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儿童霍奇金淋巴瘤低剂量放疗和化疗后幸存者的第二恶性肿瘤。

Second malignant neoplasms in survivors of pediatric Hodgkin's lymphoma treated with low-dose radiation and chemotherapy.

机构信息

Department of Pediatric Hematology/Oncology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Ave, MLC 7015, Cincinnati, OH 45229, USA.

出版信息

J Clin Oncol. 2010 Mar 1;28(7):1232-9. doi: 10.1200/JCO.2009.24.8062. Epub 2010 Feb 1.

Abstract

PURPOSE

Survivors of childhood Hodgkin's lymphoma (HL) are at risk for second malignant neoplasms (SMNs). It is theorized that this risk may be attenuated in patients treated with lower doses of radiation. We report the first long-term outcomes of a cohort of pediatric survivors of HL treated with chemotherapy and low-dose radiation.

PATIENTS AND METHODS

Pediatric patients with HL (n = 112) treated at Stanford from 1970 to 1990 on two combined modality treatment protocols were identified. Treatment included six cycles of chemotherapy with 15 to 25.5 Gy involved-field radiation with optional 10 Gy boosts to bulky sites. Follow-up through September 1, 2007, was obtained from retrospective chart review and patient questionnaires.

RESULTS

One hundred ten children completed HL therapy; median follow-up was 20.6 years. Eighteen patients developed one or more SMNs, including four leukemias, five thyroid carcinomas, six breast carcinomas, and four sarcomas. Cumulative incidence of first SMN was 17% (95% CI, 10.5 to 26.7) at 20 years after HL diagnosis. The standard incidence ratio for any SMN was 22.9 (95% CI, 14.2 to 35) with an absolute excess risk of 93.7 cases per 10,000 person-years. All four secondary leukemias were fatal. For those with second solid tumors, the mean (+/- SE) 5-year disease-free and overall survival were 76% +/- 12% and 85% +/- 10% with median follow-up 5 years from SMN diagnosis.

CONCLUSION

Despite treatment with low-dose radiation, children treated for HL remain at significant risk for SMN. Sarcomas, breast and thyroid carcinomas occurred with similar frequency and latency as found in studies of children with HL who received high-dose radiation.

摘要

目的

儿童霍奇金淋巴瘤(HL)幸存者存在发生第二恶性肿瘤(SMN)的风险。据推测,接受低剂量辐射治疗的患者风险可能会降低。我们报告了一组接受化疗和低剂量放疗的 HL 儿科幸存者的队列的首批长期结果。

患者和方法

从 1970 年至 1990 年,在斯坦福大学,根据两种联合治疗方案,确定了 112 名患有 HL 的儿科患者。治疗包括 6 个周期的化疗,采用 15 至 25.5 Gy 的受累野放疗,对大肿块部位可选加用 10 Gy 的增量。通过回顾病历和患者问卷调查获得截至 2007 年 9 月 1 日的随访情况。

结果

110 名患儿完成 HL 治疗;中位随访时间为 20.6 年。18 名患者发生了一种或多种 SMN,包括 4 例白血病、5 例甲状腺癌、6 例乳腺癌和 4 例肉瘤。HL 诊断后 20 年,首次 SMN 的累积发生率为 17%(95%CI,10.5%至 26.7%)。任何 SMN 的标准化发病比为 22.9(95%CI,14.2%至 35%),绝对超额风险为每 10,000 人年 93.7 例。所有 4 例继发性白血病均致命。对于那些发生第二实体肿瘤的患者,无疾病和总生存的 5 年平均(+/- SE)率分别为 76% +/- 12%和 85% +/- 10%,SMN 诊断后中位随访时间为 5 年。

结论

尽管接受了低剂量放疗,接受 HL 治疗的儿童仍存在发生 SMN 的重大风险。肉瘤、乳腺癌和甲状腺癌的发生率和潜伏期与接受高剂量放疗的 HL 儿童研究中发现的相似。

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