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[接受强化化疗联合或不联合放疗的小细胞肺癌患者中的双原发癌]

[Double cancer in small cell lung cancer patients treated with intensive chemotherapy with or without radiation therapy].

作者信息

Segawa Y, Ohnoshi T, Ueoka H, Miyake K, Takigawa N, Kimura I, Hiraki S, Fujii M, Machida K, Moritaka T

机构信息

Second Department of Internal Medicine, Okayama University Medical School, Japan.

出版信息

Nihon Kyobu Shikkan Gakkai Zasshi. 1991 Nov;29(11):1432-8.

PMID:1663179
Abstract

Development of double cancer was evaluated in 311 small cell lung cancer patients who had received intensive chemotherapy with or without radiotherapy. Of those, 10 patients (3.2%) developed a second malignancy:stomach cancer in four, non-small cell lung cancer in three, acute myelogenous leukemia in two, and liver cancer in one. The cumulative risk for the development of double cancer was 1.0% at 1-year, 17.0% at 3-years, and 100% at 8.1 years. The relative risk for the development of double cancer calculated by person-year method utilizing age and sex adjusted cancer incidence in Japan was 2.96-fold (p less than 0.01). The risk of non-small cell lung cancer (6.65-fold) and acute myelogenous leukemia (54.9-fold) was particularly high. Of 21 patients who survived disease-free for more than 2 years, 8 patients died; four patients (50%) died of second malignancy, two died of infectious disease, and only two patients died from recurrent small cell lung cancer. These results indicate that a cautious follow-up program for the detection of double cancer is indicated in patients surviving small cell lung cancer.

摘要

对311例接受过强化化疗(无论是否接受放疗)的小细胞肺癌患者的双原发癌发生情况进行了评估。其中,10例患者(3.2%)发生了第二种恶性肿瘤:4例为胃癌,3例为非小细胞肺癌,2例为急性髓细胞白血病,1例为肝癌。双原发癌发生的累积风险在1年时为1.0%,3年时为17.0%,8.1年时为100%。利用日本年龄和性别调整后的癌症发病率,通过人年法计算出的双原发癌发生的相对风险为2.96倍(p<0.01)。非小细胞肺癌(6.65倍)和急性髓细胞白血病(54.9倍)的风险尤其高。在21例无病生存超过2年的患者中,8例死亡;4例患者(50%)死于第二种恶性肿瘤,2例死于传染病,仅2例患者死于小细胞肺癌复发。这些结果表明,对于小细胞肺癌幸存者,应开展谨慎的双原发癌监测随访计划。

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