Furukawa T, Kubota T, Tanino H, Oura S, Yuasa S, Murate H, Morita K, Kozakai K, Yano T, Hoffman R M
Immunochemical Laboratory, Eiken Chemical Co., Ltd., Japan.
Anticancer Res. 2000 Sep-Oct;20(5C):3657-8.
Lymph node metastasis is often the first indication of the aggressiveness of breast cancer. Effective chemotherapy in breast cancer depends on targeting the metastatic component of the disease. In order to optimize chemotherapy in the metastatic target of breast cancer, the histoculture drug response assay (HDRA) was performed on surgical specimens of primary tumor and axillary lymph node metastasis from 30 breast cancer patients. The surgical specimens were cut into approximately 10 mg pieces, and placed onto the collagen gel sponges in the medium containing previously-determined cutoff concentrations of doxorubicin (DXR), 5-fluorouracil (5-FU), cisplatin (DDP), and mitomycin C (MMC). After incubation for 7 days, the chemosensitivity of the tumor fragments was evaluated with the 3-(4,5-dimethythiazol2yl)-2,5-diphenyl-2H tetrazolium bromide (MTT) endpoint. The lymph node metastases were more resistant than the primary tumor for DXR, 5-FU, and MMC (p < 0.05) but not for CDDP. The data suggest that both primary tumor and metastases from individual patients should be tested in the HDRA to enhance clinical efficacy of chemotherapy.
淋巴结转移通常是乳腺癌侵袭性的首个指征。乳腺癌的有效化疗取决于针对疾病的转移成分。为了优化乳腺癌转移靶点的化疗,对30例乳腺癌患者的原发性肿瘤和腋窝淋巴结转移的手术标本进行了组织培养药物反应测定(HDRA)。将手术标本切成约10毫克的小块,置于含有预先确定的阿霉素(DXR)、5-氟尿嘧啶(5-FU)、顺铂(DDP)和丝裂霉素C(MMC)临界浓度的培养基中的胶原凝胶海绵上。孵育7天后,用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基-2H四唑溴盐(MTT)终点法评估肿瘤碎片的化疗敏感性。对于DXR、5-FU和MMC,淋巴结转移比原发性肿瘤更具耐药性(p<0.05),但对顺铂不耐药。数据表明,应在HDRA中对个体患者的原发性肿瘤和转移灶进行检测,以提高化疗的临床疗效。