multidisciplinary therapy

多学科治疗
  • 文章类型: Journal Article
    本研究旨在评估多学科治疗对接受根治性胃切除术的局部晚期胃癌(LAGC)患者的疗效。
    比较单独手术效果的随机对照试验(RCT),辅助化疗(CT),辅助放疗(RT),辅助放化疗(CRT),新辅助CT,新辅助RT,新辅助CRT,对LAGC的围手术期CT和腹腔热化疗(HIPEC)进行了搜索。总生存期(OS),无病生存率(DFS),复发和转移,长期死亡率,不良事件(≥3级),手术并发症和R0切除率作为Meta分析的结果指标。
    最终分析了45个RCT,共10077名参与者。辅助CT的OS(风险比[HR]=0.74,95%可信区间[CI]=0.66-0.82)和DFS(HR=0.67,95%CI=0.60-0.74)高于单独手术组。围手术期CT(比值比[OR]=2.56,95%CI=1.19-5.50)和辅助CT(OR=0.48,95%CI=0.27-0.86)均比HIPEC辅助CT具有更多的复发和转移,而辅助CRT的复发和转移倾向于比辅助CT(OR=1.76,95%CI=1.29-2.42)和甚至辅助RT(OR=1.83,95%CI=0.98-3.40)更少。此外,HIPEC+辅助CT的死亡率低于辅助RT(OR=0.28,95%CI=0.11-0.72),辅助CT(OR=0.45,95%CI=0.23-0.86)和围手术期CT(OR=2.39,95%CI=1.05-5.41)。不良事件(≥3级)分析显示,任何两个辅助治疗组之间均无统计学差异。
    HIPEC与辅助CT的组合似乎是最有效的辅助疗法,这有助于减少肿瘤复发,转移和死亡率-没有增加与毒性相关的手术并发症和不良事件。与单纯CT或RT相比,CRT可以减少复发,转移和死亡率,但增加不良事件。此外,新辅助治疗能有效提高根治性切除率,但新辅助CT往往会增加手术并发症。
    UNASSIGNED: This study aimed to evaluate the efficacy of multidisciplinary treatment for patients with locally advanced gastric cancer (LAGC) who underwent radical gastrectomy.
    UNASSIGNED: Randomised controlled trials (RCTs) comparing the effectiveness of surgery alone, adjuvant chemotherapy (CT), adjuvant radiotherapy (RT), adjuvant chemoradiotherapy (CRT), neoadjuvant CT, neoadjuvant RT, neoadjuvant CRT, perioperative CT and hyperthermic intraperitoneal chemotherapy (HIPEC) for LAGC were searched. Overall survival (OS), disease-free survival (DFS), recurrence and metastasis, long-term mortality, adverse events (grade ≥3), operative complications and R0 resection rate were used as outcome indicators for meta-analysis.
    UNASSIGNED: Forty-five RCTs with 10077 participants were finally analysed. Adjuvant CT had higher OS (hazard ratio [HR] = 0.74, 95% credible interval [CI] = 0.66-0.82) and DFS (HR = 0.67, 95% CI = 0.60-0.74) than surgery-alone group. Perioperative CT (odds ratio [OR] = 2.56, 95% CI = 1.19-5.50) and adjuvant CT (OR = 0.48, 95% CI = 0.27-0.86) both had more recurrence and metastasis than HIPEC + adjuvant CT, while adjuvant CRT tended to have less recurrence and metastasis than adjuvant CT (OR = 1.76, 95% CI = 1.29-2.42) and even adjuvant RT (OR = 1.83, 95% CI = 0.98-3.40). Moreover, the incidence of mortality in HIPEC + adjuvant CT was lower than that in adjuvant RT (OR = 0.28, 95% CI = 0.11-0.72), adjuvant CT (OR = 0.45, 95% CI = 0.23-0.86) and perioperative CT (OR = 2.39, 95% CI = 1.05-5.41). Analysis of adverse events (grade ≥3) showed no statistically significant difference between any two adjuvant therapy groups.
