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Microvessel Density (MVD) in Patients with Osteosarcoma: A Systematic Review and Meta-Analysis. 骨肉瘤患者的微血管密度 (MVD):系统回顾与元分析》。
IF 1.8 4区 医学 Q3 ONCOLOGY Pub Date : 2024-01-01 Epub Date: 2024-02-12 DOI: 10.1080/07357907.2024.2311266
Konstantinos Perivoliotis, Panagiotis Ntellas, Katerina Dadouli, Athina A Samara, Sotirios Sotiriou, Maria Ioannou, Konstantinos Tepetes

A meta-analysis was designed and conducted to estimate the effect of tumoral microvessel density (MVD) on the survival of patients with osteosarcoma. There was no difference between high and low MVD regarding the overall (OS) and disease-free (DFS) survival. Low MVD tumors displayed a lower DFS at the third year of follow-up. Although primary metastases did not affect the mean MVD measurements, tumors with a good chemotherapy response had a higher MVD value. Although no significant differences between tumoral MVD, OS and DFS were found, good adjuvant therapy responders had a significant higher vascularization pattern.

我们设计并进行了一项荟萃分析,以估计肿瘤微血管密度(MVD)对骨肉瘤患者生存期的影响。在总生存期(OS)和无病生存期(DFS)方面,高MVD和低MVD之间没有差异。低MVD肿瘤在随访第三年的DFS较低。虽然原发转移瘤不影响平均MVD测量值,但化疗反应良好的肿瘤MVD值较高。虽然在肿瘤MVD、OS和DFS之间没有发现明显差异,但辅助治疗反应良好的肿瘤的血管化模式明显更高。
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引用次数: 0
The Nature, Origin and Evolution of Life: Part I The Fundamental Logic and Organization of Life. 生命的本质、起源与进化:第一部分生命的基本逻辑与组织。
IF 2.4 4区 医学 Q3 ONCOLOGY Pub Date : 2024-01-01 Epub Date: 2023-09-28 DOI: 10.1080/07357907.2023.2262122
Gary H Lyman, Christopher H Lyman, Nicole M Kuderer
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引用次数: 0
Single Nucleotide Polymorphisms Associated with Prostate Cancer Progression: A Systematic Review. 与前列腺癌进展相关的单核苷酸多态性:系统综述。
IF 1.8 4区 医学 Q3 ONCOLOGY Pub Date : 2024-01-01 Epub Date: 2023-12-18 DOI: 10.1080/07357907.2023.2291776
Daniel Felipe Mendivelso González, Santiago Andrés Sánchez Villalobos, Andrea Estefanía Ramos, Wendy Johana Montero Ovalle, Martha Lucía Serrano López

Background: New biomarkers of progression in patients with prostate cancer (PCa) are needed to improve their classification and clinical management. This systematic review investigated the relationship between single nucleotide polymorphisms (SNPs) and PCa progression.

Methods: A keyword search was performed in Pubmed, EMBASE, Scopus, Web of Science, and Cochrane for publications between 2007 and 2022. We included articles with adjusted and significant associations, a median follow-up greater than or equal to 24 months, patients taken to radical prostatectomy (RP) as a first therapeutic option, and results presented based on biochemical recurrence (BCR).

Results: In the 27 articles selected, 73 SNPs were identified in 39 genes, organized in seven functional groups. Of these, 50 and 23 SNPs were significantly associated with a higher and lower risk of PCa progression, respectively. Likewise, four haplotypes were found to have a significant association with PCa progression.

Conclusion: This article highlights the importance of SNPs as potential markers of PCa progression and their possible functional relationship with some genes relevant to its development and progression. However, most variants were identified only in cohorts from two countries; no additional studies reproduce these findings.

