leukopenia

白细胞减少症
  • 文章类型: Journal Article
    背景:冬虫夏草(CS)是一种寄生于鳞翅目幼虫的真菌,常用于治疗肺部疾病和调节免疫功能。
    目的:本综述旨在评估CS辅助治疗肺癌的疗效。
    方法:截至2022年6月,电子数据库搜索在PubMed进行,EMBASE,科克伦图书馆,中国生物医学文献数据库(CBM),中国国家知识基础设施(CNKI),万方数据库和中国科学杂志数据库(VIP数据库)。包括评估CS作为肺癌辅助治疗功效的随机临床试验(RCT)。经过质量评价,采用Stata16.0软件进行Meta分析。
    结果:本次荟萃分析共确定了12个RCT,928例患者,这表明作为一种辅助治疗,CS在肺癌治疗中具有以下优势:(1)改善肿瘤反应率(TRR)(RR:1.17,95CI:1.05-1.29,P=0.00);(2)改善免疫功能,包括增加的CD4(MD:4.98,95CI:1.49-8.47,P=0.01),CD8(MD:1.60,95CI:0.40-2.81,P=0.01,I2=0.00%),NK(MD:4.17,95CI:2.26-6.08,P=0.00),IgA(MD:1.29,95CI:0.35-2.24,P=0.01),IgG(MD:3.95,95CI:0.98-6.92,P=0.01)和IgM(MD:6.44,95CI:0.63-12.26,P=0.03);(3)根据Karnofsky表现状态(KPS)的平均值±SD(MD:8.20,95CI:6.87-9.53,P=0.00)改善了患者的生活质量;(4)减少了药物不良反应的发生率(ADR)包括骨髓抑制的发生率(RR:0.38,95CI:0.19-0.75,P=0.01),白细胞减少症(RR:0.76,95CI:0.63-0.92,P=0.00),和血小板减少(RR:0.52,95CI:0.31-0.86,P=0.01)(5)降低了放射性肺炎的发生率(RR:0.74,95CI:0.62-0.88,P=0.00)。然而,基于KPS的改善患者数量(RR:1.47,95CI:0.98-2.20,P=0.06)在两组之间相似,肝肾损害(RR:0.32,95CI:0.09~1.10,P=0.07)和胃肠道不良反应(RR:0.80,95CI:0.47~1.37,P=0.42)。亚组分析显示,CS在6g/d和21天/3-4个周期的治疗中可以增加TRR。
    结论:与常规治疗相比,肺癌CS辅助治疗不仅能提高TRR,QOL和免疫功能,还能降低ADR和放射性肺炎的发生率。最佳使用可以是6g/d和21天/3至4个周期。
    CRD42022333681。
    BACKGROUND: Cordyceps sinensis (CS) is a fungus parasitic on lepidopteran larvae which is often used to treat lung diseases and regulate immune function.
    OBJECTIVE: This review aimed to evaluate the efficacy of CS in the adjuvant treatment of lung cancer.
    METHODS: As of June 2022, the electronic database search was conducted in PubMed, EMBASE, Cochrane Library, China Biomedical Literature Database (CBM), China National Knowledge Infrastructure (CNKI), Wanfang Database and China Science Journal Database (VIP database). Randomized clinical trials (RCTs) that evaluated the efficacy of CS as an adjuvant treatment for lung cancer were included. After the quality evaluation, meta-analysis was performed with Stata 16.0 software.
    RESULTS: A total of 12 RCTs with 928 patients were identified for this meta-analysis, which showed that as an adjuvant treatment, CS has the following advantages in the treatment of lung cancer: (1) Improved tumor response rate (TRR) (RR: 1.17, 95%CI: 1.05-1.29,P = 0.00); (2) improved immune function, including increased CD4 (MD: 4.98, 95%CI: 1.49-8.47, P = 0.01), CD8 (MD: 1.60, 95%CI: 0.40-2.81, P = 0.01, I2 = 0.00%), NK (MD: 4.17, 95%CI: 2.26-6.08, P = 0.00), IgA (MD: 1.29, 95%CI: 0.35-2.24, P = 0.01), IgG (MD: 3.95, 95%CI: 0.98-6.92, P = 0.01) and IgM (MD: 6.44, 95%CI: 0.63-12.26, P = 0.03); (3) improved patients\' quality of life based on the mean ± SD of Karnofsky Performance Status (KPS) (MD: 8.20, 95%CI: 6.87-9.53, P = 0.00); (4) reduced the incidence of adverse drug reactions (ADRs), including the incidence of myelosuppression (RR: 0.38, 95%CI: 0.19-0.75, P = 0.01), leukopenia (RR: 0.76, 95%CI: 0.63-0.92, P = 0.00), and thrombocytopenia (RR: 0.52, 95%CI: 0.31-0.86, P = 0.01) (5) reduced the incidence of radiation pneumonitis (RR: 0.74, 95%CI: 0.62-0.88, P = 0.00). However, the number of improved patients based on KPS (RR: 1.47, 95%CI: 0.98-2.20, P = 0.06) were similar between two groups, liver and renal damage (RR: 0.32, 95%CI: 0.09-1.10, P = 0.07) and gastrointestinal adverse reactions (RR: 0.80, 95%CI: 0.47-1.37, P = 0.42) as well. Subgroup analysis showed that CS could increase the TRR in the treatment with 6 g/d and 21 days/3-4 cycles.
