disease-free survival

无病生存
  • 文章类型: Journal Article
    目的:乳腺癌的新辅助系统治疗(NAT)可以使肿瘤可切除或减少局部晚期癌症所需的手术范围。它还可以更好地预防远处复发,并可能通过根据对NAT的反应调整辅助治疗(AD)来调节药物治疗。通过升级或降级治疗。然而,目前缺少改善结局的明确证据.这里,我们报告了在我们机构接受NAT治疗的乳腺癌患者。
    方法:回顾性分析了2004年至2021年在我们放射肿瘤科接受治疗的127例患者。所有患者均患有局部或局部晚期乳腺癌,用NAT处理,术后接受放疗。考虑的结果是总生存期(OS),局部区域无复发生存率(LRRFS),和无远处转移生存期(DMFS)。在同一时期和同一中心用AD治疗的匹配患者群体用于比较。
    结果:5年预测的OS在NAT组中为87%,在AD组中为81.5%(p值=0.179),NAT组LRRFS为93.2%,AD组为100%(p=0.005)。NAT组的5年预测DMFS为84.6%,AD患者为82.1%(p=0.367)。在NAT组中,唯一与改善预后显着相关的预后因素是病理淋巴结反应,无残留淋巴结疾病患者的OS为95.6%,而有残留淋巴结疾病证据的患者为75.1%。
    结论:我们的研究,尽管少数患者的局限性及其回顾性性质,证实了以前较大研究的数据。在DMFS和OS方面,NAT至少和AD一样有效。NAT代表了在节点阳性乳腺癌患者中个性化调节治疗的绝佳机会。
    OBJECTIVE: Neoadjuvant systemic therapy (NAT) in breast cancer can make tumors resectable or reduce the extent of surgery needed for locally advanced cancers. It can also better prevent distant relapse and possibly modulate drug therapy by adjusting adjuvant therapy (AD) based on the response to NAT, either by escalating or de-escalating the treatment. However, clear evidence of improved outcomes is currently missing. Here, we report on breast cancer patients treated with NAT at our institution.
    METHODS: One hundred twenty-seven patients treated at our Radiation Oncology department between 2004 and 2021 were retrospectively analyzed. All patients had localized or locally advanced breast cancer, were treated with NAT, and received postoperative radiotherapy. The outcomes considered were overall survival (OS), loco-regional recurrence-free survival (LRRFS), and distant metastases-free survival (DMFS). A matched patient population treated with AD during the same period and at the same center was used for comparison.
    RESULTS: The 5-year predicted OS was 87% in the NAT group and 81.5% in the AD group (p-value=0.179), while LRRFS was 93.2% in the NAT group and 100% in the AD group (p=0.005). The 5-year predicted DMFS was 84.6% in the NAT group and 82.1% in AD patients (p=0.367). In the NAT group, the only prognostic factor significantly related to improved outcomes was the pathological node response, with an OS of 95.6% in patients without residual node disease compared to 75.1% in patients with evidence of residual node disease.
    CONCLUSIONS: Our study, despite the limitations of a small number of patients and its retrospective nature, confirms the data of previous larger studies. In terms of DMFS and OS, NAT is at least as effective as AD. NAT represents a great opportunity for personalized modulation of treatment in node-positive breast cancer patients.
