Sparano J A
Department of Breast Medical Oncology, Albert Einstein Cancer Center, Montefiore Medical Center, Bronx, NY 10467, USA.
Semin Oncol. 1998 Dec;25(6 Suppl 13):10-5.
Doxorubicin and docetaxel (Taxotere; Rhône-Poulenc Rorer, Antony, France) are the most active cytotoxic agents in the treatment of advanced breast cancer. In the pre-taxane era, randomized trials demonstrated that doxorubicin-containing chemotherapy regimens are associated with higher response rates and improved survival compared with non-doxorubicin-containing regimens. Doxorubicin-containing regimens were therefore considered the standard of care at that time. Because of the substantial activity of the taxanes in anthracyline-resistant breast cancer, there is a clear rationale for combining doxorubicin with the taxanes as initial therapy for patients with metastatic disease. The combination of doxorubicin plus paclitaxel has been extensively studied. Impressive response rates were noted in at least two studies, although the treatment also resulted in an unacceptably high risk of congestive heart failure. Paclitaxel is known to perturb the metabolism of doxorubicin, thereby increasing drug exposure and augmenting the cardiotoxicity of the anthracycline. The cardiotoxicity of the combination may be ameliorated by restricting the cumulative doxorubicin dose to less than 360 mg/m2, by increasing the interval between administration of the two drugs to at least 4 hours, or by adding the cardioprotective agent dexrazoxane. The Eastern Cooperative Oncology Group performed a randomized phase III trial comparing doxorubicin alone, paclitaxel alone, or the doxorubicin/paclitaxel combination in patients with metastatic breast cancer. Although the response rate and time to treatment failure improved with the combination, survival did not. There have been two phase II trials investigating the combination of doxorubicin plus docetaxel. The regimen was highly effective and did not seem to be associated with an increased risk of congestive heart failure. These findings justify further evaluation of the doxorubicin/docetaxel combination in patients with advanced and operable breast cancer. Such trials are currently in progress and will define the role for this combination in the management of patients with breast cancer.
多柔比星和多西他赛(泰索帝;法国罗纳普朗克乐安公司,安东尼)是治疗晚期乳腺癌最有效的细胞毒性药物。在紫杉烷类药物出现之前的时代,随机试验表明,与不含多柔比星的化疗方案相比,含多柔比星的化疗方案具有更高的缓解率和更长的生存期。因此,含多柔比星的方案在当时被视为标准治疗方案。由于紫杉烷类药物在蒽环类耐药乳腺癌中具有显著活性,将多柔比星与紫杉烷类药物联合作为转移性疾病患者的初始治疗方案有明确的理论依据。多柔比星加紫杉醇的联合方案已得到广泛研究。至少两项研究中观察到了令人印象深刻的缓解率,尽管该治疗也导致了不可接受的高充血性心力衰竭风险。已知紫杉醇会干扰多柔比星的代谢,从而增加药物暴露并增强蒽环类药物的心脏毒性。通过将多柔比星的累积剂量限制在360mg/m2以下、将两种药物的给药间隔增加到至少4小时或添加心脏保护剂右丙亚胺,可能会减轻联合用药的心脏毒性。东部肿瘤协作组进行了一项随机III期试验,比较了转移性乳腺癌患者单独使用多柔比星、单独使用紫杉醇或多柔比星/紫杉醇联合方案的疗效。尽管联合方案提高了缓解率和治疗失败时间,但生存期并未改善。有两项II期试验研究了多柔比星加多西他赛的联合方案。该方案非常有效,且似乎与充血性心力衰竭风险增加无关。这些发现为进一步评估多柔比星/多西他赛联合方案治疗晚期可手术乳腺癌患者提供了依据。此类试验目前正在进行,将确定该联合方案在乳腺癌患者管理中的作用。