Blazevic Ilfad, Vaillant Willy, Basso Maud, Salignon Karine
Medical Oncology Department, University Cancer Institute Toulouse Oncopole, Toulouse, France.
Medical Oncology Department, Auch Hospital Center, Auch, France.
Contemp Oncol (Pozn). 2020;24(3):150-156. doi: 10.5114/wo.2020.100222. Epub 2020 Oct 30.
Combinations of 5-fluorouracil/leucovorin (5-FU/LV) with oxaliplatin (FOLFOX) or irinotecan (FOLFIRI) are part of standard treatments for metastatic colorectal cancer (mCRC). For these molecules, the impact of a low relative dose intensity (RDI) on survival is not sufficiently known in real-life.
Data were collected retrospectively from patients treated in our center for an unresectable mCRC with FOLFOX or FOLFIRI as a first-line treatment. To study the impact on progression-free survival (PFS) and overall survival (OS), patients were divided into high and low RDI according to the median RDI of 5-FU on one end, and the median RDI of oxaliplatin or irinotecan (OXA-IRI) on the other.
In our population of 75 patients, the median age was 67.1 years and 77% of patients were treated with FOLFIRI. Patients with high RDI for OXA-IRI had better PFS compared to patients with low RDI (hazard ratio [HR], 0.58; = 0.03). There was no statistically significant difference in PFS for patients with high RDI for 5-FU (HR, 0.66; = 0.09). No difference was found in overall survival according to the RDI of OXA-IRI (HR, 0.72; = 0.18) or 5-FU (HR, 0.77; = 0.29). RDI had no significant impact on toxicities.
Our analysis suggests that a low RDI of oxaliplatin and irinotecan has a negative effect on PFS. RDI had no significant effect on OS in our cohort. The clinical benefit of maintaining high RDI in these patients appears low.
5-氟尿嘧啶/亚叶酸钙(5-FU/LV)与奥沙利铂(FOLFOX)或伊立替康(FOLFIRI)联合使用是转移性结直肠癌(mCRC)标准治疗方案的一部分。对于这些药物,在实际临床中,低相对剂量强度(RDI)对生存的影响尚不明确。
回顾性收集在我们中心接受FOLFOX或FOLFIRI一线治疗不可切除mCRC患者的数据。为研究对无进展生存期(PFS)和总生存期(OS)的影响,根据一端5-FU的中位RDI以及另一端奥沙利铂或伊立替康(OXA-IRI)的中位RDI,将患者分为高RDI组和低RDI组。
在我们75例患者的队列中,中位年龄为67.1岁,77% 的患者接受FOLFIRI治疗。与低RDI的患者相比,OXA-IRI高RDI的患者PFS更好(风险比[HR]为0.58;P = 0.03)。5-FU高RDI的患者PFS无统计学显著差异(HR为0.66;P = 0.09)。根据OXA-IRI(HR为0.72;P = 0.18)或5-FU(HR为0.77;P = 0.29)的RDI在总生存期方面未发现差异。RDI对毒性无显著影响。
我们的分析表明,奥沙利铂和伊立替康的低RDI对PFS有负面影响。RDI在我们的队列中对OS无显著影响。在这些患者中维持高RDI的临床获益似乎较低。