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  • 文章类型: Case Reports
    恶性梭形细胞黑色素瘤是一种罕见的癌症,由于公开的病例报道有限,预后可疑。本文讨论了一名男性患者,有Spindle细胞黑色素瘤病史,Rt鞋跟,在我们的OPD中观察到的3级(Gr3)阶段2(St2),支持阿育吠陀药物的草药-矿物质组合。这种类型的癌症是令人担忧的,并且可能对患者更麻烦。患者最初的主诉是右足跟明显的玉米样生长,当时手术切除了。当它在一年后复发时,经过彻底调查,发现它是恶性的,然后再次操作。病人第二次手术后来找我们。经过基于阿育吠陀和现代参数的适当分析,患者接受了Ayurved治疗。由于肿瘤学家没有建议其他治疗方法,他只接受阿育吠陀的支持性治疗。阿育吠陀治疗持续2年。治疗模块显示症状完全缓解(100%),治疗结束时。随访PET扫描显示进一步改善,并且观察到残留疾病的完全逆转。最后一次PET扫描没有显示任何异常的证据。迄今为止,在过去的近5年中,患者没有复发,并且生活完全正常(karnofsky评分90/100)。可以得出结论,添加阿育吠陀治疗可能有助于该恶性梭形细胞黑色素瘤患者消退残留病,迄今为止预防转移,和良好的生活质量。我们观察到该患者5年以上的无病生存和接近正常的生活质量,并且仍在进行中。
    Malignant spindle cell melanoma is a rare cancer with a questionable prognosis because of limited published case reports. This article discusses a male patient with a history of Spindle cell melanoma tumor, Rt heel, Grade 3 (Gr 3) Stage 2 (St 2) seen in our OPD treated with supporting herbo-mineral combination of Ayurvedic medicine. Such types of cancers are of concern and can be more troublesome to the patient. The initial chief complaint of the patient was a palpable corn-like growth in the right heel, which was surgically removed at that time. When it recurred after one year, it was investigated thoroughly and it was found malignant, and then operated again. The patient came to us after his second operation. After appropriate analysis based on Ayurvedic and modern parameters, the patient was treated with Ayurved treatment. As there was no other treatment suggested by oncologists, he was on supportive Ayurvedic treatment only. Ayurvedic treatment continued for 2 years afterwards. The treatment module showed complete relief in the symptoms (100%), by the end of treatment. Follow-up PET scans showed further improvement and a complete reversal of residual disease was observed. The last PET scan did not show any evidence of abnormality. To date, there has been no recurrence and the patient has been living completely normally for the last almost 5 years (karnofsky score 90/100). It can be concluded that the addition of Ayurvedic treatment might have helped this patient of malignant spindle cell melanoma for regression of residual disease, prevention of metastasis to date, and a good quality of life. We have observed 5+ years of disease-free survival and near-normal quality of life for this patient, and still ongoing.
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  • 文章类型: Journal Article
    目的:我们旨在研究卵巢癌(OC)患者肥胖与生存之间的关系,将混杂因素计入疾病阶段,组织学,和合并症。
    方法:对连续患者进行回顾性配对病例对照研究,上皮OC。肥胖(体重指数[BMI]≥35kgm-2)患者与根据疾病分期具有较低BMI(BMI<35kgm-2)的患者以1:4的比例进行匹配。细胞还原状态,肿瘤组织学和ASA评分。我们通过Kaplan-Meier生存曲线和Cox比例风险比较了3年和总无复发生存率和总生存率。
    结果:总体而言,纳入153例连续患者,其中32人(20.9%)的BMI≥35。和121个BMI<35。中位随访时间为39个月(四分位距18-67)。两个研究组在多个预后因素方面相似,包括美国麻醉医师协会的身体状况,完成细胞减少,组织学和疾病分期(分别为p=0.981,p=0.992,p=0.740和p=0.984)。95例(62.1%)患者接受了机器人手术,从机器人到剖腹手术的转换率在肥胖组2(6.3%)和6(5.0%)在低BMI患者中,p=0.673。在随访期间,两组的复发率相似;肥胖组21例(65.6%)与68(57.1%),p=0.387,死亡事件发生率相似;肥胖组16例(50.0%)与49(40.5%),p=0.333)。肥胖组的3年OS较高(logrankp=0.042),但两组的3年RFS相似(logrankp=0.556)。两组肥胖患者62个月(95%置信区间25-98个月)的中位总OS相似。低BMI组67个月(95%置信区间15-118),对数秩p=0.822。两组的中位RFS相似;肥胖组61个月(95%置信区间47-74),vs.54(95%置信区间43-64),对数秩p=0.842。在OS的Cox回归分析中,包括肥胖,年龄,开腹手术和新辅助治疗-仅新辅助治疗与较长的OS:比值比1.82(95%置信区间1.09-3.05)和较长的RFS:比值比2.16(95%置信区间1.37-3.41)独立相关.
