metastases

转移
  • 文章类型: Journal Article
    脑转移瘤(BM)的术前放射外科(SRS)旨在实现腔局部控制,与术后SRS相比,软脑膜复发(LMD)减少,并且没有额外的放射性坏死。我们介绍了在神经外科切除脑转移瘤(PREOP-1)之前进行基于直线加速器的立体定向放射外科(SRS)的前瞻性可行性试验的最终结果。
    合格标准包括用于选择性切除的直径最大为4cm的BM。主要终点是在预期的大体肿瘤切除之前在所有患者中提供基于直线加速器的术前SRS的可行性。次要终点包括LMD率,局部控制和总体生存率。探索性终点是免疫学和增殖标志物的表达水平。
    招募了13名中位年龄65岁(范围41-77)的患者。12例(92%)患者接受术前放射外科和转移瘤切除术,1例患者直接手术并接受术后SRS,因此未达到主要终点.转诊与术前SRS的中位时间为6.5个工作日(1-10),从SRS到神经外科手术的中位时间为1天(0-5)。中位处方剂量为16Gy(14-19),中位计划目标体积为12.7cm3(5.9-26.1)。5例患者在术前SRS后完成了12个月的随访,无局部复发或软脑膜疾病。接受术后FSRT的患者在六个月后发展为LMD。有一种短暂的毒性(2级脱发),9名患者死于颅外原因。患者在6个月时报告了运动无力的显着改善(P=0.04)。没有观察到标记表达变化的模式。
    在没有颅内压升高的大型脑转移患者中,基于直线加速器的术前SRS在12/13例患者中是可行的,在12/12例患者中是安全的,没有任何手术延迟或颅内并发症.
    UNASSIGNED: Preoperative radiosurgery (SRS) of brain metastases (BM) aims to achieve cavity local control with a reduction in leptomeningeal relapse (LMD) and without additional radionecrosis compared to postoperative SRS. We present the final results of a prospective feasibility trial of linac-based stereotactic radiosurgery (SRS) prior to neurosurgical resection of a brain metastasis (PREOP-1).
    UNASSIGNED: Eligibility criteria included a BM up to 4 cm in diameter for elective resection. The primary endpoint was the feasibility of delivering linac-based preoperative SRS in all patients prior to anticipated gross tumour resection. Secondary endpoints included rates of LMD, local control and overall survival. Exploratory endpoints were the level of expression of immunological and proliferative markers.
    UNASSIGNED: Thirteen patients of median age 65 years (range 41-77) were recruited. Twelve patients (92 %) received preoperative radiosurgery and metastasectomy and one patient went directly to surgery and received postoperative SRS, thus the primary endpoint was not met. The median time between referral and preoperative SRS was 6.5 working days (1-10) and from SRS to neurosurgery was 1 day (0-5). The median prescribed dose was 16 Gy (14-19) to a median planning target volume of 12.7 cm3 (5.9-26.1). Five patients completed 12-month follow-up after preoperative SRS without local recurrence or leptomeningeal disease. The patient who received postoperative FSRT developed LMD after six months. There was one transient toxicity (grade 2 alopecia) and nine patients have died from extracranial causes. Patients reported significant improvement in motor weakness at 6 months (P = 0.04). No pattern in changes of marker expression was observed.
    UNASSIGNED: In patients with large brain metastasis without raised intracranial pressure, linac-based preoperative SRS was feasible in 12/13 patients and safe in 12/12 patients without any surgical delay or intracranial complications.
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  • 文章类型: Journal Article
    背景:严重疾病对话可以帮助患者避免不必要的治疗。我们先前为患有急性髓细胞性白血病和骨髓增生异常综合征的老年人试行了远程健康严重疾病护理计划(SICP)。
    目的:在本研究中,我们旨在从临床医生的角度了解远程医疗SICP的经验。
    方法:我们研究了10名临床医生,他们向20名患有急性髓细胞性白血病或骨髓增生异常综合征的老年人提供了远程医疗SICP。定量结果包括置信度和可接受性。使用22项调查(范围1-7;得分越高越好)来衡量信心。使用11项调查(5点Likert量表)测量可接受性。由于试点性质和样本量小,在α=.10(2尾)进行了假设检验。临床医生在研究结束时参加了音频记录的定性访谈,以讨论他们的经验。
    结果:共有8名临床医生完成了置信度测量,7名临床医生完成了可接受性测量。我们发现总体置信度有统计学上的显着增加(平均增加0.5,SD0.6;P=0.03)。信心增加最大的是帮助家庭和解和告别(平均1.4,标准差1.5;P=.04)。大多数临床医生同意该格式简单(6/7,86%)且易于使用(6/7,86%)。临床医生认为远程医疗SICP可有效了解患者对临终关怀的价值(7/7,100%)。总共出现了三个定性主题:(1)远程医疗SICP加深了关系并重新建立了信任;(2)每次远程医疗SICP访问都以积极的方式感到独特和个性化;(3)不间断,不匆忙的时间优化了访问体验。
    结论:远程医疗SICP增加了进行严重疾病对话的信心,同时加深了患者与临床医生的关系。
    背景:ClinicalTrials.govNCT04745676;https://www.临床试验.gov/研究/NCT04745676。
    BACKGROUND: Serious illness conversations may help patients avoid unwanted treatments. We previously piloted the telehealth Serious Illness Care Program (SICP) for older adults with acute myeloid leukemia and myelodysplastic syndrome.