背景:前列腺癌(PCa)患者的病情进展需要新的生物标志物来改进分类和临床治疗。本系统综述研究了单核苷酸多态性(SNPs)与 PCa 进展之间的关系:在 Pubmed、EMBASE、Scopus、Web of Science 和 Cochrane 中对 2007 年至 2022 年间的出版物进行了关键词检索。我们纳入了调整后具有显著关联、中位随访时间大于或等于24个月、将根治性前列腺切除术(RP)作为首选治疗方案的患者,以及根据生化复发(BCR)得出结果的文章:在所选的 27 篇文章中,在 39 个基因中发现了 73 个 SNPs,分为 7 个功能组。其中,分别有 50 个和 23 个 SNP 与 PCa 进展的较高风险和较低风险显著相关。同样,还发现 4 个单倍型与 PCa 进展有显著相关性:本文强调了 SNPs 作为 PCa 进展潜在标志物的重要性,以及它们与 PCa 发展和进展相关基因之间可能存在的功能关系。然而,大多数变异仅在两个国家的队列中发现;没有其他研究再现这些发现。
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引用次数: 0
One Heresy and One Orthodoxy: On Dialetheism, Dimathematism, and the Non-normativity of Logic. 一个异端和一个正统:论 Dialetheism、Dimathematism 和逻辑的非规范性。
IF 0.9 4区 医学 Q3 ONCOLOGY Pub Date : 2024-01-01 Epub Date: 2022-03-09 DOI: 10.1007/s10670-022-00528-8
Heinrich Wansing

In this paper, Graham Priest's understanding of dialetheism, the view that there exist true contradictions, is discussed, and various kinds of metaphysical dialetheism are distinguished between. An alternative to dialetheism is presented, namely a thesis called 'dimathematism'. It is pointed out that dimathematism enables one to escape a slippery slope argument for dialetheism that has been put forward by Priest. Moreover, dimathematism is presented as a thesis that is helpful in rejecting the claim that logic is a normative discipline.

本文讨论了格雷厄姆-普里斯特对 "二律背反"(即存在真正矛盾的观点)的理解,并区分了各种形而上学的 "二律背反"。他还提出了拨神论的替代方案,即 "二律背反论"。论文指出,二律背反论使人们摆脱了普利斯特为辩证神论提出的滑坡论证。此外,"二律背反论 "还有助于驳斥逻辑学是一门规范性学科的说法。
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引用次数: 0
Comorbidity in Small Cell Lung Cancer: Prognostic Impacts of Hypertension/Coronary Artery Disease, Diabetes Mellitus, and Chronic Obstructive Pulmonary Disease. 小细胞肺癌的合并症:高血压/冠状动脉疾病、糖尿病和慢性阻塞性肺病的预后影响。
IF 2.4 4区 医学 Q3 ONCOLOGY Pub Date : 2024-01-01 Epub Date: 2024-02-01 DOI: 10.1080/07357907.2024.2310574
Faruk Tas, Akin Ozturk, Kayhan Erturk

Comorbidity, the most important components of which are hypertension/coronary artery disease (HTN/CAD), diabetes mellitus (DM), and chronic obstructive pulmonary disease (COPD), is frequently encountered in small cell lung cancer (SCLC) patients. We aimed to assess the possible impacts of these major comorbidities on the prognoses of SCLC patients. A total of 378 SCLC patients were analyzed retrospectively. We did not ascertain the effect of comorbidity on survival in SCLC patients in general; and similarly, the presence of HTN/CAD and COPD did not adversely affect the outcome. However, lower survival rates were observed in patients with SCLC coexisting with DM.

合并症是小细胞肺癌(SCLC)患者的常见病,其中最重要的组成部分是高血压/冠状动脉疾病(HTN/CAD)、糖尿病(DM)和慢性阻塞性肺疾病(COPD)。我们旨在评估这些主要合并症对 SCLC 患者预后可能产生的影响。我们对 378 名 SCLC 患者进行了回顾性分析。我们没有确定合并症对一般 SCLC 患者生存率的影响;同样,存在高血压/冠心病和慢性阻塞性肺病也不会对预后产生不利影响。然而,我们观察到,SCLC 患者同时患有糖尿病的存活率较低。
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引用次数: 0
Human Mycobiota and Its Role in Cancer Progression, Diagnostics and Therapeutics: A Link Lesser-Known. 人类霉菌生物群及其在癌症进展、诊断和治疗中的作用:鲜为人知的联系
IF 2.4 4区 医学 Q3 ONCOLOGY Pub Date : 2024-01-01 Epub Date: 2024-01-07 DOI: 10.1080/07357907.2024.2301733
Souvik Roy, Dhrisaj Ray, Ishani Laha, Lopamudra Choudhury