    CONCLUSIONS: Compared with conventional treatment, adjuvant treatment with CS of lung cancer not only improve TRR, QOL and immune function, but also reduce the incidence of ADRs and radiation pneumonitis. The optimal usage may be 6 g/d and 21 days/3 to 4 cycles.
    UNASSIGNED: CRD42022333681.
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  • 文章类型: Meta-Analysis
    化疗引起的白细胞减少是细胞毒性抗癌药物的常见副作用。它可以剥夺患者的治疗机会,导致延迟,reduction,或停止化疗或其他抗癌药物给药。两名研究人员搜索了英文,中文,日本人,和韩国电子数据库,在不限制时间段和语言的情况下,使用诸如“Bojungikgi,\"\"WBC,\"\"luko,\"和\"中性。“在对接受化疗的患者给予Bojingikgi-tang的人体随机对照研究中,选择报告白细胞减少症相关结局的研究,和数据提取,偏差风险评估,并对所选论文进行荟萃分析。选择了十项研究,并进行了系统评价和荟萃分析。在中国发表了9篇论文,参与者总数为715。由于给这些患者服用了Bojungikgi-tang,化疗诱导的白细胞减少患者数量显著减少(OR:0.41,95%CI:0.27-0.61,P=0.0001,I2=35%).Further,白细胞计数与对照组比较,并显示出预防效果(MD:0.64,95%CI:0.46-0.83,P<.00001,I2=90%)。观察到明显的效果,尤其是在基于模式识别的诊断后进行时,如气虚。(OR:0.32,95%CI:0.18-0.58,P=.0002,I2=0%)。然而,由于非致盲,所有研究都有很高的偏倚风险,大多数研究在创建随机分配顺序并隐藏它们时存在很高或不确定的偏差风险。Bojingikgi-tang对预防和治疗化疗引起的白细胞减少症具有作用。正确诊断后给药可提高有效率,不良反应和副作用的可能性低于粒细胞集落刺激因子(G-CSF)注射液。Bojungikgi-tang似乎可用于治疗和预防由细胞毒性抗癌药物引起的白细胞减少症。然而,未来有必要进行高质量的临床研究,考虑到当地和语言偏见的可能性,癌的异质性和干预,以及偏见的风险。注册:PROSPEROCRD4202341054。
    Chemotherapy-induced leukopenia is a common side effect of cytotoxic anticancer drugs. It can deprive patients of treatment opportunities, resulting in the delay, reduction, or discontinuation of chemotherapy or other anticancer drug administration. Two researchers searched English, Chinese, Japanese, and Korean electronic databases, without limiting the time period and language, using search terms such as \"Bojungikgi,\" \"WBC,\" \"leuko,\" and \"neutrop.\" Among the human randomized controlled studies in which Bojungikgi-tang was administered to patients who underwent chemotherapy, studies reporting leukopenia-related outcomes were selected, and data extraction, bias risk assessment, and meta-analysis were performed on the selected papers. Ten studies were selected, and a systematic review with meta-analysis was conducted. Nine papers were published in China and the total number of participants was 715. As a result of administering Bojungikgi-tang to these patients, the number of patients with chemotherapy-induced leukopenia significantly decreased (OR: 0.41, 95% CI: 0.27-0.61, P = .0001, I2 = 35%). Further, white blood cell counts were compared with that of the control group, and it showed an effect on prevention (MD: 0.64, 95% CI: 0.46-0.83, P < .00001, I2 = 90%). A pronounced effect was observed, especially when administered after a diagnosis based on the pattern identification, such as Qi deficiency. (OR: 0.32, 95% CI: 0.18-0.58, P = .0002, I2 = 0%). However, all studies had a high risk of bias due to non-blinding, and most studies had a high or uncertain risk of bias in creating random assignment orders and concealing them. Bojungikgi-tang has an effect on the prevention and treatment of chemotherapy-induced leukopenia. The effect rate can be increased when administered after proper diagnosis, and the possibility of adverse reactions and side effects is lower than that of Granulocyte-Colony Stimulating Factor (G-CSF) injection. Bojungikgi-tang appears to be useful in the treatment and prevention of leukopenia caused by cytotoxic anticancer drugs. However, it is necessary to conduct high-quality clinical studies in the future, considering the possibility of local and language bias, heterogeneity of carcinoma and intervention, and the risk of bias.Registration: PROSPERO CRD4202341054.