    结论:在本连续卵巢癌病例的研究中,肥胖似乎与结局无关,除了明显改善的3年生存率,此后逐渐消失。
    OBJECTIVE: We aimed to study the association between obesity and survival in ovarian cancer (OC) patients, accounting for confounders as disease stage, histology, and comorbidities.
    METHODS: Retrospective matched case-control study of consecutive patients, with epithelial OC. Obese (body mass index [BMI] ≥ 35 kg m-2) patients were matched in a 1:4 ratio with patients having lower BMIs (BMI < 35 kg m-2) based on disease stage, cytoreduction state, tumor histology and ASA score. We compared the 3-year and total recurrence-free survival and overall survival through Kaplan-Meier survival curves and Cox proportional hazards.
    RESULTS: Overall, 153 consecutive patients were included, of whom 32 (20.9%) had a BMI ≥ 35. and 121 a BMI < 35. The median follow-up time was 39 months (interquartile range 18-67). Both study groups were similar in multiple prognostic factors, including American Society of Anesthesiologists physical status, completion of cytoreduction, histology and stage of disease (p = 0.981, p = 0.992, p = 0.740 and p = 0.984, respectively). Ninety-five (62.1%) patients underwent robotic surgery and conversion rate from robotic to laparotomy was similar in both groups 2 (6.3%) in obese group vs. 6 (5.0%) in lower BMI patients, p = 0.673. During the follow-up time, the rate of recurrence was similar in both groups; 21 (65.6%) in obese group vs. 68 (57.1%), p = 0.387 and the rate of death events was similar; 16 (50.0%) in obese group vs. 49 (40.5%), p = 0.333). The 3-year OS was higher in the obese group (log rank p = 0.042) but the 3-year RFS was similar in both groups (log rank p = 0.556). Median total OS was similar in both groups 62 months (95% confidence interval 25-98 months) in obese vs. 67 months (95% confidence interval 15-118) in the lower BMI group, log rank p = 0.822. Median RFS was similar in both groups; 61 months (95% confidence interval 47-74) in obese, vs. 54 (95% confidence interval 43-64), log rank p = 0.842. In Cox regression analysis for OS, including obesity, age, laparotomy and neoadjuvant treatment - only neoadjuvant treatment was independently associated with longer OS: odds ratio 1.82 (95% confidence interval 1.09-3.05) and longer RFS: odds ratio 2.16 (95% confidence interval 1.37-3.41).
    CONCLUSIONS: In the present study on consecutive cases of ovarian cancer, obesity did not seem to be associated with outcome, except for an apparent improved 3-year survival that faded away thereafter.
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  • 文章类型: Case Reports
    肺肝样腺癌(HAL)是一种罕见的侵袭性肺癌亚型。HAL患者的预后普遍较差,目前,只有有限的治疗选择。这里,我们介绍了一例47岁的男性患者,该患者被诊断为局部晚期HAL,在接受新辅助和辅助卡利珠单抗联合化疗和手术治疗后,获得了非常长的无病生存期.该病例强调了免疫化疗加手术在改善HAL患者预后方面的潜力。
    Hepatoid adenocarcinoma of the lung (HAL) is a rare and aggressive subtype of lung cancer. The prognosis for patients with HAL is generally poor and currently, there are only limited treatment options. Here, we present a case of a 47-year-old male diagnosed with locally advanced-stage HAL who achieved a remarkably long disease-free survival after receiving neoadjuvant and adjuvant camrelizumab plus chemotherapy and surgery. This case highlights the potential of immunochemotherapy plus surgery in improving outcomes for patients with HAL.
