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Ki67和4F2抗原表达以及DNA合成可预测低度B细胞淋巴瘤复发/肿瘤进展时的生存率。

Ki67 and 4F2 antigen expression as well as DNA synthesis predict survival at relapse/tumour progression in low-grade B-cell lymphoma.

作者信息

Holte H, de Lange Davies C, Beiske K, Stokke T, Marton P F, Smeland E B, Høie J, Kvaløy S

机构信息

Department of Pathology, Norwegian Radium Hospital, Oslo.

出版信息

Int J Cancer. 1989 Dec 15;44(6):975-80. doi: 10.1002/ijc.2910440605.

Abstract

Previous work has shown that parameters of cell activation studied on lymphoma biopsies can be used to discriminate between low-grade and high-grade non-Hodgkin's lymphomas and to predict prognosis in the low-grade malignancy group alone. We have now examined expression of several activation antigens and indicators of DNA synthesis in 29 patients with low-grade malignant B-cell lymphomas at the time of primary diagnosis and later at relapse and/or tumour progression. At both times, the level of 4F2 antigen expression examined by flow cytometry on cells in suspension as well as the number of Ki67 antigen-positive cells examined by immunohistochemistry were predictive of patient survival. DNA synthesis estimated by (3H-TdR) thymidine incorporation was of prognostic value at the second biopsy only. These parameters were more sensitive than histological demonstration of morphological transformation in secondary high-grade lymphomas in identifying high-risk patients at repeated biopsy. We propose that Ki67 or 4F2 expression or a marker of DNA synthesis (such as 3H-TdR incorporation or labelling index) should be evaluated when repeated biopsies are performed, in order to select patients for whom aggressive chemotherapy may be considered.

摘要

先前的研究表明,在淋巴瘤活检中所研究的细胞活化参数可用于区分低度和高度非霍奇金淋巴瘤,并且仅能预测低度恶性组的预后。我们现已检测了29例低度恶性B细胞淋巴瘤患者在初次诊断时以及后来复发和/或肿瘤进展时几种活化抗原的表达及DNA合成指标。在这两个时间点,通过流式细胞术检测悬浮细胞上的4F2抗原表达水平以及通过免疫组织化学检测的Ki67抗原阳性细胞数量均可预测患者生存。仅在第二次活检时,通过(3H-TdR)胸苷掺入法估算的DNA合成具有预后价值。在重复活检时,这些参数在识别高危患者方面比继发性高度淋巴瘤形态学转化的组织学表现更敏感。我们建议,在进行重复活检时应评估Ki67或4F2表达或DNA合成标志物(如3H-TdR掺入或标记指数),以便选择可考虑进行积极化疗的患者。

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