    UNASSIGNED: A combination of HIPEC with adjuvant CT seems to be the most effective adjuvant therapy, which contributes to reducing tumour recurrence, metastasis and mortality - without increasing surgical complications and adverse events related to toxicity. Compared with CT or RT alone, CRT can reduce recurrence, metastasis and mortality but increase adverse events. Moreover, neoadjuvant therapy can effectively improve the radical resection rate, but neoadjuvant CT tends to increase surgical complications.
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  • 文章类型: Journal Article
    背景:产生甲胎蛋白的胃癌(AFPGC)是一种罕见的侵袭性胃癌(GC),预后不佳。我们介绍了一名AFPGC患者,他通过多学科方法获得了长期生存。
    方法:一名67岁的晚期GC患者被转诊到我院进行全身化疗。他被诊断为cStageIVBAFPGC。在二线治疗期间,我们无法控制GC本身的出血。完全切除后,化疗期间,发现门静脉癌栓(PVTT)和肝转移。纳武单抗和伊立替康,PVTT和肝转移消失。23个月没有免疫治疗和化疗,患者至今已存活48个月,无GC复发.
    结论:AFPGC的长期生存可以通过使用几种不同的方法来实现,比如手术,免疫疗法,和化疗。
    BACKGROUND: Alpha-fetoprotein-producing gastric cancer (AFPGC) is a rare type of aggressive gastric cancer (GC) with a dismal prognosis. We present a patient with AFPGC who achieved long-term survival through a multidisciplinary approach.
    METHODS: A 67-year-old man with advanced GC was referred to our hospital for systemic chemotherapy. He was diagnosed with cStage IVB AFPGC. During 2nd-line treatment, we could not control bleeding from the GC itself. After complete resection, during chemotherapy, portal venous tumor thrombi (PVTTs) and liver metastases were identified. With nivolumab followed by irinotecan, the PVTTs and liver metastases disappeared. Without immunotherapy and chemotherapy for 23 months, the patient has survived for 48 months so far with no recurrence of GC.
    CONCLUSIONS: Long-term survival with AFPGC can be accomplished by using several different approaches, such as surgery, immunotherapy, and chemotherapy.
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  • 文章类型: Case Reports
    BACKGROUND: Liver metastasis is the most common form of distant metastasis in colorectal cancer, and the only possible curative treatment for patients with colorectal liver metastases (CRLM) is hepatectomy. However, approximately 25% of patients with CRLM have indications for liver resection at the initial diagnosis. Strategies aimed at downstaging large or multifocal tumors to enable curative resection are appealing.
    METHODS: A 42-year-old man was diagnosed with ascending colon cancer and liver metastases. Due to the huge lesion size and compression of the right portal vein, the liver metastases were initially diagnosed as unresectable lesions. The patient was treated with preoperative transcatheter arterial chemoembolization (TACE) consisting of 5-fluorouracil/Leucovorin/oxaliplatin/Endostar®. After four courses, radical right-sided colectomy and ileum transverse colon anastomosis were performed. Postoperatively, the pathological analysis revealed moderately differentiated adenocarcinoma with necrosis and negative margins. Thereafter, S7/S8 partial hepatectomy was performed after two courses of neoadjuvant chemotherapy. Pathological examination of the resected specimen revealed a pathologically complete response (pCR). Intrahepatic recurrence was detected more than two months after the operation, and the patient was then treated with TACE consisting of irinotecan/Leucovorin/fluorouracil therapy plus Endostar®. Subsequently, the patient was treated with a γ-knife to enhance local control. Notably, a pCR was reached, and the patient\'s overall survival time was > 9 years.
    CONCLUSIONS: Multidisciplinary treatment can promote the conversion of initially unresectable colorectal liver metastasis and facilitate complete pathological remission of liver lesions.