Although not as well studied as the bacterial component of the human microbiota, the commensal fungi or mycobiota play important roles in maintaining our health by augmenting our immune system. This mycobiota is also associated with various fatal diseases like opportunistic mycoses, and even cancer, with different cancers having respective type-specific mycobiota. The different fungal species which comprise these different intratumoral mycobiota play important roles in cancer progression. The aim of this review paper is to decipher the association between mycobiota and cancer, and shed light on new avenues in cancer diagnosis, and the development of new anti-cancer therapeutics.

共生真菌或真菌生物群虽然不像人类微生物群中的细菌成分那样得到深入研究,但它们通过增强我们的免疫系统,在维护我们的健康方面发挥着重要作用。真菌生物群还与各种致命疾病有关,如机会性真菌病,甚至癌症,不同的癌症有各自特定类型的真菌生物群。组成这些不同瘤内真菌生物群的不同真菌种类在癌症进展中发挥着重要作用。这篇综述旨在解读真菌生物群与癌症之间的关系,为癌症诊断和开发新的抗癌疗法提供新的思路。
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引用次数: 0
Efficacy of Adjuvant First-Generation TKIs versus Chemotherapy in Patients with Completely Resected EGFR-Mutant Non-Small Cell Lung Cancer: A Meta-Analysis. 完全切除的表皮生长因子受体突变非小细胞肺癌患者第一代 TKIs 辅助治疗与化疗的疗效对比:一项 Meta 分析。
IF 2.4 4区 医学 Q3 ONCOLOGY Pub Date : 2024-01-01 Epub Date: 2024-01-15 DOI: 10.1080/07357907.2024.2303311
Bin Shen, Dongping Wu, Jianjiang Liu, Yang Yang

Background: The use of adjuvant first-generation epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKIs) in patients with resected EGFR-mutant non-small cell lung cancer (NSCLC) remains controversial. Therefore, we performed a systematic review with meta-analysis to investigate the overall survival (OS) in patients with resected NSCLC.

Methods: Relevant studies were identified from the PubMed and EMBASE databases, and pooled hazard risks were obtained by random-effects models.

Results: Three prospective phase III and one phase II randomized controlled trials were identified, including a total of 839 patients who had undergone resection of EGFR-sensitive mutation in our analysis, 429 of whom received adjuvant first-generation TKIs therapy. For all patients with complete resection, adjuvant first-generation TKIs therapy was associated with improved disease-free survival (DFS) [hazard ratio (HR): 0.50, 95% confidence interval (CI): 0.30-0. 82] but not OS (HR: 0.78, 95% CI: 0.48-1.27) compared with adjuvant chemotherapy. In addition, we reconstructed the OS curves of the ADJUVANT and IMPACT studies, and the pooled 3- and 5-year OS rates of stage II-III patients in the TKI group and chemotherapy group were 80% vs. 79% and 66% vs. 64%, respectively. We also reconstructed the DFS curves based on the ADJUVANT, IMPACT, and EVIDENCE studies, and the pooled 1-, 3- and 5-year DFS rates of stage II-III patients in the TKI group and chemotherapy group were 87% vs. 70%, 49% vs. 37% and 28% vs. 29%, respectively.

Conclusions: In patients with completely resected EGFR-mutant NSCLC, adjuvant first-generation TKIs may delay disease progression but still fail to improve long-term survival compared with conventional chemotherapy.