    OBJECTIVE: In this study, we aimed to understand the experience of the telehealth SICP from the clinician\'s perspective.
    METHODS: We studied 10 clinicians who delivered the telehealth SICP to 20 older adults with acute myeloid leukemia or myelodysplastic syndrome. Quantitative outcomes included confidence and acceptability. Confidence was measured using a 22-item survey (range 1-7; a higher score is better). Acceptability was measured using an 11-item survey (5-point Likert scale). Hypothesis testing was performed at α=.10 (2-tailed) due to the pilot nature and small sample size. Clinicians participated in audio-recorded qualitative interviews at the end of the study to discuss their experience.
    RESULTS: A total of 8 clinicians completed the confidence measure and 7 clinicians completed the acceptability measure. We found a statistically significant increase in overall confidence (mean increase of 0.5, SD 0.6; P=.03). The largest increase in confidence was in helping families with reconciliation and goodbye (mean 1.4, SD 1.5; P=.04). The majority of clinicians agreed that the format was simple (6/7, 86%) and easy to use (6/7, 86%). Clinicians felt that the telehealth SICP was effective in understanding their patients\' values about end-of-life care (7/7, 100%). A total of three qualitative themes emerged: (1) the telehealth SICP deepened relationships and renewed trust; (2) each telehealth SICP visit felt unique and personal in a positive way; and (3) uninterrupted, unrushed time optimized the visit experience.
    CONCLUSIONS: The telehealth SICP increased confidence in having serious illness conversations while deepening patient-clinician relationships.
    BACKGROUND: ClinicalTrials.gov NCT04745676; https://www.clinicaltrials.gov/study/NCT04745676.
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  • 文章类型: Journal Article
    背景:Nivolumab是欧洲第一个被批准用于治疗晚期肾细胞癌(aRCC)的免疫检查点抑制剂。证人是一个持续的,prospective,旨在评估纳武单抗在法国现实生活(或常规实践)中治疗的aRCC患者中的有效性和安全性的观察性研究(ClinicalTrials.gov标识符:NCT03455452).
    方法:本研究包括确诊为aRCC的成年患者,这些患者在1-2次抗血管生成治疗后开始使用纳武单抗。终点包括总生存期(OS),无进展生存期(PFS),治疗持续时间(DOT),响应持续时间(DOR),总反应率(ORR),亚组分析,和治疗相关不良事件(TRAEs)。这里提供了中位随访12.3个月后的结果。
    结果:共纳入325例aRCC患者,其中38.2%的Karnofsky评分<80,77.8%的人接受nivolumab作为二线治疗,69.5%曾接受过肾切除术。在总人口中,中位OS为20.5个月[95%置信区间(CI)17.6~25.0]个月,中位PFS为5.2个月(95%CI4.5~5.9).ORR为34.5%,中位数DOT为3.8个月,中位DOR为16.5个月。Nivolumab在不同的亚组中有效,包括骨或腺转移患者以及接受基线皮质类固醇的患者。此外,无论之前的肾切除术和治疗路线如何,均观察到有效性.没有发现新的安全性信号;32.0%的患者报告了任何等级的TRAE,≥3级和严重TRAE各占11.1%,和TRAEs导致8.9%的停药。
    结论:正在进行的WITNESS研究的初步结果证实了纳武单抗单药治疗先前治疗过的aRCC患者的真实世界有效性和安全性。治疗益处与关键III期CheckMate025随机临床试验中观察到的益处相似,尽管范围更广,现实生活中的研究人群。
    BACKGROUND: Nivolumab is the first immune checkpoint inhibitor approved in Europe for the treatment of advanced renal cell carcinoma (aRCC) in patients resistant to prior antiangiogenic therapy. WITNESS is an ongoing, prospective, observational study designed to evaluate the effectiveness and safety of nivolumab in patients with aRCC treated in real life (or routine practice) in France (ClinicalTrials.gov identifier: NCT03455452).
