clinically node-positive

  • 文章类型: Multicenter Study
    目的:本研究的目的是评估欧洲临床淋巴结阳性乳腺癌患者使用新辅助系统疗法(NST)的临床实践异质性。
    方法:这项研究是在国际多中心III期OPBC-03/TAXIS试验(ClinicalTrials.govIdentifier:NCT03513614)中预先计划的,纳入了前500名在手术时确诊淋巴结疾病的随机患者。TAXIS研究的务实设计允许根据当地研究者的偏好进行新辅助和辅助设置,他们被鼓励连续登记符合条件的患者。
    结果:从2018年8月至2022年6月,共有500名患者被纳入六个欧洲国家的44个乳腺中心,其中165名(33%)接受了NST。中位年龄为57岁(四分位数范围[IQR],48-69).大多数患者绝经后(68.4%)患有2级和3级激素受体阳性和人表皮生长因子受体2阴性乳腺癌,中位肿瘤大小为28mm(IQR20-40)。NST的使用在各国差异显著(p<0.001)。奥地利(55.2%)和瑞士(35.8%)接受NST的患者比例最高,匈牙利(18.2%)最低。多年来,NST的管理显着增加(OR1.42;p<0.001),并且在2018年至2022年之间从20%增加到46.7%。
    结论:在欧洲,使用NST治疗HR+/HER2-乳腺癌存在显著异质性。虽然严格的指南适用于三阴性和HER2+乳腺癌,对于HR+/HER2-乳腺癌,需要制定并坚持明确的建议.
    OBJECTIVE: The aim of this study was to evaluate clinical practice heterogeneity in use of neoadjuvant systemic therapy (NST) for patients with clinically node-positive breast cancer in Europe.
    METHODS: The study was preplanned in the international multicenter phase-III OPBC-03/TAXIS trial (ClinicalTrials.gov Identifier: NCT03513614) to include the first 500 randomized patients with confirmed nodal disease at the time of surgery. The TAXIS study\'s pragmatic design allowed both the neoadjuvant and adjuvant setting according to the preferences of the local investigators who were encouraged to register eligible patients consecutively.
    RESULTS: A total of 500 patients were included at 44 breast centers in six European countries from August 2018 to June 2022, 165 (33%) of whom underwent NST. Median age was 57 years (interquartile range [IQR], 48-69). Most patients were postmenopausal (68.4%) with grade 2 and 3 hormonal receptor-positive and human epidermal growth factor receptor 2-negative breast cancer with a median tumor size of 28 mm (IQR 20-40). The use of NST varied significantly across the countries (p < 0.001). Austria (55.2%) and Switzerland (35.8%) had the highest percentage of patients undergoing NST and Hungary (18.2%) the lowest. The administration of NST increased significantly over the years (OR 1.42; p < 0.001) and more than doubled from 20 to 46.7% between 2018 and 2022.
    CONCLUSIONS: Substantial heterogeneity in the use of NST with HR+/HER2-breast cancer exists in Europe. While stringent guidelines are available for its use in triple-negative and HER2+ breast cancer, there is a need for the development of and adherence to well-defined recommendations for HR+/HER2-breast cancer.
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  • 文章类型: Journal Article
    未经批准:探讨cN1M0前列腺癌(PCa)局部治疗(LT)的预后价值。
    未经证实:从监测中提取诊断为cN1M0PCa的患者,流行病学,和最终结果(SEER)数据库。使用Kaplan-Meier(KM)曲线比较接受和未接受LT治疗的患者的生存结果。Further,在接受LT的患者中,KM分析还用于研究根治性前列腺切除术(RP)和放射治疗(RT)患者的生存差异。进行倾向评分匹配(PSM)分析,以平衡各组患者的基本特征,并在探索不同治疗类型的生存影响时具有可比性。最后,在该人群中,采用单变量和多变量Cox比例风险模型来确定与总生存期(OS)和癌症特异性生存期(CSS)相关的独立预后因素.
