McQuade Rachel M, Stojanovska Vanesa, Bornstein Joel C, Nurgali Kulmira
College of Health and Biomedicine, Victoria University, Melbourne. Australia.
Department of Physiology, Melbourne University, Melbourne. Australia.
Curr Med Chem. 2017;24(15):1537-1557. doi: 10.2174/0929867324666170111152436.
Colorectal cancer (CRC) is one the greatest contributors to cancer related mortality. Although 5 year survival rate for patients at the early stage of CRC (stages I and II) is above 60%, more than 50% of patients are diagnosed at or beyond stage III when distant metastasis has already occurred, in which case 5 year survival rate drops to 10%. Chemotherapeutic intervention coupled with surgery is the backbone of metastatic CRC treatment and the only means of enhanced survival. For decades following its discovery, an antimetabolite 5- fluorouracil (5-FU) was the only chemotherapeutic agent available to successfully improve 12 month survival in CRC patients. Treatment of metastatic CRC has been considered palliative for many years; aiming to increase the duration and quality of the patient's remaining life, with little hope of cure, highlighting the need for novel DNA and RNA targeted therapies in the treatment of CRC. Over the last several decades, combinations of several chemotherapeutic agents have been incorporated into routine clinical practice. Combination regimes incorporating irinotecan, a semisynthetic inhibitor of topoisomerase, oxaliplatin, a third-generation platinum compound that causes mitotic arrest via the formation of DNA adducts, and capecitabine, a 5-FU prodrug, are now all established options for use as first-line, second-line and sequential treatment of CRC. This review provides a brief overview of the evolution of CRC chemotherapy as well as new and emerging treatment options.
结直肠癌(CRC)是导致癌症相关死亡的主要原因之一。尽管CRC早期(I期和II期)患者的5年生存率超过60%,但超过50%的患者在诊断时已处于III期或更晚期,此时已发生远处转移,5年生存率降至10%。化疗联合手术是转移性CRC治疗的核心,也是提高生存率的唯一手段。在发现抗代谢物5-氟尿嘧啶(5-FU)后的几十年里,它是唯一能成功提高CRC患者12个月生存率的化疗药物。多年来,转移性CRC的治疗一直被视为姑息性治疗;旨在延长患者剩余生命的时长并提高其质量,治愈的希望渺茫,这凸显了在CRC治疗中需要新型DNA和RNA靶向疗法。在过去几十年里,几种化疗药物的联合应用已纳入常规临床实践。包含伊立替康(一种拓扑异构酶的半合成抑制剂)、奥沙利铂(一种通过形成DNA加合物导致有丝分裂停滞的第三代铂类化合物)和卡培他滨(一种5-FU前药)的联合方案,现在都是作为CRC一线、二线及序贯治疗的既定选择。本综述简要概述了CRC化疗的演变以及新出现的治疗选择。