long-term survival

长期生存
  • 文章类型: Journal Article
    性别对冠状动脉旁路移植术(CABG)早期和长期结局的影响尚不明确。目的:本研究旨在使用KROK注册中心的数据评估性别对CABG术后早期和长期死亡率的影响。方法:2009年1月1日至2019年12月31日在波兰接受CABG的所有133,973例成年患者均纳入波兰国家心脏外科手术注册(KROK注册)。该研究纳入了90,541例患者:符合纳入标准的男性68,401例(75.55%)和女性22,140例(24.45%)。然后,30天死亡率,1年死亡率,并比较了长期死亡率。结果:高龄,加拿大心血管学会(CCS)和纽约心脏协会(NYHA)等级较高,糖尿病,高胆固醇血症,动脉高血压,体重指数BMI>35kg/m2,肾功能衰竭,在倾向匹配之前,在女性中更常见。女性更经常接受紧急手术,包括单移植和双移植手术,和非泵送CABG(OPCAB)(p<0.001)。在倾向匹配的群体中,女性的早期死亡率(30天)明显更高(3.4%对2.8%,p<0.001)。该组的年死亡率仍然较高(6.6%对6.0%,p=0.025)。然而,两组之间的长期死亡率差异显着,男性组较高(男性为33.0%,女性为28.8%,p<0.001)。结论:在整个人群中,两种性别之间的长期死亡率没有明显差异。在倾向匹配的患者中,男性的早期死亡率较低,但是发现女性的长期生存率更好。
    The influence of gender on both early and long-term outcomes of coronary artery bypass grafting (CABG) is not clearly defined. Objectives: This study aimed to assess the impact of gender on early and long-term mortality after CABG using data from the KROK Registry. Methods: All 133,973 adult patients who underwent CABG in Poland between 1 January 2009 and 31 December 2019 were included in the Polish National Registry of Cardiac Surgical Procedures (KROK Registry). The study enrolled 90,541 patients: 68,401 men (75.55%) and 22,140 women (24.45%) who met the inclusion criteria. Then, 30-day mortality, 1-year mortality, and long-term mortality rates were compared. Results: Advanced age, higher Canadian Cardiovascular Society (CCS) and New York Heart Association (NYHA) grade, diabetes, hypercholesterolemia, arterial hypertension, body mass index BMI > 35 kg/m2, and renal failure, before the propensity matching, were more frequently observed in women. Women more frequently underwent urgent surgery, including single and double graft surgery, and off-pump CABG (OPCAB) (p < 0.001). In propensity-matched groups, early mortality (30 days) was significantly higher in women (3.4% versus 2.8%, p < 0.001). The annual mortality remained higher in this group (6.6% versus 6.0%, p = 0.025). However, long-term mortality differed significantly between the groups and was higher in the male group (33.0% men versus 28.8% women, p < 0.001). Conclusions: There are no apparent differences in long-term mortality between the two sexes in the entire population. In propensity-matched patients, early mortality was lower for men, but the long-term survival was found to be better in women.
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  • 文章类型: Case Reports
    小细胞肺癌(SCLC)仍然是一种预后不良的疾病,特别是在广泛阶段SCLC(ES-SCLC)。目前的标准治疗包括铂类药物化疗和依托泊苷+阿特珠单抗或durvalumab免疫治疗,在临床试验中,其平均总生存期为12-13个月。然而,ES-SCLC的长期生存,即使增加了免疫疗法,仍然是罕见的。我们介绍了一名诊断为ES-SCLC的中年男性患者,该患者接受了四个周期的诱导化疗(卡铂和依托泊苷)和阿特珠单抗治疗,此后每21天开始阿替珠单抗维持治疗,和胸部放疗。9个月后,他经历了轻微的疾病进展,并接受了6个周期的卡铂和依托泊苷治疗,并继续接受阿特珠单抗治疗。随后的成像显示几乎完全的疾病消退,此后一直持续。自诊断以来,他继续使用阿替珠单抗维持治疗,总生存期为60个月,无进展生存期为44个月。在整个治疗过程中,他保持了较高的功能能力,仅经历了一次与免疫相关的不良事件。我们的患者代表了能够实现对免疫疗法的持久反应的一小部分,他的病例强调需要进一步研究以阐明驱动这种反应的临床和生物学因素。
    Small-cell lung cancer (SCLC) remains a disease with poor prognosis, particularly in extensive-stage SCLC (ES-SCLC). Current standard-of-care treatment includes chemotherapy with platinum agents and etoposide plus immunotherapy with atezolizumab or durvalumab, which has achieved a mean overall survival of 12-13 months in clinical trials. However, long-term survival in ES-SCLC, even with the addition of immunotherapy, continues to be rare. We present the case of a middle-aged male patient diagnosed with ES-SCLC who was treated with four cycles of induction chemotherapy (carboplatin and etoposide) and atezolizumab, starting maintenance atezolizumab every 21 days thereafter, and thoracic radiotherapy. After 9 months, he experienced mild disease progression and was rechallenged with six cycles of carboplatin and etoposide with continued atezolizumab. Subsequent imaging showed near-complete disease resolution which has been sustained since. He has continued on maintenance atezolizumab since diagnosis and has achieved 60 months overall survival and 44 months progression-free survival. Throughout treatment, he has maintained a high functional capacity and only experienced one immune-related adverse event. Our patient is representative of a small subset who are capable of achieving durable responses to immunotherapy and his case highlights the need for further research to elucidate the clinical and biological factors driving this response.
