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肢体软组织肉瘤淋巴结转移患者的可治愈性。

Curability of patients with lymph node metastases from extremity soft-tissue sarcoma.

机构信息

Musculoskeletal Oncology Unit, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.

Maisonneuve-Rosemont Hospital, Montreal, Quebec, Canada.

出版信息

Cancer. 2020 Dec 1;126(23):5098-5108. doi: 10.1002/cncr.33189. Epub 2020 Sep 10.

Abstract

BACKGROUND

Lymph node metastases (LNM) rarely occur in adult extremity soft-tissue sarcoma (STS), affecting approximately 5% of patients. To the authors' knowledge, few studies to date have evaluated the prognosis and survival of patients with LNM.

METHODS

A retrospective review was performed of a single-center, prospectively collected STS database. Demographic, treatment, and oncologic data for patients with STS of the extremity with LNM were obtained from clinical and radiographic records.

RESULTS

Of 2689 patients with extremity STS, a total of 120 patients (4.5%) were diagnosed with LNM. LNM occurred most frequently among patients diagnosed with clear cell sarcoma (27.6%), epithelioid sarcoma (21.9%), rhabdomyosarcoma (17.3%), angiosarcoma (14.0%), and extraskeletal myxoid chondrosarcoma (9.3%). A total of 98 patients (81.7%) underwent LNM surgical resection. Patients with isolated LNM had a greater 5-year overall survival (57.3%) compared with patients with American Joint Committee on Cancer (AJCC) eighth edition stage IV STS with only systemic metastases (14.6%) or both LNM and systemic disease (0%; P < .0001). Patients with isolated LNM had an overall survival rate (52.9%) similar to that of patients with localized AJCC stage III tumors (ie, large, high-grade tumors) (49.3%) (P = .8). Patients with late, isolated, metachronous LNM had a 5-year overall survival rate (61.2%) that was similar to that of patients with isolated synchronous LNM at the time of presentation (53.6%) (P = .4).

CONCLUSIONS

Many different types of STS develop LNM. Patients with extremity STS with isolated LNM should not be considered as having stage IV disease as they are according to the current AJCC eighth edition classification because they have significantly better survival than those with systemic metastases. Patients with isolated, late, metachronous LNM have a survival similar to that of patients with isolated synchronous LNM at the time of presentation.

LAY SUMMARY

The results of the current study demonstrated that patients diagnosed with isolated lymph node metastases have a prognosis similar to that of patients diagnosed with localized American Joint Committee on Cancer stage III soft-tissue sarcomas, which also equates to a significantly better overall survival compared with patients with systemic metastases. Therefore, the authors recommend modifications to the most recent eighth edition of the American Joint Committee on Cancer staging system to clearly distinguish patients with isolated lymph node metastases to acknowledge their better prognosis compared with those with systemic metastases.

摘要

背景

淋巴结转移(LNM)在成人肢体软组织肉瘤(STS)中很少发生,约占患者的 5%。据作者所知,迄今为止,很少有研究评估 LNM 患者的预后和生存情况。

方法

对单中心前瞻性收集的 STS 数据库进行回顾性分析。从临床和影像学记录中获取 LNM 患者的 STS 患者的人口统计学、治疗和肿瘤学数据。

结果

在 2689 例肢体 STS 患者中,共有 120 例(4.5%)被诊断为 LNM。LNM 最常发生于透明细胞肉瘤(27.6%)、上皮样肉瘤(21.9%)、横纹肌肉瘤(17.3%)、血管肉瘤(14.0%)和骨外黏液样软骨肉瘤(9.3%)患者中。共有 98 例(81.7%)患者接受了 LNM 手术切除。孤立性 LNM 患者的 5 年总生存率(57.3%)高于美国癌症联合委员会(AJCC)第八版分期为 IV 期且仅存在全身转移(14.6%)或同时存在 LNM 和全身疾病(0%)的患者(P<0.0001)。孤立性 LNM 患者的总生存率(52.9%)与 AJCC 局部 III 期肿瘤(即大、高级别肿瘤)患者的总生存率(49.3%)相似(P=0.8)。孤立性、晚期、异时性 LNM 患者的 5 年总生存率(61.2%)与初诊时孤立性同步 LNM 患者相似(53.6%)(P=0.4)。

结论

许多不同类型的 STS 会发生 LNM。根据当前的 AJCC 第八版分类,肢体 STS 患者伴有孤立性 LNM 不应被视为 IV 期疾病,因为他们的生存率明显高于全身转移患者。孤立性、晚期、异时性 LNM 患者的生存率与初诊时孤立性同步 LNM 患者相似。

背景

淋巴结转移(LNM)在成人肢体软组织肉瘤(STS)中很少发生,约占患者的 5%。据作者所知,迄今为止,很少有研究评估 LNM 患者的预后和生存情况。

方法

对单中心前瞻性收集的 STS 数据库进行回顾性分析。从临床和影像学记录中获取 LNM 患者的 STS 患者的人口统计学、治疗和肿瘤学数据。

结果

在 2689 例肢体 STS 患者中,共有 120 例(4.5%)被诊断为 LNM。LNM 最常发生于透明细胞肉瘤(27.6%)、上皮样肉瘤(21.9%)、横纹肌肉瘤(17.3%)、血管肉瘤(14.0%)和骨外黏液样软骨肉瘤(9.3%)患者中。共有 98 例(81.7%)患者接受了 LNM 手术切除。孤立性 LNM 患者的 5 年总生存率(57.3%)高于美国癌症联合委员会(AJCC)第八版分期为 IV 期且仅存在全身转移(14.6%)或同时存在 LNM 和全身疾病(0%)的患者(P<0.0001)。孤立性 LNM 患者的总生存率(52.9%)与 AJCC 局部 III 期肿瘤(即大、高级别肿瘤)患者的总生存率(49.3%)相似(P=0.8)。孤立性、晚期、异时性 LNM 患者的 5 年总生存率(61.2%)与初诊时孤立性同步 LNM 患者相似(53.6%)(P=0.4)。

结论

许多不同类型的 STS 会发生 LNM。根据当前的 AJCC 第八版分类,肢体 STS 患者伴有孤立性 LNM 不应被视为 IV 期疾病,因为他们的生存率明显高于全身转移患者。孤立性、晚期、异时性 LNM 患者的生存率与初诊时孤立性同步 LNM 患者相似。

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