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  • 文章类型: Review
    拉莫三嗪的不良反应更可能伴随使用抗癫痫药物,快速剂量滴定,和多种药物的使用,强调测量其浓度的重要性。这里,1名具有这些危险因素的20岁双相女性患者在第三次mRNA疫苗接种后第1天接受拉莫三嗪.白细胞减少症发生在第12天,没有快速浓度增加,但白细胞在22周后逐渐恢复,没有停药拉莫三嗪。第二次mRNA接种不诱导白细胞减少症。可能,同时接种疫苗和拉莫三嗪引起白细胞减少症的协同免疫反应,随着反应减弱而恢复。在mRNA接种后立即启动拉莫三嗪可能是白细胞减少症的危险因素。
    Adverse lamotrigine effects are more likely with concomitant use of antiepileptic drugs, rapid dose titration, and multiple drug use, highlighting the importance of measuring its concentration. Here, lamotrigine was administered the day after the third mRNA vaccination to a 20-year-old bipolar woman with these risk factors. Leukopenia occurred on day 12 without rapid concentration increase, but leukocytes gradually recovered after 22 weeks without discontinuation of lamotrigine. The second mRNA vaccination did not induce leukopenia. Possibly, a synergetic immune response to simultaneous vaccination and lamotrigine caused leukopenia, which recovered as the response weakened. Lamotrigine initiation immediately after mRNA vaccination may be a leukopenia risk factor.
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  • 文章类型: Journal Article
    周期性中性粒细胞减少症是一种罕见的血液疾病,其特征是中性粒细胞计数的周期性波动。周期为21天。临床表现从轻度到重度不等,随着反复发烧的发作,痛苦的口腔溃疡,复发性细菌感染,腹膜炎,和感染性休克。粒细胞集落刺激因子(G-CSF)的可用性彻底改变了这种疾病的管理和自然史,调节增殖,分化,和祖细胞的成熟,并减少中性粒细胞减少症的持续时间。炎症性肠病(IBD),包括克罗恩病(CD)和溃疡性结肠炎(UC),是一组影响胃肠道的慢性病变。这两种疾病的发病可能在年轻时(甚至在童年或青春期),临床表现可能导致误诊,由于类似的特征,如反复感染,口腔溃疡,肛周脓肿,和不孕症。此外,这两种病理很少相关,有不同的管理和治疗选择。这里,我们描述了两例因诊断为复杂CD而接受手术的患者的病例报告.手术后,由于持续的中性粒细胞减少,血液学家顾问证实了周期性中性粒细胞减少症的怀疑,G-CSF治疗开始时受益,强调正确鉴别诊断的重要性。
    Cyclic neutropenia is a rare hematological condition characterized by periodic fluctuations in neutrophil counts, with a 21-day periodicity. Clinical presentation varies from mild to severe forms of the disease, with the onset of recurrent fever, painful oral ulcers, recurrent bacterial infections, peritonitis, and septic shock. The availability of granulocyte colony-stimulating factor (G-CSF) has revolutionized the management and natural history of this disease, regulating the proliferation, differentiation, and maturation of the progenitor cells, and reducing the duration of neutropenia. Inflammatory bowel disease (IBD), including Crohn\'s disease (CD) and ulcerative colitis (UC), is a group of chronic pathologies that affect the gastrointestinal tract. The onset of both diseases may be at a young age (even during childhood or adolescence), and clinical manifestations may lead to misdiagnosis, due to similar characteristics such as recurrent infections, oral ulcers, perianal abscesses, and infertility. Moreover, the two pathologies are rarely associated, with different management and therapeutic options. Here, we describe two case reports of patients who underwent surgery because of diagnosis of complicated CD. After surgery, due to persistent neutropenia, the hematologist consultant confirmed suspicions of cyclic neutropenia, and G-CSF therapy was started with benefits, underlining the crucial importance of proper differential diagnosis.
