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小细胞肺癌强化化疗后发生的急性非淋巴细胞白血病、白血病前期及实体瘤。

Acute nonlymphocytic leukemia, preleukemia, and solid tumors following intensive chemotherapy of small cell carcinoma of the lung.

作者信息

Pedersen-Bjergaard J, Osterlind K, Hansen M, Philip P, Pedersen A G, Hansen H H

出版信息

Blood. 1985 Dec;66(6):1393-7.

PMID:2998512
Abstract

Six of 796 patients treated with intensive combination chemotherapy for small cell carcinoma of the lung developed overt acute nonlymphocytic leukemia (ANLL) (three patients) or preleukemia with severe refractory cytopenia and clonal cytogenetic abnormalities in bone marrow cells (three patients). The latent period to development of preleukemia or leukemia was less than two years in four of the six patients. The cumulative risk of preleukemia and leukemia according to a Kaplan-Meier estimate was 14.0% +/- 6.9% (mean +/- SE) four years after the start of treatment. The relative risk of overt ANLL was 77, since three cases were observed v 0.039 cases expected, based on the age- and sex-specific incidence of acute nonlymphocytic leukemia in the general Danish population. The risk of secondary solid tumors was not increased. The possible causes of the exceptionally early appearance and very high cumulative risk of leukemic complications found in the present study, as compared to previous experience in other malignant diseases, is discussed, including the implications for future therapy of patients with small cell lung cancer.

摘要

796例接受强化联合化疗的小细胞肺癌患者中有6例发生了明显的急性非淋巴细胞白血病(ANLL)(3例)或骨髓细胞出现严重难治性血细胞减少和克隆性细胞遗传学异常的白血病前期(3例)。6例患者中有4例发生白血病前期或白血病的潜伏期不到两年。根据Kaplan-Meier估计,治疗开始后四年白血病前期和白血病的累积风险为14.0%±6.9%(均值±标准误)。明显ANLL的相对风险为77,因为观察到3例,而根据丹麦普通人群急性非淋巴细胞白血病的年龄和性别特异性发病率预期为0.039例。继发性实体瘤的风险没有增加。本文讨论了与其他恶性疾病以往经验相比,本研究中白血病并发症出现异常早且累积风险非常高的可能原因,包括对小细胞肺癌患者未来治疗的影响。

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