major entities included non-small cell lung cancer (n = 2,550), breast cancer (n = 1,119), pancreatic cancer (n = 466), and urothelial cancer (n = 161)). For the incidence of severe lung toxicity (common toxicity criteria [CTC] grades 3-5), we found a combined estimate of 2.70% (95% CI 2.26, 3.14). The estimate for the proportion of fatal cases was 0.35% (95% CI 0.21, 0.58). We found that the sequence of the chemotherapy schedule had no influence on the incidence of severe pulmonary adverse events (F-test F = 0.65, df = 3,113, P = 0.58) nor did the study phase, treatment line or ethnicity of the participants. We found that patients with breast cancer, compared to lung cancer patients, developed severe lung toxicity less frequently (OR = 0.18, 95% CI (0.09, 0.36)).
We could not demonstrate that a particular chemotherapy sequence of docetaxel-gemcitabine is associated with excess pulmonary toxicity. Patients with lung cancer are at a higher risk for severe pulmonary side effects with docetaxel-gemcitabine than are patients with breast cancer.
多西他赛联合吉西他滨已在肺癌、乳腺癌、胰腺癌和其他肿瘤实体患者的多项研究中进行了测试。一些研究报告了严重甚至致命的肺毒性病例,导致一些试验提前终止。我们创建了一个已发表研究的荟萃分析模型,以确定与多西他赛-吉西他滨相关的肺毒性的解释因素。
我们在 MEDLINE/Pubmed、EMBASE 和 Cochrane 临床试验数据库中搜索了使用多西他赛和吉西他滨治疗恶性疾病的计划的前瞻性全文研究。我们使用反正弦变换对比例进行荟萃分析,并使用基于二项分布和对数链接的广义线性混合模型进行荟萃回归。
我们纳入了 103 项试验,共 113 个治疗臂,包括 5065 名患者(主要实体包括非小细胞肺癌(n=2550)、乳腺癌(n=1119)、胰腺癌(n=466)和尿路上皮癌(n=161))。对于严重肺毒性(常见毒性标准[CTC]等级 3-5)的发生率,我们发现综合估计值为 2.70%(95%CI 2.26,3.14)。致命病例的比例估计值为 0.35%(95%CI 0.21,0.58)。我们发现化疗方案的顺序对严重肺部不良事件的发生率没有影响(F 检验 F=0.65,df=3,113,P=0.58),研究阶段、治疗线或参与者的种族也没有影响。我们发现,与肺癌患者相比,乳腺癌患者发生严重肺毒性的频率较低(OR=0.18,95%CI(0.09,0.36))。
我们无法证明多西他赛-吉西他滨的特定化疗顺序与肺毒性增加有关。与乳腺癌患者相比,肺癌患者接受多西他赛-吉西他滨治疗时发生严重肺部副作用的风险更高。