Gori Stefania, Inno Alessandro, Rossi Valentina, Turazza Monica, Fiorio Elena, Fabi Alessandra, Bisagni Giancarlo, Foglietta Jennifer, Santini Daniele, Pavese Ida, Pellegrino Arianna, Zambelli Alberto, Vici Patrizia, Leonardi Vita, Barni Sandro, Saracchini Silvana, Bogina Giuseppe, Marchetti Fabiana, Duranti Simona, Lunardi Gianluigi, Montemurro Filippo
Medical Oncology, Sacro Cuore Don Calabria Hospital, Negrar, Verona, Italy.
Medical Oncology, Ospedale Civile di Saluzzo, Saluzzo, Italy.
PLoS One. 2016 May 25;11(5):e0156221. doi: 10.1371/journal.pone.0156221. eCollection 2016.
There are no validated predictive markers for lapatinib and capecitabine in patients with trastuzumab-resistant HER2 positive metastatic breast cancer.
Data of 148 consecutive patients treated with lapatinib and capecitabine from March 2007 to December 2013 were collected from 13 Italian institutions. Estimates of progression-free survival (PFS) and overall survival (OS) were obtained with the Kaplan-Meier method and compared with logrank test. The association of clinicopathological variables and the outcome was studied by binary logistic regression analysis and Cox proportional hazard analysis.
At a median follow-up of 41 months, median PFS and OS were 7 and 21 months, respectively. Patents with a PFS longer than 7 months had a significantly longer OS, compared with patients with a PFS equal to or shorter than 7 months (36 vs 15 months; p<0.001). Multivariate analysis revealed the benefit of lapatinib-based therapy in terms of PFS and OS was significantly associated with time-to-progression (TTP) on prior first-line trastuzumab-based therapy. In particular, each additional month on first-line trastuzumab based therapy was associated with a reduction in hazard of progression and death after the initiation of lapatinib-based therapy of 2% and 4%, respectively.
A longer TTP to first line trastuzumab seems to predict a prolonged PFS and OS with subsequent lapatinib and capecitabine.
对于曲妥珠单抗耐药的HER2阳性转移性乳腺癌患者,尚无经证实的拉帕替尼和卡培他滨预测标志物。
收集了2007年3月至2013年12月期间在13家意大利机构接受拉帕替尼和卡培他滨治疗的148例连续患者的数据。采用Kaplan-Meier方法获得无进展生存期(PFS)和总生存期(OS)的估计值,并通过对数秩检验进行比较。通过二元逻辑回归分析和Cox比例风险分析研究临床病理变量与结局的关联。
中位随访41个月时,中位PFS和OS分别为7个月和21个月。PFS长于7个月的患者与PFS等于或短于7个月的患者相比,OS显著更长(36个月对15个月;p<0.001)。多变量分析显示,基于拉帕替尼的治疗在PFS和OS方面的获益与既往一线基于曲妥珠单抗治疗的疾病进展时间(TTP)显著相关。特别是,一线基于曲妥珠单抗治疗每增加一个月,与拉帕替尼治疗开始后疾病进展风险和死亡风险分别降低2%和4%相关。
一线曲妥珠单抗治疗的TTP较长似乎可预测后续使用拉帕替尼和卡培他滨时PFS和OS延长。