腰高比与肺腺癌患者术后化疗粒细胞减少的相关性研究
Study on the Correlation between Waist-to-Height Ratio and Neutropenia after Chemotherapy in Patients with Lung Adenocarcinoma
DOI: 10.12677/acm.2026.1682941, PDF,   
作者: 刘 佳:咸宁市中心医院肿瘤科,湖北 咸宁
关键词: 腰高比;肺癌;顺铂;培美曲塞;粒细胞减少;Waist-to-Height Ratio; Lung Cancer; Cisplatin; Pemetrexed; Neutropenia
摘要: 目的:探讨腰高比(waist-to-height ratio, WHtR)与肺腺癌患者术后接受顺铂 + 培美曲塞方案辅助化疗所致粒细胞减少的相关性。方法:回顾性连续纳入300例肺腺癌术后接受顺铂 + 培美曲塞方案辅助化疗的腺癌患者(IIA~IIIB期)。测量化疗前身高、体重、腰围,并计算腰高比(WHtR)、BMI等。依据WHtR是否≥0.5将患者分为高WHtR组和低WHtR组。主要结局指标为化疗期间≥3级粒细胞减少的发生率。使用Log-rank检验进行组间比较,Kaplan-Meier法绘制粒细胞减少的累积发生率曲线,采用多因素COX回归模型分析WHtR与粒细胞减少的独立关联。结果:300例患者中,共72例(24.0%)发生粒细胞减少。低WHtR组粒细胞减少发生率为34.8%,高WHtR组为11.5%,差异有统计学意义。多因素COX回归显示,WHtR是粒细胞减少的独立保护因素(作为连续变量时:HR < 0.001,95% CI: 0.000~0.001,P < 0.001;作为二分类变量时:HR = 0.279,95% CI: 0.160~0.486,P < 0.001)。结论:WHtR与肺腺癌患者术后顺铂 + 培美曲塞化疗所致粒细胞减少相关,WHtR作为一种简便、无创的人体测量指标,可成为化疗前的风险评估工具。
Abstract: Objective: To investigate the correlation between waist-to-height ratio (WHtR) and granulocytopenia induced by cisplatin plus pemetrexed adjuvant chemotherapy in patients with lung adenocarcinoma postoperatively. Method: A retrospective study consecutively enrolled 300 patients with lung adenocarcinoma (stages IA-IB) who received adjuvant chemotherapy with cisplatin plus pemetrexed postoperatively. Pre-treatment measurements of height, weight, and waist circumference were recorded, and parameters such as waist-to-height ratio (WHtR) and body mass index (BMI) were calculated. Patients were classified into a high WHtR group and a low WHtR group based on whether their WHtR was ≥0.5. The primary outcome measure was the incidence of grade ≥3 granulocytopenia during chemotherapy. Intergroup comparisons were performed using the Log-rank test; cumulative incidence curves for granulocytopenia were plotted using the Kaplan-Meier method; and a multivariate Cox regression model was employed to analyze the independent association between WHtR and granulocytopenia. Results: Among the 300 patients, granulocytopenia occurred in 72 cases (24.0%). The incidence of granulocytopenia was 34.8% in the low WHtR group and 11.5% in the high WHtR group, with a statistically significant difference. Multivariate COX regression analysis demonstrated that WHtR was an independent protective factor for granulocytopenia (as a continuous variable: HR < 0.001, 95% CI: 0.000~0.001, P < 0.001; as a binary variable: HR = 0.279, 95% CI: 0.160~0.486, P <0.001). Conclusion: WHtR exhibits a significant negative correlation with neutropenia induced by cisplatin plus pemetrexed chemotherapy in lung adenocarcinoma patients postoperatively. As a simple and non-invasive anthropometric parameter, WHtR can serve as a risk assessment tool prior to chemotherapy.
文章引用:刘佳. 腰高比与肺腺癌患者术后化疗粒细胞减少的相关性研究[J]. 临床医学进展, 2026, 16(8): 1617-1623. https://doi.org/10.12677/acm.2026.1682941

参考文献

[1] Sung, H., Ferlay, J., Siegel, R.L., Laversanne, M., Soerjomataram, I., Jemal, A., et al. (2021) Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA: A Cancer Journal for Clinicians, 71, 209-249.
https://doi.org/10.3322/caac.21660
[2] National Comprehensive Cancer Network (2025) NCCN Clinical Practice Guidelines in Oncology: Non-Small Cell Lung Cancer (Version 5.2024).
