胃肠道恶性肿瘤化疗患者当日给药Pegfilgrastim的安全性和有效性。

Cancer medicine journal Pub Date : 2021-04-01 Epub Date: 2020-05-18
Robert M Matera, Valerie Relias, Muhammad Wasif Saif
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引用次数: 0

摘要

背景:Pegfilgrastim通常在化疗后24小时给药;然而,由于工作或交通原因,一些患者不能或不愿意再来进行额外的检查,特别是在输注5-FU的情况下。当天给药消除了额外访问的需要。其他肿瘤类型的先前研究结果不确定,因为很少支持当天给药,而其他研究则表现出自卑。本研究的目的是确定胃肠道(GI)恶性肿瘤患者在化疗当日给予聚非格拉西汀的安全性和有效性。方法:对2014年1月至2017年1月69例胃肠道恶性肿瘤患者进行单机构回顾性分析,这些患者在化疗完成后1小时内接受化疗和当日pegfilgrastim (6mg)。根据机构指南,患者在给药前被告知当日服用pegfilgrastim的风险。将这些患者与70名在完成胃肠道肿瘤化疗后24小时接受pegfilgrastim治疗的患者进行比较。结果:共分析69例患者536个化疗周期。所有周期的绝对中性粒细胞计数中位数最低点为4538/uL(范围:1160 - 25168)。536个周期中有6个(1%)出现1级和2级中性粒细胞减少症。3例(4%)患者出现骨痛。无3级或4级中性粒细胞减少或发热性中性粒细胞减少发作。没有人因中性粒细胞减少而减少剂量、化疗延迟、住院或使用抗生素。结论:我们相信我们的研究是第一个在胃肠道恶性肿瘤中报告当天给药pegfilgrastim可能与第二天给药一样有效和安全,使患者受益并可能降低成本的研究。
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Safety and Efficacy of Same-Day Administration of Pegfilgrastim in Patients Receiving Chemotherapy for Gastrointestinal Malignancies.

Background: Pegfilgrastim is typically administered 24 hours after chemotherapy per package insert; however some patients are unable or unwilling to return for this additional visit due to work or transportation especially with regimens consisting of infusional 5-FU. Same-day dosing eliminates need for this additional visit. Results from prior studies in other tumor types are inconclusive as few support same-day dosing whereas others show inferiority. Purpose of our study was to determine safety and efficacy of administering pegfilgrastim on same day as chemotherapy in patients with gastrointestinal (GI) malignancies.

Method: A single-institution retrospective review was conducted of 69 patients with GI malignancies who received chemotherapy and same-day pegfilgrastim (6 mg) within 1 hour of completion of chemotherapy from Jan 2014 through Jan 2017. As per institutional guidelines, patients were counseled on risks of same-day pegfilgrastim prior to its administration. These patients were compared with a set of 70 patients who received pegfilgrastim 24-hours after completing the chemotherapy for GI cancers.

Result: A total of 536 chemotherapy cycles in 69 patients were analyzed. Median absolute neutrophil count nadir for all cycles was 4538/uL (Range: 1160 - 25168). Grade 1 and 2 neutropenia developed in 6 of 536 (1%) cycles. Bone pain reported in 3 patients (4%). There were no episodes of grade 3 or 4 neutropenia or febrile neutropenia. None had dose reductions, chemotherapy delays, hospitalizations, or antibiotic use due to neutropenia.

Conclusion: We believe our study is the first in GI malignancies to report that same-day pegfilgrastim administration may be as effective and safe as next-day administration, benefiting patients and might reduce costs.

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