    UNASSIGNED:接受LT治疗的患者的OS(P<0.0001)和CSS(P<0.0001)明显优于未接受LT治疗的患者,以及在大多数子群中,除了非白人患者,或那些与ISUP等级组1或T3阶段。值得注意的是,接受RP治疗的患者的OS(P=0.00012)和CSS(P=0.0045)也明显优于单纯接受RT治疗的患者,尤其是在年龄≥75岁的人群中,前列腺特异性抗原(PSA)10-20ng/mL,ISUP1-3级或非白人患者。最后,临床T分期,在cN1M0PCa患者中,ISUP分级组和LT的给药被确定为OS和CSS的独立预后因素。
    UNASSIGNED:接受LT治疗的cN1M0PCa患者的生存率显著提高。在接受LT的患者中,在大多数亚组中,与单纯RT相比,RP和PLND联合治疗可导致更好的预后.在权衡治疗的益处和风险后,有必要制定个性化的治疗策略。
    UNASSIGNED: To investigate the prognostic value of local therapy (LT) in cN1M0 prostate cancer (PCa).
    UNASSIGNED: Patients diagnosed with cN1M0 PCa were extracted from the surveillance, epidemiology, and end results (SEER) database. Kaplan-Meier (KM) curve was used to compare the survival outcomes between patients treated with and without LT. Further, among patients receiving LT, KM analysis was also applied to investigate the survival differences in patients with radical prostatectomy (RP) and radiation therapy (RT). Propensity score matching (PSM) analysis was performed to balance the basic characteristics of patients in each group and make it comparable when exploring the survival impact of different treatment types. Finally, uni- and multivariable Cox proportional-hazards models were utilized to identify independent prognostic factors associated with overall survival (OS) and cancer-specific survival (CSS) in this population.
    UNASSIGNED: Patients treated with LT had significantly better OS (P<0.0001) and CSS (P<0.0001) than those without LT, as well as in most subgroups, except for non-White patients, or those with ISUP grade group 1 or T3 stage. Notably, patients receiving RP also had significantly better OS (P=0.00012) and CSS (P=0.0045) than those treated with RT alone, especially in those aged ≥75 years old, prostate-specific antigen (PSA) 10-20 ng/mL, ISUP grade 1-3 or non-white patients. Finally, clinical T stage, ISUP grade group and the administration of LT were identified to be independent prognostic factors for OS and CSS among cN1M0 PCa patients.
    UNASSIGNED: The cN1M0 PCa patients treated with LT were associated with significantly better survival. Among patients receiving LT, the combination of RP and PLND could lead to a better prognosis compared to RT alone in most subgroups. An individualized treatment strategy is warranted to be developed after weighing the benefits and risks of treatment.
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  • 文章类型: Journal Article
    背景:研究支持前哨淋巴结阳性患者省略腋窝淋巴结清扫术(ALND),对于存在临床阳性淋巴结的患者,建议使用ALND。这里,我们评估接受ALND的雌激素受体阳性(ER+)乳腺癌患者的患者和肿瘤特征以及病理淋巴结分期,以确定是否存在基于淋巴结表现的差异.
