Significance of histopathological evaluation in primary therapy for breast cancer -Recent trends in primary modality with pathological complete response (pCR) as endpoint

被引:27
作者
Kurosumi M. [1 ]
机构
[1] Department of Pathology, Saitama Cancer Center, Kitaadachi-gun, Saitama 362-0806
关键词
Breast cancer; Chemotherapy; Pathological complete response; PCR; Primary therapy;
D O I
10.1007/BF02968293
中图分类号
学科分类号
摘要
In recent years, primary therapy has been used to improve the prognosis of patients with locally advanced breast cancer and to expand the indication for breast conserving treatment for patients with a relatively early stage of breast cancer. In addition, the therapeutic efficacy of primary therapy has been evaluated on the basis of pathological findings and pathological complete response (pCR) is considered to be a main target of primary therapy. The results of NSABP protocol B-18 and B-27, and the Aberdeen trials confirmed the prognostic significance of pCR in primary therapy and indicated the significance of minute pathological assessment. However, the criteria of pathological response is not yet universal, but the evaluation of the main invasive tumor, intraductal component and the regional lymph nodes, is thought to be necessary, shown by the "Histopathological Criteria for Assessment of Therapeutic Response in Breast Cancer" compiled by the Japanese Breast Cancer Society. Among these criteria, there exist methodological variations as to the evaluation of residual disease of intraductal carcinoma, thus some controversies exist. The presence of intraductal component might be negligible with regard to prognosis, but might be an important risk factor for local recurrence after breast conserving therapy. In the future, participation by the pathologist in the field of primary therapy for breast cancer will be a matter of course in most clinical studies. © Springer, Part of Springer Science+Business Media.
引用
收藏
页码:139 / 147
页数:8
相关论文
共 32 条
[21]  
Bear G.S., Emerging role of taxanes in adjuvant and neoadjuvant therapy for breast cancer: The potential and the questions, Surg Clin North Am, 83, pp. 943-971, (2003)
[22]  
Olson J.E., Gray R., Sponzo R.W., Damsker J.I., Tormey D.C., Cummings F.J., Management of nonresectable locally advanced (Stage III) breast cancer. An ECOG trial, Breast Cancer Res Treat, 8, (1986)
[23]  
Mauriac L., Durand M., Avil A., Dilhuydy J.M., Effect of primary chemotherapy in conservative treatment of breast cancer patients with operable tumors larger than 3 cm, Ann Oncol, 2, pp. 347-354, (1991)
[24]  
Mauriac L., MacGrogan G., Avril A., Durand M., Floquet A., Debled M., Dilhuydy J.M., Bonichon F., Neoadjuvant chemotherapy for operable breast carcinoma larger than 3 cm: A unicentre randomized trial with a 124-month median follow-up, Annals of Oncology, 10, 1, pp. 47-52, (1999)
[25]  
Bear H.D., Anderson S., Brown A., Smith R., Mamounas E.P., Fisher B., Margolese R., Theoret H., Soran A., Lawrence Wickerham D., Wolmark N., The effect on tumor response of adding sequential preoperative docetaxel to preoperative doxorubicin and cyclophosphamide: Preliminary results from National Surgical Adjuvant Breast and Bowel Project Protocol B-27, Journal of Clinical Oncology, 21, 22, pp. 4165-4174, (2003)
[26]  
Heys S.D., Hutcheon A.W., Sarkar T.K., Ogston K.N., Miller I.D., Payne S., Smith I., Walker L.G., Eremin O., Neoadjuvant docetaxel in breast cancer: 3-year survival results from the Aberdeen trial, Clin Breast Cancer, 2, pp. 69-74, (2002)
[27]  
Frabzen S., Zajicek J., Aspiration biopsy in diagnosis of palpable lesions of the breast, Acta Radiol, 7, pp. 241-262, (1968)
[28]  
Smith I.C., Miller I.D., Issues involved in research into the neoadjuvant treatment of breast cancer, Anti-Cancer Drugs, 12, pp. 525-529, (2001)
[29]  
Parker S.H., Lovin J.D., Jobe W.E., Burke B.J., Hopper K.D., Yakes W.F., Nonpalpable breast lesions
[30]  
stereotactic automated large-core biopsies, Radiology, 180, pp. 403-407, (1991)