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  • 文章类型: Meta-Analysis
    这篇综述通过荟萃分析总结了影响COVID-19疫苗在LTR中的疗效和安全性的因素,希望为疫苗的使用提供策略。
    筛选电子数据库以进行LTR中mRNA疫苗的研究。主要结果是合并血清转换率,次要结局是不良事件的发生率+突破性感染.亚组分析基于BMI,相关的合并症,基线白细胞减少症的存在,移植以来的时间,和使用的药物。
    总共,包括31篇文章。至少两剂SARS-CoV-2疫苗接种后的合并血清转化率为72%(95%CI[0.52-0.91)。研究间的显著异质性I2=99.9%,血清转化率约为72%(95CI[0.66-0.75]),从报告两剂疫苗的研究中得出,比报告三剂疫苗的研究高出约75%(95CI[0.29-1.22])。BMI低到正常组的合并血清转换率为74%(95%CI[0.22-1.27],Pi=0.005)对67%(95%CI[0.52-0.81],高BMI组的Pi=0.000)。白细胞减少阳性组的合并血清转换率最低,59%。白细胞减少可能影响LTR中疫苗的血清转换率。从移植后的分析时间开始,设定7年为截止点,至少两剂COVID-19疫苗接种后的合并血清转化率为53%(95%CI[0.18-0.83],<7岁组的P=0.003,I2=99.6%)和83%(95%CI[0.76-0.90],P=0.000I2=95.7%)>7岁组。自移植以来唯一一次达到统计学意义,被认为是血清学反应不良的危险因素预测因子(OR=1.2795CI[1.03-1.55],P=0.024)。疫苗接种后的突破感染率很低2%(95%CI0.01-0.03,I2=63.0%),以及不良事件的总体发生率,主要包括注射部位的疼痛和疲劳,为18%(95CI[0.11-0.25],I2=98.6%,Pi=0.000)。
    用至少两剂COVID-19mRNA疫苗接种的LTR的血清转化率可能会受到疫苗类型的显着影响,使用免疫抑制剂,BMI,白细胞减少症,相关的合并症,和移植后的时间。然而,LTR仍建议使用加强剂量。
    This review summarizes the factors influencing the efficacy and safety of the COVID-19 vaccine in LTR through meta-analysis, hoping to provide strategies for vaccine use.
    Electronic databases were screened for studies on mRNA vaccines in LTR. The primary outcome was the pooled seroconversion rate, and the secondary outcome was the incidence of adverse events+breakthrough infections. Subgroup analyses were made based on BMI, associated comorbidities, presence of baseline leukopenia, time since transplant, and drugs used.
    In total, 31 articles got included. The pooled seroconversion rate after at least two doses of SARS-CoV-2 vaccination was 72% (95% CI [0.52-0.91). With significant heterogeneity among studies I2 = 99.9%, the seroconversion rate was about 72% (95%CI [0.66-0.75]), from the studies reporting two doses of vaccine slightly higher around 75%(95%CI [0.29-1.22]) from studies reporting three doses. The pooled seroconversion rate within the lower to normal BMI group was 74% (95% CI [0.22-1.27], Pi=0.005) against 67% (95% CI [0.52-0.81], Pi=0.000) in the high BMI group. The pooled seroconversion rate in the \'\'positive leukopenia\'\' group was the lowest, 59%. Leukopenia could influence the vaccine seroconversion rate in LTR. From the time since transplant analysis after setting seven years as cut off point, the pooled seroconversion rate after at least two doses of COVID-19 vaccination was 53% (95% CI [0.18-0.83], P=0.003, I2 = 99.6%) in <7years group and 83% (95% CI [0.76-0.90], P=0.000 I2 = 95.7%) in > 7years group. The only time since transplantation had reached statistical significance to be considered a risk factor predictor of poor serological response (OR=1.27 95%CI [1.03-1.55], P=0.024). The breakthrough infection rate after vaccination was very low2% (95% CI 0.01-0.03, I2 = 63.0%), and the overall incidence of adverse events, which included mainly pain at the injection site and fatigue, was 18% (95%CI [0.11-0.25], I2 = 98.6%, Pi=0.000).
