Dr B.R. Ambedkar Institute Rotary Cancer Hospital, All India Institute of Medical Sciences, New Delhi, India.
J Clin Oncol. 2010 Oct 20;28(30):4581-6. doi: 10.1200/JCO.2010.29.3605. Epub 2010 Sep 20.
We designed this study to evaluate efficacy of modified gemcitabine and oxaliplatin (mGEMOX) over best supportive care (BSC) or fluorouracil (FU) and folinic acid (FA) in unresectable gall bladder cancer (GBC).
Patients with unresectable GBC were enrolled for single center randomized study. Arm A, BSC; arm B, FU 425 mg/m(2) and FA 20 mg/m(2) intravenous (IV) bolus weekly for 30 weeks (FUFA); arm C, gemcitabine 900 mg/m(2) and oxaliplatin 80 mg/m(2) IV infusion on days 1 and 8 every 3 weeks for maximum of six cycles. Eighty-one patients were randomly assigned, arms A (n = 27), B (n = 28), and C (n = 26).
Complete response plus partial response in the three groups was 0 (0%), four (14.3%), and eight (30.8%) respectively (P < .001). Two patients in the mGEMOX arm and one patient in the FUFA arm underwent curative resection after chemotherapy. One patient in the mGEMOX arm had complete pathologic response. Median overall survival (OS) was 4.5, 4.6, and 9.5 months for the BSC, FUFA, and mGEMOX arms (P = .039), respectively. Progression-free survival (PFS) was 2.8, 3.5, and 8.5 months for the three groups (P < .001). There was no difference in grade 3/4 toxicities in the chemotherapy arms except transaminitis, which was more prevalent in mGEMOX arm (P = .04). Two patients in the FUFA arm and 10 patients in the mGEMOX arm had grade 3 or 4 myelosuppression. Two patients in the mGEMOX group had neutropenic fever that resolved with antibiotics.
This randomized controlled trial confirmed the efficacy of chemotherapy (mGEMOX) compared with BSC and FUFA in improving OS and PFS in unresectable GBC.
我们设计这项研究旨在评估改良吉西他滨和奥沙利铂(mGEMOX)对比最佳支持治疗(BSC)或氟尿嘧啶(FU)和亚叶酸(FA)在不可切除的胆囊癌(GBC)中的疗效。
我们招募了不可切除的 GBC 患者进行单中心随机研究。A 组为 BSC;B 组为 FU 425mg/m²静脉推注联合 FA 20mg/m²每周 30 周(FUFA);C 组为吉西他滨 900mg/m²和奥沙利铂 80mg/m²静脉输注,每 3 周一次,最多 6 个周期。81 名患者被随机分配到 A 组(n=27)、B 组(n=28)和 C 组(n=26)。
三组的完全缓解+部分缓解率分别为 0(0%)、4(14.3%)和 8(30.8%)(P<0.001)。mGEMOX 组的 2 名患者和 FUFA 组的 1 名患者在化疗后接受了根治性切除术。mGEMOX 组的 1 名患者有完全的病理缓解。BSC、FUFA 和 mGEMOX 组的中位总生存期(OS)分别为 4.5、4.6 和 9.5 个月(P=0.039)。无进展生存期(PFS)分别为 2.8、3.5 和 8.5 个月(P<0.001)。化疗组除转氨血症外,3/4 级毒性无差异,mGEMOX 组更为常见(P=0.04)。FUFA 组有 2 名患者和 mGEMOX 组有 10 名患者发生 3 或 4 级骨髓抑制。mGEMOX 组有 2 名患者出现中性粒细胞减少性发热,经抗生素治疗后缓解。
这项随机对照试验证实了化疗(mGEMOX)与 BSC 和 FUFA 相比,可改善不可切除的 GBC 患者的 OS 和 PFS。