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  • 文章类型: Journal Article
    背景:细胞减灭术(CRS)联合腹腔热化疗(HIPEC)是结直肠腹膜癌(CPC)的主要治疗方法。目的是确定接受CRS-HIPEC治疗的CPC患者的无病生存率(DFS)和总生存率(OS)以及与长期生存率(LTS)相关的因素。
    方法:纳入2007年至2021年在HIPEC中心接受CRS-HIPEC的连续CPC患者。计算了实际生存率,和Cox比例风险模型用于识别与OS相关的因素,DFS和LTS。
    结果:有125例CPC患者接受了原发性CRS-HIPEC,平均年龄54.5岁。中位随访时间为31个月。术中平均PCI为11,完全细胞减灭术(CC-0)达到96.8%。中位OS为41.6个月(6-196)。2年和5年OS分别为68%和24.8%,分别,两年DFS为28.8%。与OS较差相关的因素包括HIPEC系统治疗前,同步腹膜外转移,PCI≥20(p<0.05)。CRS-HIPEC之前的进展与更差的DFS相关(p<0.05)。更低的PCI,更少的并发症,较低的复发和较长的DFS与LTS相关(p<0.05).
    结论:CRS和HIPEC可改善CPC患者的OS,但其疾病复发率较高。结果取决于术前治疗反应,腹膜外转移,和腹膜疾病负担。
    BACKGROUND: Cytoreductive surgery (CRS) combined with hyperthermic intraperitoneal chemotherapy (HIPEC) is a major treatment of colorectal peritoneal carcinomatosis (CPC). The aim was to determine the disease-free survival (DFS) and overall survival (OS) of patients undergoing CRS-HIPEC for CPC and factors associated with long-term survival (LTS).
    METHODS: consecutive CPC patients who underwent CRS-HIPEC at a HIPEC center between 2007 and 2021 were included. Actual survival was calculated, and Cox proportional hazards models were used to identify factors associated with OS, DFS and LTS.
    RESULTS: there were 125 patients with CPC who underwent primary CRS-HIPEC, with mean age of 54.5 years. Median follow-up was 31 months. Average intraoperative PCI was 11, and complete cytoreduction (CC-0) was achieved in 96.8%. Median OS was 41.6 months (6-196). The 2-year and 5-year OS were 68% and 24.8%, respectively, and the 2-year DFS was 28.8%. Factors associated with worse OS included pre-HIPEC systemic therapy, synchronous extraperitoneal metastasis, and PCI ≥ 20 (p < 0.05). Progression prior to CRS-HIPEC was associated with worse DFS (p < 0.05). Lower PCI, fewer complications, lower recurrence and longer DFS were associated with LTS (p < 0.05).
    CONCLUSIONS: CRS and HIPEC improve OS in CPC patients but they have high disease recurrence. Outcomes depend on preoperative therapy response, extraperitoneal metastasis, and peritoneal disease burden.
