Litviakov Nikolai V, Ibragimova Marina K, Tsyganov Matvey M, Kazantseva Polina V, Doroshenko Artem V, Garbukov Eugeniy Yu, Frolova Irina G, Slonimskaya Elena M
Cancer Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences, 634050 Tomsk, Russia.
J Pers Med. 2021 May 11;11(5):397. doi: 10.3390/jpm11050397.
In this prospective study, a new strategy for the prescription of neoadjuvant chemotherapy (NAC) was prospectively tested and depended on the presence of stemness gene amplifications in the tumor before treatment, which in our early studies showed a connection with metastasis. The study included 92 patients with grade IIA-IIIB luminal B breast cancer. Patients underwent a biopsy before treatment, and with the use of a CytoScan HD Array microarray (Affymetrix, Santa Clara, CA, USA), the presence of stemness gene amplifications (3q, 5p, 6p, 7q, 8q, 13q, 9p, 9q, 10p, 10q21.1, 16p, 18chr, 19p) in the tumor was determined. In group 1 ( = 41), in the presence of two or more amplifications, patients were prescribed a personalized NAC regimen. In group 2 ( = 21), if there was no amplification of stemness genes in the tumor, then patients were not prescribed NAC, and treatment began with surgery. Group 3 ( = 30) served as a historical control. The frequency of an objective response to NAC in groups 1 and 3 was 79%. Nonmetastatic survival was found in 100% of patients in group 2, who did not undergo NAC. In patients in group 1, the frequency of metastasis was 10% (4/41). At the same time, in patients in group 3, who received NAC, the rate of metastasis was 47% (14/30). The differences between group 1 and group 3 and between group 2 and group 3 were statistically significant, both by Fisher's criterion and a log-rank test. The appointment of NAC was most feasible in patients with clones with stemness gene amplifications in the primary tumor, while in the absence of amplifications, preoperative chemotherapy led to a sharp decrease in metastasis-free survival. This strategy of NAC prescription allowed us to achieve 93% metastatic survival in patients with breast cancer.
在这项前瞻性研究中,一种新的新辅助化疗(NAC)处方策略得到了前瞻性测试,该策略取决于治疗前肿瘤中干性基因扩增的存在情况,在我们早期的研究中显示其与转移有关。该研究纳入了92例IIA-IIIB期管腔B型乳腺癌患者。患者在治疗前接受活检,并使用CytoScan HD Array微阵列(美国加利福尼亚州圣克拉拉市Affymetrix公司)确定肿瘤中干性基因扩增(3q、5p、6p、7q、8q、13q、9p、9q、10p、10q21.1、16p、18chr、19p)的存在情况。在第1组(n = 41)中,若存在两个或更多扩增,则为患者开具个性化的NAC方案。在第2组(n = 21)中,如果肿瘤中不存在干性基因扩增,则不给患者开具NAC,治疗从手术开始。第3组(n = 30)作为历史对照。第1组和第3组中对NAC的客观缓解频率为79%。未接受NAC的第2组患者的无转移生存率为100%。在第1组患者中,转移频率为10%(4/41)。与此同时,在接受NAC的第3组患者中,转移率为47%(14/30)。根据Fisher检验和对数秩检验,第1组与第3组之间以及第2组与第3组之间的差异均具有统计学意义。对于原发性肿瘤中有干性基因扩增克隆的患者,开具NAC最为可行,而在不存在扩增的情况下,术前化疗会导致无转移生存率急剧下降。这种NAC处方策略使我们在乳腺癌患者中实现了93%的转移生存率。