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慢性淋巴细胞白血病患者的二次癌症

Second cancers in patients with chronic lymphocytic leukemia.

作者信息

Travis L B, Curtis R E, Hankey B F, Fraumeni J F

机构信息

Epidemiology and Biostatistics Program, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.

出版信息

J Natl Cancer Inst. 1992 Sep 16;84(18):1422-7. doi: 10.1093/jnci/84.18.1422.

Abstract

BACKGROUND

Reports to date have provided widely divergent estimates of the risk of second malignant neoplasms in patients with chronic lymphocytic leukemia (CLL), ranging from cancer deficits to excesses of twofold to threefold.

PURPOSE

Our purpose was to estimate the risk of second primary cancers following CLL, utilizing population-based tumor registries, and to determine whether site-specific excesses might be associated with type of initial treatment for CLL.

METHODS

We analyzed data for 9456 patients diagnosed with CLL as a first primary cancer between 1973 and 1988, who were reported to one of nine tumor registries participating in the National Cancer Institute's Surveillance, Epidemiology, and End Results (SEER) Program and who survived 2 or more months. SEER files were searched for invasive primary malignancies that developed at least 2 months after the initial CLL diagnosis.

RESULTS

Compared with the general population, CLL patients demonstrated a significantly increased risk of developing all second cancers (840 observed; observed-to-expected ratio [O/E] = 1.28; 95% confidence interval [CI] = 1.19-1.37). Significant excesses were noted for cancers of the lung (O/E = 1.90), brain (O/E = 1.98), and eye (intraocular melanoma) (O/E = 3.97) as well as malignant melanoma (O/E = 2.79) and Hodgkin's disease (O/E = 7.69). Cancer risk, which did not vary according to initial treatment category, was also constant across all time intervals after CLL diagnosis.

CONCLUSION

CLL patients are at a significantly increased risk of developing a second malignant neoplasm. The pattern of cancer excesses suggests a susceptibility state permitting the development of selected second malignancies in patients with CLL, perhaps because of shared etiologic factors, immunologic impairment, and/or other influences. Although our results do not suggest a strong treatment effect, more detailed studies of second tumors in CLL are needed to investigate the role of radiation therapy and chemotherapy.

摘要

背景

迄今为止的报告对慢性淋巴细胞白血病(CLL)患者发生第二原发性恶性肿瘤的风险给出了差异很大的估计,范围从癌症发生率不足到高出两到三倍。

目的

我们的目的是利用基于人群的肿瘤登记处来估计CLL后发生第二原发性癌症的风险,并确定特定部位的发生率过高是否可能与CLL的初始治疗类型有关。

方法

我们分析了1973年至1988年间被诊断为第一原发性癌症CLL的9456例患者的数据,这些患者被报告给参与美国国立癌症研究所监测、流行病学和最终结果(SEER)计划的九个肿瘤登记处之一,并且存活了2个月或更长时间。在SEER文件中搜索在初始CLL诊断至少2个月后发生的侵袭性原发性恶性肿瘤。

结果

与一般人群相比,CLL患者发生所有第二癌症的风险显著增加(观察到840例;观察与预期比率[O/E]=1.28;95%置信区间[CI]=1.19-1.37)。肺癌(O/E=1.90)、脑癌(O/E=1.98)、眼癌(眼内黑色素瘤)(O/E=3.97)以及恶性黑色素瘤(O/E=2.79)和霍奇金病(O/E=7.69)的发生率显著过高。癌症风险并不因初始治疗类别而异,在CLL诊断后的所有时间间隔内也保持不变。

结论

CLL患者发生第二原发性恶性肿瘤的风险显著增加。癌症发生率过高的模式表明存在一种易感性状态,使得CLL患者有可能发生某些特定的第二恶性肿瘤,这可能是由于共同的病因、免疫损害和/或其他影响。虽然我们的结果并未表明有很强的治疗效果,但需要对CLL中的第二肿瘤进行更详细的研究,以调查放射治疗和化疗的作用。

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