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骨未分化多形性肉瘤的临床特征及辅助化疗对患者的影响:基于人群的队列研究。

Clinical characteristics of undifferentiated pleomorphic sarcoma of bone and the impact of adjuvant chemotherapy on the affected patients: a population-based cohort study.

机构信息

The University of Tokyo, Department of Orthopaedic Surgery, Bunkyo-ku, Tokyo, Japan.

Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital Department of Musculoskeletal Oncology, Bunkyo-ku, Tokyo, Japan.

出版信息

Jpn J Clin Oncol. 2022 May 31;52(6):589-598. doi: 10.1093/jjco/hyac017.

Abstract

BACKGROUND

Clinical characteristics of undifferentiated pleomorphic sarcoma of bone are not elucidated. Herein, we clarify its clinical features and analyze the efficacy of adjuvant chemotherapy in patients with undifferentiated pleomorphic sarcoma of bone.

METHODS

Prognostic factors and estimated disease-specific survival in 247 patients with primary undifferentiated pleomorphic sarcoma of bone were identified from a registry in Japan. The effect of adjuvant chemotherapy was evaluated in localized resectable cases, and the characteristics of the two groups treated with or without chemotherapy were adjusted using propensity score matching.

RESULTS

The 5-year disease-specific survival rates were 47.4% in the entire cohort and 56.4 and 16.9% in the M0 and M1 groups, respectively. Multivariate disease-specific survival analysis revealed that metastasis on initial presentation and age ≥ 65 years were poor prognostic factors. Overall, 132 localized and resectable primary lesions were extracted. Adjuvant chemotherapy administration was a favorable prognostic factor (hazard ratio: 0.43, P = 0.04), and it significantly prolonged disease-specific survival compared with no adjuvant chemotherapy (5-year disease-specific survival: 78.8% vs. 51.8%, P = 0.008). Adjuvant chemotherapy prolonged disease-specific survival in patients with tumor size <8 cm (5-year disease-specific survival: 100% vs. 54.6%, P = 0.02); however, its efficacy decreased in those with tumor size ≥8 cm (5-year disease-specific survival: 68.7% vs. 42%, P = 0.09). After propensity score matching, adjuvant chemotherapy was significantly associated with good disease-specific survival (P = 0.02).

CONCLUSIONS

Metastasis in the initial presentation was the poorest prognostic factor. On evaluating localized and resectable cases only, adjuvant chemotherapy significantly improved disease-specific survival, although its effect decreased in cases with large tumors.

摘要

背景

骨未分化多形性肉瘤的临床特征尚不清楚。在此,我们阐明其临床特征,并分析骨未分化多形性肉瘤患者辅助化疗的疗效。

方法

从日本的一个登记处确定了 247 例原发性骨未分化多形性肉瘤患者的预后因素和估计的疾病特异性生存率。评估了局限性可切除病例的辅助化疗效果,并使用倾向评分匹配调整了未接受化疗和接受化疗两组患者的特征。

结果

整个队列的 5 年疾病特异性生存率为 47.4%,M0 组和 M1 组分别为 56.4%和 16.9%。多变量疾病特异性生存分析显示,初诊时转移和年龄≥65 岁是不良预后因素。总体上,提取了 132 例局限性和可切除的原发性病变。辅助化疗的应用是一个有利的预后因素(危险比:0.43,P=0.04),与未接受辅助化疗相比,显著延长了疾病特异性生存(5 年疾病特异性生存率:78.8%比 51.8%,P=0.008)。辅助化疗延长了肿瘤直径<8cm 患者的疾病特异性生存(5 年疾病特异性生存率:100%比 54.6%,P=0.02);然而,在肿瘤直径≥8cm 的患者中,其疗效降低(5 年疾病特异性生存率:68.7%比 42%,P=0.09)。经过倾向评分匹配后,辅助化疗与良好的疾病特异性生存显著相关(P=0.02)。

结论

初诊时转移是最差的预后因素。仅评估局限性可切除病例时,辅助化疗显著提高了疾病特异性生存率,尽管在肿瘤较大的病例中其效果降低。

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