Giovanni Imbimbo , Marica Pellegrini , Simone Scagnoli , Simona Pisegna , Veronica Rizzo , Carmen Gallicchio , Andrea Botticelli , Alessio Molfino
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Therefore, we evaluated in MBC treated with CDK4/6 inhibitors changes in adiposity and muscularity before and after treatment and whether the changes in these parameters were associated with toxicities, dose reduction or treatment discontinuation.</div></div><div><h3>Methods</h3><div>We considered ER+/HER2- MBC patients undergoing treatment with CDK 4/6 inhibitors, collected clinical data and registered the number and type of toxicities, dose reduction due to adverse events and the rate of discontinuation. We analyzed CT scan images before treatment (T0) and at the first follow-up visit (T1), calculating SAT, VAT, TAT (adipose tissue), SMA and SMI (skeletal muscle mass).</div></div><div><h3>Results</h3><div>70 MBC patients were enrolled. Median time of observation at T1 was 4 months (3; 12); 68 (97 %) patients experienced at least one G1-G2 adverse event, whereas 37 (53 %) at least one G3-G4. Dose reduction due to toxicity was registered in 17 patients (24 %), whereas discontinuation in 24 (34 %) patients. SMA at baseline inversely correlated with the number of adverse events (G3-G4) (r = −0.30; p = 0.039). Changes in body composition were not associated with G3-G4 toxicities. However, in patients with dose reduction, we observed overtime (T0-T1) an increase in median VAT (118 vs 135; p = 0.023) (median Delta VAT<sub>T0-T1</sub> 3.9 %). In patients not discontinuing the treatment, we observed overtime an increase in mean SMA (127 ± 23 vs 131 ± 22, p < 0.05) and median VAT (119 vs 131, p < 0.05). We observed greater reduction in median VAT (Δ%) in patients who discontinued the therapy (p < 0.05). ΔVAT (%) (reduction) was more pronounced in those patients who discontinued therapy for disease progression (p = 0.01).</div></div><div><h3>Conclusion</h3><div>Changes in muscularity and adiposity with not univocal direction were associated with toxicities, treatment discontinuation or dose reduction among patients with breast cancer treated with CDK4/6 inhibitors.</div></div>","PeriodicalId":10517,"journal":{"name":"Clinical nutrition","volume":"47 ","pages":"Pages 242-247"},"PeriodicalIF":7.4000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Association between body composition parameters and treatment-related toxicities in patients with metastatic breast cancer receiving cyclin-dependent kinase 4 and 6 inhibitors\",\"authors\":\"Giovanni Imbimbo , Marica Pellegrini , Simone Scagnoli , Simona Pisegna , Veronica Rizzo , Carmen Gallicchio , Andrea Botticelli , Alessio Molfino\",\"doi\":\"10.1016/j.clnu.2025.02.031\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background & aims</h3><div>Nowadays, limited data or no data are available on body composition changes and the development of treatment-related toxicities in metastatic breast cancer (MBC) patients treated with innovative and promising anticancer therapies, including cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors. Therefore, we evaluated in MBC treated with CDK4/6 inhibitors changes in adiposity and muscularity before and after treatment and whether the changes in these parameters were associated with toxicities, dose reduction or treatment discontinuation.</div></div><div><h3>Methods</h3><div>We considered ER+/HER2- MBC patients undergoing treatment with CDK 4/6 inhibitors, collected clinical data and registered the number and type of toxicities, dose reduction due to adverse events and the rate of discontinuation. We analyzed CT scan images before treatment (T0) and at the first follow-up visit (T1), calculating SAT, VAT, TAT (adipose tissue), SMA and SMI (skeletal muscle mass).</div></div><div><h3>Results</h3><div>70 MBC patients were enrolled. Median time of observation at T1 was 4 months (3; 12); 68 (97 %) patients experienced at least one G1-G2 adverse event, whereas 37 (53 %) at least one G3-G4. Dose reduction due to toxicity was registered in 17 patients (24 %), whereas discontinuation in 24 (34 %) patients. SMA at baseline inversely correlated with the number of adverse events (G3-G4) (r = −0.30; p = 0.039). Changes in body composition were not associated with G3-G4 toxicities. However, in patients with dose reduction, we observed overtime (T0-T1) an increase in median VAT (118 vs 135; p = 0.023) (median Delta VAT<sub>T0-T1</sub> 3.9 %). In patients not discontinuing the treatment, we observed overtime an increase in mean SMA (127 ± 23 vs 131 ± 22, p < 0.05) and median VAT (119 vs 131, p < 0.05). We observed greater reduction in median VAT (Δ%) in patients who discontinued the therapy (p < 0.05). ΔVAT (%) (reduction) was more pronounced in those patients who discontinued therapy for disease progression (p = 0.01).