小淋巴细胞性淋巴瘤与肺癌并发发展:二例报告及文献复习。

IF 0.9 Q4 HEMATOLOGY
Kensuke Nakao, Momoko Nishikori, Masakazu Fujimoto, Hiroshi Arima, Hironori Haga, Akifumi Takaori-Kondo
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引用次数: 0

摘要

小淋巴细胞性淋巴瘤(Small lymphocytic lymphoma, SLL)是一种罕见的疾病亚型,与慢性淋巴细胞性白血病(chronic lymphocytic leukemia, CLL)具有相同的形态学和免疫表型特征,但不表现淋巴细胞增生,主要生长于淋巴结和脾脏。与CLL一样,SLL患者往往表现出免疫异常,并与发展为第二原发性恶性肿瘤的风险增加有关。我们在此报告两例SLL并发肺癌的病例。这两例患者的生物学和临床特征非常相似;他们都患有SLL伴12三体,缺乏淋巴细胞增多症或细胞减少症。SLL细胞累及肺腺癌附近表达PD-L1的淋巴结区。1例患者接受了包括纳武单抗和伊匹单抗在内的针对肺癌的免疫化疗,值得注意的是,在第二周期免疫化疗后,SLL出现了一过性恶化,同时发生了免疫相关不良事件。患者SLL样本免疫组化分析显示肿瘤细胞CTLA-4阳性,提示ipilimumab可能通过阻断CTLA-4介导的抑制信号诱导SLL细胞活化。这些临床发现提示SLL与肺癌之间潜在的生物学关系。根据这些观察结果,我们希望引起人们对免疫检查点抑制剂用于治疗SLL患者恶性肿瘤时SLL恶化的可能性的关注。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Concurrent development of small lymphocytic lymphoma and lung cancer: A report of two cases and a review of the literature.

Concurrent development of small lymphocytic lymphoma and lung cancer: A report of two cases and a review of the literature.

Concurrent development of small lymphocytic lymphoma and lung cancer: A report of two cases and a review of the literature.

Concurrent development of small lymphocytic lymphoma and lung cancer: A report of two cases and a review of the literature.

Small lymphocytic lymphoma (SLL) is a rare disease subtype which has the same morphological and immunophenotypic features as chronic lymphocytic leukemia (CLL) but does not demonstrate lymphocytosis and grows mainly in the lymph nodes and spleen. As with CLL, SLL patients tend to present with immune abnormalities, and are associated with an increased risk for developing second primary malignancies. We report here two cases of SLL who developed lung cancer concurrently. The biological and clinical features of these two patients were very similar to each other; they both developed SLL with trisomy 12 and lacked lymphocytosis or cytopenia. SLL cells involved nodal areas adjacent to lung adenocarcinoma which expressed PD-L1. One patient received immunochemotherapy including nivolumab and ipilimumab against lung cancer, and notably, transient deterioration of SLL occurred after the second cycle of immunochemotherapy along with the development of immune related adverse events. Immunohistochemical analysis of the SLL samples of the patient revealed that the tumor cells were positive for CTLA-4, suggesting that ipilimumab might have potentially induced the activation of SLL cells by blocking the inhibitory signal mediated by CTLA-4. These clinical findings indicate the potential biological relationship between SLL and lung cancer. According to these observations, we would like to draw attention to the possibility of deterioration of SLL when immune checkpoint inhibitors are used for the treatment of malignancies developed in SLL patients.

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来源期刊
CiteScore
2.00
自引率
6.70%
发文量
25
审稿时长
11 weeks
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