Dollner Ralph, Granzow Christof, Neudert Marcus, Dietz Andreas
Klinik und Poliklinik für Hals-, Nasen-, Ohrenheilkunde/Plastische Operationen der Universität Leipzig, Leipzig, Germany.
Anticancer Res. 2006 Mar-Apr;26(2B):1651-5.
Previous studies focusing on response prediction to chemotherapy by chemosensitivity testing of tumor explants has focused on the response determination of single cytostatic drugs, in contrast to the common clinical application of cytostatic drug combinations. Therefore, the present study was aimed at determining the quantitative ex vivo chemoreactivity of epithelial cells from head and neck squamous cell carcinoma (HNSCC) specimens to cytostatic drug combinations. Specimens from 12 histologically-confirmed HNSCC were investigated. According to a previously established ex vivo colony formation assay, the individual cellular chemoreactivity was determined quantitatively for combinations of 4 cytostatic drugs: cis-platinum (cis-DDP), carboplatin (CBDCA), 5-Fluorouracil (5-FU) and docetaxel (DTX). The tests were performed using drug combinations according to recent clinical therapy regimens in the treatment of solid tumors: i) cis-DDP + 5FU, ii) CBDCA + 5FU, iii) cis-DDP + DTX and iv) CBDCA + DTX. The approach provides individual drug response patterns of epithelial as well as of stromal cells. Individual, selective sensitivities were found for each drug combination tested. The stromal and epithelial chemoreactivity profiles differed in most of the specimens. Moreover, stromal cell chemoresistance dominated selective epithelial chemosensitivities in the majority of cases. The determination of the epithelial ex vivo chemoreactivity identified individual chemosensitivities which were verified by the clinical history of the patient. Therefore, the described protocol to determine the ex vivo chemoresponse of HNSCC specimens to cytostatic drug combinations may help to provide clinicaly useful information concerning the individual chemoresponse of HNSCC with regard to individualization of oncological decision making.
以往通过肿瘤外植体的化疗敏感性测试来预测化疗反应的研究主要集中在单一细胞毒性药物的反应测定上,这与细胞毒性药物联合使用的临床常见应用形成对比。因此,本研究旨在确定头颈部鳞状细胞癌(HNSCC)标本中的上皮细胞对细胞毒性药物组合的体外化学活性。对12例经组织学确诊的HNSCC标本进行了研究。根据先前建立的体外集落形成试验,对4种细胞毒性药物的组合定量测定了个体细胞化学活性:顺铂(cis-DDP)、卡铂(CBDCA)、5-氟尿嘧啶(5-FU)和多西他赛(DTX)。测试使用的药物组合依据近期实体瘤治疗的临床治疗方案:i)顺铂+5氟尿嘧啶;ii)卡铂+5氟尿嘧啶;iii)顺铂+多西他赛;iv)卡铂+多西他赛。该方法提供了上皮细胞和基质细胞的个体药物反应模式。对于每种测试的药物组合都发现了个体选择性敏感性。在大多数标本中,基质和上皮细胞的化学活性谱不同。此外,在大多数情况下,基质细胞的化学抗性主导了选择性上皮细胞的化学敏感性。上皮细胞体外化学活性的测定确定了个体化学敏感性,并通过患者的临床病史得到验证。因此,所描述的用于确定HNSCC标本对细胞毒性药物组合的体外化疗反应的方案可能有助于提供有关HNSCC个体化疗反应的临床有用信息,以实现肿瘤决策的个体化。