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Soft‐tissue sarcoma in adolescents and young adults compared with older adults: A report among 5000 patients from the Scandinavian Sarcoma Group Central Register

机译:青少年和年轻成人的软组织肉瘤与老年人相比:斯堪的纳维亚赛马岛集团中央登记册中的5000名患者

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Background In recent years, there has been growing awareness of the distinct characteristics of adolescents and young adults (AYA) diagnosed with cancer. Soft‐tissue sarcoma (STS) accounts for approximately 1% of all cancers diagnosed in adults and 8% of cancers diagnosed in AYA. To the best of our knowledge, only a few sarcoma registers include data regarding histological subtype, age at diagnosis, and detailed clinical information. Therefore, little is known regarding clinical presentation and outcomes in AYA diagnosed with STS. Methods Using the Scandinavian Sarcoma Group Central Register, data were obtained regarding 4977 patients who were diagnosed with STS for the period between 1986 and 2011. AYA (those aged 18‐39?years) were compared with older adults (OA; those aged 40‐80?years) with respect to clinical presentation, treatment, and outcome. Results There were 868 AYA and 4109 OA. Overall and by STS subtype, there were significant differences noted between AYA and OA with regard to presentation, treatment, and survival. The distribution of STS subtypes was different between OA and AYA (eg, OA were more likely to be diagnosed with malignant fibrous histiocytoma compared with AYA [34% vs 16%; P ??.001]). OA also were more likely to have tumors measuring ≥5?cm (68% vs 56%; P ??.001) and a higher malignancy grade (75% vs 67%; P ??.001). In the majority of STS subtypes AYA had significantly better overall survival and less disease recurrence compared with OA, but this finding was not true for those with malignant peripheral nerve sheath tumors. Conclusions There are several differences between AYA and OA with STS with regard to presentation, treatment, and survival, and such differences must be taken into consideration when designing clinical trials. Additional work also is needed to characterize the potential biological mechanisms underlying these differences.
机译:背景技术近年来,患有患有癌症的青少年和年轻成年人(AYA)的不同特征越来越意识到。软组织SARCOMA(STS)占患有成人患者的所有癌症的1%和诊断为AYA的8%的癌症。据我们所知,只有少数肉瘤寄存器包括关于组织学亚型的数据,诊断的年龄和详细的临床信息。因此,关于诊断出STS的AYA的临床介绍和结果几乎是众所周知的。方法采用斯堪的纳维亚赛马岛集团中央登记册,有关4977名诊断为1986年至2011年期间的STS患者的数据。绫(18-39岁的人)与老年人(OA; 40岁的人)进行比较80?年)关于临床介绍,治疗和结果。结果有868 AYA和4109 oA。总体而通过STS亚型,AYA和OA在介绍,治疗和生存方面有显着差异。 STS亚型的分布在OA和Aya之间不同(例如,与Aya相比,OA更可能被诊断为恶性纤维组织细胞瘤[34%Vs 16%;p≤001])。 OA还更容易具有测量≥5Ωcm的肿瘤(68%Vs 56%;p≤00.001)和更高的恶性级(75%vs 67%;p≤001)。在大多数STS亚型中,AYA与OA相比,AYA显着更好地生存和较少的疾病复发,但对于那些具有恶性周围神经鞘瘤的人来说,这种发现并不是真的。结论AYA和OA在介绍,治疗和生存方面存在若干差异,并且在设计临床试验时必须考虑这种差异。还需要额外的工作来表征这些差异的潜在生物机制。

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