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  • 文章类型: Journal Article
    背景:大约20%的直肠肿瘤在出现时局部进展并侵入相邻结构。这些可能需要手术切除超过全直肠系膜切除术(bTME)的范围以进行根治性手术。机器人bTME正在调查中。这项研究报告了机器人bTME治疗局部晚期直肠癌的围手术期和肿瘤学结果。
    方法:多中心,前瞻性收集的机器人bTME切除术的回顾性分析(2015年7月至2020年11月)。人口统计,临床病理特征,短期结果,复发,和生存进行了调查。
    结果:纳入了一百六十八个患者(八个中心)。中位年龄和BMI分别为60.0(50.0-68.7)岁和24.0(24.4-27.7)kg/m2。女性普遍存在(n=95,56.8%)。50例患者(29.6%)为ASAIII-IV。125例(74.4%)患者接受新辅助放化疗。中位手术时间为314.0(260.0-450.0)分钟。中位估计失血量为150.0(27.5-500.0)ml。向剖腹手术的转化率为4.8%。术后并发症77例(45.8%);Clavien-DindoIII和IV分别占27.3%和3.9%。分别。30天死亡率为1.2%(n=2)。R0率为92.9%。72例(42.9%)患者接受辅助化疗。中位随访时间为34.0(10.0-65.7)个月。35例(20.8%)和15例(8.9%)患者出现远处和局部复发,分别。1、3和5年总生存率(OS)分别为91.7、82.1和76.8%。1、3和5年的无病生存率(DFS)分别为84.0、74.5和69.2%。
    结论:机器人bTME在技术上是安全的,转化率相对较低,良好的操作系统,和可接受的DFS在高容量中心的经验丰富的外科医生手中。在选定的情况下,机器人方法允许bTME期间的高R0率。
    BACKGROUND: Around 20% of rectal tumors are locally advanced with invasion into adjacent structures at presentation. These may require surgical resections beyond boundaries of total mesorectal excision (bTME) for radicality. Robotic bTME is under investigation. This study reports perioperative and oncological outcomes of robotic bTME for locally advanced rectal cancers.
    METHODS: A multicentre, retrospective analysis of prospectively collected robotic bTME resections (July 2015-November 2020). Demographics, clinicopathological features, short-term outcomes, recurrences, and survival were investigated.
    RESULTS: One-hundred-sixty-eight patients (eight centres) were included. Median age and BMI were 60.0 (50.0-68.7) years and 24.0 (24.4-27.7) kg/m2. Female sex was prevalent (n = 95, 56.8%). Fifty patients (29.6%) were ASA III-IV. Neoadjuvant chemoradiotherapy was given to 125 (74.4%) patients. Median operative time was 314.0 (260.0-450.0) minutes. Median estimated blood loss was 150.0 (27.5-500.0) ml. Conversion to laparotomy was seen in 4.8%. Postoperative complications occurred in 77 (45.8%) patients; 27.3% and 3.9% were Clavien-Dindo III and IV, respectively. Thirty-day mortality was 1.2% (n = 2). R0 rate was 92.9%. Adjuvant chemotherapy was offered to 72 (42.9%) patients. Median follow-up was 34.0 (10.0-65.7) months. Distant and local recurrences were seen in 35 (20.8%) and 15 patients (8.9%), respectively. Overall survival (OS) at 1, 3, and 5-years was 91.7, 82.1, and 76.8%. Disease-free survival (DFS) at 1, 3, and 5-years was 84.0, 74.5, and 69.2%.
    CONCLUSIONS: Robotic bTME is technically safe with relatively low conversion rate, good OS, and acceptable DFS in the hands of experienced surgeons in high volume centres. In selected cases robotic approach allows for high R0 rates during bTME.
