Dipartimento di Scienze Cliniche e Biologiche, Università di Torino, Turin, Italy.
Horm Cancer. 2011 Dec;2(6):378-84. doi: 10.1007/s12672-011-0087-1.
Metronomic chemotherapy is the administration of cytotoxic drugs at low doses, on a frequent or continuous schedule, with no extended interruption. This treatment approach can target tumor cells indirectly since it can affect the endothelium of the growing tumor vasculature and stimulates the anticancer immune response. Both the antiangiogenetic and the immunomodulatory roles of metronomic chemotherapy favor a tumor dormancy, a condition that may improve the patient outcome. Prospective clinical trials conducted in several malignancies have shown that metronomic chemotherapy can obtain disease stabilization or responses in tumors that had been made resistant in vivo to conventional chemotherapeutic regimens. Three prospective phase II trials have been conducted in patients with adrenocortical carcinoma (ACC). In all of them, patients heavily pretreated with conventional chemotherapy and mitotane have been enrolled. One trial tested the activity of the association of gemcitabine and fluoropyrimidines administered on a metronomic schedule. In this trial, 40% of patients attained a disease stabilization or disease response that was long lasting in some of them. In the remaining two trials, metronomic chemotherapy was administered in association with antiangiogenetic drugs, and the results were disappointing since no response or stable disease was obtained. In conclusion, metronomic chemotherapy can delay tumor progression in advanced ACC and deserves to be further tested. The concomitant administration of antiangiogenetic drugs may be detrimental. Several important questions remain to be addressed such as the optimal dose and most effective dosing interval, when to use the metronomic approach in the natural history of the disease, the choice of cytotoxic drugs, and the most efficacious way to integrate metronomic chemotherapy with standard therapy protocols.
节拍化疗是指以低剂量、频繁或连续的方案给予细胞毒性药物,且没有延长的中断。这种治疗方法可以间接靶向肿瘤细胞,因为它可以影响生长中的肿瘤血管内皮,并刺激抗肿瘤免疫反应。节拍化疗的抗血管生成和免疫调节作用都有利于肿瘤休眠,这种情况可能改善患者的预后。在几种恶性肿瘤中进行的前瞻性临床试验表明,节拍化疗可以使体内对常规化疗方案产生耐药的肿瘤获得疾病稳定或缓解。已经在肾上腺皮质癌 (ACC) 患者中进行了三项前瞻性 II 期试验。在所有这些试验中,均招募了经过常规化疗和米托坦大量预处理的患者。一项试验测试了吉西他滨和氟嘧啶类药物联合节拍化疗的活性。在该试验中,40%的患者获得了疾病稳定或持久缓解。在其余两项试验中,节拍化疗与抗血管生成药物联合应用,但结果令人失望,因为没有获得缓解或疾病稳定。总之,节拍化疗可以延缓晚期 ACC 的肿瘤进展,值得进一步研究。同时给予抗血管生成药物可能有害。仍有几个重要问题需要解决,例如最佳剂量和最有效的给药间隔、节拍化疗在疾病自然史中的应用时机、细胞毒性药物的选择以及将节拍化疗与标准治疗方案最有效地整合的方法。