黑色素瘤对程序性死亡-1阻断的解决,但同时伴有慢性淋巴细胞白血病的快速进展。

IF 1.7 4区 医学 Q3 HEMATOLOGY Acta Haematologica Pub Date : 2023-01-01 DOI:10.1159/000527631
Melinda Burgess, Colm Keane, Joshua Wd Tobin, Soi Cheng Law, Alison Griffin, Devinder Gill, Adam D Ewing, Victoria Atkinson, Peter Mollee, Muhammed B Sabdia, Nicholas Saunders, Maher K Gandhi
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引用次数: 2

摘要

在这里,我们报告了一例新病例,慢性淋巴细胞白血病(CLL)患者接受CTLA-4和PD-1免疫检查点阻断(ICB)治疗合并转移性黑色素瘤。尽管转移性黑色素瘤对ICB有反应,但CLL进展迅速(但对ICB停止和依鲁替尼有反应)。没有新的基因突变驱动来解释改变的临床过程。在CLL B细胞、CD8+或CD4+ t细胞亚群或单核细胞中,PD-1/PD-L1/PD-L2和CTLA-4/CD80/CD86的表达均未升高。在PD-1阻断期间,患者的CLL B细胞在体外存活时间显著延长,这在ICB之前或之后或与其他患者一起采集的样本中没有观察到。据我们所知,在双重恶性肿瘤患者中,不一致的临床过程与这些生物学特征相结合尚未报道。
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Resolution of Melanoma to Programmed Death-1 Blockade but Simultaneous Rapid Progression of Concomitant Chronic Lymphocytic Leukemia.

Here, we present a novel case of a patient with chronic lymphocytic leukemia (CLL) who received CTLA-4 and then PD-1 immune-checkpoint blockade (ICB) as treatment for concomitant metastatic melanoma. Whereas the metastatic melanoma was responsive to ICB, the CLL rapidly progressed (but responded to ICB cessation and ibrutinib). There were no new genetic mutational drivers to explain the altered clinical course. PD-1/PD-L1/PD-L2 and CTLA-4/CD80/CD86 expression was not increased in CLL B cells, CD8+ or CD4+ T-cell subsets, or monocytes. The patient's CLL B cells demonstrated strikingly prolonged in vitro survival during PD-1 blockade, which was not observed in samples taken before or after ICB, or with other patients. To our knowledge, a discordant clinical course to ICB coupled with these biological features has not been reported in a patient with dual malignancies.

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来源期刊
Acta Haematologica
Acta Haematologica 医学-血液学
CiteScore
4.90
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: ''Acta Haematologica'' is a well-established and internationally recognized clinically-oriented journal featuring balanced, wide-ranging coverage of current hematology research. A wealth of information on such problems as anemia, leukemia, lymphoma, multiple myeloma, hereditary disorders, blood coagulation, growth factors, hematopoiesis and differentiation is contained in first-rate basic and clinical papers some of which are accompanied by editorial comments by eminent experts. These are supplemented by short state-of-the-art communications, reviews and correspondence as well as occasional special issues devoted to ‘hot topics’ in hematology. These will keep the practicing hematologist well informed of the new developments in the field.
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