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  • 文章类型: Journal Article
    背景:在非小细胞肺癌(NSCLC)的治疗中,5年的无病生存期(DFS)是治愈的标准.本研究旨在评估5年DFS(晚期复发性脑转移,LRBM)。
    方法:我们回顾了2014年11月至2022年12月在一家研究机构连续1,281例肺癌脑转移患者。相关文章从PubMed检索。仅包括以英文出版的同行评审期刊。
    结果:6例患者(0.47%)出现LRBM。三个是男性。肺癌诊断的中位年龄为45岁。所有患者的组织学诊断均为腺癌。在5例患者中观察到驱动基因突变。从肺癌治疗到脑转移的中位潜伏期为13年。所有患者均未转移至任何其他器官,并进行了开颅手术。开颅手术后的中位随访时间为3.5年。未观察到局部颅内复发。3例患者在开颅手术后7、2和0.6年出现颅内远端复发。5例患者在开颅手术后存活了8、4、3、2和0.3年。一名患者在开颅手术后4年肺部复发,并在3.7年后死亡。在我们的系统审查中,只有6项研究描述了NSCLC的LRBM。
    结论:LRBM在NSCLC患者中很少见。在我们的机构里,这些患者中有许多携带驱动基因突变,并通过积极的局部治疗获得长期生存。多中心分析是强制性的。
    In the treatment of nonsmall cell lung cancer (NSCLC), a disease-free survival of 5 years is a criterion for cure. This study aimed to evaluate the characteristics and outcomes of patients with brain metastases of NSCLC after a disease-free survival of 5 years (late recurrent brain metastasis [LRBM]).
    We reviewed 1281 consecutive patients with brain metastasis of lung cancer at a single institute between November 2014 and December 2022. Relevant articles were retrieved from PubMed. Only peer-reviewed journals published in English were included.
    Six patients (0.47%) showed LRBM. Three were male. The median age at lung cancer diagnosis was 45 years. The histological diagnosis of all patients was adenocarcinoma. Driver gene mutations were observed in five patients. The median latency period from lung cancer treatment to the development of brain metastasis was 13 years. All patients had no metastasis to any other organs and underwent craniotomies. The median follow-up duration after craniotomy was 3.5 years. No local intracranial recurrences were observed. Three patients had distant intracranial recurrences at 7, 2, and 0.6 years after craniotomy. Five patients survived for 8, 4, 3, 2, and 0.3 years after craniotomy. One patient experienced re-recurrence in the lung 4 years after craniotomy and died 3.7 years later. In our systematic review, only six studies described LRBM of NSCLC.
    LRBM is rare in patients with NSCLC. In our institution, many of these patients harbored driver gene mutations, and achieved long-term survival with aggressive local therapy. Multicenter analysis is mandatory.
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  • 文章类型: Case Reports
    背景:化生乳腺癌(MpBC)是一种极为罕见的实体,占所有恶性乳腺肿瘤的不到1%。主要是三阴性,他们因化学抗性而臭名昭著,复发率高,无病生存率(DFS)下降。所有这些都对BC死亡率有显著影响,并导致预后不良。有限的证据导致了针对该实体的特定治疗指南的空白,因此对于临床医生来说仍然是未知的领域。
    方法:我们报告一例46岁的绝经前女性,左侧化生三阴性T3N2aM0BC伴间质分化(高级别),我们接受新辅助化疗治疗,通过Telecobalt机器进行极端肿瘤成形术和辅助放射治疗的主要手术。与预期的疾病侵袭性病程和治疗不良预后相反,患者目前处于缓解期,随访超过2年,无进展。
    结论:在这种病理实体的管理方面的经验有限,需要对其进行更多的研究,特别关注靶向治疗。讨论定制方法的可能性,而不是一刀切的方法可能有助于为MpBC治疗的未来铺平道路。
    Metaplastic Breast Cancer (MpBC) is an exceedingly rare entity, accounting for less than 1% of all malignant breast tumours. Predominantly triple-negative, they are notorious for their chemoresistance, high rates of recurrence and decreased disease-free survival (DFS). All this contributes significantly to BC mortality and results in poor prognostic implications. Limited evidence has led to a lacuna of specific treatment guidelines for this entity and hence remains an uncharted territory for clinicians.
    We report a case of a 46 year old premenopausal female with left-sided metaplastic triple negative T3N2aM0 BC with mesenchymal differentiation (high grade) whom we treated with neoadjuvant chemotherapy, primary surgery in the form of extreme oncoplasty and adjuvant radiotherapy by Telecobalt machine. Contrary to the expected aggressive course of the disease and poor prognosis of treatment, the patient is presently in remission without progression for over 2 years of follow up.
