Ifosfamide

异环磷酰胺
  • 文章类型: Journal Article
    异环磷酰胺诱导的肾损害患者存在范可尼综合征。核型肾病/间质性肾炎(KNIN)是一种罕见的慢性肾小管间质性肾炎,最初被认为是家族性肾病。然而,关于药物诱导的KNIN的几篇报道,即,KNIN样肾病,近年来有报道。我们介绍了一名18岁男子的病例,该男子在接受包括异环磷酰胺和顺铂在内的化疗治疗右股骨肉瘤后出现Fanconi综合征和进行性肾功能障碍。肾活检显示大量萎缩的肾小管上皮细胞,多态核,最终诊断为KNIN。大多数接受异环磷酰胺治疗的KNIN样肾病患者同时接受顺铂治疗,这表明异环磷酰胺和顺铂可能协同作用,增加KNIN样肾病的风险。有必要对病例系列进行进一步研究,以揭示潜在的治疗方法并评估预后。
    Patients with ifosfamide-induced renal damage present with Fanconi syndrome. Karyomegalic nephropathy/interstitial nephritis (KNIN) is a rare form of chronic tubulo-interstitial nephritis that was initially considered a type of familial nephropathy. However, several reports of drug-induced KNIN, i.e., KNIN-like nephropathy, have been reported in recent years. We present the case of an 18-year-old man who presented with Fanconi syndrome and progressive renal dysfunction after receiving chemotherapy including ifosfamide and cisplatin for right femoral osteosarcoma. Renal biopsy revealed numerous atrophied tubular epithelial cells with large, polymorphic nuclei, and the definitive diagnosis was KNIN. Most patients with KNIN-like nephropathy who receive ifosfamide are concomitantly treated with cisplatin, indicating that ifosfamide and cisplatin might act synergistically to increase the risk for KNIN-like nephropathy. Further investigation in case series is warranted to reveal potential treatment approaches and to evaluate prognosis.
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  • 文章类型: Journal Article
    背景:治疗方案有限,铂耐药复发转移性(R/M)头颈部鳞状细胞癌(HNSCC)患者预后较差。这项研究评估了紫杉醇和异环磷酰胺(TI)方案在以铂类为基础的治疗后疾病进展的R/MHNSCC患者中的疗效和安全性。
    方法:在这项回顾性研究中,我们纳入了53例R/MHNSCC患者,他们接受了至少一个基于TI的治疗周期,铂金故障后,2020年2月至2023年8月。一些患者接受与免疫疗法和/或西妥昔单抗组合的TI方案。评估的关键指标包括客观反应率(ORR),疾病控制率,和无进展以及总生存期。
    结果:该研究观察到ORR为15.8%,疾病控制率为36.8%。整个队列的中位无进展生存期为3.3个月,中位总生存期为9.6个月.值得注意的是,TI与免疫疗法的组合产生了30.8%的更高的ORR,与单独使用TI的14.3%相比。最常见的1-2级不良事件是贫血(81%),体重减轻(68%)和高钠血症(55%)。
    结论:基于TI的方案在治疗R/MHNSCC方面表现出良好的疗效和安全性。当将其与免疫疗法相结合时,可以获得增强的结果。这项研究表明,基于TI的治疗可以作为该特定患者组的潜在挽救选择。
    BACKGROUND: Treatment options are limited, and the prognosis is poor for patients with platinum-resistant recurrent metastatic (R/M) head and neck squamous cell carcinoma (HNSCC). This study evaluated the efficacy and safety of a paclitaxel and ifosfamide (TI) regimen in patients with R/M HNSCC whose disease had progressed following platinum-based therapy.
    METHODS: In this retrospective study, we included 53 patients with R/M HNSCC who underwent at least one cycle of TI-based therapy, post platinum failure, between February 2020 and August 2023. Some patients received the TI regimen in combination with immunotherapy and/or cetuximab. Key metrics assessed included the objective response rate (ORR), disease control rate, and progression-free as well as overall survival.
    RESULTS: The study observed an ORR of 15.8% and a disease control rate of 36.8%. The median progression-free survival for the entire cohort was 3.3 months, and the median overall survival was 9.6 months. Notably, the combination of TI with immunotherapy yielded a higher ORR of 30.8%, compared to 14.3% with TI alone. The most prevalent grade 1-2 adverse events were anemia (81%), weight loss (68%) and hypernatremia (55%).
