Optimal duration of a first-line palliative chemotherapy in disseminated colorectal cancer – a review of the literature from a developing country perspective

W. Rogowski, V. Sulżyc-Bielicka
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引用次数: 6

Abstract

We still do not know whether the presently used protocol of the first-line palliative treatment of disseminated colorectal cancer (FOLFOX/FOLFIRI protocol) allows maximization of therapeutic response and minimization of side effects. No-one has verified whether continuation of the first-line chemotherapy despite the lack of progression is reflected by improved prognosis or significant risk of toxicity. This issue is of vital importance in the case of developing countries where targeted therapies are not available due to financial shortages. We have identified three potential strategies of the palliative therapy of disseminated colorectal cancer: 1) discontinuation of chemotherapy after a fixed number of cycles with its restart on progression (stop-and-go strategy), 2) intermittent protocol of chemotherapy, and 3) continuation of chemotherapy with discontinuation of the most toxic agent. None of the studies proved the superiority of the most commonly used standard, i.e. 12 cycles of the FOLFOX or FOLFIRI regimen. Although longer duration of this treatment may be associated with higher response rates and longer progression-free survival, these improvements frequently prove insignificant on statistical analysis.
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播散性结直肠癌一线姑息性化疗的最佳持续时间——从发展中国家角度的文献综述
我们仍然不知道目前使用的弥散性结直肠癌一线姑息治疗方案(FOLFOX/FOLFIRI方案)是否允许治疗反应最大化和副作用最小化。没有人证实在没有进展的情况下继续一线化疗是否反映在预后改善或明显的毒性风险上。对于发展中国家来说,这个问题至关重要,因为这些国家由于资金短缺而无法获得靶向治疗。我们已经确定了播散性结直肠癌姑息治疗的三种潜在策略:1)在固定周期后停止化疗并根据进展重新开始(走走停停策略),2)间歇化疗方案,以及3)继续化疗并停止毒性最强的药物。没有一项研究证明最常用的标准,即12个周期的FOLFOX或FOLFIRI方案的优越性。虽然较长的治疗时间可能与较高的缓解率和较长的无进展生存期相关,但这些改善在统计分析中往往被证明是微不足道的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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