    Limited experience in management of this pathological entity warrants the need for more research on it, with a special focus on targeted therapy. Discussing possibilities of a tailored approach, rather than a one-size-fits-all approach may aid in paving the path for the future of MpBC treatment.
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  • 文章类型: Case Reports
    背景:肺癌是全球流行和致命的疾病。非小细胞肺癌(NSCLC)是最常见的亚型,占85%的病例。
    方法:一位65岁的男性前吸烟者出现夜间咳嗽。各种调查显示他患有转移性NSCLC,为此他接受了顺铂和吉西他滨的化疗,随后用Nivolumab进行免疫治疗。他对治疗有完全反应,并且自最初诊断以来已超过7年没有复发。
    结论:转移性NSCLC的治疗仍然是一个重大的治疗挑战,但是新治疗技术的实施扩大了实现彻底和持久根除这种疾病的可能性。
    Lung cancer is a prevalent and deadly disease globally. Non-small cell lung cancer (NSCLC) is the most common subtype, comprising 85% of cases.
    A 65-year-old male ex-smoker presented to our facility with a nocturnal cough. Various investigations revealed that he had metastatic NSCLC, for which he underwent chemotherapy with cisplatin and gemcitabine, followed by immunotherapy with Nivolumab. He achieved a complete response to the therapy and has remained free from recurrence for over 7 years since the initial diagnosis.
    The treatment of metastatic NSCLC remains a significant therapeutic challenge, but the implementation of new therapeutic techniques has expanded the possibilities of achieving complete and durable eradication of the disease.
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  • 文章类型: Journal Article
    背景:多发性骨软骨瘤是一种遗传性疾病,其特征是形成多个良性软骨覆盖的骨肿瘤,骨软骨瘤,在骨骼发育过程中。最可怕的并发症是继发性外周软骨肉瘤,由先前存在的骨软骨瘤的软骨帽引起的恶性软骨瘤。我们对1960年至2019年诊断和随访的患者进行了一项回顾性队列研究,以描述多发性骨软骨瘤受周围软骨肉瘤影响的个体的临床和病理特征。评估随访信息和个体结局,并将结果与文献进行比较。数据,包括年龄,性别,site,组织学分级,软骨帽厚度,手术治疗,手术切缘,我们从医院电子健康记录和多发性骨软骨瘤登记处获取了基因型突变状态和治疗细节.此外,病理学家对所有苏木精和伊红(H&E)染色切片进行了完整的组织学检查.
    结果:本研究纳入了105例筛查病例。诊断SPC的年龄范围为13至63岁,诊断时的中位年龄为34岁。最常受到恶性变性影响的部位是骨盆(46例,44%),男性患者发病率较高(男性32例,女性14例)。第二个是下肢(包括股骨,腓骨,或胫骨),在35名患者中确定。组织学信息-可用于103名患者-显示:59名患者为1级;40名患者为2级,4名患者为3级。最常见的手术治疗是完全切除,接着是剔除,截肢和部分切除。大多数病例没有复发。无病生存的结果突出表明,病程较差与组织学2级或3级以及部分切除手术有关。在大多数分析病例(94%)中,发现了致病变异。
    结论:结论:本研究概述了继发性外周软骨肉瘤,确认这种疾病代表了多个骨软骨瘤患者的影响并发症,并表明恶性转化也可能发生在年轻患者中,在一些并非无关紧要的案件中。
    BACKGROUND: Multiple osteochondromas is genetic disorder characterized by the formation of multiple benign cartilage-capped bone tumors, named osteochondromas, during skeletal development. The most feared complication is the secondary peripheral chondrosarcoma, a malignant cartilaginous neoplasm that arises from the chondroid cap of pre-existent osteochondromas. We conducted a retrospective cohort study on patients diagnosed and followed up from 1960 to 2019 to describe the clinical and pathological features of individuals affected by peripheral chondrosarcoma in multiple osteochondromas, to evaluate follow up information and individual outcome and to compare the results with literature. Data, including age, gender, site, histological grade, cartilage cap thickness, surgical treatments, surgical margins, genotype mutational status as well as treatment details were captured from the hospital electronic health records and from Registry of Multiple Osteochondromas. In addition, a complete histological review of all hematoxylin and eosin (H&E)-stained sections has been performed by expert pathologists.
