首页> 美国卫生研究院文献>Case Reports in Oncology >Beneficial Treatment Management with Trifluridine/Tipiracil in a Patient with Metastatic Colorectal Cancer and Pronounced Hematological Event History during Previous Treatments
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Beneficial Treatment Management with Trifluridine/Tipiracil in a Patient with Metastatic Colorectal Cancer and Pronounced Hematological Event History during Previous Treatments

机译:转移性结直肠癌和先前治疗期间有明显血液事件史的患者以三氟吡啶/替吡拉西进行有益治疗

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摘要

Trifluridine/tipiracil (FTD/TPI) significantly improves overall survival in patients with metastatic colorectal cancer (mCRC). The most common treatment-related event (grade ≥3) was hematological toxicity. We here report long-term disease-stabilizing FTD/TPI treatment of an mCRC patient (KRAS wild-type, ECOG performance status 1 at baseline and at the end of FTD/TPI therapy) with multifocal synchronous metastases and a longstanding history of extensive hematological events during previous treatments. Finally, this 62-year-old male patient was treated for 10 months with FTD/TPI by consecutive alteration of treatment parameters: (i) initial daily dose reduction to 80 mg (72% of the recommended dose), (ii) 20 days dose delay, (iii) a second and later third dose reduction to 70 mg and 60 mg (about 64% and 55%, respectively, of the recommended dose), and (iv) 30 µg per day of granulocyte colony-stimulating factor administration first for 3 days, and later for 5 days, for each treatment cycle.
机译:Trifluridine / tipiracil(FTD / TPI)可显着提高转移性​​结直肠癌(mCRC)患者的总体生存率。最常见的治疗相关事件(≥3级)是血液学毒性。我们在此报告了具有多灶性同步转移和长期广泛血液病史的mCRC患者的长期稳定疾病的FTD / TPI治疗(KRAS野生型,基线和FTD / TPI治疗结束时ECOG表现为1)先前治疗期间发生的事件。最后,通过连续更改治疗参数,对这名62岁的男性患者进行了FTD / TPI治疗10个月:(i)初始每日剂量降低至80 mg(建议剂量的72%),(ii)20天延迟剂量;(iii)将第二和第三次剂量减至70 mg和60 mg(分别为推荐剂量的约64%和55%),以及(iv)每天服用30μg粒细胞集落刺激因子对于每个治疗周期,先进行3天,然后进行5天。

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