    METHODS: This study includes adult patients with a confirmed diagnosis of aRCC who have initiated nivolumab after 1-2 prior lines of antiangiogenic therapy. Endpoints include overall survival (OS), progression-free survival (PFS), duration of treatment (DOT), duration of response (DOR), overall response rate (ORR), subgroup analyses, and treatment-related adverse events (TRAEs). Results after a median follow-up of 12.3 months are presented here.
    RESULTS: A total of 325 patients with aRCC were included, of whom 38.2% had a Karnofsky score <80, 77.8% received nivolumab as second-line therapy, and 69.5% had undergone a previous nephrectomy. In the overall population, median OS was 20.5 [95% confidence interval (CI) 17.6-25.0] months and median PFS was 5.2 (95% CI 4.5-5.9) months. ORR was 34.5%, median DOT was 3.8 months, and median DOR was 16.5 months. Nivolumab was effective in different subgroups including patients with bone or glandular metastases and those receiving baseline corticosteroids. Moreover, effectiveness was observed irrespective of prior nephrectomy and line of treatment. No new safety signals were identified; TRAEs of any grade were reported in 32.0% of patients, grade ≥3 and serious TRAEs in 11.1% each, and TRAEs leading to discontinuation in 8.9%.
    CONCLUSIONS: Preliminary results of the ongoing WITNESS study confirm the real-world effectiveness and safety of nivolumab monotherapy in previously treated patients with aRCC. Treatment benefits were similar to those observed in the pivotal phase III CheckMate 025 randomized clinical trial, despite a broader, real-life study population.
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  • 文章类型: Journal Article
    胰腺癌(PC)是一种致命的疾病,尤其是转移性PC。它可以分为两种类型:头部胰腺癌(H-PC)和体尾胰腺癌(BT-PC)。先前的研究证明,它们具有不同的总体生存率(OS),应被视为PC的两个不同类别。目前,关于不同原发肿瘤位置和转移部位的OS,该领域仍然存在差距,以及与转移性PC患者的各种原发肿瘤位置相关的转移模式。因此,我们的研究旨在通过分析来自监测的大量人口的数据来解决这一差距,流行病学,和结束结果(SEER)数据库。不同原发肿瘤位置和转移部位的不同预后可能表明不同的原发位置和转移部位可能需要不同的治疗和随访策略。希望这些发现将为今后的指南更新和相关研究奠定基础。
    纳入了2010年至2015年间美国国家癌症研究所SEER计划的病理证实为IV期转移性PC的患者,排除各种肿瘤患者,不指定年龄,转移的特定部位,或操作系统。数据包括年龄,种族,性别,肿瘤大小,T级,N级,grade,网站,转移部位的数量,手术,放射治疗,从SEER数据库收集化疗和诊断年限.OS定义为从最初诊断到死亡日期的时期。比较了肿瘤不同原发位置的特定转移部位。通过Cox回归分析分析生存率。
    总的来说,14,406例转移性PC患者纳入本研究(7,104例H-PC和7,302例BT-PC)。性别比例,肿瘤大小,T级,N级,BT-PC和H-PC的原发灶手术和放疗转移部位数量不同。H-PC中只有1个转移部位的比例为68.3%,而BT-PC中为58.3%。与H-PC相比,BT-PC是肝转移的独立危险因素[比值比(OR)=1.510;95%置信区间(CI):1.320-1.727]。不管是那些有多发性转移的人,或者对于那些孤立的肝或肺转移瘤,转移性H-PC患者的OS较好(分别为P<0.001,P=0.001,P=0.04).在孤立性肝转移患者中,BT-PC的OS比H-PC更差[风险比(HR)=1.109;95%CI:1.046-1.175].
    转移性BT-PC的OS更差,罹患肝脏和多发性转移的风险增加。此外,在孤立性转移患者中,肝转移患者的生存率最差.