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  • 文章类型: Journal Article
    急性代偿性心力衰竭(ADHF)与频繁住院有关,在全球范围内构成重大的健康和经济负担。尽管在心力衰竭管理方面取得了进展,描述ADHF结局的时间趋势的研究很少。方法:在回顾性分析中,2007年至2017年在沙米尔医学中心住院的ADHF患者分为两个队列:早期(2007-2011年)和最近(2012-2017年)。临床特征,医院干预措施,并对结果进行了比较。使用具有对数秩检验的Kaplan-Meier方法进行生存分析。
    对8332名入院患者进行了分析,4366(52.4%)在早期,和3966(47.6%)在最近一段时间。在最近的队列中,缺血性心脏病显著减少(从45.2%降至34.7%),而高血压和吸烟率上升。此外,观察到出院后冠状动脉旁路移植术(从0.8%到3.5%)和β受体阻滞剂处方(从45.5%到63.4%)显著增加.然而,住院死亡率没有实质性改善(早期与早期的8.9%最近8.0%),30天(早期与早期的3.2%最近3.1%),1年(早期与早期的23.3%最近的23.8%),或5年生存率被记录在队列之间.对心内科住院患者的子集分析显示,在最近的队列中,住院死亡率显着降低(早期与早期相比为12.3%最近的6.3%),但没有相应的长期生存益处。
    在11年的研究期间,心力衰竭管理方面的进步并未显示ADHF患者的临床结局有所改善,强调将ADHF患者医疗护理的进步转化为长期生存获益的挑战。
    UNASSIGNED: Acute Decompensated Heart Failure (ADHF) is associated with frequent hospitalizations, posing a significant health and economic burden globally. Despite advancements in heart failure management, studies delineating temporal trends in ADHF outcomes are sparse.Methods: in this retrospective analysis, ADHF patients admitted to Shamir Medical Center from 2007 to 2017 were categorized into two cohorts: early (2007-2011) and recent (2012-2017). Clinical characteristics, in-hospital interventions, and outcomes were compared. Survival analysis was performed using Kaplan-Meier methods with log-rank tests.
    UNASSIGNED: 8332 admitted patients were analyzed, 4366 (52.4 %) in the early period, and 3966 (47.6 %) in the recent period. In the recent cohort, ischemic heart disease decreased significantly (from 45.2 % to 34.7 %), while hypertension and smoking rates increased. Additionally, a significant increase in coronary artery bypass grafting (from 0.8 % to 3.5 %) and beta-blockers prescription (from 45.5 % to 63.4 %) post-discharge was observed. However, no substantial improvement in in-hospital mortality (8.9 % in early vs. 8.0 % in recent), 30-day (3.2 % in early vs. 3.1 % in recent), 1-year (23.3 % in early vs. 23.8 % in recent), or 5-year survival rates was noted between cohorts. A subset analysis of patients admitted to cardiology departments showed a significant reduction in in-hospital mortality in the recent cohort (12.3 % in early vs. 6.3 % in recent), yet without a corresponding long-term survival benefit.
    UNASSIGNED: Advancements in heart failure management over the 11-year study period did not demonstrate an improvement in clinical outcomes for ADHF patients, highlighting the challenge of translating advancements in the medical care of ADHF patients into long-term survival benefits.
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  • 文章类型: Case Reports
    免疫检查点抑制剂(ICIs)是非小细胞肺癌(NSCLC)患者的标准治疗方法。自从nivolumab被FDA批准用于NSCLC患者以来,已经过去了近十年。然而,个别病例的长期结局和临床特征仍不清楚.假性进展是ICI治疗下众所周知的矛盾放射学反应模式,当明显的初始进展后肿瘤指标病变消退时发生。我们在此报告了一个独特的NSCLC病例,在使用纳武单抗单一疗法治疗8.5年的晚期重复假性进展。
    一名56岁男性,诊断为非sqNSCLC临床分期IVA,在左上叶原发灶。原发灶为PD-L1阴性,无致癌驱动突变。他有多发性肺转移和左肾上腺转移,随后,接受nivolumab作为三线治疗.nivolumab开始后,肺部病变和肾上腺转移迅速缩小;然而,患者在纵隔淋巴结(LN)出现3次晚期假性进展.该患者仍在接受无症状和PS0的nivolumab。对于仅LN的寡进展患者,应仔细判断获得性耐药,以避免不必要的局部治疗和对治疗的误判。
    UNASSIGNED: Immune check point inhibitors (ICIs) are standard treatment for patients with non-small cell lung cancer (NSCLC). Nearly a decade has passed since nivolumab was approved by the FDA for NSCLC patients. However, long-term outcomes and clinical features remain unclear for individual cases. Pseudo-progression is a well-known paradoxical radiological response pattern under ICI treatment which occurs when tumor index lesions regress after apparent initial progression. We herein report a unique case of NSCLC with repeating pseudo-progression in late phase treated with nivolumab monotherapy for 8.5 years.