    The seroconversion rate in LTR vaccinated with at least two doses of mRNA COVID-19 vaccine could be significantly affected by the vaccine type, immunosuppressant used, BMI, leukopenia, associated comorbidities, and time since transplantation. Nevertheless, booster doses are still recommended for LTR.
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  • 文章类型: Systematic Review
    背景:抗磷脂综合征(APS)是一种全身性自身免疫性疾病,临床上与血栓性和产科事件相关。其他表现与APS有关,如弥漫性肺泡出血(DAH)。我们旨在总结所有可用的证据来描述呈现的临床特征,他们的预后因素,以及短期和长期结果。
    方法:我们采用混合方法,将多中心队列与APS相关DAH患者的系统文献综述(SLR)相结合。我们描述了他们的临床特征,治疗,预后因素,和结果(复发,死亡率,和机械通风要求[MV])。Kaplan-Meier方法用于估计复发率和死亡率,以及Cox和logistic回归模型用于评估适当的相关因素。
    结果:我们纳入了219例发生APS相关DAH的患者(61例来自梅奥诊所,158例来自SLR)。中位年龄为39.5岁,51%是女性,29%患有系统性红斑狼疮,34%的人出现了灾难性的APS(CAPS)。74%的患者有血栓性事件史,26%的女性有妊娠病史;一半的患者有血小板减少病史,三分之一患有瓣膜病。在DAH之前,55%的患者进行了抗凝治疗。在DAH发作时,65%的患者出现咯血。6个月复发率为47%,1年复发率为52%。三阳性(HR4.22,95%CI1.14-15.59)与六个月时的复发相关。估计一年和五年的死亡率分别为30.3%和45.8%。与死亡率相关的因素是严重的血小板减少症(<50K/μL)(HR3.10,95%CI1.39-6.92),瓣膜植被(HR3.22,95%CI1.14-9.07),CAPS(HR3.80,95%CI1.84-7.87),和MV要求(HR2.22,95%CI1.03-4.80)。42%的患者在发生DAH发作时需要MV。出现严重血小板减少症(OR6.42,95%CI1.77-23.30)或CAPS(OR4.30,95%CI1.65-11.16)的患者更可能需要MV。
    结论:APS相关的DAH与高发病率和高死亡率相关,特别是当呈现三重积极性时,血小板减少症,瓣膜受累,和CAPS。
    Antiphospholipid syndrome (APS) is a systemic autoimmune disease clinically associated with thrombotic and obstetric events. Additional manifestations have been associated with APS, like diffuse alveolar hemorrhage (DAH). We aimed to summarize all the evidence available to describe the presenting clinical features, their prognostic factors, and short- and long-term outcomes.
    We performed a mixed-method approach combining a multicenter cohort with a systematic literature review (SLR) of patients with incident APS-associated DAH. We described their clinical features, treatments, prognostic factors, and outcomes (relapse, mortality, and requirement of mechanical ventilation [MV]). Kaplan-Meier methods were used to estimate relapse and mortality rates, and Cox and logistic regression models were used to assess the factors associated as appropriate.
    We included 219 patients with incident APS-associated DAH (61 from Mayo Clinic and 158 from SLR). The median age was 39.5 years, 51% were female, 29% had systemic lupus erythematosus, and 34% presented with catastrophic APS (CAPS). 74% of patients had a history of thrombotic events, and 26% of women had a history of pregnancy morbidity; half of the patients had a history of thrombocytopenia, and a third had valvulopathy. Before DAH, 55% of the patients were anticoagulated. At DAH onset, 65% of patients presented hemoptysis. The relapse rate was 47% at six months and 52% at one year. Triple positivity (HR 4.22, 95% CI 1.14-15.59) was associated with relapse at six months. The estimated mortality at one and five years was 30.3% and 45.8%. Factors associated with mortality were severe thrombocytopenia (< 50 K/μL) (HR 3.10, 95% CI 1.39-6.92), valve vegetations (HR 3.22, 95% CI 1.14-9.07), CAPS (HR 3.80, 95% CI 1.84-7.87), and requirement of MV (HR 2.22, 95% CI 1.03-4.80). Forty-two percent of patients required MV on the incident DAH episode. Patients presenting with severe thrombocytopenia (OR 6.42, 95% CI 1.77-23.30) or CAPS (OR 4.30, 95% CI 1.65-11.16) were more likely to require MV.