    UNASSIGNED: Pancreatic cancer (PC) is a lethal disease, especially metastatic PC. And it can be divided into two types: head pancreatic cancer (H-PC) and body and tail pancreatic cancer (BT-PC). Prior studies have proved that they have different overall survival (OS) and should be regarded as two different categories of PC. At present, there remains a gap in the field regarding OS across different primary tumor locations and metastatic sites, as well as the metastatic patterns associated with various primary tumor locations in patients with metastatic PC. Thus, our study aims to address this gap by analyzing data from a large population sourced from the Surveillance, Epidemiology, and End Results (SEER) database. The different prognosis of different primary tumor locations and metastatic sites may indicate that different primary locations and metastatic sites may require different therapy and follow-up strategy. It is hoped that these findings will lay the groundwork for future guideline updates and related research.
    UNASSIGNED: Patients with pathologically confirmed stage IV metastatic PC from the National Cancer Institute\'s SEER program between 2010 and 2015 were included, excluding patients with various tumors, without specifying age, specific sites of metastasis, or OS. Data including age, race, gender, tumor size, T stage, N stage, grade, sites, number of metastatic sites, surgery, radiotherapy, chemotherapy and years of diagnoses were collected from the SEER database. OS was defined as the period from initial diagnosis to the date of death. Specific metastatic sites for the different primary locations of tumor were compared. Survival was analyzed by Cox regression analyses.
    UNASSIGNED: Overall, 14,406 patients with metastatic PC were included in this research (7,104 of H-PC and 7,302 of BT-PC). Gender proportion, tumor size, T stage, N stage, number of metastatic sites surgery of the primary lesions and radiotherapy were different between BT-PC and H-PC. The proportion of only 1 metastatic site was 68.3% in H-PC compared with 58.3% in the BT-PC. The BT-PC was an independent risk factor for liver metastases compared with the H-PC [odds ratio (OR) =1.510; 95% confidence interval (CI): 1.320-1.727]. No matter for those with multiple metastases, or for those with solitary liver or lung metastases, patients with metastatic H-PC showed better OS (P<0.001, P=0.001, P=0.04, respectively). In patients with solitary liver metastases, worse OS was observed in the BT-PC than the H-PC [hazard ratio (HR) =1.109; 95% CI: 1.046-1.175].
    UNASSIGNED: The metastatic BT-PC had worse OS and increased risk to suffer from liver and multiple metastases. Moreover, in patients with solitary metastases, those with liver metastases presented poorest survival.
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  • 文章类型: Journal Article
    对于一些无法手术的转移性结直肠癌患者,氟嘧啶单药治疗是一种选择。不像贝伐单抗,增加了aflibercept,作为抗血管生成剂的抗体,从未在这种情况下进行过评估。该研究的目的是确定阿柏西普是否可以增加氟嘧啶单药治疗的疗效而不增加毒性。这项多中心II期非比较试验评估了在不适合接受双重细胞毒性化疗的患者中,在输注5-氟尿嘧啶/亚叶酸(LV5FU2方案)中添加阿柏西普作为一线治疗。主要终点是6个月无进展生存期(PFS)。临床假设预期6个月的PFS率超过40%(预期60%)。共有117名患者,平均年龄为81岁,包括:A组59例(LV5FU2-aflibercept)和B组58例(仅LV5FU2)。两组的6个月PFS为54.7%(两组的90%CI为42.5-66.5)。中位总生存期为21.8个月(A组)和25.1个月(B组)。总体毒性在A组中更为常见:≥3级毒性为82%对58.2%。鉴于6个月的PFS,这项研究可以被认为是积极的。然而,阿柏西普在这个人群中的毒性很高,并且不打算将试验延续至III期.
    Fluropyrimidine monotherapy is an option for some patients with inoperable metastatic colorectal cancer. Unlike bevacizumab, the addition of aflibercept, an antibody acting as an anti-angiogenic agent, has never been evaluated in this context. The aim of the study was to determine whether aflibercept could increase the efficacy of fluoropyrimidine monotherapy without increasing toxicity. This multicenter phase II non-comparative trial evaluated the addition of aflibercept to infusional 5-fluorouracil/folinic acid (LV5FU2 regimen) as first-line treatment in patients unfit to receive doublet cytotoxic chemotherapy. The primary endpoint was 6-month progression-free survival (PFS). The clinical hypotheses expected a PFS rate at 6 months of over 40% (60% expected). A total of 117 patients, with a median age of 81 years, were included: 59 in arm A (LV5FU2-aflibercept) and 58 in arm B (LV5FU2 alone). Six-month PFS was 54.7% in both arms (90% CI 42.5-66.5 in both). Median overall survival was 21.8 months (arm A) and 25.1 months (arm B). Overall toxicity was more common in arm A: grade ≥ 3 toxicity in 82% versus 58.2%. Given the 6-month PFS, the study can be considered positive. However, the toxicity of aflibercept in this population was high, and continuation of the trial into phase III is not envisaged.
