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吉西他滨联合顺铂诱导治疗局部晚期肝门部胆管癌患者(IMPACCA):一项前瞻性注册研究。

Gemcitabine-cisplatin induction treatment in patients with locally advanced perihilar cholangiocarcinoma (IMPACCA): A prospective registration study.

作者信息

Ten Haaft Britte H E A, Sickmann Mélise M T, Nooijen Lynn E, Ali Mahsoem, Wilmink Johanna W, Klümpen Heinz-Josef, Swijnenburg Rutger-Jan, Zonderhuis Barbara M, Besselink Marc G, Kazemier Geert, Erdmann Joris I

机构信息

Amsterdam UMC, Location University of Amsterdam, Department of Surgery, Amsterdam, the Netherlands; Cancer Center Amsterdam, Amsterdam, the Netherlands.

Amsterdam UMC, Location Vrije Universiteit Amsterdam, Department of Surgery, Amsterdam, the Netherlands.

出版信息

Eur J Surg Oncol. 2025 Jun;51(6):109358. doi: 10.1016/j.ejso.2024.109358. Epub 2024 Nov 6.

Abstract

BACKGROUND

Induction treatment may be beneficial in patients with unresectable locally advanced perihilar cholangiocarcinoma (LAPCCA). Prospective studies are currently lacking. This study aimed to assess the feasibility and efficacy of gemcitabine and cisplatin as induction treatment in patients with unresectable LAPCCA.

METHODS

In this prospective single-center registration study, consecutive patients with unresectable LAPCCA who received induction treatment with gemcitabine and cisplatin in an intent to downsize the tumor to allow for resection were included. The primary outcomes were resection rate and overall survival.

RESULTS

Overall, 265 patients with perihilar cholangiocarcinoma were screened between January 2020 and June 2023, of whom 23 patients (9%) with unresectable LAPCCA met the eligibility criteria. Eight patients (35%) became eligible for resection, of whom six ultimately underwent resection (resection rate, 26% (11-42%)). Two out of 23 patients (9%) experienced adverse events grade≥3, forcing one to stop induction treatment. Compared to baseline, CA19.9 levels decreased by 42% (95 % CI, -65 to -5%; P = 0.039) and 8% (-44 to 112%; P = 0.80) at the first and second restaging, respectively. Tumor size did not significantly decrease after chemotherapy. Median overall survival was 19 months (12 to not available (NA)), with NA (19 to NA) in the resected group vs. 15 (11 to NA) in the unresected group (P=0.127). Two-year survival rates were 67% (38 to 100) and 31% (15 to 67), respectively.

CONCLUSION

Patients with LAPCCA frequently tolerate induction gemcitabine-cisplatin, leading to a 26% resection rate with an improved two-year survival rate of 67%. These findings support routine re-staging after three to six cycles of palliative treatment, and lay the groundwork for future prospective trials in this patient group.

摘要

背景

诱导治疗可能对不可切除的局部晚期肝门部胆管癌(LAPCCA)患者有益。目前缺乏前瞻性研究。本研究旨在评估吉西他滨和顺铂作为诱导治疗在不可切除的LAPCCA患者中的可行性和疗效。

方法

在这项前瞻性单中心注册研究中,纳入了连续的不可切除LAPCCA患者,这些患者接受吉西他滨和顺铂诱导治疗的目的是缩小肿瘤以便进行切除。主要结局是切除率和总生存期。

结果

总体而言,在2020年1月至2023年6月期间筛选了265例肝门部胆管癌患者,其中23例(9%)不可切除的LAPCCA患者符合纳入标准。8例(35%)患者符合切除条件,其中6例最终接受了切除(切除率为26%(11 - 42%))。23例患者中有2例(9%)发生≥3级不良事件,其中1例被迫停止诱导治疗。与基线相比,在首次和第二次重新分期时,CA19.9水平分别下降了42%(95%CI,-65至-5%;P = 0.039)和8%(-44至112%;P = 0.80)。化疗后肿瘤大小无显著减小。中位总生存期为19个月(12至不可用(NA)),切除组为NA(19至NA),未切除组为15个月(11至NA)(P = 0.127)。两年生存率分别为67%(38至100)和31%(15至67)。

结论

LAPCCA患者通常能耐受吉西他滨 - 顺铂诱导治疗,切除率为26%,两年生存率提高至67%。这些发现支持在三至六个周期的姑息治疗后进行常规重新分期,并为该患者群体未来的前瞻性试验奠定了基础。

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