背景:切除的表皮生长因子受体突变非小细胞肺癌(NSCLC)患者辅助使用第一代表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)仍存在争议。因此,我们进行了一项系统综述和荟萃分析,研究切除的非小细胞肺癌患者的总生存率(OS):方法:从PubMed和EMBASE数据库中筛选出相关研究,并通过随机效应模型得出汇总危险风险:结果:共发现3项前瞻性III期和1项II期随机对照试验,我们的分析共包括839例接受了表皮生长因子受体敏感突变切除术的患者,其中429例接受了第一代TKIs辅助治疗。对于所有完全切除的患者,与辅助化疗相比,第一代TKIs辅助治疗与无病生存期(DFS)的改善相关[危险比(HR):0.50,95%置信区间(CI):0.30-0.82],但与OS(HR:0.78,95%置信区间(CI):0.48-1.27)无关。此外,我们还重建了ADJUVANT和IMPACT研究的OS曲线,TKI组和化疗组II-III期患者的3年和5年总OS率分别为80% vs. 79%和66% vs. 64%。我们还根据ADJUVANT、IMPACT和EVIDENCE研究重建了DFS曲线,TKI组和化疗组II-III期患者的汇总1年、3年和5年DFS率分别为87% vs. 70%、49% vs. 37%和28% vs. 29%:结论:对于完全切除的表皮生长因子受体突变型NSCLC患者,第一代TKIs辅助治疗可延缓疾病进展,但与传统化疗相比,仍无法改善长期生存率。
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引用次数: 0
Comparative Analysis of miRNA and EMT Markers in Metastatic Colorectal Cancer. 转移性结直肠癌miRNA和EMT标志物的比较分析。
IF 2.4 4区 医学 Q3 ONCOLOGY Pub Date : 2023-12-01 Epub Date: 2024-01-02 DOI: 10.1080/07357907.2023.2283495
Veronika Hanusova, Petra Matouskova, Monika Manethova, Jiri Soukup, Stanislav John, Martin Zofka, Hana Vošmikova, Lukas Krbal, Emil Rudolf

Colorectal cancer (CRC) is the fourth most commonly diagnosed malignant condition in the world. Micro RNAs (miRNAs) as well as epithelial to mesenchymal transition (EMT) play an important role in the pathogenesis of CRC. We performed a comparative analysis of the expression of selected miRNA genes and EMT markers in bioptic samples from patients (n = 45) with primary CRC or metastatic (m)CRC to the regional lymph node using reverse transcription-quantitative PCR and IHC staining. Results: Out of all miRNA analyzed, the miR-17 expression was most significantly different and associated with lower risk of CRC spread to the lymph node. In addition, significant relationships were found between the tumor side localization and several miRNAs expressions (miR-9, miR-29b, miR-19a, miR-19b, miR-21, miR-106a, miR-20a and miR-17). In addition, of the examined EMT markers, only VEGFA expression correlated with tumor progression (tumor grade G2). In the examined set of patient samples and their matched healthy tissue, several specific molecular markers (miRNAs associated with EMT and tumor progression) were identified with a promising prognostic potential. Their further examination in larger patient cohorts is planned to validate the present data.

结直肠癌(CRC)是世界上第四大最常诊断的恶性疾病。微rna (miRNAs)和上皮到间充质转化(EMT)在结直肠癌的发病机制中起重要作用。我们使用逆转录定量PCR和免疫组化染色对原发性结直肠癌或转移性结直肠癌患者(n = 45)的活检样本中选定的miRNA基因和EMT标志物的表达进行了比较分析。结果:在所分析的所有miRNA中,miR-17的表达差异最为显著,并与结直肠癌扩散到淋巴结的风险较低相关。此外,肿瘤侧定位与几种mirna表达(miR-9、miR-29b、miR-19a、miR-19b、miR-21、miR-106a、miR-20a和miR-17)之间存在显著相关性。此外,在所检测的EMT标志物中,只有VEGFA表达与肿瘤进展相关(肿瘤分级G2)。在检查的患者样本及其匹配的健康组织中,几个特定的分子标记(与EMT和肿瘤进展相关的mirna)被确定为具有良好的预后潜力。他们计划在更大的患者队列中进行进一步的检查,以验证目前的数据。
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引用次数: 0
Genomic Alterations of Signaling and DNA Damage Repair Pathways in Non-Muscle Invasive Bladder Cancer. 非肌肉浸润性膀胱癌信号通路和DNA损伤修复途径的基因组改变。
IF 2.4 4区 医学 Q3 ONCOLOGY Pub Date : 2023-12-01 Epub Date: 2024-01-02 DOI: 10.1080/07357907.2023.2288640
Serdar Celik, Tekincan Aktas, Ozde Gokbayrak, Aylin Erol, Kutsal Yorukoglu, Batuhan Yilmaz, Hilmi Sari, Zekiye Altun, Mehmet Ugur Mungan, Ilhan Celebi, Guven Aslan, Safiye Aktas