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  • 文章类型: Journal Article
    背景:使用不同翻转角演化(SPACE)的应用优化对比度的对比后T1采样完美是评估脑转移的首选3DT1自旋回波序列,无论延长的扫描时间。
    目的:评估加速对比后T1-SPACE与迭代去噪(ID)在肿瘤患者颅内增强病变中的应用。
    方法:对于颅内病变的评估,108例患者在相同的成像过程中接受了标准和加速T1-SPACE。两名神经放射科医生评估了整体图像质量,神器,增强程度,平均对比度-噪声比/薄壁组织,以及无ID的标准和加速T1-SPACE的增强病变数量。
    结果:尽管没有ID的标准和加速的T1-SPACE与有和没有ID的加速SPACE在整体图像质量和平均对比度噪声比/薄壁组织方面存在显著差异,标准和加速T1-SPACE与ID之间没有显着差异。加速的T1-SPACE比标准的T1-SPACE表现出更多的伪影;然而,带ID的加速T1-SPACE显示出比不带ID的加速T1-SPACE明显更少的伪影。无ID的加速T1-SPACE显示的增强病变数量明显低于有ID的标准和加速T1-SPACE;然而,标准T1-SPACE和加速T1-SPACE与ID之间没有显着差异,无论病变大小。
    结论:虽然T1-SPACE加速显著缩短了扫描时间,与标准T1-SPACE相比,它显示出更低的整体图像质量和病变可检测性.将ID应用于加速的T1-SPACE可产生与标准T1-SPACE相当的整体图像质量和脑实质中增强病变的检测。具有ID的加速T1-SPACE可能是标准T1-SPACE的有希望的替代品。
    BACKGROUND: Post-contrast T1-Sampling Perfection with Application-optimized Contrasts using different flip angle Evolutions (SPACE) is the preferred 3D T1 spin-echo sequence for evaluating brain metastases, regardless of the prolonged scan time.
    OBJECTIVE: To evaluate the application of accelerated post-contrast T1-SPACE with iterative denoising (ID) for intracranial enhancing lesions in oncologic patients.
    METHODS: For evaluation of intracranial lesions, 108 patients underwent standard and accelerated T1-SPACE during the same imaging session. Two neuroradiologists evaluated the overall image quality, artifacts, degree of enhancement, mean contrast-to-noise ratiolesion/parenchyma, and number of enhancing lesions for standard and accelerated T1-SPACE without ID.
    RESULTS: Although there was a significant difference in the overall image quality and mean contrast-to-noise ratiolesion/parenchyma between standard and accelerated T1-SPACE without ID and accelerated SPACE with and without ID, there was no significant difference between standard and accelerated T1-SPACE with ID. Accelerated T1-SPACE showed more artifacts than standard T1-SPACE; however, accelerated T1-SPACE with ID showed significantly fewer artifacts than accelerated T1-SPACE without ID. Accelerated T1-SPACE without ID showed a significantly lower number of enhancing lesions than standard- and accelerated T1-SPACE with ID; however, there was no significant difference between standard and accelerated T1-SPACE with ID, regardless of lesion size.
    CONCLUSIONS: Although accelerated T1-SPACE markedly decreased the scan time, it showed lower overall image quality and lesion detectability than the standard T1-SPACE. Application of ID to accelerated T1-SPACE resulted in comparable overall image quality and detection of enhancing lesions in brain parenchyma as standard T1-SPACE. Accelerated T1-SPACE with ID may be a promising replacement for standard T1-SPACE.
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  • 文章类型: Journal Article
    脊柱多发性骨髓瘤(MM)和转移瘤是两种常见的癌症类型,具有相似的影像学特征,需要进行鉴别诊断以确保精确治疗。这项研究的目的是建立放射组学模型,以有效区分它们。
    参加这项研究的是来自两个医疗机构的263名患者,其中脊柱MM127例,脊柱转移瘤136例。其中,来自机构I的210名患者被用作内部训练队列,来自机构II的53名患者被用作外部验证队列。收集并回顾了对比增强T1加权成像(CET1)和T2加权成像(T2WI)序列。基于从CET1和T2WI图像中提取的1037个影像组学特征,逻辑回归(LR),AdaBoost(AB),支持向量机(SVM)随机森林(RF),构造了基于多核学习的支持向量机(MKL-SVM)。通过五次交叉验证来调整超参数。通过准确度(ACC)比较了不同影像组学模型之间的诊断效率,灵敏度(SEN),特异性(SPE),ROC曲线下面积(AUC),YI,阳性预测值(PPV),负预测值(NPY),和F1得分。
    基于单序列,RF模型优于所有其他模型。所有基于T2WI图像的模型都比基于CET1的模型表现更好。通过整合CET1和T2WI序列提高了所有模型的效率,MKL-SVM模型与ACC实现了最佳性能,AUC,F1评分分别为0.862、0.870和0.874。
    基于MRI构建的影像组学模型在鉴别脊柱MM和转移瘤方面取得了令人满意的诊断性能,为个体化诊疗提供了广阔的应用前景。
    UNASSIGNED: Spinal multiple myeloma (MM) and metastases are two common cancer types with similar imaging characteristics, for which differential diagnosis is needed to ensure precision therapy. The aim of this study is to establish radiomics models for effective differentiation between them.
