结肠癌患者术后化疗相对剂量强度与总生存率。

IF 2.7 4区 医学 Q3 ONCOLOGY Cancer Chemotherapy and Pharmacology Pub Date : 2024-09-01 Epub Date: 2024-03-23 DOI:10.1007/s00280-024-04665-5
Justin C Brown, Jeffrey A Meyerhardt, Shengping Yang, Bette J Caan
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引用次数: 0

摘要

目的量化化疗相对剂量强度(RDI)与总生存期之间的关系,可使改善化疗RDI的支持性护理干预措施估算出其潜在临床获益的程度:这项队列研究纳入了533名II-III期结肠癌患者,这些患者开始了12个周期的5-氟尿嘧啶、亮霉素和奥沙利铂(FOLFOX)化疗计划。主要暴露指标为化疗RDI。主要结果为总生存期。限制性三次样条估计了危险比(HR):化疗方案 RDI 与总生存期呈 L 型相关(线性 P = 0.006;非线性 P = 0.057);死亡风险在 85% 以上持平,但在 85% 以下呈线性增长。例如,RDI从85%降至75%与死亡风险增加有关[HR:1.20(95% CI:1.08,1.52)],而RDI从85%增至95%与死亡风险无关[HR:1.06(95% CI:0.82,1.38)]:如果化疗RDI被认为是总生存期的潜在替代指标,那么改善化疗RDI的支持治疗干预措施可能会给这一人群带来潜在的临床获益。
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Postoperative chemotherapy relative dose intensity and overall survival in patients with colon cancer.

Purpose: Quantifying the association of chemotherapy relative dose intensity (RDI) with overall survival may enable supportive care interventions that improve chemotherapy RDI to estimate their magnitude of potential clinical benefit.

Methods: This cohort study included 533 patients with stage II-III colon cancer who initiated a planned regimen of 12 cycles of 5-fluorouracil, leucovorin, and oxaliplatin (FOLFOX) chemotherapy. The primary exposure was chemotherapy RDI. The primary outcome was overall survival. Restricted cubic splines estimated hazard ratios (HR).

Results: Chemotherapy regimen RDI was associated with overall survival in an L-shaped pattern (linear P = 0.006; nonlinear P = 0.057); the risk of death was flat above 85% but increased linearly below 85%. For example, a decrease in RDI from 85 to 75% was associated with an increased risk of death [HR: 1.20 (95% CI: 1.08, 1.52)], whereas an increase in RDI from 85 to 95% was not associated with the risk of death [HR: 1.06 (95% CI: 0.82, 1.38)].

Conclusion: If chemotherapy RDI is considered a potential surrogate of overall survival, supportive care interventions that improve chemotherapy RDI might confer a potential clinical benefit in this population.

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来源期刊
CiteScore
6.10
自引率
3.30%
发文量
116
审稿时长
2.5 months
期刊介绍: Addressing a wide range of pharmacologic and oncologic concerns on both experimental and clinical levels, Cancer Chemotherapy and Pharmacology is an eminent journal in the field. The primary focus in this rapid publication medium is on new anticancer agents, their experimental screening, preclinical toxicology and pharmacology, single and combined drug administration modalities, and clinical phase I, II and III trials. It is essential reading for pharmacologists and oncologists giving results recorded in the following areas: clinical toxicology, pharmacokinetics, pharmacodynamics, drug interactions, and indications for chemotherapy in cancer treatment strategy.
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