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霍奇金淋巴瘤后实体瘤风险分析。

Analysis of the risk of solid tumor following Hodgkin's disease.

作者信息

Maurizi Enrici R, Anselmo A P, Osti M F, Santoro M, Tombolini V, Mandelli F, Biagini C

机构信息

Chair of Radiation Oncology, Hospital S. Maria di Collemaggio, University of L'Aquila, Rome, Italy.

出版信息

Haematologica. 1997 Jan-Feb;82(1):57-63.

PMID:9107084
Abstract

BACKGROUND AND OBJECTIVE

This study examines the occurrence of solid tumor (ST) in relation to the different types of therapy (radiotherapy, chemotherapy and radiochemotherapy; splenectomy or splenic irradiation vs no splenectomy-no splenic irradiation) received by patients treated for Hodgkin's disease (HD).

METHODS

The study included 1,045 HD patients treated at the Department of Radiation Oncology, the Institute of Radiology and the Department of Human Biopathology, Hematology Section, University of Rome, "La Sapienza", from 1972 to 1992. For 23% of the patients the follow-up period was longer than 10 years. The average follow-up period was 72 months. For a more accurate calculation of the risk of ST occurrence, the patients were first divided into 3 subgroups according to initial treatment and then according to the total treatment they had received. Moreover, to establish a probable connection between solid tumor and splenic treatment the patients were also divided into 3 subgroups (splenectomy, splenic irradiation and no splenectomy/no splenic irradiation).

RESULTS

We recorded twenty-four cases of ST after initial treatment. Secondary solid tumor showed a cumulative risk of 0.2% and 13.4% at 5 and 20 years, respectively. After initial treatment with radiotherapy (RT) alone, the cumulative risk was 1.7% and 5.2% at 10 and 20 years, respectively; in the chemotherapy (CT) group, it was 2.4% and 18.1%; in the CT(+)RT group, it was 1.7% and 9%. No statistically significant differences were observed among the different types of treatment (splenectomy, splenic irradiation or no splenectomy/no splenic irradiation) as regards the occurrence of ST. According to multivariate analysis, the most important factor in the risk of ST was age (> 40). Relative risk was 5.2, p = 0.0001.

INTERPRETATION AND CONCLUSIONS

We conclude that an age of over 40 at diagnosis and treatment with CT alone greatly increase the risk of solid tumor occurrence.

摘要

背景与目的

本研究探讨了接受霍奇金病(HD)治疗的患者中,实体瘤(ST)的发生与不同类型治疗(放疗、化疗及放化疗;脾切除术或脾区照射与未行脾切除术及未行脾区照射)之间的关系。

方法

该研究纳入了1972年至1992年期间在罗马“La Sapienza”大学放射肿瘤学系、放射学研究所及人体生物病理学系血液科接受治疗的1045例HD患者。23%的患者随访期超过10年。平均随访期为72个月。为更准确计算ST发生风险,患者首先根据初始治疗分为3个亚组,然后根据其接受的总体治疗进一步分组。此外,为确定实体瘤与脾脏治疗之间的可能联系,患者还被分为3个亚组(脾切除术、脾区照射及未行脾切除术/未行脾区照射)。

结果

初始治疗后我们记录到24例ST病例。继发性实体瘤在5年和20年时的累积风险分别为0.2%和13.4%。仅接受放疗(RT)初始治疗后,10年和20年时的累积风险分别为1.7%和5.2%;化疗(CT)组分别为2.4%和18.1%;放化疗(CT+RT)组分别为1.7%和9%。在ST发生方面,不同类型治疗(脾切除术、脾区照射或未行脾切除术/未行脾区照射)之间未观察到统计学显著差异。根据多变量分析,ST风险中最重要的因素是年龄(>40岁)。相对风险为5.2,p = 0.0001。

解读与结论

我们得出结论,诊断时年龄超过40岁且仅接受CT治疗会大大增加实体瘤发生风险。

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