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  • 文章类型: Case Reports
    促甲状腺激素分泌腺瘤(TSH-oma)是一种非常罕见的功能性垂体腺瘤,尤其是在青少年中发生的。然而,其潜在的临床和治疗特征仍然未知。
    本研究旨在总结青少年型TSH-oma患者的临床和治疗特点。
    我们回顾性分析了2012年1月至2020年10月在我院确诊为TSH-oma的148例患者中的6例(4.1%)青少年TSH-oma病例。对PubMed在线数据库进行了文献综述,并检索到14例青少年发病TSH-oma病例。然后,临床表现的特点,治疗结果,并与成年TSH-oma患者进行随访分析和比较。
    总之,本研究包括20例青少年发病病例,平均发病年龄为13.4±3.3岁。在我们的研究中发现雄性稍微占优势(M:F=1.5:1)。TSH的基线水平中位数,青少年发病病例中的FT3和FT4为6.30[四分位距(IQR)9.82]µIU/ml,9.18(IQR11.61)pg/ml,和3.22(IQR1.90)ng/dl,分别,均明显高于我院成年患者。此外,青少年发病病例显示更大的肿瘤比率(36.8%vs.9.3%,p=0.007)与成年患者相比。与文献中所有年龄段的患者相比,在青少年发病患者中,SSA的生化缓解率(57.1%)和TSS的缓解率(38.9%)明显较低。而复发率(44.4%)明显较高。
    青少年TSH-oma患者的TSH和甲状腺激素水平较高,更大的肿瘤,治疗结果比成人更差。因此,早期诊断,多学科治疗,应重视密切随访以改善预后。
    Thyrotropin-secreting adenoma (TSH-oma) is a very rare kind of functional pituitary adenoma, especially that which occurs in adolescents. However, its potential clinical and therapeutic characteristics are still unknown.
    The study was aimed to summarize the clinical and therapeutic characteristics of patients with adolescent-onset TSH-oma.
    We retrospectively analyzed six (4.1%) adolescent-onset TSH-oma cases from 148 patients who were diagnosed with TSH-oma at our hospital between January 2012 and October 2020. A literature review was performed on the PubMed online database, and 14 adolescent-onset TSH-oma cases were retrieved. Then, the characteristics of clinical manifestations, treatment outcomes, and follow-ups were analyzed and compared to the adult TSH-oma patients.
    Altogether, 20 adolescent-onset cases were included in this study having mean onset age of 13.4 ± 3.3 years. Males were found to be slightly predominant (M: F = 1.5:1) in our study. The median baseline levels of TSH, FT3, and FT4 in adolescent-onset cases were found to be 6.30 [interquartile range (IQR) 9.82] µIU/ml, 9.18 (IQR 11.61) pg/ml, and 3.22 (IQR 1.90) ng/dl, respectively, which were all significantly higher than the adult patients of our hospital. Also, the adolescent-onset cases showed more large tumor ratio (36.8% vs. 9.3%, p = 0.007) compared to the adult patients. Compared to the patients of all ages in the literature, the biochemical remission rate of SSAs (57.1%) and remission rate of TSS (38.9%) were found to be considerably lower in adolescent-onset patients, while the recurrence rate (44.4%) was found to be considerably higher.
    Adolescent-onset TSH-oma patients showed higher TSH and thyroid hormone levels, more large tumors, and worse treatment outcomes than adult cases. Hence, early diagnosis, multidisciplinary therapy, and close follow-up should be highlighted to improve the prognosis.
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  • 文章类型: Case Reports
    OBJECTIVE: The aim of this case report and review was to determine the characteristics of retinoblastoma.
    METHODS: One case report was introduced along with previous reports on retinoblastoma metastasizing to the mandible.
    RESULTS: Sixteen cases from 14 reports were included in this study. Including the present case, 11 of 16 patients died within 8 months.
    CONCLUSIONS: Retinoblastoma rarely metastasizes to the mandible. However, metastasis to other organs should be considered, and specialists should be consulted if retinoblastoma metastasis to the mandible is observed. Moreover, it is necessary to follow up patients after multidisciplinary therapy is completed, because subsequent complications of the teeth and jawbones associated with therapy could occur.
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