Murta E F, de Andrade J M, Falcão R P, Bighetti S
Department of Gynecology and Obstetrics, Faculty of Medicine of Ribeirão Preto, Brazil.
Tumori. 2000 Sep-Oct;86(5):403-7. doi: 10.1177/030089160008600507.
There is an enhanced immune response in patients with breast cancer after the use of chemotherapy. The objective of this study was therefore to investigate alterations in the number of peripheral lymphocytes in patients with breast cancer after neoadjuvant chemotherapy (NC) and the relationship with prognosis.
Thirty women were analyzed. Their UICC staging was IIb (only T3N0 included) and III (N3 not included). Sample analysis was performed using flow cytometry before the first cycle and 18 to 21 days after the last cycle of NC. The lymphocyte subsets studied were: T (CD3, CD4, CD8), B (CD19, CD23), natural killer (NK) (CD56, CD16), and interleukin-2 (CD25). CD3, CD56, CD8, and CD16 lymphocytes were analyzed with double marking. After x = 3.8 +/- 1.3 cycles of 5-fluorouracil, epirubicin and cyclophosphamide (FEC), 16 patients showed a complete or partial response (group 1). After three cycles 14 showed no response or tumor progression (group 2). A control group of healthy women was used for pretreatment analysis.
Before NC there was a significant increase in B lymphocytes and NK cells in comparison to the control group. After NC there was a significant percentage increase in CD3, CD4, CD8, CD25 and CD3+CD56+ cells and a decrease in CD19, CD23, CD56, CD16 and CD16+CD8+ cells. There was a significant fall in the absolute number of CD4, CD19, CD23, CD56, CD16 and CD16+CD8+ lymphocytes and an increase in CD3+CD56+ lymphocytes. Before NC the ratio CD4/CD8 in group 1 was 2.25 +/- 0.5 and in group 2 it was 1.79 +/- 0.5 (P <0.05).
Patients with advanced breast cancer showed increases in B and NK lymphocytes. Neoadjuvant chemotherapy (FEC) caused an increase in CD3+CD56+ and a decrease in B lymphocytes. Patients with an increased CD4/CD8 ratio have a better chance of responding to neoadjuvant chemotherapy.
乳腺癌患者在接受化疗后免疫反应增强。因此,本研究的目的是调查新辅助化疗(NC)后乳腺癌患者外周淋巴细胞数量的变化及其与预后的关系。
对30名女性进行分析。她们的国际抗癌联盟(UICC)分期为IIb期(仅包括T3N0)和III期(不包括N3)。在NC的第一个周期之前以及最后一个周期后的18至21天,使用流式细胞术进行样本分析。研究的淋巴细胞亚群包括:T细胞(CD3、CD4、CD8)、B细胞(CD19、CD23)、自然杀伤(NK)细胞(CD56、CD16)和白细胞介素-2(CD25)。对CD3、CD56、CD8和CD16淋巴细胞进行双重标记分析。在接受5-氟尿嘧啶、表柔比星和环磷酰胺(FEC)进行x = 3.8 +/- 1.3个周期的化疗后,16例患者显示出完全或部分缓解(第1组)。三个周期后,14例患者无反应或肿瘤进展(第2组)。使用一组健康女性作为对照组进行预处理分析。
与对照组相比,NC前B淋巴细胞和NK细胞显著增加。NC后,CD3、CD4、CD8、CD25和CD3 + CD56 +细胞的百分比显著增加,而CD19、CD23、CD56、CD16和CD16 + CD8 +细胞减少。CD4、CD19、CD23、CD56、CD16和CD16 + CD8 +淋巴细胞的绝对数量显著下降,而CD3 + CD56 +淋巴细胞增加。NC前,第1组的CD4/CD8比值为2.25 +/- 0.5,第2组为1.79 +/- 0.5(P <0.05)。
晚期乳腺癌患者的B淋巴细胞和NK淋巴细胞增加。新辅助化疗(FEC)导致CD3 + CD56 +增加,B淋巴细胞减少。CD4/CD8比值升高的患者对新辅助化疗有更好的反应机会。