首页> 外文期刊>Journal of Clinical Oncology >Chemotherapy-phased imatinib pulses improve long-term outcome of adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia: Northern Italy Leukemia Group protocol 09/00.
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Chemotherapy-phased imatinib pulses improve long-term outcome of adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia: Northern Italy Leukemia Group protocol 09/00.

机译:化学治疗阶段的伊马替尼脉冲改善了费城染色体阳性急性淋巴细胞白血病成年患者的长期预后:意大利北部白血病小组协议09/00。

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PURPOSE: Short imatinib pulses were added to chemotherapy to improve the long-term survival of adult patients with Philadelphia chromosome (Ph) -positive acute lymphoblastic leukemia (ALL), to optimize complete remission (CR) and stem-cell transplantation (SCT) rates. PATIENTS AND METHODS: Of 94 total patients (age range, 19 to 66 years), 35 represented the control cohort (ie, imatinib-negative [IM-negative] group), and 59 received imatinib 600 mg/d orally for 7 consecutive days (ie, imatinib-positive [IM-positive] group), starting from day 15 of chemotherapy course 1 and from 3 days before chemotherapy during courses 2 to 8. Patients in CR were eligible for allogeneic SCT or, alternatively, for high-dose therapy with autologous SCT followed by long-term maintenance with intermittent imatinib. RESULTS: CR and SCT rates were greater in the IM-positive group (CR: 92% v 80.5%; P = .08; allogeneic SCT: 63% v 39%; P = .041). At a median observation time of 5 years (range, 0.6 to 9.2 years), 22 patients in the IM-positive group versus five patients in the IM-negative group were alive in first CR (P = .037). Patients in the IM-positive group had significantly greater overall and disease-free survival probabilities (overall: 0.38 v 0.23; P = .009; disease free: 0.39 v 0.25; P = .044) and a lower incidence of relapse (P = .005). SCT-related mortality was 28% (ie, 15 of 54 patients), and postgraft survival probability was 0.46 overall. CONCLUSION: This imatinib-based protocol improved long-term outcome of adult patients with Ph-positive ALL. With SCT, post-transplantation mortality and relapse remain the major hindrance to additional therapeutic improvement. Additional intensification of imatinib therapy should warrant a better molecular response and clinical outcome, both in patients selected for SCT and in those unable to undergo this procedure.
机译:目的:将短的伊马替尼脉冲添加到化疗中,以改善费城染色体(Ph)阳性急性淋巴细胞白血病(ALL)的成年患者的长期存活率,以优化完全缓解(CR)和干细胞移植(SCT)率。患者与方法:在94名患者(年龄在19至66岁之间)中,有35名代表对照组(即伊马替尼阴性[IM阴性]组),还有59名连续7天口服伊马替尼600 mg / d (即伊马替尼阳性[IM阳性]组),从化疗1疗程的第15天开始,到疗程2至8的化疗前3天开始。CR患者符合异基因SCT或高剂量治疗的条件自体SCT治疗,然后长期维持间断伊马替尼治疗。结果:IM阳性组的CR和SCT发生率更高(CR:92%对80.5%; P = 0.08;同种异体SCT:63%对39%; P = .041)。中位观察时间为5年(范围为0.6到9.2年),IM阳性组中22例患者与IM阴性组中5例患者在首次CR中存活(P = .037)。 IM阳性组患者的总体生存率和无疾病生存率显着更高(总体:0.38 v 0.23; P = .009;无疾病:0.39 v 0.25; P = .044),复发率更低(P = .005)。 SCT相关的死亡率为28%(即54例患者中的15例),并且移植后的生存概率总体为0.46。结论:基于伊马替尼的方案改善了成年Ph阳性的ALL患者的长期预后。使用SCT,移植后的死亡率和复发率仍然是进一步改善治疗的主要障碍。伊马替尼治疗的进一步强化,无论对于选择进行SCT的患者还是无法进行此手术的患者,都应具有更好的分子反应和临床效果。

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