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转移性或不可切除的胆道癌的治疗进展。

Advances in the treatment of metastatic or unresectable biliary tract cancer.

机构信息

Christie Hospital/The University of Manchester, Manchester, UK.

出版信息

Ann Oncol. 2010 Oct;21 Suppl 7:vii345-8. doi: 10.1093/annonc/mdq420.

Abstract

The prognosis for advanced/inoperable biliary tract cancer is poor and the management of biliary obstruction and sepsis remains the cornerstone of best supportive care (BSC). Many phase II studies have reported some activity of chemotherapy, usually involving one or more of a fluoropyrimidine, a platinum agent and gemcitabine. No adequately powered study has shown conclusively a benefit for chemotherapy compared with BSC alone although three small randomized studies have suggested an improved survival. Results from the randomized phase III ABC-02 study demonstrated a survival advantage of cisplatin and gemcitabine doublet-chemotherapy over gemcitabine monotherapy {median survival of 11.7 compared with 8.1 months, hazard ratio (HR), 0.64 [95% confidence interval (CI) 0.52 to 0.80]; log rank P < 0.001} as well as a significantly longer progression-free survival [median 8 compared with 5 months; HR 0.63 (95% CI 0.51 to 0.77); log rank P < 0.001]. A similar magnitude of benefit was seen in Japanese patients in a second study using the same treatment regimens (the BT-22 study). Ongoing studies are underway evaluating other chemotherapy regimens in first-line although attention is turning to the addition of targeted therapies; these will be reviewed. Pivotal to success in this process is both the identification of appropriate targets across this heterogeneous group of malignancies (e.g. EGFR, VEGF, MEK inhibition, amongst others) and collaboration between investigators to deliver relevant, timely and adequately powered studies.

摘要

晚期/不可切除胆道癌的预后较差,胆道梗阻和脓毒症的治疗仍然是最佳支持治疗(BSC)的基石。许多二期研究报告了化疗的一些活性,通常涉及一种或多种氟嘧啶、铂剂和吉西他滨。尽管三项小型随机研究表明化疗与单独 BSC 相比具有生存优势,但没有一项充分有力的研究明确证明化疗优于单独 BSC。来自随机 III 期 ABC-02 研究的结果表明,顺铂和吉西他滨联合化疗与吉西他滨单药治疗相比具有生存优势(中位生存期分别为 11.7 个月和 8.1 个月,风险比(HR)为 0.64 [95%置信区间(CI)为 0.52 至 0.80];对数秩 P<0.001),无进展生存期也显著延长(中位生存期分别为 8 个月和 5 个月;HR 为 0.63 [95%CI 为 0.51 至 0.77];对数秩 P<0.001)。在第二项使用相同治疗方案的日本患者研究(BT-22 研究)中也观察到了类似的获益幅度。目前正在进行评估一线中其他化疗方案的研究,尽管注意力转向添加靶向治疗;这些将进行综述。在这一过程中取得成功的关键是在这组异质性恶性肿瘤(例如 EGFR、VEGF、MEK 抑制等)中识别出合适的靶点,并进行合作,开展相关、及时和充分有力的研究。

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