The aim of the study was to demonstrate the most common genetic alterations and evaluate possible targets involving phosphatidylinositol-3-OH kinase (PIK3)/AKT/mammalian target of rapamycin (mTOR) signaling and DNA damage repair (DDR) pathways for personalized treatment in patients with non-muscle invasive bladder cancer (NMIBC). Alterations of these pathways were observed in 89.5% and 100% of patients, respectively. Among them, BARD1 was more frequently altered in low/intermediate-risk cases, but PARP4 was more frequently affected in intermediate/high-risk patients. The possible target feasibility of BARD1 and PARP4 alterations should be evaluated for personalized treatment using PARP-inhibitors in NMIBC. It is important to detect high tumor mutation burden (TMB) in patients in terms of immunotherapy.

该研究的目的是证明最常见的遗传改变,并评估涉及PIK3/AKT/mTOR信号传导和DNA损伤修复(DDR)途径的可能靶点,以用于NMIBC患者的个性化治疗。这些通路的改变分别在89.5%和100%的患者中观察到。其中,BARD1在低/中危患者中改变较多,而PARP4在中危患者中改变较多。应该评估BARD1和PARP4改变的可能靶标可行性,以便在NMIBC中使用parp抑制剂进行个性化治疗。在免疫治疗方面,检测患者的高肿瘤突变负荷是很重要的。
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引用次数: 0
Recurrence Patterns and Clinical Management after a Positive Sentinel Node Biopsy in Melanoma Patients. 黑色素瘤患者前哨淋巴结活检阳性后的复发模式和临床管理。
IF 2.4 4区 医学 Q3 ONCOLOGY Pub Date : 2023-12-01 Epub Date: 2024-01-02 DOI: 10.1080/07357907.2023.2283459
Jacqueline N de Menezes, Dante A S M Arra, Matheus M Lôbo, Clovis A L Pinto, João P S N Lima, Milton J B Silva, João P Duprat Neto, Eduardo Bertolli

Introduction melanoma patients who become stage III after a positive sentinel node biopsy (SNB) may have several patterns of recurrence patients and methods retrospective analysis of melanoma patients who have undergone SNB in a single institution from 2000 to 2015. Results There were 111 recurrences (45.1%) among 246 (20.3%) SNB positive patients and median DRFS was 77.7 months. After initial treatment, further recurrences occurred in 68 (77.3%) patients, regardless the site of initial recurrence conclusions multimodal strategies are recommended to achieve better results when managing stage III melanoma patients after a positive SNB.

在前哨淋巴结活检(SNB)阳性后进入III期的黑色素瘤患者可能有几种复发模式,患者和方法对2000年至2015年在同一机构接受SNB的黑色素瘤患者进行回顾性分析。结果246例(20.3%)SNB阳性患者中有111例(45.1%)复发,中位DRFS为77.7个月。在初始治疗后,68例(77.3%)患者发生了进一步复发,无论初始复发部位如何。结论:在治疗SNB阳性的III期黑色素瘤患者时,推荐采用多模式策略以获得更好的结果。
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引用次数: 0
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Cancer Investigation
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