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Supplement Material: Selective Internal Radiation Therapy with Yttrium-90 Resin Microspheres Followed by Gemcitabine plus Cisplatin for Unresectable Intrahepatic Cholangiocarcinoma: A Phase 2 Single-Arm Multicenter Clinical Trial

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DataCite Commons2023-11-09 更新2024-08-18 收录
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https://karger.figshare.com/articles/dataset/Supplement_Material_Selective_Internal_Radiation_Therapy_with_Yttrium-90_Resin_Microspheres_Followed_by_Gemcitabine_plus_Cisplatin_for_Unresectable_Intrahepatic_Cholangiocarcinoma_A_Phase_2_Single-Arm_Multicenter_Clinical_Trial/24532723
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<em><strong>Introduction:</strong></em> This investigator-initiated clinical trial aims to study the efficacy and safety of administering selective internal radiation therapy with resin yttrium-90 microspheres (SIRT) followed by standard chemotherapy in unresectable intrahepatic cholangiocarcinoma (ICC). <em><strong>Methods:</strong></em> A phase 2 single-arm multicenter study was conducted in patients with unresectable ICC (NCT02167711). SIRT was administered at dose of 120 Gy targeted at tumor followed by commencement of gemcitabine 1,000 mg/m2 and cisplatin 25 mg/m2 on days one and eight of a 21-day cycle. The primary endpoint was overall survival (OS), and the secondary endpoints include progression-free survival (PFS), response rate according to Response Evaluation Criteria in solid tumors 1.1, toxicity, and time from SIRT to commencement of chemotherapy. <em><strong>Results:</strong></em> Total 31 patients were screened and twenty-four were recruited. All patients completed SIRT and 16 of them underwent subsequent chemotherapy. The median cycle of chemotherapy was 5 (range: 1–8). The median OS was 13.6 months (95% CI: 5.4–21.6) for the intent-to-treat population. Among 16 patients undergoing chemotherapy, the median OS was 21.6 months (95% CI: 7.3–25.2) and the median PFS was 9 months (95% CI: 3.2–13.1). The response rate was 25% (95% CI: 3.8–46.2%), and the disease control rate was 75% (95% CI: 53.8–96.2%). No new safety signal was observed, with fewer than 10% of patients suffering from grade 3 or higher treatment-related adverse events. The median time from SIRT to chemotherapy was 29 (range: 7–42) days. Eight patients could not receive chemotherapy due to rapid progressive disease (<em>n</em> = 4), underlying treatment unrelated comorbidities (<em>n</em> = 2), and withdrawal of consent due to personal reasons (<em>n</em> = 2). <em><strong>Conclusions:</strong></em> Treatment of SIRT followed by standard gemcitabine and cisplatin chemotherapy is feasible and effective for unresectable ICC. Further studies are required to study the optimal sequence of SIRT and chemotherapy.
提供机构:
Karger Publishers
创建时间:
2023-11-09
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