</div></div><div><h3>Conclusion</h3><div>Changes in muscularity and adiposity with not univocal direction were associated with toxicities, treatment discontinuation or dose reduction among patients with breast cancer treated with CDK4/6 inhibitors.</div></div>\",\"PeriodicalId\":10517,\"journal\":{\"name\":\"Clinical nutrition\",\"volume\":\"47 \",\"pages\":\"Pages 242-247\"},\"PeriodicalIF\":7.4000,\"publicationDate\":\"2025-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical nutrition\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0261561425000664\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/3/1 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"NUTRITION & DIETETICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical nutrition","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0261561425000664","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/1 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"NUTRITION & DIETETICS","Score":null,"Total":0}
引用次数: 0
摘要
背景,目前,关于转移性乳腺癌(MBC)患者接受创新和有前景的抗癌疗法(包括细胞周期蛋白依赖性激酶4和6 (CDK4/6)抑制剂)治疗的体成分变化和治疗相关毒性发展的数据有限或没有数据。因此,我们评估了接受CDK4/6抑制剂治疗的MBC患者治疗前后脂肪和肌肉的变化,以及这些参数的变化是否与毒性、剂量减少或停止治疗有关。方法选取接受cdk4 /6抑制剂治疗的ER+/HER2- MBC患者,收集临床资料,记录毒副反应的数量和类型、不良事件引起的剂量减少和停药率。我们分析治疗前(T0)和第一次随访时(T1)的CT扫描图像,计算SAT、VAT、TAT(脂肪组织)、SMA和SMI(骨骼肌质量)。结果共纳入70例MBC患者。T1时的中位观察时间为4个月(3;12);68例(97%)患者至少经历一次G1-G2不良事件,而37例(53%)患者至少经历一次G3-G4不良事件。17例(24%)患者因毒性而减少剂量,而24例(34%)患者停药。基线SMA与不良事件数量(G3-G4)负相关(r = - 0.30;p = 0.039)。体成分的变化与G3-G4毒性无关。然而,在剂量减少的患者中,我们观察到随着时间的推移(T0-T1)中位VAT增加(118 vs 135;p = 0.023)(中位δ VATT0-T1为3.9%)。在未停止治疗的患者中,我们观察到平均SMA随时间增加(127±23 vs 131±22),p <;0.05)和增值税中位数(119 vs 131, p <;0.05)。我们观察到停止治疗的患者中位VAT (Δ%)有更大的降低(p <;0.05)。ΔVAT(%)(降低)在因疾病进展而停止治疗的患者中更为明显(p = 0.01)。结论在接受CDK4/6抑制剂治疗的乳腺癌患者中,肌肉和脂肪的变化方向不明确,与毒性、停药或剂量减少有关。
Association between body composition parameters and treatment-related toxicities in patients with metastatic breast cancer receiving cyclin-dependent kinase 4 and 6 inhibitors
Background & aims
Nowadays, limited data or no data are available on body composition changes and the development of treatment-related toxicities in metastatic breast cancer (MBC) patients treated with innovative and promising anticancer therapies, including cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors. Therefore, we evaluated in MBC treated with CDK4/6 inhibitors changes in adiposity and muscularity before and after treatment and whether the changes in these parameters were associated with toxicities, dose reduction or treatment discontinuation.
Methods
We considered ER+/HER2- MBC patients undergoing treatment with CDK 4/6 inhibitors, collected clinical data and registered the number and type of toxicities, dose reduction due to adverse events and the rate of discontinuation. We analyzed CT scan images before treatment (T0) and at the first follow-up visit (T1), calculating SAT, VAT, TAT (adipose tissue), SMA and SMI (skeletal muscle mass).
Results
70 MBC patients were enrolled. Median time of observation at T1 was 4 months (3; 12); 68 (97 %) patients experienced at least one G1-G2 adverse event, whereas 37 (53 %) at least one G3-G4. Dose reduction due to toxicity was registered in 17 patients (24 %), whereas discontinuation in 24 (34 %) patients. SMA at baseline inversely correlated with the number of adverse events (G3-G4) (r = −0.30; p = 0.039). Changes in body composition were not associated with G3-G4 toxicities. However, in patients with dose reduction, we observed overtime (T0-T1) an increase in median VAT (118 vs 135; p = 0.023) (median Delta VATT0-T1 3.9 %). In patients not discontinuing the treatment, we observed overtime an increase in mean SMA (127 ± 23 vs 131 ± 22, p < 0.05) and median VAT (119 vs 131, p < 0.05). We observed greater reduction in median VAT (Δ%) in patients who discontinued the therapy (p < 0.05). ΔVAT (%) (reduction) was more pronounced in those patients who discontinued therapy for disease progression (p = 0.01).
Conclusion
Changes in muscularity and adiposity with not univocal direction were associated with toxicities, treatment discontinuation or dose reduction among patients with breast cancer treated with CDK4/6 inhibitors.
期刊介绍:
Clinical Nutrition, the official journal of ESPEN, The European Society for Clinical Nutrition and Metabolism, is an international journal providing essential scientific information on nutritional and metabolic care and the relationship between nutrition and disease both in the setting of basic science and clinical practice. Published bi-monthly, each issue combines original articles and reviews providing an invaluable reference for any specialist concerned with these fields.