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儿童骨肉瘤幸存者 20 年随访:来自儿童癌症幸存者研究的报告。

Twenty years of follow-up of survivors of childhood osteosarcoma: a report from the Childhood Cancer Survivor Study.

机构信息

Division of Hematology/Oncology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA.

出版信息

Cancer. 2011 Feb 1;117(3):625-34. doi: 10.1002/cncr.25446. Epub 2010 Oct 4.

Abstract

BACKGROUND

Osteosarcoma survivors have received significant chemotherapy and have undergone substantial surgeries. Their very long-term outcomes (20 year) are reported here.

METHODS

The authors assessed the long-term outcomes of 733 5-year survivors of childhood osteosarcoma diagnosed from 1970 to 1986 to provide a comprehensive evaluation of medical and psychosocial outcomes for survivors enrolled in the Childhood Cancer Survivor Study (CCSS). Outcomes evaluated included overall survival, second malignant neoplasms (SMNs), recurrent osteosarcoma, chronic health conditions, health status (general and mental health and functional limitations), and psychosocial factors. Outcomes of osteosarcoma survivors were compared with general-population statistics, other CCSS survivors, and CCSS siblings.

RESULTS

Survivors had a mean follow-up of 21.6 years. The overall survival of children diagnosed with osteosarcoma who survived 5 years at 20 years from original diagnosis was 88.6% (95% confidence interval [CI], 86.6%-90.5%). The cumulative incidence of SMNs at 25 years was 5.4%, with a standardized incidence ratio of 4.79 (95% CI, 3.54-6.33; P<.01). Overall, 86.9% of osteosarcoma survivors experienced at least 1 chronic medical condition, and >50% experienced ≥2 conditions. Compared with survivors of other cancers, osteosarcoma survivors did not differ in their reported general health status (odds ratio [OR], 0.9; 95% CI, 0.7-1.2), but were more likely to report an adverse health status in at least 1 domain (OR, 1.9; 95% CI, 1.6-2.2), with activity limitations (29.1%) being the most common.

CONCLUSIONS

Childhood osteosarcoma survivors in this cohort did relatively well, considering their extensive treatment, but are at risk of experiencing chronic medical conditions and adverse health status. Survivors warrant life-long follow-up.

摘要

背景

骨肉瘤幸存者接受了大量的化疗,并经历了大量的手术。本研究报告了他们的非常长期(20 年)结果。

方法

作者评估了 1970 年至 1986 年期间诊断为儿童骨肉瘤的 733 名 5 年幸存者的长期结果,为参加儿童癌症幸存者研究(CCSS)的幸存者提供了对医疗和社会心理结果的全面评估。评估的结果包括总生存率、第二恶性肿瘤(SMN)、复发性骨肉瘤、慢性健康状况、健康状况(一般和心理健康以及功能限制)和社会心理因素。将骨肉瘤幸存者的结果与一般人群统计数据、其他 CCSS 幸存者和 CCSS 兄弟姐妹进行比较。

结果

幸存者的平均随访时间为 21.6 年。在原始诊断后 20 年,诊断为骨肉瘤且存活 5 年的儿童的总生存率为 88.6%(95%置信区间[CI],86.6%-90.5%)。25 年时 SMN 的累积发生率为 5.4%,标准化发病率比为 4.79(95%CI,3.54-6.33;P<.01)。总体而言,86.9%的骨肉瘤幸存者至少患有 1 种慢性疾病,超过 50%的幸存者患有≥2 种疾病。与其他癌症幸存者相比,骨肉瘤幸存者在一般健康状况报告方面没有差异(比值比[OR],0.9;95%CI,0.7-1.2),但在至少 1 个领域更有可能报告不良健康状况(OR,1.9;95%CI,1.6-2.2),活动受限(29.1%)是最常见的。

结论

在本队列中,这些儿童骨肉瘤幸存者的治疗效果相当好,考虑到他们广泛的治疗,但存在患有慢性疾病和不良健康状况的风险。幸存者需要终身随访。

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