    APS-associated DAH is associated with high morbidity and mortality, particularly when presenting with triple positivity, thrombocytopenia, valvular involvement, and CAPS.
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  • 文章类型: Review
    Copper deficiency can present as myelopathy by the manifestation of sensory ataxia, secondary to demyelination of the posterior cords of the spinal cord, accompanied by cytopenia, mainly anemia, and leukopenia. Case series study of three patients with myelopathy due to copper deficiency, diagnosed and managed from 2020 to 2022 in a highly complex university hospital in Colombia. Regarding gender, two cases were female patients. The age range was between 57 and 68 years. In all three cases serum copper levels were decreased, and in two of these, different causes of myelopathy affecting the posterior cords of the spinal cord were ruled out, such as vitamin B12, vitamin E and folic acid deficiency, tabes dorsalis, myelopathy due to human immunodeficiency virus, multiple sclerosis and infection by the human lymphotropic virus type I and II, among others. However, at the moment of the myelopathy diagnosis, one patient had vitamin B12 deficiency associated with copper insufficiency. All three cases presented sensory ataxia, and in two, paraparesis was the initial motor deficit. The diagnostic approach must include copper levels assessment in every case of patients with chronic gastrointestinal pathology, chronic diarrhea, malabsorption syndrome, or significant reduction in dietary intake; and the development of neurological symptoms that may suggest cord involvement. It has been reported that a delay in diagnosis can lead to poor neurological outcomes.
    El déficit de cobre puede presentarse como una mielopatía y manifestarse como una ataxia sensorial secundaria a una desmielinización de los cordones posteriores de la médula espinal. Puede acompañarse de citopenias, principalmente anemia y leucopenia. Se presenta una serie de casos de tres pacientes con mielopatía por déficit de cobre, diagnosticados y manejados desde el año 2020 al 2022 en un hospital universitario de alta complejidad en Colombia. Dos de los casos eran mujeres. El rango de edad fue entre 57 y 68 años. En los tres casos, los niveles séricos de cobre estaban disminuidos y en dos de ellos, se descartaron diferentes causas de mielopatía que afectan los cordones posteriores de la médula espinal como el déficit de vitamina B12, vitamina E y ácido fólico, tabes dorsal, mielopatía por virus de la inmunodeficiencia humana, esclerosis múltiple e infección por el virus linfotrópico humano de tipo I y II, entre otras. Sin embargo, un paciente tenía deficiencia de vitamina B12 asociada con de cobre en el momento del diagnóstico de la mielopatía. En los tres casos hubo ataxia sensitiva y en dos, la paraparesia fue el déficit motor inicial.
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  • 文章类型: Meta-Analysis
    目的:Nudix水解酶15[NUDT15]遗传变异增加了硫嘌呤诱导的白细胞减少症[TIL]的风险;然而,他们在炎症性肠病[IBD]患者中的全球患病率未知.我们旨在评估IBD患者中NUDT15变异的全球患病率和这些患者中TIL的发生率。
    方法:从开始到2022年7月搜索了六个数据库。包括报告具有这些变异的成年IBD患者中任何NUDT15变异的频率和/或白细胞减少症的频率的研究。进行了随机效应模型来估计变体的合并患病率,早期[≤8周]和晚期[>8周]白细胞减少症的发生率,和白细胞减少症的相对风险。
    结果:纳入20项研究,包括5232名患者。*1/*3c.415C>TC/T复型的合并患病率为13%(95%置信区间[CI]:10-18%),*3/*3c.415C>TT/T复型为2%[95%CI:1-2%],*1/*5c.52G/A复型为2%[95%CI:1-3%],*1/*6c.36_37insGGAGTCins/-二倍体为7%[95%CI:4-12%]。*1/*3的合并患病率在日本很高[20%,95%CI:16-24%]和中国患者[18%,95%CI:12-27%]。*1/*3患者早期白细胞减少症发生率为20%[95%CI:16-26%],*3/*3患者的99%[95%CI:7-100%],*1/*6例患者为49%[95%CI:29-69%]。在*1/*3患者中,晚期白细胞减少症的发生率为36%[95%CI:26-49%]。
    结论:NUDT15变异体在IBD患者中很常见并能强烈预测TIL。治疗前NUDT15基因分型应特别考虑在亚洲人群中,指导硫嘌呤给药和预防骨髓毒性。
    OBJECTIVE: Nudix hydrolase 15 [NUDT15] genetic variants confer an increased risk of thiopurine-induced leukopenia [TIL]; however, their global prevalence in inflammatory bowel disease [IBD] patients is unknown. We aimed to evaluate the global prevalence of NUDT15 variants in IBD patients and incidence of TIL in these patients.