[3] Scagliotti, G.V., Parikh, P., von Pawel, J., Biesma, B., Vansteenkiste, J., Manegold, C., et al. (2008) Phase III Study Comparing Cisplatin Plus Gemcitabine with Cisplatin Plus Pemetrexed in Chemotherapy-Naive Patients with Advanced-Stage Non-Small-Cell Lung Cancer. Journal of Clinical Oncology, 26, 3543-3551.
https://doi.org/10.1200/jco.2007.15.0375
[4] Lyman, G.H., Michels, S.L., Reynolds, M.W., Barron, R., Tomic, K.S. and Yu, J. (2010) Risk of Mortality in Patients with Cancer Who Experience Febrile Neutropenia. Cancer, 116, 5555-5563.
https://doi.org/10.1002/cncr.25332
[5] Lyman, G.H., Abella, E. and Pettengell, R. (2014) Risk Factors for Febrile Neutropenia among Patients with Cancer Receiving Chemotherapy: A Systematic Review. Critical Reviews in Oncology/Hematology, 90, 190-199.
https://doi.org/10.1016/j.critrevonc.2013.12.006
[6] de Jong, C., Chargi, N., Herder, G.J.M., van Haarlem, S.W.A., van der Meer, F., van Lindert, A.S.R., et al. (2022) The Association between Skeletal Muscle Measures and Chemotherapy‐Induced Toxicity in Non‐Small Cell Lung Cancer Patients. Journal of Cachexia, Sarcopenia and Muscle, 13, 1554-1564.
https://doi.org/10.1002/jcsm.12967
[7] Ashwell, M. and Gibson, S. (2016) Waist-to-Height Ratio as an Indicator of ‘Early Health Risk’: Simpler and More Predictive than Using a ‘Matrix’ Based on BMI and Waist Circumference. BMJ Open, 6, e010159.
https://doi.org/10.1136/bmjopen-2015-010159
[8] Zhang, C., Rexrode, K.M., van Dam, R.M., Li, T.Y. and Hu, F.B. (2008) Abdominal Obesity and the Risk of All-Cause, Cardiovascular, and Cancer Mortality: Sixteen Years of Follow-Up in US Women. Circulation, 117, 1658-1667.
https://doi.org/10.1161/circulationaha.107.739714
[9] Sparreboom, A., Wolff, A.C., Mathijssen, R.H.J., Chatelut, E., Rowinsky, E.K., Verweij, J., et al. (2007) Evaluation of Alternate Size Descriptors for Dose Calculation of Anticancer Drugs in the Obese. Journal of Clinical Oncology, 25, 4707-4713.
https://doi.org/10.1200/jco.2007.11.2938
[10] Browning, L.M., Hsieh, S.D. and Ashwell, M. (2010) A Systematic Review of Waist-to-Height Ratio as a Screening Tool for the Prediction of Cardiovascular Disease and Diabetes: 0·5 Could Be a Suitable Global Boundary Value. Nutrition Research Reviews, 23, 247-269.
https://doi.org/10.1017/s0954422410000144
[11] Lennon, H., Sperrin, M., Badrick, E. and Renehan, A.G. (2016) The Obesity Paradox in Cancer: A Review. Current Oncology Reports, 18, Article No. 56.
https://doi.org/10.1007/s11912-016-0539-4
[12] Di Leone, A., Filippone, A., Maggiore, C., Rossi, M.M., Rossi, C., Di Micco, A., et al. (2024) The Role of Body Composition in Neurological and Hematologic Toxicity in a Retrospective Analysis of 120 Breast Cancer Patients Undergoing Neoadjuvant Chemotherapy: The COMBOTOX Study. Breast Cancer Research and Treatment, 210, 205-213.
https://doi.org/10.1007/s10549-024-07553-x
[13] Lyv, J., Shi, Y., Liu, Z., et al. (2025) Sarcopenia, Elevated Body Mass Index, and Platinum-Associated Adverse Events in Patients with Lung Cancer. Journal of the National Comprehensive Cancer Network, 23, 407-414.
[14] Kershaw, E.E. and Flier, J.S. (2004) Adipose Tissue as an Endocrine Organ. The Journal of Clinical Endocrinology & Metabolism, 89, 2548-2556.
https://doi.org/10.1210/jc.2004-0395