    UNASSIGNED: A 56-year-old male diagnosed with Non-sq NSCLC clinical stage IVA, at the left upper lobe primary lesion. The primary lesion was PD-L1 negative with no oncogenic driver mutations. He had multiple pulmonary metastases and a left adrenal gland metastasis, and subsequently, received nivolumab as third-line therapy. After initiation of nivolumab, the lung lesion and adrenal metastasis shrank rapidly; however, the patient experienced three late-phase pseudo-progressions in the mediastinal lymph node (LN). This patient is still receiving nivolumab with no symptoms and PS 0. Acquired resistance should be judged carefully in patients with LN-only oligo-progression to avoid unnecessary local therapies and the misjudgment of treatment.
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  • 文章类型: Journal Article
    背景:晚期胃癌(AGC)的预后相对较差,长期生存取决于及时的干预。目前,预测生存率仍然是一个热门话题。影像组学和免疫组织化学相关技术在癌症研究中的应用日益广泛。然而,它们在预测AGC患者长期生存率方面的整合尚未得到充分探索.
    方法:收集2015-2019年大连大学附属中山医院诊断为AGC的患者150例。遵循严格的纳入和排除标准,90例患者纳入分析。我们收集了入选患者的术后病理标本,使用免疫组织化学技术分析MAOA的表达水平,并将这些水平量化为MAOAHScore。获得患者腹部普通CT图像,描绘了L3椎体水平的感兴趣区域,并提取了影像组学特征。LassoCox回归用于选择重要特征以建立放射学风险评分,将其转换为名为风险的分类变量,并使用Cox回归来识别独立的预测因子以构建临床预测模型。ROC,DCA,和校准曲线验证了模型的性能。
    结果:入选患者的平均年龄为65.71岁,包括70名男性和20名女性。多因素Cox回归分析显示风险(P=0.001,HR=3.303),MAOAHScore(P=0.043,HR=2.055),和TNM分期(P=0.047,HR=2.273)是3年总生存期(OS)的独立预后危险因素,在3年疾病特异性生存期(DSS)的分析中也发现了类似的结果。开发的列线图可以预测3年的OS和DSS率,ROC曲线下面积(AUC)分别为0.81和0.797。联合校准和决策曲线分析(DCA)证实了列线图的良好预测性能和临床实用性。
    结论:结合免疫组织化学和肌肉脂肪特征可以更准确地预测胃癌患者的长期生存。本研究为更深入地理解AGC中的生存预测提供了新的视角和方法。
    BACKGROUND: The prognosis of advanced gastric cancer (AGC) is relatively poor, and long-term survival depends on timely intervention. Currently, predicting survival rates remains a hot topic. The application of radiomics and immunohistochemistry-related techniques in cancer research is increasingly widespread. However, their integration for predicting long-term survival in AGC patients has not been fully explored.
    METHODS: We Collected 150 patients diagnosed with AGC at the Affiliated Zhongshan Hospital of Dalian University who underwent radical surgery between 2015 and 2019. Following strict inclusion and exclusion criteria, 90 patients were included in the analysis. We Collected postoperative pathological specimens from enrolled patients, analyzed the expression levels of MAOA using immunohistochemical techniques, and quantified these levels as the MAOAHScore. Obtained plain abdominal CT images from patients, delineated the region of interest at the L3 vertebral body level, and extracted radiomics features. Lasso Cox regression was used to select significant features to establish a radionics risk score, convert it into a categorical variable named risk, and use Cox regression to identify independent predictive factors for constructing a clinical prediction model. ROC, DCA, and calibration curves validated the model\'s performance.
    RESULTS: The enrolled patients had an average age of 65.71 years, including 70 males and 20 females. Multivariate Cox regression analysis revealed that risk (P = 0.001, HR = 3.303), MAOAHScore (P = 0.043, HR = 2.055), and TNM stage (P = 0.047, HR = 2.273) emerged as independent prognostic risk factors for 3-year overall survival (OS) and The Similar results were found in the analysis of 3-year disease-specific survival (DSS). The nomogram developed could predict 3-year OS and DSS rates, with areas under the ROC curve (AUCs) of 0.81 and 0.797, respectively. Joint calibration and decision curve analyses (DCA) confirmed the nomogram\'s good predictive performance and clinical utility.