    METHODS: Six databases were searched from inception until July 2022. Studies reporting the frequency of any NUDT15 variant and/or frequency of leukopenia in adult IBD patients with these variants were included. A random effects model was performed to estimate the pooled prevalence of variants, incidence of early [≤8 weeks] and late [>8 weeks] leukopenia, and relative risk of developing leukopenia.
    RESULTS: Twenty studies comprising 5232 patients were included. The pooled prevalence of the *1/*3 c.415C > T C/T diplotype was 13% (95% confidence interval [CI]: 10-18%), *3/*3 c.415C > T T/T diplotype was 2% [95% CI: 1-2%], *1/*5 c.52G > A G/A diplotype was 2% [95% CI: 1-3%], and *1/*6 c.36_37insGGAGTC ins/- diplotype was 7% [95% CI: 4-12%]. The pooled prevalence of *1/*3 was high in Japanese [20%, 95% CI: 16-24%] and Chinese patients [18%, 95% CI: 12-27%]. The incidence of early leukopenia was 20% [95% CI: 16-26%] in *1/*3 patients, 99% [95% CI: 7-100%] in *3/*3 patients, and 49% [95% CI: 29-69%] in *1/*6 patients. The incidence of late leukopenia was 36% [95% CI: 26-49%] in *1/*3 patients.
    CONCLUSIONS: NUDT15 variants are common and strongly predict TIL in IBD patients. Pre-treatment NUDT15 genotyping should be considered particularly in Asian populations, to guide thiopurine dosing and prevent myelotoxicity.
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  • 文章类型: Systematic Review
    背景:巨细胞病毒(CMV)是实体器官移植(SOT)后常见的感染性并发症。考虑到医疗保健系统的显著差异,进行了系统评价来描述流行病学,管理,以及欧洲和北美以外选定国家的CMV后SOT负担。
    方法:MEDLINE,Embase,并在Cochrane数据库中搜索了亚洲地区15个国家的SOT接受者的观察性研究,太平洋,和拉丁美洲(搜索期:2011年1月1日至2021年9月17日)。结果包括CMV感染/疾病的发生率,复发,危险因素,CMV相关死亡率,治疗模式和指南,耐火和/或抗性CMV,患者报告的结果,和经济负担。
    结果:在确定的2708项研究中,49人符合条件(n=43/49;成人为87.8%;n=34/49,肾脏接受者为69.4%)。在整个研究中,CMV预防策略的选择基于CMV血清状态。总的来说,CMV感染率(1年内)和CMV疾病后SOT分别为,10.3%-63.2%(9项研究)和0%-19.0%(17项研究)。复发发生在35.4%-41.0%的病例中(3项研究),高达5.3%的受者死于CMV相关原因(11项研究)。CMV感染/疾病的常规治疗包括更昔洛韦(GCV)或伐更昔洛韦。高达4.4%的患者对治疗耐药(3项研究);没有关于难治性CMV的研究报道。GCV治疗相关的不良事件包括中性粒细胞减少症(2%-29%),贫血(13%-48%),白细胞减少症(11%-37%),和血小板减少(13%-24%)。关于经济负担的数据很少。
    结论:在北美和欧洲以外,SOT后CMV感染/疾病的发生率高度可变,并且CMV复发频繁。CMV耐药和治疗相关的不良事件,包括骨髓抑制,突出常规治疗未满足的需求。
    BACKGROUND: Cytomegalovirus (CMV) is a frequent infectious complication following solid organ transplantation (SOT). Considering significant differences in healthcare systems, a systematic review was conducted to describe the epidemiology, management, and burden of CMV post-SOT in selected countries outside of Europe and North America.
    METHODS: MEDLINE, Embase, and Cochrane databases were searched for observational studies in SOT recipients across 15 countries in the regions of Asia, Pacific, and Latin America (search period: January 1, 2011 to September 17, 2021). Outcomes included incidence of CMV infection/disease, recurrence, risk factors, CMV-related mortality, treatment patterns and guidelines, refractory and/or resistant CMV, patient-reported outcomes, and economic burden.
