Dang S P, Liberman B A, Shepherd F A, Messner H, Tweeddale M, Gardner H A, Colgan T, Rose T H, Evans W K
Arch Intern Med. 1986 Sep;146(9):1689-94.
The bone marrow of 11 patients with small-cell lung cancer, who survived more than two years following combined-modality therapy, was subjected to morphologic, cytogenetic, and bone marrow culture studies. One patient, after a prodrome of anemia and thrombocytopenia, developed acute leukemia 60 months after the start of chemotherapy. Four months before frank leukemia developed, bone marrow culture studies showed a marked inability to form colonies. Cytogenetic studies demonstrated an abnormal clone of cells that included the deletion of the long arm of chromosome 5. No morphologic abnormalities were noted in the bone marrow of any other long-term survivor; however, the mean corpuscular volume of peripheral red blood cells was greater than normal in three of four patients who remain alive and disease free. In one of these patients marrow culture studies also failed to grow colonies. The other patients showed a decreased ability to form multilineage colonies and colonies of the granulocyte-macrophage lineage in vitro compared with a control population. All patients showed some degree of aneuploidy on cytogenetic analysis; in two cases approximately 50% of cells were aneuploid. However, no clonal abnormality was detected in any patient. Follow-up for the development of secondary acute leukemia and other long-term complications continues in these patients.
对11例采用综合治疗后存活超过两年的小细胞肺癌患者的骨髓进行了形态学、细胞遗传学和骨髓培养研究。1例患者在出现贫血和血小板减少前驱症状后,化疗开始60个月后发生急性白血病。在明显发生白血病的4个月前,骨髓培养研究显示形成集落的能力明显下降。细胞遗传学研究证明存在一个异常细胞克隆,其中包括5号染色体长臂缺失。其他长期存活者的骨髓未发现形态学异常;然而,4例存活且无疾病的患者中有3例外周红细胞平均体积大于正常。其中1例患者的骨髓培养研究也未能生长出集落。与对照人群相比,其他患者在体外形成多谱系集落和粒细胞-巨噬细胞谱系集落的能力下降。所有患者在细胞遗传学分析中均显示出一定程度的非整倍体;在2例病例中,约50%的细胞为非整倍体。然而,未在任何患者中检测到克隆异常。这些患者仍在继续随访继发性急性白血病和其他长期并发症的发生情况。