    UNASSIGNED: Enrolled in this study were 263 patients from two medical institutions, including 127 with spinal MM and 136 with spinal metastases. Of them, 210 patients from institution I were used as the internal training cohort and 53 patients from Institution II were used as the external validation cohort. Contrast-enhanced T1-weighted imaging (CET1) and T2-weighted imaging (T2WI) sequences were collected and reviewed. Based on the 1037 radiomics features extracted from both CET1 and T2WI images, Logistic Regression (LR), AdaBoost (AB), Support Vector Machines (SVM), Random Forest (RF), and multiple kernel learning based SVM (MKL-SVM) were constructed. Hyper-parameters were tuned by five-fold cross-validation. The diagnostic efficiency among different radiomics models was compared by accuracy (ACC), sensitivity (SEN), specificity (SPE), area under the ROC curve (AUC), YI, positive predictive value (PPV), negative predictive value (NPY), and F1-score.
    UNASSIGNED: Based on single-sequence, the RF model outperformed all other models. All models based on T2WI images performed better than those based on CET1. The efficiency of all models was boosted by incorporating CET1 and T2WI sequences, and the MKL-SVM model achieved the best performance with ACC, AUC, and F1-score of 0.862, 0.870, and 0.874, respectively.
    UNASSIGNED: The radiomics models constructed based on MRI achieved satisfactory diagnostic performance for differentiation of spinal MM and metastases, demonstrating broad application prospects for individualized diagnosis and treatment.
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  • 文章类型: Journal Article
    肺癌是全球男性死亡的首要原因,也是女性癌症相关死亡的第二大原因。非小细胞肺癌(NSCLC)病例是在晚期发现的,在疾病管理和生存结果方面提出了重大挑战。本研究旨在调查IIIB期和IV期NSCLC患者的临床发现和管理,以便更好地做出决策。疾病管理,以及对这种致命疾病的理解。
    在这项针对340名患者的队列研究中,共有140例(41.2%)被诊断为晚期NSCLC,平均年龄为64岁.从利雅得的两家三级医院检索了符合纳入标准的2015年至2021年患者的电子数据,沙特阿拉伯,并使用Excel表记录变量。患者数据,包括所有分类变量,如性别,舞台,转移,ALK,EGFR,ROS,等。,检索并分析了年龄和体重指数(BMI)等连续变量。
    多变量Cox回归模型表明,吸烟是三分之二男性吸烟者(37.9%)死亡的重要危险因素,中位生存时间为123天。胸膜和脑转移的疾病进展更高,局部转移在75%的患者中最高。治疗的意图主要是姑息治疗,然而,同时使用化疗和免疫治疗具有统计学意义.如果将化疗维持在相同剂量而不中断剂量,则患者对一线治疗的反应显着改善。
    非小细胞肺癌的总体治愈率和生存率仍然很低,特别是在转移性疾病中。因此,需要继续研究新药和联合疗法,以便更好地做出决策,将临床获益扩大到更广泛的患者群体,并改善NSCLC的预后.
    UNASSIGNED: Lung cancer is the top cause of mortality in males and the second largest cause of cancer-related fatalities in women worldwide. Non-small cell lung cancer (NSCLC) cases are discovered at an advanced stage, raising major challenges in disease management and survival outcomes. This study aimed to investigate the clinical findings and management of stage IIIB and IV NSCLC patients for better decision-making, disease management, and understanding of this fatal disease.
