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首页> 外文期刊>Supportive care in cancer: official journal of the Multinational Association of Supportive Care in Cancer >Single-dose palonosetron for prevention of chemotherapy-induced nausea and vomiting in patients with aggressive non-Hodgkin's lymphoma receiving moderately emetogenic chemotherapy containing steroids: results of a phase II study from the Gruppo Italiano per lo Studio dei Linfomi (GISL).
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Single-dose palonosetron for prevention of chemotherapy-induced nausea and vomiting in patients with aggressive non-Hodgkin's lymphoma receiving moderately emetogenic chemotherapy containing steroids: results of a phase II study from the Gruppo Italiano per lo Studio dei Linfomi (GISL).

机译:单剂量帕洛诺司琼用于预防中度致癌的含类固醇激素的侵袭性非霍奇金淋巴瘤患者的化疗引起的恶心和呕吐:Gruppo Italiano per lo Studio dei Linfomi(GISL)的II期研究结果。

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PURPOSE: The control of nausea and vomiting induced by chemotherapy is paramount for overall treatment success in cancer patients. Antiemetic therapy during chemotherapy in lymphoma patients generally consists of anti-serotoninergic drugs and dexamethasone. The aim of this trial was to evaluate the efficacy of a single dose of palonosetron, a second-generation serotonin type 3 (5-HT(3)) receptor antagonist, in patients with aggressive non-Hodgkin's lymphoma receiving moderately emetogenic chemotherapy (MEC) containing steroids. METHODS: Patients received a single intravenous bolus of palonosetron (0.25 mg) before administration of chemotherapy. Complete response (CR) defined as no vomiting and no rescue therapy during overall phase (0-120 h) was the primary endpoint. Complete control (CC) defined as CR and only mild nausea was a secondary endpoint. RESULTS: Eighty-six evaluable patients entered in the study. A CR was observed in 74 patients (86.0%) during the overall phase; the CR during the acute (0-24 h) and delayed (24-120 h) phases was 90.7% and 88.4%, respectively. CC was 89.5% during the acute and 84.9% during the delayed phase; the overall CC was 82.6%. CONCLUSIONS: This was the first trial, which demonstrated the efficacy of a single dose of palonosetron in control CINV in patients with aggressive non-Hodgkin's lymphoma receiving MEC regimen containing steroids.
机译:目的:控制化疗引起的恶心和呕吐对于癌症患者的整体治疗成功至关重要。淋巴瘤患者化疗期间的止吐药通常由抗5-羟色胺能药物和地塞米松组成。该试验的目的是评估单剂量帕洛诺司琼(第二代3型血清素(5-HT(3))受体拮抗剂)在接受中度致癌化疗(MEC)的侵袭性非霍奇金淋巴瘤患者中的疗效含有类固醇。方法:患者在化疗前接受了单剂量的帕洛诺司琼静脉推注(0.25 mg)。主要终点是完全缓解(CR),其定义为在整个阶段(0-120小时)内无呕吐且无急救疗法。完全对照(CC)定义为CR,只有轻度恶心是次要终点。结果:八十六名可评估的患者进入了研究。在整个阶段中,有74例患者(86.0%)观察到CR;急性期(0-24 h)和延迟期(24-120 h)的CR分别为90.7%和88.4%。急性期CC为89.5%,延迟期CC为84.9%;整体CC为82.6%。结论:这是第一项试验,证明单剂量帕洛诺司琼对接受含类固醇的MEC方案的侵袭性非霍奇金淋巴瘤患者的对照CINV有效。

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