    CONCLUSIONS: The TI-based regimen demonstrated favorable efficacy and safety profile in treating R/M HNSCC. Enhanced outcomes may be attainable when combining it with immunotherapy. This study suggests that TI-based therapy could serve as a potential salvage option for this specific patient group.
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  • 文章类型: Journal Article
    目的:关于腹膜后软组织肉瘤的全身治疗的证据有限,而目前的日本指导方针未能提出明确的建议。这里,我们报告了我们的Mesna联合化疗的经验,阿霉素,异环磷酰胺,和达卡巴嗪(MAID)在该人群中。
    方法:我们回顾性回顾了8例患者(3例男性和5例女性)的记录,这些患者在2019年10月至2022年1月期间因病理诊断为转移性不可切除的腹膜后肉瘤(平滑肌肉瘤或多形性肉瘤)而接受MAID。治疗效果,耐受性(需要减少剂量),和安全性概况进行评估和总结.
    结果:开始时,中位年龄为56.0岁,体重指数为20.0kg/cm26例患者的东部肿瘤协作组表现状态评分为0。净临床获益是三名(37.5%)患者的部分反应,4例疾病稳定(50.0%),和进行性疾病之一(12.5%)。在中位90.8周的随访期间,五名患者的病情进展,导致中位无进展生存期为48.4周,发生了5人死亡,导致95.1周的总生存期。常见的不良事件是中性粒细胞减少症(8例),贫血(8名患者),血小板计数下降(7名患者),这导致6名患者的剂量减少(60-80%)。
    结论:MAID联合治疗可能是晚期腹膜后肉瘤的可接受选择;然而,由于其毒性并非微不足道,因此必须仔细评估其益处。
    OBJECTIVE: There is limited evidence regarding the systemic treatment of retroperitoneal soft-tissue sarcoma, and the current Japanese guidelines fail to make definitive suggestions. Here, we report our experience with combination chemotherapy of mesna, doxorubicin, ifosfamide, and dacarbazine (MAID) in this population.
    METHODS: We retrospectively reviewed the records of eight patients (three male and five female) who received MAID for pathologically diagnosed metastatic unresectable retroperitoneal sarcoma (either leiomyosarcoma or pleomorphic sarcoma) between October 2019 and January 2022. Treatment efficacy, tolerability (need for dose reduction), and safety profiles were evaluated and summarized.
    RESULTS: At initiation, the median age was 56.0 years, and the body mass index was 20.0 kg/cm2 Six patients had Eastern Cooperative Oncology Group performance status scores of 0. The net clinical benefit was a partial response in three (37.5%) patients, stable disease in four (50.0%), and progressive disease in one (12.5%). During the median 90.8 weeks of follow-up, disease in five patients progressed, resulting in a median progression-free survival of 48.4 weeks, and five deaths occurred, resulting in an overall survival of 95.1 weeks. Commonly observed adverse events were neutropenia (eight patients), anemia (eight patients), and decreased platelet count (seven patients), which led to dose reduction (60-80%) in six patients.
    CONCLUSIONS: MAID combination therapy may be an acceptable option for advanced retroperitoneal sarcoma; however, its benefits must be carefully assessed owing to its not insignificant toxicity.
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  • 文章类型: Journal Article
    背景:复发/难治性骨肉瘤(R/ROS)患者的预后仍然不佳,但未就全身治疗达成一致。在R/ROS患者中,在门诊环境(14-IFO)中使用大剂量异环磷酰胺(14g/sqm)与外部泵(14-IFO)是有限的。这项研究代表了第一个回顾性队列分析,重点是评估14-IFO在这种情况下的活性和毒性。
    方法:这项研究调查了14-IFO活性,在根据RECIST1.1标准的肿瘤反应方面,以及存活率和毒性,根据CTCAEv.5
    结果:该试验纳入了26例R/ROS患者。总有效率(ORR)和疾病控制率(DCR)分别为23%和57.5%,分别。与难治性患者相比,复发OS患者表现出更高的ORR(45%)和DCR(82%),无论接受的先前治疗行的数量如何。通过14-IFO给药实现疾病控制,使27%的患者接受了新的局部治疗。所有患者的4个月无进展生存率(PFS)为54%,复发OS亚组为82%。中位总生存期(OSurv)为13.7个月,所有患者的1年OSurv为51%,复发患者为71%。年龄超过18岁和难治性疾病的存在被确定为该患者队列的负面预后因素。总共评估了101个周期的毒性评估,没有3-4级非血液毒性的耐受性。
    结论:14-IFO应被视为R/ROS的可行治疗选择,特别是由于其良好的耐受性毒性特征和家庭管理的潜力,这可以提高患者的生活质量而不影响疗效。
    BACKGROUND: The prognosis of patients with Relapsed/Refractory Osteosarcoma (R/R OS) remains dismal without an agreement on systemic therapy. The use of High-Dose Ifosfamide (14 g/sqm) with an external pump in outpatient setting (14-IFO) in R/R OS patients is limited. This study represents the first retrospective cohort analysis focused on evaluating the activity and toxicity of 14-IFO in this setting.