    RESULTS: Of 2708 studies identified, 49 were eligible (n = 43/49; 87.8% in adults; n = 34/49, 69.4% in kidney recipients). Across studies, selection of CMV preventive strategy was based on CMV serostatus. Overall, rates of CMV infection (within 1 year) and CMV disease post-SOT were respectively, 10.3%-63.2% (9 studies) and 0%-19.0% (17 studies). Recurrence occurred in 35.4%-41.0% cases (3 studies) and up to 5.3% recipients died of CMV-associated causes (11 studies). Conventional treatments for CMV infection/disease included ganciclovir (GCV) or valganciclovir. Up to 4.4% patients were resistant to treatment (3 studies); no studies reported on refractory CMV. Treatment-related adverse events with GCV included neutropenia (2%-29%), anemia (13%-48%), leukopenia (11%-37%), and thrombocytopenia (13%-24%). Data on economic burden were scarce.
    CONCLUSIONS: Outside of North America and Europe, rates of CMV infection/disease post-SOT are highly variable and CMV recurrence is frequent. CMV resistance and treatment-associated adverse events, including myelosuppression, highlight unmet needs with conventional therapy.
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  • 文章类型: Meta-Analysis
    背景:程序性细胞死亡蛋白1(PD-1)和程序性细胞死亡配体1(PD-L1)的抑制剂最近已用于治疗复发性和难治性霍奇金淋巴瘤(R/RHL)。为了进一步了解PD-1/PD-L1抑制剂在R/RHL中的安全性和有效性,我们进行了这项荟萃分析.
    方法:到2022年3月,已经系统地搜索了数据库和临床注册平台的相关研究。对于安全分析,评估任何级别和3级或更高级别不良反应(AE)的发生率和表现.此外,严重不良事件(SAE),治疗相关死亡,总结了导致治疗中断的AE。总反应率(ORR),完全反应(CR)率,部分响应(PR)率,无进展生存期(PFS),总生存期(OS),并计算缓解持续时间(DOR)进行疗效分析.所有过程主要通过R4.1.2软件的Meta和MetaSurv包实现。
    结果:共纳入20项研究和1440例患者。任何级别和3级或更高级别AE的合并发生率分别为92%和26%,分别。汇集的ORR,CR率和PR率分别为79%,44%和34%,分别。最常见的不良事件是神经病(29%),恶心(27%),发热(26%),和白细胞减少症(25%),最常见的3级或更高的不良事件包括白细胞减少症(10%),输液反应(8%),体重增加(3%),和中性粒细胞减少(2.7%)。在生存分析中,与纳武单抗单药治疗相比,派姆单抗单药治疗的效果似乎更好.
    结论:PD-1/PD-L1抑制剂在R/RHL的治疗中显示出良好的疗效和可耐受的不良事件。
    BACKGROUND: Inhibitors of programmed cell death protein 1 (PD-1) and programmed cell death ligand 1 (PD-L1) have been used in the treatment of relapsed and refractory Hodgkin\'s lymphoma (R/R HL) recently. To further understand the safety and efficacy of PD-1/PD-L1 inhibitors in R/R HL, we conducted this meta-analysis.
    METHODS: Databases and the Clinical Registration Platforms have been systematically searched for related studies by March 2022. For safety analysis, the incidence and exhibition of any grade and grade 3 or higher adverse effects (AEs) were evaluated. Besides, severe AEs (SAEs), treatment-related deaths, and AEs leading to treatment discontinuation were summarized. The overall response rate (ORR), complete response (CR) rate, partial response (PR) rate, progression-free survival (PFS), overall survival (OS), and duration of response (DOR) were calculated for efficacy analysis. All processes were implemented mainly through the package Meta and MetaSurv of software R 4.1.2.
    RESULTS: Overall 20 studies and 1440 patients were enrolled. The pooled incidence of any grade and grade 3 or higher AEs were 92% and 26%, respectively. The pooled ORR, CR rate and PR rate were 79%, 44% and 34%, respectively. The most common AEs were neuropathy (29%), nausea (27%), pyrexia (26%), and leukopenia (25%), and the most common grade 3 or higher AEs included leukopenia (10%), infusion reaction (8%), weight gain (3%), and neutropenia (2.7%). In survival analysis, pembrolizumab monotherapy appeared to perform better compared to nivolumab monotherapy.
    CONCLUSIONS: PD-1/PD-L1 inhibitors show promising efficacy and tolerable AEs in the treatment of R/R HL.
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