关键词: Body composition Sarcopenia Tislelizumab Toxicity Tumor response Urothelial carcinoma

Mesh : Humans Male Female Middle Aged Sarcopenia / chemically induced Cisplatin / administration & dosage adverse effects therapeutic use Leukopenia / chemically induced Deoxycytidine / analogs & derivatives administration & dosage adverse effects Gemcitabine Antineoplastic Combined Chemotherapy Protocols / adverse effects administration & dosage therapeutic use Aged Antibodies, Monoclonal, Humanized / adverse effects administration & dosage therapeutic use Retrospective Studies Carcinoma, Transitional Cell / drug therapy complications Urinary Bladder Neoplasms / drug therapy pathology complications Adult Urologic Neoplasms / drug therapy complications pathology

来  源:   DOI:10.1007/s10147-023-02448-1   PDF(Pubmed)

Abstract:
BACKGROUND: In the era of combination therapy, there has been limited research on body composition. Specific body composition, such as sarcopenia, possesses the potential to serve as a predictive biomarker for toxic effects and clinical response in patients with urothelial carcinoma (UC) undergoing tislelizumab combined with gemcitabine and cisplatin (T + GC).
METHODS: A total of 112 UC patients who received T + GC were selected at the Affiliated Hospital of Xuzhou Medical University from April 2020 to January 2023. Baseline patient characteristics and detailed hematological parameters were collected using the electronic medical system and laboratory examinations. The computed tomography images of patients were analyzed to calculate psoas muscle mass index (PMI). We evaluated the association between sarcopenia (PMI < 4.5 cm2/m2 in men; PMI < 3.3 cm2/m2 in women) and both hematological toxicity and tumor response.
RESULTS: Overall, of the 112 patients (65.2% male, median age 56 years), 43 (38.4%) were defined as sarcopenia. Patients with sarcopenia were notably older (p = 0.037), more likely to have hypertension (p = 0.009), and had poorer ECOG-PS (p = 0.027). Patients with sarcopenia were more likely to develop leukopenia (OR 2.969, 95% CI 1.028-8.575, p = 0.044) after receiving at least two cycles of T + GC. However, these significant differences were not observed in thrombocytopenia and anemia. There were no significant differences in the tumor response and grade 3-4 hematological toxicity between patients with sarcopenia and those without sarcopenia.
CONCLUSIONS: Patients with sarcopenia were more likely to develop leukopenia after receiving T + GC. There were no notable alterations observed in relation to anemia or thrombocytopenia. No significant difference was found between the sarcopenia group and non-sarcopenia group in terms of tumor response and grade 3-4 hematological toxicity.
摘要:
背景:在联合治疗时代,对身体成分的研究有限。特定的身体成分,比如肌肉减少症,在接受tislelizumab联合吉西他滨和顺铂(T+GC)治疗的尿路上皮癌(UC)患者中,具有作为毒性作用和临床反应的预测生物标志物的潜力。
方法:选择2020年4月至2023年1月在徐州医科大学附属医院接受T+GC治疗的UC患者112例。使用电子医疗系统和实验室检查收集基线患者特征和详细血液学参数。分析患者的计算机断层扫描图像以计算腰大肌质量指数(PMI)。我们评估了肌肉减少症(男性PMI<4.5cm2/m2;女性PMI<3.3cm2/m2)与血液学毒性和肿瘤反应之间的关系。
结果:总体而言,112名患者中(65.2%为男性,中位年龄56岁),43(38.4%)被定义为肌肉减少症。患有肌少症的患者明显年龄较大(p=0.037),更有可能患有高血压(p=0.009),ECOG-PS较差(p=0.027)。在接受至少两个周期的T+GC治疗后,肌肉减少症患者更容易发生白细胞减少症(OR2.969,95%CI1.028-8.575,p=0.044)。然而,在血小板减少症和贫血中未观察到这些显著差异.肌少症患者和无肌少症患者之间的肿瘤反应和3-4级血液学毒性没有显着差异。
结论:患有肌少症的患者在接受T+GC后更容易出现白细胞减少。没有观察到与贫血或血小板减少有关的显著改变。在肿瘤反应和3-4级血液学毒性方面,肌肉减少组和非肌肉减少组之间没有发现显着差异。
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