    METHODS: The study investigated 14-IFO activity, in terms of tumour response according to RECIST 1.1 criteria, as well as survival rates and toxicity, according to CTCAE v.5.
    RESULTS: The trial enrolled 26 patients with R/R OS. The Overall Response Rate (ORR) and Disease Control Rate (DCR) obtained was 23% and 57.5%, respectively. Patients with relapsed OS showed a higher ORR (45%) and DCR (82%) compared to refractory patients, irrespective of the number of prior treatment lines received. The achievement of disease control with 14-IFO administration enabled 27% of patients to undergo new local treatment. Four-month Progression-Free Survival (PFS) was 54% for all patients and 82% for the relapsed OS sub-group. Median Overall Survival (OSurv) was 13.7 months, with 1-year OSurv of 51% for all patients and 71% for relapsed patients. Age over 18 years and the presence of refractory disease were identified as negative prognostic factors for this patient cohort. A total of 101 cycles were evaluated for toxic assessment, demonstrating a tolerable profile without grade 3-4 non-haematological toxicities.
    CONCLUSIONS: 14-IFO should be considered a viable treatment option for R/R OS, particularly due to its well tolerated toxicity profile and the potential for home-administration, which can improve patient quality of life without compromising efficacy.
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  • 文章类型: Journal Article
    这项研究调查了两种最广泛食用的抗肿瘤药物的慢性影响,异环磷酰胺(IF)和顺铂(CDDP),在当前(17°C)和预测的变暖条件(21°C)下的双壳类动物Mytilusgalloprovincialis。伴随着全球癌症发病率的预期增长,预计水生环境中的抗肿瘤物质检测也将上升。将贻贝暴露于不同浓度的IF(10、100、500ng/L)和CDDP(10、100、1000ng/L)28天。生化分析侧重于代谢能力,抗氧化和生物转化能力,细胞损伤,和神经毒性。结果显示生化反应的温度依赖性变化。代谢能力在IF下保持稳定,而CDDP暴露在两个温度下都增加了1000ng/L。抗氧化酶活性不受IF的影响,但是CDDP激活了它们,特别是在21°CIF的生物转化能力不变,但CDDP增强了生物转化能力。然而,CDDP浓度高于100ng/L时发生细胞损伤,不管温度。综合生物标志物反应突出了CDDP的更大影响,强调温度在塑造生物体反应中的关键作用,并强调环境压力源相互作用的复杂性。
    This study investigates the chronic impact of two of the most widely consumed antineoplastic drugs, Ifosfamide (IF) and Cisplatin (CDDP), on the bivalve species Mytilus galloprovincialis under current (17 °C) and predicted warming conditions (21 °C). Accompanying the expected increase in worldwide cancer incidence, antineoplastics detection in the aquatic environment is also expected to rise. Mussels were exposed to varying concentrations of IF (10, 100, 500 ng/L) and CDDP (10, 100, 1000 ng/L) for 28 days. Biochemical analyses focused on metabolic, antioxidant and biotransformation capacities, cellular damage, and neurotoxicity. Results showed temperature-dependent variations in biochemical responses. Metabolic capacity remained stable in mussels exposed to IF, while CDDP exposure increased it at 1000 ng/L for both temperatures. Antioxidant enzyme activities were unaffected by IF, but CDDP activated them, particularly at 21 °C. Biotransformation capacity was unchanged by IF but enhanced by CDDP. Nevertheless, cellular damage occurred at CDDP concentrations above 100 ng/L, regardless of temperature. Integrated biomarker responses highlighted CDDP\'s greater impact, emphasizing the critical role of temperature in shaping organismal responses and underscoring the complexity of environmental stressor interactions.
