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帕洛诺司琼单药预防含类固醇中度致吐性化疗方案治疗侵袭性非霍奇金淋巴瘤患者化疗所致恶心呕吐的Ⅱ期临床研究:来自意大利淋巴瘤研究组(GISL)的研究结果。

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).

机构信息

UO di Ematologia e Trapianto di Cellule Staminali, Ospedale Vito Fazzi, Piazza Filippo Muratore, 73100 Lecce, Italy.

出版信息

Support Care Cancer. 2011 Oct;19(10):1505-10. doi: 10.1007/s00520-010-0974-y. Epub 2010 Aug 8.

Abstract

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.

摘要

目的

控制癌症患者化疗引起的恶心和呕吐对于整体治疗成功至关重要。淋巴瘤患者化疗期间的止吐治疗通常包括抗血清素药物和地塞米松。本试验的目的是评估帕洛诺司琼单次剂量在接受含类固醇中度致吐化疗(MEC)的侵袭性非霍奇金淋巴瘤患者中的疗效。

方法

患者在接受化疗前接受帕洛诺司琼(0.25 毫克)单次静脉推注。完全缓解(CR)定义为整个阶段(0-120 小时)无呕吐且无解救治疗,为主要终点。完全控制(CC)定义为 CR 且仅有轻度恶心,为次要终点。

结果

86 例可评估患者入组本研究。在整个阶段,74 例患者(86.0%)观察到 CR;急性(0-24 小时)和延迟(24-120 小时)阶段的 CR 分别为 90.7%和 88.4%。急性和延迟阶段的 CC 分别为 89.5%和 84.9%;总体 CC 为 82.6%。

结论

这是第一项证明在接受含类固醇 MEC 方案治疗的侵袭性非霍奇金淋巴瘤患者中,单次给予帕洛诺司琼可有效控制 CINV 的试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/347e/3166604/8c84eba7a984/520_2010_974_Fig1_HTML.jpg

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