Adhikaree Jason, Madhusudan Srinivasan
Academic Unit of Oncology, Division of Cancer and Stem Cells, School of Medicine, Nottingham University Hospitals, University of Nottingham, Nottingham, NG51PB, UK.
Med Oncol. 2014 Jul;31(7):46. doi: 10.1007/s12032-014-0046-0. Epub 2014 Jun 10.
The clinical benefit of second-line chemotherapy in advanced biliary tract cancers is currently unknown. We investigated the role of platinum re-challenge in a selected cohort of patients who progressed after first-line gemcitabine/cisplatin (GemCis) chemotherapy. We retrospectively analysed seventy-four patients treated between January 2008 and September 2012 at Nottingham University Hospitals. Demographics, treatment data, radiological response and survival data were captured. Univariate and multivariate analysis of survival outcomes were evaluated. Platinum sensitive disease was defined as tumours that progress after 12 weeks of completion of first-line GemCis chemotherapy. Seventy-four patients (median age = 67 years) had received first-line chemotherapy (gemcitabine alone = 21/74, Gem/Cis combination = 53/74). Best response to GemCis chemotherapy was as follows; partial response (PR) (17 %), stabilisation of disease (SD) (39.6 %), disease control rate (DCR) (56.6 %) and disease progression (43.4 %). 18/74 patients received second-line chemotherapy [GemCis (12/18), 5-FU/cisplatin (4/18), gemcitabine (2/8)]. Best response to GemCis second-line chemotherapy was as follows: PR (33.3 %), SD (33.3 %) and DCR (66.6 %). The median overall survival in patients who received second-line chemotherapy was 29 months compared to 10.6 months in patients who received first-line therapy only (p = 0.00001). The data suggest that patients who progress after 12 weeks of completion of first-line therapy may remain platinum sensitive and benefit from second-line platinum re-challenge. Prospective multicentre studies are warranted to explore this possibility further.
二线化疗在晚期胆管癌中的临床获益目前尚不清楚。我们在一组一线吉西他滨/顺铂(GemCis)化疗后病情进展的特定患者队列中研究了铂类再挑战的作用。我们回顾性分析了2008年1月至2012年9月在诺丁汉大学医院接受治疗的74例患者。收集了人口统计学、治疗数据、放射学反应和生存数据。对生存结果进行了单因素和多因素分析。铂敏感疾病定义为一线GemCis化疗完成12周后病情进展的肿瘤。74例患者(中位年龄 = 67岁)接受了一线化疗(单纯吉西他滨 = 21/74,吉西他滨/顺铂联合 = 53/74)。对GemCis化疗的最佳反应如下:部分缓解(PR)(17%)、病情稳定(SD)(39.6%)、疾病控制率(DCR)(56.6%)和疾病进展(43.4%)。18/74例患者接受了二线化疗[GemCis(12/18)、5-氟尿嘧啶/顺铂(4/18)、吉西他滨(2/8)]。对GemCis二线化疗的最佳反应如下:PR(33.3%)、SD(33.3%)和DCR(66.6%)。接受二线化疗患者的中位总生存期为29个月,而仅接受一线治疗的患者为10.6个月(p = 0.00001)。数据表明,一线治疗完成12周后病情进展的患者可能仍对铂类敏感,并从二线铂类再挑战中获益。有必要进行前瞻性多中心研究以进一步探索这种可能性。