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  • 文章类型: Journal Article
    背景:在回顾性分析中,儿科肿瘤组[POG)和联邦国家癌症中心(FNCLCC)组织学分级预测小儿非横纹肌肉瘤软组织肉瘤(NRSTS)的预后,但是关于分级的前瞻性数据,临床特征,低等级NRSTS的结果有限。
    方法:我们分析了30岁以下儿童肿瘤组(COG)研究ARST0332(NCT00346164)患者的POG1级或2级NRSTS。低风险患者仅接受手术治疗。中危/高危患者接受异环磷酰胺/多柔比星和放疗,在放化疗12周之前或之后进行明确切除。
    结果:估计的5年无事件生存率和总生存率分别为90%和100%低风险(n=80),55%和78%的中间风险(n=15),25%和25%的高风险(n=4)。在低风险患者中,只有10%的患者出现局部复发;边缘大于1mm的患者均未出现局部复发.17例完成新辅助放化疗的中/高危患者中有16例接受了全肿瘤切除,80%的负利润率。中间/高风险组事件包括1例局部复发和7例转移性复发。如果FNCLCC分级系统用于指导治疗,29%的低风险(仅手术)患者会接受放疗±化疗。
    结论:大多数完全切除POG低级别NRSTS的低风险患者仅通过手术即可成功治疗,和手术边缘大于1毫米可能足以防止局部复发。中危和高危低级别NRSTS患者的预后与高级别组织学患者相似,需要更有效的治疗方法.使用当前的FNCLCC分级系统可能会导致仅通过手术即可治愈的低风险NRSTS的过度治疗。
    BACKGROUND: In retrospective analyses, the Pediatric Oncology Group [POG) and the Federation National des Centres de Lutte Contre le Cancer (FNCLCC) histologic grade predict outcome in pediatric non-rhabdomyosarcoma soft tissue sarcoma (NRSTS), but prospective data on grading, clinical features, and outcomes of low-grade NRSTS are limited.
    METHODS: We analyzed patients less than 30 years of age enrolled on Children\'s Oncology Group (COG) study ARST0332 (NCT00346164) with POG grade 1 or 2 NRSTS. Low-risk patients were treated with surgery alone. Intermediate-/high-risk patients received ifosfamide/doxorubicin and radiotherapy, with definitive resection either before or after 12 weeks of chemoradiotherapy.
    RESULTS: Estimated 5-year event-free and overall survival were 90% and 100% low risk (n = 80), 55% and 78% intermediate risk (n = 15), and 25% and 25% high risk (n = 4). In low-risk patients, only local recurrence was seen in 10%; none with margins greater than 1 mm recurred locally. Sixteen of 17 intermediate-/high-risk patients who completed neoadjuvant chemoradiotherapy underwent gross total tumor resection, 80% with negative margins. Intermediate-/high-risk group events included one local and seven metastatic recurrences. Had the FNCLCC grading system been used to direct treatment, 29% of low-risk (surgery alone) patients would have received radiotherapy ± chemotherapy.
    CONCLUSIONS: Most low-risk patients with completely resected POG low-grade NRSTS are successfully treated with surgery alone, and surgical margins greater than 1 mm may be sufficient to prevent local recurrence. Patients with intermediate- and high-risk low-grade NRSTS have outcomes similar to patients with high-grade histology, and require more effective therapies. Use of the current FNCLCC grading system may result in overtreatment of low-risk NRSTS curable with surgery alone.
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  • 文章类型: Journal Article
    背景:先前的研究表明,基于阿霉素的化疗在诊断和早期淋巴细胞恢复时的中性粒细胞与淋巴细胞(NLR)比率,可能会影响骨肉瘤(OST)患者的预后。这项研究旨在评估接受大剂量甲氨蝶呤和依托泊苷/异环磷酰胺(M-EI)化疗的OST患者的血象参数的预后价值。
    方法:我们回顾性分析了在法国OS2006试验中纳入并接受M-EI化疗的OST患者的大量连续队列中,各种血象参数在诊断和治疗期间的预后价值。
    结果:共分析了164例患者。中位年龄为14.7岁(四分位距[IQR]:11.7-17)。中位随访时间为5.6年(IQR:3.3-7.7年)。三年无事件生存率(EFS)和总生存率(OS)分别为71.5%(95%置信区间[CI]:64%-78%)和86.4%(95%CI:80%-91%),分别。在单变量分析中,诊断时的血细胞计数参数和第14天的早期淋巴细胞恢复未发现对生存结局的预后影响.相比之下,在单变量(p=.0044)和多变量分析(危险比[HR]=1.3,95%CI:1.1-1.5;p=.002)中,首次EI化疗(NLR-W4)第1天的NLR比率增加与OS降低相关,虽然不是EFS。在调整组织学反应和转移状态后,NLR-W4比值增加1与死亡风险增加30%相关.