    CONCLUSIONS: Integrating immunohistochemistry and muscle fat features provides a more accurate prediction of long-term survival in gastric cancer patients. This study offers new perspectives and methods for a deeper understanding of survival prediction in AGC.
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  • 文章类型: Journal Article
    目的:罕见胰腺肿瘤的生物学,不同于导管胰腺癌,需要更多的关注。尽管大多数罕见的胰腺肿瘤是良性的,如果不完全切除病变,很难确定是否存在侵入性成分,尽管在诊断方面取得了相当大的进展。我们正在调查大量经组织学证实的胰腺上皮非导管非神经内分泌肿瘤患者。
    方法:在这里,我们分析了患者的长期生存率,接受组织学证实的胰腺上皮非导管非神经内分泌肿瘤切除术的患者。1月1日之间在我们部门,1999年和12月31日,2019.中位随访时间为61(范围0-168)个月。所有统计分析均使用SPSS26.0(IBM,芝加哥,IL,美国)软件。
    结果:46例(48%)随访5年以上,18例(19%)患者10年以上。罕见的非侵袭性胰腺肿瘤的5年和10年生存率分别为72%和55%。在1999年至2019年期间,我们的诊所中罕见肿瘤实体(非导管和非神经内分泌)的比例从4.2%连续增加到12.3%(p=0.004)。如果还没有侵入性生长,在疾病的过程中,恶性变性的风险各不相同。因此,胰腺切除的适应症仍是讨论的主题.
    结论:R0切除后的罕见上皮性胰腺肿瘤的长期预后-即使它们已经是恶性的-比导管胰腺癌的预后要好得多。
    OBJECTIVE: The biology of rare pancreatic tumours, which differs from that of ductal pancreatic cancer, requires increased attention. Although the majority of rare pancreatic tumours are benign, it is difficult to decide whether an invasive component exists without complete removal of the lesion, despite considerable progress in diagnosis. We are investigating a large cohort of patients with histologically confirmed epithelial non-ductal non-neuroendocrine neoplasms of the pancreas.
    METHODS: Here we analyze long-term survival from patients, who underwent resection of histologically confirmed epithelial non-ductal non-neuroendocrine neoplasms of the pancreas. At our department between Jan 1st, 1999, and Dec 31st, 2019. The median follow-up was 61 (range 0-168) month. All statistical analyses were performed using SPSS 26.0 (IBM, Chicago, IL, USA) software.
    RESULTS: 46 patients (48%) were followed up for more than 5 years, 18 patients (19%) for more than 10 years. The 5-year and 10-year survival rates for rare non-invasive pancreatic tumours were 72% and 55% respectively. The proportion of rare tumour entities (non-ductal and non-neuroendocrine) increased continuously and statistically significantly (p = 0.004) from 4.2 to 12.3% in our clinic between 1999 and 2019. If there is no invasive growth yet, there is a varying risk of malignant degeneration in the course of the disease. Therefore, the indication for pancreatic resection is still the subject of discussion.
    CONCLUSIONS: The long-term prognosis of rare epithelial pancreatic tumours after R0 resection-even if they are already malignant-is much better than that of ductal pancreatic cancer.
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  • 文章类型: Case Reports
    伴有发育迟缓和黑棘皮病的严重软骨发育不全(SADDAN)是由成纤维细胞生长因子受体3(FGFR3)的致病性变体引起的骨发育不良。FGFR3中的致病性变异也会导致嗜血性发育不良(TD)和软骨发育不全。尽管胎儿期和新生儿期的SADDAN和TD的发现相似,他们的长期预后不同。我们对一名男性患者进行了FGFR3分析,因为在新生儿期难以区分SADDAN和TD。我们发现病人有致病变异,p.Lys650Met,这与先前报道的SADDAN患者相似。关于SADDAN患者长期生存的报告很少,也没有关于GH治疗的报道。我们给予GH治疗明显身材矮小。治疗后,4年来,他的身高每年增加4厘米,因呼吸衰竭而住院的频率减少,和健康改善。FGFR3分析可用于在新生儿早期诊断SADDAN。GH治疗可能有助于患者的长期生存。
    Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN) is a bone dysplasia caused by a pathogenic variant of fibroblast growth factor receptor 3 (FGFR3). Pathogenic variants in FGFR3 also cause thanatophoric dysplasia (TD) and achondroplasia. Although the findings of SADDAN and TD during the fetal and neonatal periods are similar, they differ in their long-term prognoses. We conducted FGFR3 analysis in one male patient because of the difficulty in differentiating SADDAN from TD during the neonatal period. We found that the patient had a pathogenic variant, p. Lys650Met, which was similar to that previously reported in patients with SADDAN. Reports on long-term survival in patient with SADDAN are scarce, and there have been no reports of treatment with GH. We administered GH therapy for a markedly short stature. After treatment, his height increased by 4 cm each year for 4 years, the frequency of hospitalizations due to respiratory failure decreased, and the health improved. FGFR3 analysis is useful for diagnosing SADDAN during the early neonatal period. GH therapy may have contributed to the patient\'s long-term survival.
