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对于复发性非小细胞肺癌患者,在接受多西他赛联合雷莫芦单抗治疗时,减少多西他赛剂量可避免使用培非格司亭。

Dose reduction of docetaxel avoids the usage of pegfilgrastim in docetaxel plus ramucirumab therapy for recurrent nonsmall cell lung cancer.

机构信息

Department of Respiratory Medicine, Hiroshima Prefectural Hospital, Hiroshima, Japan.

Department of Respiratory Medicine, Hiroshima General Hospital, Hiroshima, Japan.

出版信息

Cancer Rep (Hoboken). 2023 Apr;6(4):e1793. doi: 10.1002/cnr2.1793. Epub 2023 Feb 2.

Abstract

BACKGROUND

Pegfilgrastim is recommended in docetaxel plus ramucirumab (DTX + RAM) therapy for recurrent nonsmall cell lung cancer (NSCLC) because of the associated frequency of febrile neutropenia (FN). However, the FN occurs less frequently when the dose of DTX is reduced because of other adverse events, such as appetite loss and oral mucositis.

METHODS AND RESULTS

Twenty-two patients with recurrent NSCLC who received DTX + RAM therapy at the Hiroshima Prefectural Hospital. The cut-off value which is the most unlikely to cause FN without the combined use of pegfilgrastim was set using a receiver operating characteristic (ROC) curve. This was created according to the dose of DTX and the presence or absence of the onset of FN. We compared the incidence of FN when a DTX dose above and below the cut-off value was used. The ROC curve showed that 48 mg/m was the best cut-off value that predicted whether FN was likely to occur when pegfilgrastim was not used concurrently. The incidence of FN was 26.1% for DTX ≥48 mg/m and 5.1% for DTX <48 mg/m .

CONCLUSIONS

Pegfilgrastim can be discontinued when the dose of DTX is reduced to <48 mg/m due to nonhematological toxicities.

摘要

背景

培非格司亭在多西他赛联合雷莫芦单抗(DTX+RAM)治疗复发性非小细胞肺癌(NSCLC)中的推荐使用,是因为其与发热性中性粒细胞减少症(FN)的发生频率相关。然而,当由于其他不良反应(如食欲下降和口腔黏膜炎)而减少 DTX 剂量时,FN 的发生频率较低。

方法和结果

22 名在广岛县立医院接受 DTX+RAM 治疗的复发性 NSCLC 患者。使用受试者工作特征(ROC)曲线设置了最不可能在不联合使用培非格司亭的情况下引起 FN 的截止值。这是根据 DTX 剂量和 FN 发生的有无来创建的。我们比较了在使用高于和低于截止值的 DTX 剂量时 FN 的发生率。ROC 曲线显示,48mg/m 是预测在不联合使用培非格司亭时 FN 是否可能发生的最佳截止值。DTX≥48mg/m 时 FN 的发生率为 26.1%,DTX<48mg/m 时 FN 的发生率为 5.1%。

结论

当由于非血液学毒性而将 DTX 剂量减少至<48mg/m 时,可以停止使用培非格司亭。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/697f/10075288/9b2dd14e9d0b/CNR2-6-e1793-g002.jpg

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