    方法:2010年至2019年的回顾性图表回顾定义了三组ER+乳腺癌患者,这些患者接受了ALND的阳性淋巴结:SLN+(SLN活检发现的阳性淋巴结),cNUS(异常的术前US和活检),和cNpalp(明显的腺病)。排除接受新辅助化疗或腋窝复发的患者。
    结果:在191名患者中,94个是SLN+,40个是cNUS,57人是cNpalp。与cNpalp相比,SLN+患者更年轻(56岁vs64岁,p<0.01),更常在绝经前(41%vs14%,p<0.01),和白色(65%对39%,p=0.01),低度肿瘤更多(36%vs8%,p<0.01)。PR+的比率(p=0.16),Ki67表达水平(p=0.07)和LVI水平(p=0.06)在组间没有显著差异.患有SLN+疾病的患者,与cNUS的38%(p=0.1)和cNpalp的40%(p=0.01)相比,64%患有pN1疾病。关于单变量分析,肿瘤大小(p=0.01)和组织学(p=0.04)与pN1疾病显着相关,在多变量分析中,大小仍然是独立的预测因子(p=0.02)。
    结论:从历史上看,较高的风险特征归因于临床阳性淋巴结排除ALND的患者,但是当限制对ER+乳腺癌患者的评估时,只有肿瘤大小与较高的淋巴结分期相关。
    BACKGROUND: Studies support omission of axillary lymph node dissection (ALND) for patients with sentinel node-positive disease, with ALND recommended for patients who present with clinically positive nodes. Here, we evaluate patient and tumor characteristics and pathologic nodal stage of patients with estrogen receptor-positive (ER +) breast cancer who undergo ALND to determine if differences exist based on nodal presentation.
    METHODS: Retrospective chart review from 2010 to 2019 defined three groups of patients with ER + breast cancer who underwent ALND for positive nodes: SLN + (positive node identified at SLN biopsy), cNUS (abnormal preoperative US and biopsy), and cNpalp (palpable adenopathy). Patients who received neoadjuvant chemotherapy or presented with axillary recurrence were excluded.
    RESULTS: Of 191 patients, 94 were SLN + , 40 were cNUS, and 57 were cNpalp. Patients with SLN + compared with cNpalp were younger (56 vs 64 years, p < 0.01), more often pre-menopausal (41% vs 14%, p < 0.01), and White (65% vs 39%, p = 0.01) with more tumors that were low-grade (36% vs 8%, p < 0.01). Rates of PR + (p = 0.16), levels of Ki67 expression (p = 0.07) and LVI (p = 0.06) did not differ significantly among groups. Of patients with SLN + disease, 64% had pN1 disease compared to 38% of cNUS (p = 0.1) and 40% of cNpalp (p = 0.01). On univariable analysis, tumor size (p = 0.01) and histology (p = 0.04) were significantly associated with pN1 disease, with size remaining an independent predictor on multivariable analysis (p = 0.02).
    CONCLUSIONS: Historically, higher risk features have been attributed to patients with clinically positive nodes precluding omission of ALND, but when restricting evaluation to patients with ER + breast cancer, only tumor size is associated with higher nodal stage.
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  • 文章类型: Comparative Study
    支持前列腺癌根治术(RP)治疗临床淋巴结阳性(cN+)前列腺癌(PC)的证据有限。在美国国家数据库中,我们确定了在2000-2015年期间诊断为cN+非转移性PC的741名男性,他们接受了RP的明确局部治疗(n=78),放疗(RT)与新辅助雄激素剥夺治疗(ADT)(n=193),单独使用ADT(n=445)或观察(n=25)的非确定性治疗。我们使用多变量Fine-Gray竞争风险回归和Cox回归比较了PC特异性死亡率(PCSM)和全因死亡率(ACM),分别。与非确定性治疗相比,RP与更好的PCSM(亚分布风险比[SHR]0.32,95%置信区间[CI]0.16-0.66;p=0.002)和ACM(HR0.36,95%CI0.21-0.61;p<0.001)相关。与RT相比,RP与PCSM(SHR0.47,95%CI0.19-1.17;p=0.1)或ACM(HR0.88,95%CI0.46-1.70;p=0.71)的显着差异无关。这些数据表明,RP与良好的生存结果相关,似乎优于未接受确定性治疗的患者,并且与接受确定性ADT/RT的患者相当。需要多模式治疗手术的随机试验。患者总结:我们发现,在临床淋巴结阳性前列腺癌中,与非确定性治疗相比,根治性前列腺切除术与癌症特异性和总体生存获益相关.需要进行随机临床试验以确定该患者人群的最佳治疗方法。
    Evidence supporting radical prostatectomy (RP) for men with clinically node-positive (cN+) prostate cancer (PC) is limited. In a US national database, we identified 741 men with cN+ nonmetastatic PC diagnosed during 2000-2015 who underwent definitive local therapy with RP (n=78), radiotherapy (RT) with neoadjuvant androgen deprivation therapy (ADT) (n=193), or nondefinitive therapy with ADT alone (n=445) or observation (n=25). We compared PC-specific mortality (PCSM) and all-cause mortality (ACM) using multivariable Fine-Gray competing risk regression and Cox regression, respectively. Compared to nondefinitive therapy, RP was associated with significantly