Kamada Teppei, Ohdaira Hironori, Aida Takashi, Yamagishi Daisuke, Hashimoto Ryu, Kawashima Takeru, Takahashi Junji, Nakashima Keigo, Hata Taigo, Eto Ken, Suzuki Yutaka
Department of Surgery, International University of Health and Welfare Hospital, Nasushiobara, Japan.
Department of Pharmacy, International University of Health and Welfare Hospital, Nasushiobara, Japan.
J Anus Rectum Colon. 2024 Oct 25;8(4):383-392. doi: 10.23922/jarc.2024-052. eCollection 2024.
The prognostic significance of a high visceral fat area (VFA) in metastatic colorectal cancer (mCRC) remains unclear. We evaluated the prognostic impact of high-VFA on the long-term outcomes of patients with mCRC who underwent chemotherapy.
Ninety patients with metastatic CRC who underwent chemotherapy were included. VFA measurement was performed by pre-treatment computed tomography using image analysis system. Overall survival (OS) and progression-free survival (PFS) rates were analyzed using the Cox proportional hazards model and Kaplan-Meier curves with the log-rank test.
High-VFA was identified in 39 patients. The OS (2-year OS rates: 51.6% vs 33.3%, p=0.0023) and PFS rates (2-year PFS rates: 18.0% vs 2.7%, p=0.012) were significantly lower in the high-VFA group than in the low-VFA group. In multivariate analysis, the independent significant predictors of OS were carbohydrate antigen 19-9 (CA19-9) ≥37.0 U/mL (HR: 1.99, 95%CI [1.20-3.31], p=0.007), Glasgow prognostic score (GPS) of 1 or 2 (HR: 2.65, 95%CI [1.53-4.58], p<0.001), and high-VFA (HR: 3.09, 95%CI [1.81-5.25], p<0.001). Similarly, the independent significant predictors of PFS were CA19-9 ≥37.0 U/mL (HR: 2.02, 95%CI [1.21-3.38], p=0.007), GPS of 1 or 2 (HR: 1.87, 95%CI [1.17-2.99], p=0.008), and high-VFA (HR: 2.65, 95% CI [1.61-4.35], p<0.001).
We demonstrated that pre-treatment high-VFA and high-GPS were significantly associated with worse OS and PFS rates in patients with mCRC who underwent chemotherapy.
高内脏脂肪面积(VFA)在转移性结直肠癌(mCRC)中的预后意义尚不清楚。我们评估了高VFA对接受化疗的mCRC患者长期预后的影响。
纳入90例接受化疗的转移性结直肠癌患者。使用图像分析系统通过治疗前计算机断层扫描进行VFA测量。使用Cox比例风险模型和带有对数秩检验的Kaplan-Meier曲线分析总生存期(OS)和无进展生存期(PFS)率。
39例患者被确定为高VFA。高VFA组的OS(2年OS率:51.6%对33.3%,p = 0.0023)和PFS率(2年PFS率:18.0%对2.7%,p = 0.012)显著低于低VFA组。在多变量分析中,OS的独立显著预测因素是糖类抗原19-9(CA19-9)≥37.0 U/mL(HR:1.99,95%CI[1.20 - 3.31],p = 0.007)、格拉斯哥预后评分(GPS)为1或2(HR:2.65,95%CI[1.53 - 4.58],p<0.001)以及高VFA(HR:3.09,95%CI[1.81 - 5.25],p<0.001)。同样,PFS的独立显著预测因素是CA19-9≥37.0 U/mL(HR:2.02,95%CI[1.21 - 3.38],p = 0.007)、GPS为1或2(HR:1.87,95%CI[1.17 - 2.99],p = 0.008)以及高VFA(HR:2.65,95%CI[1.61 - 4.35],p<0.001)。
我们证明,在接受化疗的mCRC患者中,治疗前高VFA和高GPS与较差的OS和PFS率显著相关。