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本文引用的文献

1
Pathological prognostic factors in breast cancer.乳腺癌的病理预后因素
Crit Rev Oncol Hematol. 1999 Aug;31(3):209-23. doi: 10.1016/s1040-8428(99)00034-7.
2
Assessment of pathologic prognostic factors in breast core needle biopsies.乳腺粗针穿刺活检中病理预后因素的评估
Mod Pathol. 1999 Oct;12(10):941-5.
3
An immunohistochemical examination of the expression of E-cadherin, alpha- and beta/gamma-catenins, and alpha2- and beta1-integrins in invasive breast cancer.浸润性乳腺癌中E-钙黏蛋白、α-和β/γ-连环蛋白以及α2-和β1-整合素表达的免疫组织化学检查
J Pathol. 1999 Apr;187(5):523-9. doi: 10.1002/(SICI)1096-9896(199904)187:5<523::AID-PATH296>3.0.CO;2-3.
4
The pathologist as optimist: cancer grade deflation in prostatic needle biopsies.作为乐观主义者的病理学家:前列腺穿刺活检中的癌症分级降低
Am J Surg Pathol. 1998 Oct;22(10):1169-70. doi: 10.1097/00000478-199810000-00001.
5
Gleason scores from prostate biopsies obtained with 18-gauge biopsy needles poorly predict Gleason scores of radical prostatectomy specimens.用18号活检针获取的前列腺活检组织的Gleason评分,对前列腺根治性切除标本的Gleason评分预测效果不佳。
Eur Urol. 1998;33(3):261-70. doi: 10.1159/000019578.
6
Routine audit of breast fine needle aspiration (FNA) cytology specimens and aspirator inadequate rates.乳腺细针穿刺(FNA)细胞学标本的常规审计及抽吸器不足率。
Cytopathology. 1997 Aug;8(4):236-47. doi: 10.1046/j.1365-2303.1997.8682086.x.
7
Diagnosis of breast cancer with core-biopsy and fine needle aspiration cytology.通过粗针活检和细针穿刺细胞学检查诊断乳腺癌。
Aust N Z J Surg. 1996 Sep;66(9):592-4. doi: 10.1111/j.1445-2197.1996.tb00825.x.
8
The role of pre-operative diagnosis in breast cancer.术前诊断在乳腺癌中的作用。
Histopathology. 1996 Jun;28(6):563-6. doi: 10.1046/j.1365-2559.1996.d01-465.x.
9
Histological precision of stereotactic core biopsy in diagnosis of malignant and premalignant breast lesions.立体定向芯针活检在乳腺良恶性病变诊断中的组织学准确性
Histopathology. 1996 Jun;28(6):537-41. doi: 10.1046/j.1365-2559.1996.d01-463.x.
10
The impact of core-biopsy on pre-operative diagnosis rate of screen detected breast cancers.粗针活检对筛查发现的乳腺癌术前诊断率的影响。
Clin Radiol. 1996 Aug;51(8):562-5. doi: 10.1016/s0009-9260(96)80136-x.

乳腺癌预后因素的术前评估。

Preoperative assessment of prognostic factors in breast cancer.

作者信息

Denley H, Pinder S E, Elston C W, Lee A H, Ellis I O

机构信息

Department of Histopathology, Nottingham City Hospital NHS Trust, Hucknall Road, Nottingham NG5 1PB, UK.

出版信息

J Clin Pathol. 2001 Jan;54(1):20-4. doi: 10.1136/jcp.54.1.20.

DOI:10.1136/jcp.54.1.20
PMID:11271783
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1731277/
Abstract

The adoption of preoperative diagnostic strategies involving fine needle aspiration cytology (FNAC) or core biopsy is well established, allowing the planning of operating lists and bed occupancy and patient involvement in therapeutic management. In addition to diagnosis, however, pathologists are increasingly being asked to provide pathological prognostic information from preoperative samples. This leader describes techniques for predicting prognosis and response to treatment on these specimens and some of the problems inherent in the determination of prognosis on small samples. For example, although histological grade can be assessed relatively reliably on either core or FNAC samples, the evaluation of tumour type (which includes an overall assessment of the architecture of a given tumour) may be less reliable on small preoperative samples. Other well recognised histological prognostic factors, such as vascular channel invasion or tumour size, cannot be determined accurately on small preoperative samples. For those patients who might benefit from neoadjuvant treatment, predicting the response to such treatments--for example, by the assessment of oestrogen receptor status--can readily be performed on either core biopsy or FNAC. In the future, other molecular markers such as C-erbB-2 might also prove beneficial in predicting response to newly developed treatments.

摘要

采用包括细针穿刺抽吸细胞学检查(FNAC)或粗针活检在内的术前诊断策略已得到广泛认可,这有助于安排手术日程、规划床位占用情况并让患者参与治疗管理。然而,除了诊断之外,病理学家越来越多地被要求从术前样本中提供病理预后信息。本社论介绍了预测这些标本预后及对治疗反应的技术,以及在小样本上确定预后所固有的一些问题。例如,虽然在粗针或FNAC样本上相对可靠地评估组织学分级,但在术前小样本上评估肿瘤类型(包括对特定肿瘤结构的全面评估)可能不太可靠。其他公认的组织学预后因素,如血管侵犯或肿瘤大小,在术前小样本上无法准确确定。对于那些可能从新辅助治疗中获益的患者,预测对这类治疗的反应——例如,通过评估雌激素受体状态——可以很容易地在粗针活检或FNAC上进行。未来,其他分子标志物,如C-erbB-2,在预测对新开发治疗的反应方面可能也会被证明是有益的。