better PCSM (subdistribution hazard ratio [SHR] 0.32, 95% confidence interval [CI] 0.16-0.66; p=0.002) and ACM (HR 0.36, 95% CI 0.21-0.61; p<0.001). Compared to RT, RP was not associated with a significant difference in PCSM (SHR 0.47, 95% CI 0.19-1.17; p=0.1) or ACM (HR 0.88, 95% CI 0.46-1.70; p=0.71). These data suggest that RP is associated with favorable survival outcomes that appear to be superior to those for patients who did not receive definitive therapy and comparable to those for patients receiving definitive ADT/RT. Randomized trials of surgery with multimodal therapy are needed. PATIENT SUMMARY: We found that in clinically node-positive prostate cancer, radical prostatectomy was associated with a cancer-specific and overall survival benefit compared to nondefinitive therapy. Randomized clinical trials are required to determine the best treatment approach in this patient population.
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  • 文章类型: Clinical Trial Protocol
    BACKGROUND: Complete lymph node removal through conventional axillary dissection (ALND) has been standard treatment for breast cancer patients for almost a century. In the 1990s, however, and in parallel with the advent of the sentinel lymph node (SLN) procedure, ALND came under increasing scrutiny due to its association with significant patient morbidity. Several studies have since provided evidence to suggest omission of ALND, often in favor of axillary radiation, in selected clinically node-negative, SLN-positive patients, thus supporting the current trend in clinical practice. Clinically node-positive patients, by contrast, continue to undergo ALND in many cases, if only for the lack of studies re-assessing the indication for ALND in these patients. Hence, there is a need for a clinical trial to evaluate the optimal treatment for clinically node-positive breast cancer patients in terms of surgery and radiotherapy. The TAXIS trial is designed to fill this gap by examining in particular the value of tailored axillary surgery (TAS), a new technique for selectively removing positive lymph nodes.
    METHODS: In this international, multicenter, phase-III, non-inferiority, randomized controlled trial (RCT), including 34 study sites from four different countries, we plan to randomize 1500 patients to either receive TAS followed by ALND and regional nodal irradiation excluding the dissected axilla, or receive TAS followed by regional nodal irradiation including the full axilla. All patients undergo adjuvant whole-breast irradiation after breast-conserving surgery and chest-wall irradiation after mastectomy. The main objective of the trial is to test the hypothesis that treatment with TAS and axillary radiotherapy is non-inferior to ALND in terms of disease-free survival of clinically node-positive breast cancer patients in the era of effective systemic therapy and extended regional nodal irradiation. The trial was activated on 31 July 2018 and the first patient was randomized on 7 August 2018.
    CONCLUSIONS: Designed to test the hypothesis that TAS is non-inferior to ALND in terms of curing patients and preventing recurrences, yet is significantly superior in reducing patient morbidity, this trial may establish a new worldwide treatment standard in breast cancer surgery. If found to be non-inferior to standard treatment, TAS may significantly contribute to reduce morbidity in breast cancer patients by avoiding surgical overtreatment.
    BACKGROUND: ClinicalTrials.gov, ID: NCT03513614. Registered on 1 May 2018. www.kofam.ch , ID: NCT03513614 . Registered on 17 June 2018. EudraCT No.: 2018-000372-14.
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