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  • 文章类型: Case Reports
    尽管转移性结直肠癌(mCRC)患者的长期生存率有限,现在建议使用三线和后期治疗.我们描述了一名患者,当他们接受三氟尿苷/替吡草胺(FTD/TPI)的三线治疗时,他们获得了长期生存。
    诊断为右结肠腺癌(T3/N0/M1)并向肺转移的52岁女性,肝脏,子房,和其他软组织接受以氟嘧啶为基础的一线化疗(FOLFOX/FOLFIRI加贝伐单抗)间歇性约8.5年,疾病总体稳定,和二线FOLFIRI加放疗。在二线治疗进展后,患者在每个28天周期的第1-5天和第8-12天开始使用FTD/TPI35mg/m2每日2次治疗.在34个月的时间里,她总共收到了38个周期的FTD/TPI,实现了部分响应,保持的性能状态,提高了生活质量。中性粒细胞减少症通过FTD/TPI剂量延迟或减少成功治疗。
    这位经过大量预处理的mCRC患者在FTD/TPI治疗下表现出令人印象深刻的长期生存率和良好的生活质量。
    UNASSIGNED: Although long-term survival in patients with metastatic colorectal cancer (mCRC) is limited, treatments for third-line and later treatment are now recommended. We describe a patient who achieved long-term survival when they received third-line treatment with trifluridine/tipiracil (FTD/TPI).
    UNASSIGNED: The woman who was 52 years old at diagnosis of adenocarcinoma of the right colon (T3/N0/M1) with metastases to the lung, liver, ovary, and other soft tissues received first-line fluoropyrimidine-based chemotherapy (FOLFOX/FOLFIRI plus bevacizumab) intermittently for approximately 8.5 years with generally stable disease, and second-line FOLFIRI plus radiotherapy. After progression on second-line therapy, the patient initiated treatment with FTD/TPI 35 mg/m2 twice daily on days 1-5 and 8-12 of each 28-day cycle. She received a total of 38 cycles of FTD/TPI over a period of 34 months achieving a partial response, maintained performance status, and improved quality of life. Neutropenia was successfully managed with FTD/TPI dose delays or reductions.
    UNASSIGNED: This heavily pre-treated patient with mCRC demonstrated impressive long-term survival and maintenance of good quality of life with FTD/TPI treatment.
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  • 文章类型: Case Reports
    包括胸腔积液或血浆的液体活检通常用于晚期非小细胞肺癌(NSCLC)和胸腔积液(PE)的患者,以指导治疗。ALK-TKIs是ALK阳性突变患者的首选方案,ALK-TKIs与血管生成剂联合使用可能会提高生存率。我们在这里报告了一例ALK阳性肺腺癌,其中患者在接受精确的胸腔积液NGS并在多线ALK-TKI耐药后接受贝伐单抗联合治疗后,获得了97个月的延长的无进展生存期(PFS)。
    Liquid biopsies including pleural fluid or plasma are commonly applied for patients with advanced non-small cell lung cancer (NSCLC) and pleural effusion (PE) to guide the treatment. ALK-TKIs are the first options for patients with ALK-positive mutations and combining ALK-TKIs with angiogenic agents may improve survival. We report here one case with ALK-positive lung adenocarcinoma in which the patient achieved a prolonged progression-free survival (PFS) of 97 months after undergoing precise pleural effusion NGS and receiving combined bevacizumab treatment following multiple-line ALK-TKI resistance.
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