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肉瘤的大小很关键!

Size matters for sarcomas!

作者信息

Grimer Robert J

机构信息

Oncology Service, Royal Orthopaedic Hospital, Birmingham, UK.

出版信息

Ann R Coll Surg Engl. 2006 Oct;88(6):519-24. doi: 10.1308/003588406X130651.

DOI:10.1308/003588406X130651
PMID:17059708
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1963770/
Abstract

INTRODUCTION

By the time of diagnosis, sarcomas have frequently reached a large size and many patients have a long history of symptoms prior to diagnosis. The aim of this study was to assess whether size of tumour at presentation or duration of symptoms was a significant factor affecting outcome.

PATIENTS AND METHODS

A prospective database recording patient, tumour, treatment and outcome factors was reviewed. A total of 1460 patients with newly diagnosed sarcomas and with > 3 years of follow-up were included for analysis.

RESULTS

The mean size of sarcomas presenting to our unit was 10.7 cm at the time of diagnosis. Bone sarcomas averaged 11.3 cm with little variation by age or diagnosis, whilst subcutaneous soft tissue sarcomas averaged 10 cm. The incidence of metastases at diagnosis increased almost linearly with increasing size and the prognosis, even for patients without metastases at diagnosis became steadily worse with increasing size for all tumours, independent of other factors. Duration of symptoms did not correlate with size but patients with symptoms > 1 year had a slightly better prognosis than those with a shorter duration.

CONCLUSIONS

The author makes a plea for greater awareness of potential malignancy in lumps and bumps, particularly those over the size of a golf ball (4.27 cm), making the point that the smaller the tumour at diagnosis the better the prognosis.

摘要

引言

在确诊时,肉瘤通常已长得很大,而且许多患者在确诊前已有很长时间的症状史。本研究的目的是评估就诊时肿瘤大小或症状持续时间是否是影响预后的重要因素。

患者与方法

回顾了一个记录患者、肿瘤、治疗及预后因素的前瞻性数据库。共纳入1460例新诊断的肉瘤患者且随访时间超过3年进行分析。

结果

我院就诊的肉瘤确诊时平均大小为10.7厘米。骨肉瘤平均为11.3厘米,在年龄或诊断方面变化不大,而皮下软组织肉瘤平均为10厘米。确诊时转移的发生率几乎随肿瘤大小增加呈线性上升,并且对于所有肿瘤而言,即使是确诊时无转移的患者,其预后也随着肿瘤大小增加而逐渐变差,与其他因素无关。症状持续时间与肿瘤大小无关,但症状持续超过1年的患者预后略好于症状持续时间较短的患者。

结论

作者呼吁对肿块尤其是那些超过高尔夫球大小(4.27厘米)的肿块可能存在的恶性肿瘤提高认识,指出确诊时肿瘤越小预后越好。

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本文引用的文献

1
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2
Testicular cancer: perils of very late presentation.睾丸癌:极晚期就诊的风险
Lancet. 2002 May 11;359(9318):1632-3. doi: 10.1016/S0140-6736(02)08544-6.
3
Risk factors for survival and local control in chondrosarcoma of bone.骨肉瘤生存及局部控制的危险因素。 (注:你提供的原文中chondrosarcoma是软骨肉瘤,不是骨肉瘤,按照正确的软骨肉瘤翻译为:骨软骨肉瘤生存及局部控制的危险因素。 )
J Bone Joint Surg Br. 2002 Jan;84(1):93-9. doi: 10.1302/0301-620x.84b1.11942.
4
Osteosarcoma of the limb. Amputation or limb salvage in patients treated by neoadjuvant chemotherapy.肢体骨肉瘤。接受新辅助化疗患者的截肢或保肢治疗
J Bone Joint Surg Br. 2002 Jan;84(1):88-92. doi: 10.1302/0301-620x.84b1.12211.
5
Prognostic factors in high-grade osteosarcoma of the extremities or trunk: an analysis of 1,702 patients treated on neoadjuvant cooperative osteosarcoma study group protocols.四肢或躯干高级别骨肉瘤的预后因素:对1702例接受新辅助治疗的骨肉瘤协作研究组方案患者的分析
J Clin Oncol. 2002 Feb 1;20(3):776-90. doi: 10.1200/JCO.2002.20.3.776.
6
Monitoring referral and treatment in soft tissue sarcoma: study based on 1,851 patients from the Scandinavian Sarcoma Group Register.软组织肉瘤转诊与治疗的监测:基于斯堪的纳维亚肉瘤研究组登记处1851例患者的研究
Acta Orthop Scand. 2001 Apr;72(2):150-9. doi: 10.1080/000164701317323408.
7
Prognostic factors in Ewing's tumor of bone: analysis of 975 patients from the European Intergroup Cooperative Ewing's Sarcoma Study Group.骨尤文肉瘤的预后因素:对欧洲多组合作尤文肉瘤研究组975例患者的分析
J Clin Oncol. 2000 Sep;18(17):3108-14. doi: 10.1200/JCO.2000.18.17.3108.
8
Delay in diagnosis of high-grade osteosarcoma of the extremities. Has it any effect on the stage of disease?四肢高级别骨肉瘤的诊断延迟。这对疾病分期有影响吗?
Tumori. 2000 May-Jun;86(3):204-6. doi: 10.1177/030089160008600305.
9
Initial symptoms and clinical features in osteosarcoma and Ewing sarcoma.骨肉瘤和尤因肉瘤的初始症状及临床特征。
J Bone Joint Surg Am. 2000 May;82(5):667-74. doi: 10.2106/00004623-200005000-00007.
10
Variable management of soft tissue sarcoma: regional audit with implications for specialist care.软组织肉瘤的可变管理:区域审计及其对专科护理的影响
Br J Surg. 1997 Dec;84(12):1692-6.