    结论:我们确定了NLR-W4作为一种潜在的早期生物标志物,用于观察接受M-EI化疗的OST患者的生存。需要进一步的研究来确认NLR的预后价值,并更好地确定与疾病监测有关的免疫机制。
    BACKGROUND: Previous studies have shown that neutrophil-to-lymphocyte (NLR) ratio at diagnosis and early lymphocytes recovery on doxorubicin-based chemotherapy, may impact the outcome in patients with osteosarcoma (OST). This study aimed to evaluate the prognostic value of hemogram parameters in patients with OST treated with high-dose methotrexate and etoposide/ifosfamide (M-EI) chemotherapy.
    METHODS: We retrospectively analyzed the prognostic value of various hemogram parameters at diagnosis and during therapy in a large consecutive cohort of patients with OST included in the French OS2006 trial and treated with M-EI chemotherapy.
    RESULTS: A total of 164 patients were analyzed. The median age was 14.7 years (interquartile range [IQR]: 11.7-17). Median follow-up was 5.6 years (IQR: 3.3-7.7 years). Three-year event-free survival (EFS) and overall survival (OS) were 71.5% (95% confidence interval [CI]: 64%-78%) and 86.4% (95% CI: 80%-91%), respectively. In univariate analysis, blood count parameters at diagnosis and early lymphocyte recovery at Day 14 were not found prognostic of survival outcomes. By contrast, an increase of NLR ratio at Day 1 of the first EI chemotherapy (NLR-W4) was associated with reduced OS in univariate (p = .0044) and multivariate analysis (hazards ratio [HR] = 1.3, 95% CI: 1.1-1.5; p = .002), although not with EFS. After adjustment on histological response and metastatic status, an increase of the ratio NLR-W4 of 1 was associated with an increased risk of death of 30%.
    CONCLUSIONS: We identified NLR-W4 as a potential early biomarker for survival in patients with OST treated with M-EI chemotherapy. Further studies are required to confirm the prognostic value of NLR and better identify immune mechanisms involved in disease surveillance.
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  • 文章类型: Journal Article
    在这项研究中,五种细胞抑制剂(他莫昔芬,甲氨蝶呤,卡培他滨,环磷酰胺,和异环磷酰胺)对黑头min鱼(Pimephalespromelas)幼虫进行了评估。受精后的卵暴露于浓度增加的药物中6天。测量了两种毒性遗传生物标志物和四种甲状腺激素相关基因通路的表达水平。有趣的是,结果显示,5种细胞抑制剂的所有浓度都会影响两种毒性生物标志物基因的转录水平。此外,甲状腺激素相关基因的表达水平与对照组不同,在暴露于环磷酰胺和异环磷酰胺的幼虫中观察到最显著的变化。虽然之前的一项研究发现对鱼类形态没有影响,这项研究表明,五种细胞抑制剂修饰了P.promelas的微妙分子反应,强调在整个动物生命周期中评估多生物学水平终点的重要性,以了解细胞抑制剂和其他污染物的潜在影响的完整肖像。
    In this study, the toxicogenomic effects of five cytostatics (tamoxifen, methotrexate, capecitabine, cyclophosphamide, and ifosfamide) on fathead minnow (Pimephales promelas) larvae were evaluated. Post-fertilization eggs were exposed to increasing concentrations of the drugs for six days. The expression levels of two genetic biomarkers for toxicity and four thyroid hormone-related gene pathways were measured. Interestingly, the results showed that all concentrations of the five cytostatics affect the transcription levels of both toxicity biomarker genes. Additionally, the thyroid hormone-related genes had different expression levels than the control, with the most significant changes observed in those larvae exposed to cyclophosphamide and ifosfamide. While a previous study found no effects on fish morphology, this study suggests that the five cytostatics modify subtle molecular responses of P. promelas, highlighting the importance of assessing multibiological level endpoints throughout the lifecycle of animals to understand the full portrait of potential effects of cytostatics and other contaminants.