    UNASSIGNED: In this cohort study of 340 patients, a total of 140 (41.2%) were diagnosed with advanced-stage NSCLC at a mean age of 64 years. The electronic data of patients from 2015 to 2021 who met the inclusion criteria were retrieved from two tertiary hospitals in Riyadh, Saudi Arabia, and an Excel sheet was used to record the variables. Patients\' data including all categorical variables such as gender, stage, metastasis, ALK, EGFR, and ROS, etc., and continuous variables such as age and body mass index (BMI) were retrieved and analyzed.
    UNASSIGNED: The multivariate Cox-regression model indicated that smoking was the significant risk factor of death for two-thirds of male smokers (37.9%), with a median survival time of 123 days. Disease progression was higher with pleural and brain metastasis, and localized metastasis was the highest in 75% of patients. The intent of treatment was mainly palliative, however, a statistically significant association was found with the simultaneous use of chemotherapy and immunotherapy. Patients\' response to first-line treatment revealed a significant improvement if chemotherapy treatment was maintained at the same dose without interruption of dosage.
    UNASSIGNED: The overall cure and survival rates for NSCLC remain low, particularly in metastatic disease. Therefore, continued research into new drugs and combination therapies is required for better decision-making to expand the clinical benefit to a broader patient population and to improve outcomes in NSCLC.
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  • 文章类型: Journal Article
    目的:根据淋巴结转移的发生率,探讨SiewertII型腺癌(AC)是否应解剖上纵隔和/或中纵隔淋巴结(UMMN)。此外,探讨食管受累长度(LEI)与UMMN转移之间的关系。
    方法:对一组SiewertII型AC患者进行回顾性评估,这些患者由一个常规治疗食管胃交界处(EGJ)肿瘤的外科团队进行手术,并进行食管切除术和扩大淋巴结切除术。研究的主要终点是UMMN的转移率。
    结果:共纳入2018年7月至2022年9月的94例EGJ肿瘤患者。车站106recR(6.4%,6/94)是上纵隔淋巴结(UMN)中唯一呈现阳性淋巴结的站点。107、109和108站的中纵隔淋巴结(MMN)转移分别为2.1%(2/94)和5.0%(4/80),分别。在11例MMN或UMN转移患者中,63.6%(7/11)的转移性淋巴结少于7个,54.5%(6/11)的病理N分期≤2。LEI>3cm(p=0.042)在单变量逻辑分析中显示MMN转移的风险更高。然而,未检测到纵隔淋巴结转移的独立危险因素。
    结论:这项研究表明,在可切除的SiewertII型AC中,阳性MMN和UMN的发生率相对较低,这表明没有必要对这些站进行例行解剖。LEI>3cm可能与纵隔淋巴结转移的风险增加有关。由于大多数MMN或UMN阳性的患者的转移性淋巴结数量有限,因此某些患者可以从扩大的淋巴结切除术中受益。
    OBJECTIVE: To explore whether the upper and/or middle mediastinal nodes (UMMN) should be dissected in Siewert type II adenocarcinoma (AC) according to the incidence of lymph node metastasis. Additionally, to investigate the association between the length of esophageal involvement (LEI) and the UMMN metastases.
    METHODS: A cohort with Siewert type II AC who were operated on by a surgical team that routinely treated esophagogastric junction (EGJ) tumors with esophagectomy and extended lymphadenectomy were assessed retrospectively. The primary endpoint of the research was the metastasis rate of UMMN.
    RESULTS: A total of 94 patients with EGJ tumor from July 2018 to September 2022 were enrolled. Station 106recR (6.4%, 6/94) was the only station among upper mediastinal nodes (UMN) that presented positive nodes. Middle mediastinal nodes (MMN) metastases of station 107, 109 and station 108 were 2.1% (2/94) and 5.0% (4/80), respectively. Among the 11 patients with MMN or UMN metastases, 63.6% (7/11) had lesser than seven metastatic nodes, and 54.5% (6/11) had a pathological N stage ≤2. LEI >3 cm (p = 0.042) showed a higher risk for MMN metastases in univariable logistic analysis. However, no independent risk factor for mediastinal node metastases was detected.
    CONCLUSIONS: This study demonstrated that the incidence of positive MMN and UMN is relatively low in resectable Siewert type II AC, which indicated that it is not necessary to perform a routine dissection upon these stations. LEI >3 cm might be associated with higher risk for mediastinal node metastasis. Certain patients could benefit from extended lymphadenectomy since most of the patients with positive MMN or UMN have a limited number of metastatic nodes.
