Schoenberg B S
Recent Results Cancer Res. 1977;58:1-173.
Results for non-simultaneously diagnosed malignant tumors from Connecticut indicate that individuals with one malignant neoplasm have 1.29 times the risk of developing a new independent primary tumor when compared to individuals who never had cancer (P less than 0.01). However, the increased risk of multiple primary tumors is highly selective on a site-specific basis. Table 135 presents Connecticut Registry data indicating the risk of a subsequent primary malignancy by anatomic site of the later primary in patients with a first primary cancer. Tables 136 and 137 present tabulations for anatomic sites with statistically significant excesses and deficiencies, with an analysis by time interval between the two malignancies. Finally, Table 138 presents figures showing histologic confirmation for site-group paris with significant excesses of observed-over-expected later primary malignant neoplasms. The reader should bear in mind that just as the risk of subsequent primaries varies with the anatomic site of the subsequent primary (Table 135), the risk is also highly dependent upon the anatomic site of the first primary cancer (Chapters 6-12).
来自康涅狄格州的非同时诊断出的恶性肿瘤研究结果表明,与从未患过癌症的个体相比,患有一种恶性肿瘤的个体发生新的独立原发性肿瘤的风险是其1.29倍(P小于0.01)。然而,多原发性肿瘤风险的增加在特定部位具有高度选择性。表135展示了康涅狄格州登记处的数据,表明患有首例原发性癌症的患者中,后续原发性恶性肿瘤按后期原发性肿瘤的解剖部位划分的风险。表136和表137列出了具有统计学显著超额和不足的解剖部位列表,并按两种恶性肿瘤之间的时间间隔进行了分析。最后,表138给出了一些数据,显示了观察到的后期原发性恶性肿瘤超过预期显著超额的部位组对的组织学确认情况。读者应牢记,正如后续原发性肿瘤的风险随后续原发性肿瘤的解剖部位而变化(表135)一样,该风险也高度依赖于首例原发性癌症的解剖部位(第6 - 12章)。