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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Isolated tumor cells in the bone marrow (ITC-BM) of breast cancer patients before and after anthracyclin based therapy: influenced by the HER2- and Topoisomerase IIα-status of the primary tumor?
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Isolated tumor cells in the bone marrow (ITC-BM) of breast cancer patients before and after anthracyclin based therapy: influenced by the HER2- and Topoisomerase IIα-status of the primary tumor?

机译:基于蒽环素的治疗前后乳腺癌患者骨髓中分离的肿瘤细胞(ITC-BM):受原发肿瘤的HER2-和TopoisomeraseIIα状态影响吗?

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Purpose: The presence of isolated tumor cells in the bone marrow (ITC-BM) is an independent prognostic factor in all stages of breast cancer. Both the expression/amplification of human epithelial growth factor receptor 2 (HER2) and Topoisomerase IIα (TOP IIa), a key enzyme of DNA replication and main target of anthracyclins, in breast cancer tissue seem to have predictive value regarding the effectiveness of systemic therapies. Methods: To investigate the correlation between these factors and their influence on clinical outcome, tumor tissue of 54 patients who were screened for ITC-BM before and after anthracyclin-based chemotherapy (abCTX) was examined for HER2 and TOP IIa by immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH). Results: By IHC, 31% of the tumors showed positive for HER2 (2+/3+), 14.6% were amplified in FISH. TOP IIa expression (>50%) was found in 13/53 patients (25%), FISH was positive in 5/47 cases (11%). TOP IIa amplification was not seen in cases without HER2 amplification, five of the seven HER2 amplified cases also were amplified for TOP IIa (71% co-amplification). Forty-three patients had adjuvant, seven neo-adjuvant, four palliative abCTX. ITC-BM were present in 24% of patients before and 31% after CTX. Patients with HER2 (IHC, P=0.29) and TOP IIa (FISH, P=0.16) positive tumors tended to stay or become negative in BM status after abCTX and vice versa. After a median follow-up of 44 months (6–127), none of the factors reached significance for overall survival. Yet, patients with HER2 (P=0.16) and TOP IIa (P=0.09) positive tumors showed a trend towards prolonged disease-free survival. Remarkably, none of the TOP IIa FISH-positive patients developed distant metastases (P=0.099) or died (P=0.19) after CTX so far. Conclusions: HER2- and TOP IIa positivity seem to improve the effect of abCTX. The combination of the prognostic value of ITC-BM and the predictive capacity of HER2 and TOP IIa could help to stratify patients for certain therapies. The direct examination of those factors on ITC-BM is the focus of ongoing studies.
机译:目的:骨髓中分离的肿瘤细胞(ITC-BM)的存在是乳腺癌所有阶段的独立预后因素。人上皮生长因子受体2(HER2)和拓扑异构酶IIα(TOP IIa)(DNA复制的关键酶和蒽环素的主要靶标)在乳腺癌组织中的表达/扩增似乎对全身治疗的有效性具有预测价值。方法:为调查这些因素及其对临床结局的影响之间的相关性,通过免疫组织化学(IHC)检查54例基于蒽环素类化学疗法(abCTX)进行ITC-BM筛查的患者的肿瘤组织中的HER2和TOP IIa和荧光原位杂交(FISH)。结果:通过IHC,31%的肿瘤显示HER2阳性(2 + / 3 +),FISH中扩增了14.6%。在13/53例患者(25%)中发现TOP IIa表达(> 50%),在5/47例患者中(11%)FISH阳性。没有HER2扩增的病例中未见TOP IIa扩增,在7例HER2扩增病例中,有5例也被TOP IIa扩增(共扩增71%)。 43例患者接受了佐剂,7例新辅助,4例姑息性abCTX。 CTX之前和之后,有24%的患者存在ITC-BM。 HER2(IHC,P = 0.29)和TOP IIa(FISH,P = 0.16)阳性的患者在abCTX后倾向于保持BM状态或变为阴性,反之亦然。在中位随访44个月(6-127)后,所有因素均未达到总体生存的重要意义。然而,HER2(P = 0.16)和TOP IIa(P = 0.09)阳性的患者显示出无病生存期延长的趋势。值得注意的是,到目前为止,CTX后,TOP IIa FISH阳性患者均未发生远处转移(P = 0.099)或死亡(P = 0.19)。结论:HER2-和TOP IIa阳性似乎可以改善abCTX的作用。 ITC-BM的预后价值与HER2和TOP IIa的预测能力的结合可以帮助对某些疗法的患者进行分层。对这些因素在ITC-BM上的直接检查是正在进行的研究的重点。

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