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  • 文章类型: Journal Article
    目的:COVID-19大流行导致远程医疗的迅速发展。远程医疗的意义尚未在放射肿瘤学中得到严格研究,程序性专业。这项研究旨在评估在大流行之前和期间出现在大型癌症中心的当面患者(IPPs)和虚拟患者(VPs)的特征,并了解影响在我们机构接受放射治疗的可能性(产量)的变量。
    方法:纳入了2019年至2021年期间接受新会诊的17,915例患者,从2020年3月24日开始,按流行病和大流行期进行分层。远程医疗访问包括视频和电话。还比较了区域剥夺指数(ADI)。
    结果:总人口为56%的男性和93%的白人,平均年龄为63岁。大流行期间,副总裁占访问人数的21%,平均比他们的面对面(IP)同行年轻(63.3岁IPv62.4VP),住在离诊所更远的地方(215英里IPv402VP)。在经过治疗的VPs中,居住在靠近诊所的地方与更高的产量相关(比值比[OR],0.95;P<.001)。这在接受治疗的IPP中也见过(OR,0.96;P<.001);然而,IPPs与诊所的平均距离显著低于VPs(205英里IPv349VP).在VPs中更多地使用了专门的放射治疗(质子和近距离放射治疗)。IPP的ADI高于VP。在副总裁中,治疗组ADI较高(P<.001)。
    结论:患者特征和产量在IPP和VPs之间有显著差异。远程医疗扩大了对远离诊所的患者的影响,包括来自农村或医疗保健匮乏的地区,允许获得专门的放射肿瘤护理。远程医疗有可能增加其他技术和程序专业的覆盖面。
    OBJECTIVE: The COVID-19 pandemic led to rapid expansion of telemedicine. The implications of telemedicine have not been rigorously studied in radiation oncology, a procedural specialty. This study aimed to evaluate the characteristics of in-person patients (IPPs) and virtual patients (VPs) who presented to a large cancer center before and during the pandemic and to understand variables affecting likelihood of receiving radiotherapy (yield) at our institution.
    METHODS: A total of 17,915 patients presenting for new consultation between 2019 and 2021 were included, stratified by prepandemic and pandemic periods starting March 24, 2020. Telemedicine visits included video and telephone calls. Area deprivation indices (ADIs) were also compared.
    RESULTS: The overall population was 56% male and 93% White with mean age of 63 years. During the pandemic, VPs accounted for 21% of visits, were on average younger than their in-person (IP) counterparts (63.3 years IP v 62.4 VP), and lived further away from clinic (215 miles IP v 402 VP). Among treated VPs, living closer to clinic was associated with higher yield (odds ratio [OR], 0.95; P < .001). This was also seen among IPPs who received treatment (OR, 0.96; P < .001); however, the average distance from clinic was significantly lower for IPPs than VPs (205 miles IP v 349 VP). Specialized radiotherapy (proton and brachytherapy) was used more in VPs. IPPs had higher ADI than VPs. Among VPs, those treated had higher ADI (P < .001).
    CONCLUSIONS: Patient characteristics and yield were significantly different between IPPs and VPs. Telemedicine increased reach to patients further away from clinic, including from rural or health care-deprived areas, allowing access to specialized radiation oncology care. Telemedicine has the potential to increase the reach of other technical and procedural specialties.
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  • 文章类型: Case Reports
    高铁血红蛋白血症是一种潜在的危及生命的疾病,血红蛋白携氧能力减弱的罕见情况。我们介绍了一个3岁男孩接受T细胞急性淋巴细胞白血病(T-ALL)治疗的案例,该男孩因服用异环磷酰胺而出现高铁血红蛋白血症(MetHb57.1%)。由于他的病情危急,患者被转移至重症监护病房(ICU).治疗包括亚甲蓝给药,交换输血,儿茶酚胺输注,和类固醇。改善一般状况,可以在没有异环磷酰胺的情况下继续化疗,并完成HR2阻断。在治疗方案中使用异环磷酰胺时应广泛警惕高铁血红蛋白血症作为一种非常罕见的副作用。
    Methemoglobinemia is a potentially life-threatening, rare condition in which the oxygen-carrying capacity of hemoglobin is diminished. We present the case of a 3-year-old boy treated for T-cell acute lymphoblastic leukemia (T-ALL) who developed methemoglobinemia (MetHb 57.1%) as a side effect of ifosfamide administration. Due to his critical condition, the patient was transferred to the intensive care unit (ICU). The therapy included methylene blue administration, an exchange transfusion, catecholamine infusion, and steroids. Improving the general condition allowed for continuing chemotherapy without ifosfamide and completion of the HR2 block. Vigilance for methemoglobinemia as a very rare side effect should be widespread when using ifosfamide in the treatment protocols.
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