Institute for Diagnostic and Interventional Radiology, Johann Wolfgang Goethe-University Frankfurt, Theodor-Stern-Kai 7, 60590 Frankfurt am Main, Germany.
AJR Am J Roentgenol. 2011 Jan;196(1):W66-72. doi: 10.2214/AJR.09.3836.
The purpose of this study was to evaluate local tumor control and survival after use of a downstaging protocol of repeated transarterial chemoembolization (TACE) with two chemotherapeutic combinations followed by laser-induced thermotherapy in the care of patients with liver metastasis of breast cancer.
This prospective study included 161 patients with liver metastasis of breast cancer origin. TACE (mean, 3.5 [SD, 1.3] sessions per patient; range, 1-9 sessions) was performed as downstaging treatment to achieve the size and number of metastatic lesions that met the requirements for laser-induced thermotherapy (diameter < 5 cm, number ≤ 5). The TACE protocol was performed with either mitomycin C alone (n = 53) or mitomycin C in combination with gemcitabine (n = 108).
In response to TACE overall, the mean reduction in diameter based on the longest diameter of the target lesions was 27%. The difference between diameter reduction in the mitomycin C group and that in the mitomycin C-gemcitabine group was not statistically significant (p = 0.65). The mean survival time of all patients was 32.5 months, calculation starting from the first TACE treatment. The mean local tumor control period calculated as of completion of therapy was 13 months, and the mean time to progression was 8 months. In the mitomycin-gemcitabine group, mean time to progression was 10.7 months, and in the mitomycin group it was 6.9 months (p = 0.5).
TACE can be used for sufficient downstaging of liver metastatic lesions of breast cancer to allow laser-induced thermotherapy. A combination of mitomycin C and gemcitabine seems to improve the reduction achieved with TACE.
本研究旨在评估重复经动脉化疗栓塞(TACE)联合两种化疗方案降期治疗联合激光诱导热疗治疗乳腺癌肝转移患者的局部肿瘤控制和生存情况。
本前瞻性研究纳入了 161 例乳腺癌肝转移患者。TACE(平均每位患者 3.5[SD,1.3]次;范围 1-9 次)作为降期治疗,使转移瘤的大小和数量符合激光诱导热疗的要求(直径<5cm,数目≤5 个)。TACE 方案采用丝裂霉素 C 单药(n=53)或丝裂霉素 C 联合吉西他滨(n=108)。
总体而言,TACE 治疗后,基于靶病变最长直径的平均直径缩小率为 27%。丝裂霉素 C 组与丝裂霉素 C-吉西他滨组之间的直径缩小差异无统计学意义(p=0.65)。所有患者的平均生存时间为 32.5 个月,从第一次 TACE 治疗开始计算。治疗完成时的平均局部肿瘤控制期为 13 个月,平均进展时间为 8 个月。在丝裂霉素 C-吉西他滨组中,进展时间的平均值为 10.7 个月,而在丝裂霉素 C 组中为 6.9 个月(p=0.5)。
TACE 可用于充分降期乳腺癌肝转移瘤,以允许进行激光诱导热疗。丝裂霉素 C 联合吉西他滨似乎可提高 TACE 的减瘤效果。