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  • 文章类型: Journal Article
    目的:评估大量成人可疑恶性骨性病变的影像引导芯针活检(ICNB)的诊断率和准确性,评估哪些因素影响这些措施,并提供优化产量的技术建议。
    方法:完成了对2010年至2021年进行的2321个ICNB的回顾性分析。活检的诊断产量和准确性以及一系列患者,病变相关,技术因素进行回顾性分析。进行多变量统计分析以评估哪些因素与产量和准确性相关。然后测试总核心长度和核心数量的不同截断值以确定与增加的诊断产量相关的阈值。
    结果:诊断率为98.2%(2279/2321),准确率为97.6%(120/123)。总核心长度增加(比值比[OR]=2.34,95%置信区间[CI](1.41-3.90),p=0.001),核心编号(OR=1.51,95%CI(1.06-2.16),p=0.02)和原发性恶性肿瘤的存在(OR=2.81,95%CI(1.40-5.62),p=0.004)与提高的产率相关。四肢病变位置(OR=0.27,95%CI(0.11-0.68),p=0.006)并使用荧光成像指导(OR=0.33,95%CI(0.12-0.90),p=0.03)与较低的产量有关。发现与诊断产量增加相关的截止阈值为20mm的总岩心长度(边际OR=4.16,95%CI=(2.09-9.03),p<0.001),和获得的三个总岩心(边际OR=2.78,95%CI(1.34-6.54),p=0.005)。所分析的因素均不影响诊断准确性。
    结论:ICNB具有较高的诊断率和准确率。几个因素影响诊断产量;20毫米的核心长度和三个总核心优化产量。
    结论:影像引导下可疑恶性骨性病变的粗针活检是一种安全的方法,具有很高的诊断率和准确率。获得20毫米的总核心长度和三个总核心优化诊断产量。
    结论:•在一项回顾性队列研究中,对成人疑似骨性恶性病变的图像引导芯针活检被发现具有非常高的诊断率和准确率.•活检的总核心长度和核心数量增加均与诊断产量增加相关。这些关系在20毫米的总核心长度和三个总核心获得的阈值。•已知原发性恶性肿瘤的存在也与产量增加有关,而使用荧光成像指导和四肢病变位置与产量降低有关。
    OBJECTIVE: To evaluate diagnostic yield and accuracy of image-guided core needle biopsy (ICNB) of suspected malignant osseous lesions in a large cohort of adults, evaluate what factors influence these measures, and offer technical recommendations to optimize yield.
    METHODS: A retrospective analysis of 2321 ICNBs performed from 2010 to 2021 was completed. The diagnostic yield and accuracy of the biopsies as well as a series of patient, lesion-related, and technical factors were retrospectively analyzed. Multivariate statistical analysis was performed to evaluate what factors were associated with yield and accuracy. Different cutoff values of total core length and core number were then tested to determine threshold values in relation to increased diagnostic yield.
    RESULTS: Diagnostic yield was 98.2% (2279/2321) and accuracy was 97.6% (120/123). Increased total core length (odds ratio [OR] = 2.34, 95% confidence interval [CI] (1.41-3.90), p = 0.001), core number (OR = 1.51, 95% CI (1.06-2.16), p = 0.02) and presence of primary malignancy (OR = 2.81, 95% CI (1.40-5.62), p = 0.004) were associated with improved yield. Lesion location in an extremity (OR = 0.27, 95% CI (0.11-0.68), p = 0.006) and using fluoroscopic imaging guidance (OR = 0.33, 95% CI (0.12-0.90), p = 0.03) were associated with lower yield. Cutoff thresholds in relation to increased diagnostic yield were found to be 20 mm total core length (marginal OR = 4.16, 95% CI = (2.09-9.03), p < 0.001), and three total cores obtained (marginal OR = 2.78, 95% CI (1.34-6.54), p = 0.005). None of the analyzed factors influenced diagnostic accuracy.
    CONCLUSIONS: ICNB has a high rate of diagnostic yield and accuracy. Several factors influence diagnostic yield; 20 mm core length and three total cores optimize yield.
    CONCLUSIONS: Image-guided core needle biopsy of suspected malignant osseous lesions is a safe procedure with a very high rate of diagnostic yield and accuracy. Obtaining 20 mm total core length and three total cores optimizes diagnostic yield.
    CONCLUSIONS: • In a retrospective cohort study, image-guided core needle biopsy of suspected osseous malignant lesions in adults was found to have very high rates of diagnostic yield and accuracy. • Increased total core length and core number of biopsies were each associated with increased diagnostic yield, and these relationships reached thresholds at 20 mm total core length and three total cores obtained. • The presence of a known primary malignancy was also associated with increased yield while using fluoroscopic imaging guidance and lesion location in an extremity were associated with decreased yield.
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