首页> 外文期刊>Bone marrow transplantation >Pegase 03: a prospective randomized phase III trial of FEC with or without high-dose thiotepa, cyclophosphamide and autologous stem cell transplantation in first-line treatment of metastatic breast cancer.
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Pegase 03: a prospective randomized phase III trial of FEC with or without high-dose thiotepa, cyclophosphamide and autologous stem cell transplantation in first-line treatment of metastatic breast cancer.

机译:Pegase 03:FEC的前瞻性随机III期试验,有或没有高剂量的噻替帕,环磷酰胺和自体干细胞移植用于转移性乳腺癌的一线治疗。

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Pegase 03 is a multicenter prospective randomized phase III trial evaluating the impact of first-line high-dose chemotherapy (HDC) with stem cell support on overall survival (OS), disease-free survival (DFS) and response rate in 308 patients with histologically proven metastatic breast cancer responding to induction therapy. Eligible patients received four induction cycles with FEC 100 (5-fluorouracil 500 mg/m(2), epirubicin 100 mg/m(2), cyclophosphamide 500 mg/m(2)). Patients with objective response (N=179) were randomized to one cycle of HDC (cyclophosphamide 6000 mg/m(2) and thiotepa 800 mg/m(2) (CHUT)) and stem cell support (N=88), or no further treatment (N=91). All patients were observed until disease progression or death. One toxic death occurred after CHUT. Other toxicities were manageable. The response rate at 3 months was higher in the intensification arm: 82.7% (25.3% complete response (CR)) versus 59.2% (14.1% CR) (P=0.0002). Median follow-up was 48 months. Median DFS was 11 and 6.6 months in the intensification and the observation arms, respectively (P=0.0001). There was no survival difference: 33.6 versus 27.3% OS at 3 years (P=0.8) and 22.9 versus 22.3 months median time to relapse in the intensification and observation arms, respectively. In this randomized trial, HDC with CHUT improved DFS but not OS, corroborating findings from earlier trials.
机译:Pegase 03是一项多中心前瞻性随机III期临床试验,评估了采用干细胞支持的一线大剂量化疗(HDC)对308例组织学患者的总生存期(OS),无病生存期(DFS)和缓解率的影响已证实对诱导疗法有反应的转移性乳腺癌。符合条件的患者接受FEC 100(5-氟尿嘧啶500 mg / m(2),表柔比星100 mg / m(2),环磷酰胺500 mg / m(2))的四个诱导周期。有客观反应的患者(N = 179)被随机分配到一个HDC周期(环磷酰胺6000 mg / m(2)和thiotepa 800 mg / m(2)(CHUT))和干细胞支持(N = 88)进一步治疗(N = 91)。观察所有患者直至疾病进展或死亡。 CHUT后发生1例中毒死亡。其他毒性是可以控制的。强化组3个月的缓解率更高:82.7%(完全缓解(CR)为25.3%)比59.2%(完全缓解(CR)为14.1%)(P = 0.0002)。中位随访时间为48个月。强化组和观察组中位DFS分别为11个月和6.6个月(P = 0.0001)。没有生存率差异:强化组和观察组的3年生存率分别为33.6%和27.3%(P = 0.8)和22.9%和22.3个月。在这项随机试验中,采用CHUT的HDC可改善DFS,但不能改善OS,从而证实了早期试验的发现。

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