UNEXPECTED SPONTANEOUS REGRESSION IN CLL AFTER LETROZOLE TREATMENT: COINCIDENCE OR CONNECTION?

IF 1.6 Q3 HEMATOLOGY
Ennur Ramadan , Mesut Seker , Guven Cetin
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引用次数: 0

Abstract

Introduction

According to iwCLL guidelines, remissions are divided into two groups: Complete Remission (CR) and Partial Remission (PR). CR in Chronic Lymphocytic Leukemia (CLL) is defined by having peripheral blood lymphocytes less than 4 × 10^9/L, no significant lymphadenopathy (lymph nodes < 1.5 cm), no splenomegaly or hepatomegaly, absence of disease-related constitutional symptoms, and blood counts showing neutrophils ≥ 1.5 × 10^9/L and platelets ≥ 100 × 10^9/L, while PR requires at least two parameters from group A (lymphoid tumor load and constitutional symptoms) and one parameter from group B (hematopoietic system) to improve if previously abnormal. Hence, we present a case with Spontaneous Regression (SR) of CLL right after letrozole treatment.

Case presentation

A 74-year-old female was admitted to the hematology clinic in 2018 due to lymphocytosis. The complete blood count of the patient showed a leukocyte count of 9.9 10^9/L with 6 10^9/L lymphocytes, a hemoglobin concentration of 15 g/dL, and 194 10^9/L platelets. The flow cytometry revealed 23% of lymphocytes displayed CD5+, CD20+, CD22+, CD19+, CD23+, Anti-Kappa+, CD38-, HLA DR+ immunophenotypes. In the physical examination, there was no splenomegaly or lymphadenomegaly. The patient was classified as Rai stage 0 CLL and managed with observation. In 2023, the patient had a mass on the left breast. Since they had a family history of breast cancer, the patient was referred to general surgery. The breast biopsy showed invasive lobular carcinoma. The breast cancer profile was T2cN0M0 (IB), estrogen and progesterone receptors were above 95%, cErbB2 (−), and low ki-67 index (13%). The patient was administered to the oncology for treatment. The patient received letrozole 2.5 mg/day and radiotherapy, respectively. One month after letrozole initiation, the peripheral blood lymphocyte count was observed within normal limits (Table 1). Throughout the one-year follow-up period before this case was reported, the levels remained within normal limits. The last flow cytometry still presented CLL, except atypic B-cells’ count decreased to 10%. The patient’s malignancies are considered under remission and the follow-up continues.

Discussion

SR of CLL is rare and not fully understood. Estrogen is known to influence B-cell function and survival, particularly through its interaction with Estrogen Receptors (ER). The study by Ladikou et al.[1] highlights that estrogen receptors are expressed in B-cell malignancies, including CLL, and predominantly involve the ERβ isoform, which has antiproliferative effects when selectively activated. Importantly, the disruption of estrogen-mediated pathways may lead to reduced proliferation and enhanced apoptosis of malignant B-cells. To the best of our knowledge, this is the second case of SR of CLL after letrozole treatment in the literature.[2] Future studies need to focus on the genetic causes of SR of CLL.
来曲唑治疗后CLL意外自发消退:巧合还是联系?
根据iwCLL指南,缓解分为两组:完全缓解(CR)和部分缓解(PR)。慢性淋巴细胞白血病(CLL)的CR定义为外周血淋巴细胞小于4 × 10^9/L,无明显淋巴结病变(淋巴结<;1.5 cm),没有脾或肝肿大,没有疾病相关的体质症状,血液计数显示中性粒细胞≥1.5 × 10^9/L,血小板≥100 × 10^9/L,而PR需要来自A组的至少两个参数(淋巴肿瘤负荷和体质症状)和来自B组的一个参数(造血系统)才能改善,如果以前异常。因此,我们报告了一例来曲唑治疗后CLL的自发消退(SR)。病例介绍:一名74岁女性因淋巴细胞增多症于2018年入住血液科诊所。患者全血细胞计数:白细胞计数9.9 10^9/L,淋巴细胞6 10^9/L,血红蛋白浓度15 g/dL,血小板194 10^9/L。流式细胞术显示23%的淋巴细胞表现为CD5+、CD20+、CD22+、CD19+、CD23+、Anti-Kappa+、CD38-、HLA DR+免疫表型。体格检查未见脾肿大、淋巴肿大。患者被归类为Rai期CLL,观察治疗。2023年,患者左乳房出现肿块。由于他们有乳腺癌的家族史,病人被转介到普通外科。乳腺活检显示浸润性小叶癌。乳腺癌类型为T2cN0M0 (IB),雌激素和孕激素受体≥95%,cErbB2(−),ki-67指数低(13%)。病人被送到肿瘤科接受治疗。患者分别给予来曲唑2.5 mg/d和放疗。来曲唑起始治疗一个月后,外周血淋巴细胞计数正常(表1)。在报告该病例之前的一年随访期间,该水平保持在正常范围内。除非典型b细胞计数下降至10%外,末次流式细胞术仍显示CLL。患者的恶性肿瘤被认为处于缓解期,继续进行随访。CLL的sr是罕见的,并没有被完全理解。众所周知,雌激素可以影响b细胞的功能和存活,特别是通过与雌激素受体(ER)的相互作用。Ladikou等人的研究强调,雌激素受体在包括CLL在内的b细胞恶性肿瘤中表达,并且主要涉及ERβ亚型,当选择性激活时具有抗增殖作用。重要的是,雌激素介导途径的破坏可能导致恶性b细胞增殖减少和凋亡增强。据我们所知,这是文献中第二例来曲唑治疗后CLL发生SR的病例未来的研究需要关注CLL SR的遗传原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.40
自引率
4.80%
发文量
1419
审稿时长
30 weeks
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