    RESULTS: One hundred five of the screened cases were included in the present study. The age at diagnosis of SPC ranges from 13 to 63, with median age at diagnosis of 34 years. The site most frequently affected by malignant degeneration was the pelvis (46 patients, 44%) with higher incidence in male patients (32 males vs.14 females). The second one was lower limbs (including femur, fibula, or tibia), identified in 35 patients. Histological information - available for 103 patients - showed: 59 patients with grade 1; 40 patients had a grade 2 and 4 patients had a grade 3. The most common surgical treatment was the complete resection, followed by debulking, amputation and partial resection. Most of cases did not have recurrence of the disease. Outcome in disease-free survival highlights that a worse course of the disease was associated with histological grade 2 or 3, and partial resection surgery. In most of analyzed cases (94%) a pathogenic variant was identified.
    CONCLUSIONS: In conclusion, the present study gives an overview of the secondary peripheral chondrosarcomas, confirming that this disease represents an impacting complication for multiple osteochondromas patients and suggests that malignant transformation can occur also in younger patient, in a not irrelevant number of cases.
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  • 文章类型: Journal Article
    对于原发肿瘤切除后远处转移或转移性复发的结直肠癌(CRC)的治疗策略存在争议。在本研究中,本研究报告4例晚期CRC伴远处转移患者实现5年以上的无病生存(DFS),并被认为可能治愈.病例1是一名53岁的男性患者,患有直肠癌和肝转移(pT3N2bM1,pStageIV),病例2是一名58岁女性降结肠癌患者(pT3N1M1,pStageIV),在手术和术后均有肺转移。两名患者在同时或分期进行部分肝切除术或全肺切除术后化疗后达到DFS>5年。病例3是一名75岁的横结肠癌男性患者(pT3N1M0,pStageIIIB),病例4是一名73岁的乙状结肠癌男性患者(pT3N0M0,pStageIIA)。这些病例在切除原发肿瘤后发生肝转移,随后在部分肝切除术之前或之后接受化疗。实现了>5年的DFS。所有四名患者均被认为治愈。数据显示,即使是患有CRC和远处转移的患者,经过多学科治疗也可能被治愈。在本案例报告中,讨论了使这些患者被认为治愈的因素,目的是改进治疗策略,以治愈有远处转移或复发的CRC.
    The treatment strategies for colorectal cancer (CRC) with distant metastasis or metastatic recurrence after resection of the primary tumor are controversial. In the present study, four cases of patients with advanced CRC with distant metastasis who achieved disease-free survival (DFS) for >5 years and were deemed potentially cured were reported. Case 1 was that of a 53-year-old male patient with rectal cancer and liver metastases (pT3N2bM1, pStage IV), and case 2 was that of a 58-year-old female patient with descending colon cancer (pT3N1M1, pStage IV) who had lung metastases at surgery and postoperatively. Both patients achieved DFS for >5 years after simultaneous or staged partial hepatectomy or pneumonectomy followed by chemotherapy. Case 3 was that of a 75-year-old male patient with transverse colon cancer (pT3N1M0, pStage IIIB) and case 4 was that of a 73-year-old male patient with sigmoid colon cancer (pT3N0M0, pStage IIA). These cases developed liver metastases after resection of the primary tumour and were subsequently treated with chemotherapy before or after partial hepatectomy. DFS for >5 years was achieved. All four patients were considered cured. The data revealed that even patients with CRC and distant metastases can potentially be cured following multidisciplinary treatment. In the present case report, the factors that enabled these patients to be considered cured were discussed and the aim was to improve the treatment strategy to cure CRC with distant metastasis or recurrence.
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