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Effectiveness of posters in enhancement of knowledge about cancer among outpatients and caregivers: A quasi-experimental study 海报提高门诊病人和护理人员癌症知识的有效性:一项准实验研究
Pub Date : 2022-01-01 DOI: 10.4103/oji.oji_5_22
Sadhana A. Kulkarni, Bhavna Joshi, P. Nayak, Vasanti P. Kelkar
Introduction: Noncommunicable diseases are posing serious public health threats in developed as well as developing countries. Cancer has become one of the leading health problems. The lack of knowledge about cancer in the general public is a major hurdle in its prevention, early detection, and treatment. Out of various media, display of posters is a simple and cost-effective way of mass education. Hence, the effectiveness of posters in imparting knowledge regarding cancer needs to be evaluated. Materials and Methods: After ethical clearance, a quasi-experimental study was undertaken among 314 outpatients and caregivers in waiting area of outpatient department of a tertiary health-care institute. Individuals aged 18 years and above, who could read, write, and understand Marathi language, participated in the study. Written informed consent was obtained. Each of the participants was asked to fill a pretested, structured questionnaire before their entry into display area of posters. Self-paced observation of posters was allowed, after which posttest questionnaire was administered. Totally 255 completely filled forms were considered for analysis. Data were analyzed using SPSS v25.0, and Chi-square values were calculated. Results: Of the 255 participants, 175 (68.6%) were males and 80 (31.3%) were females. The number of correct responses marked increased in posttest as compared to pretest for all 13 items. The difference was found to be statistically highly significant (P ≤ 0.0001) for 9 and significant (P = 0.012, 0.005) for 2 of the total 13 items in the questionnaire. Conclusions: This study provides evidence that posters can be used as an effective tool for health communication regarding cancer among outpatients and caregivers in outpatient department.
导言:非传染性疾病在发达国家和发展中国家都构成严重的公共卫生威胁。癌症已经成为主要的健康问题之一。公众对癌症缺乏了解是癌症预防、早期发现和治疗的主要障碍。在各种媒介中,展示海报是一种简单而经济的大众教育方式。因此,海报在传授癌症知识方面的有效性需要评估。材料与方法:对某三级卫生保健机构门诊部候诊区314名门诊患者和护理人员进行准实验研究。年龄在18岁及以上,能读、写、理解马拉地语的人参加了这项研究。获得书面知情同意。每位参与者都被要求在进入海报展示区之前填写一份预先测试过的结构化问卷。允许自定进度观察海报,之后进行后测问卷调查。总共考虑了255个完整填写的表格进行分析。数据采用SPSS v25.0进行分析,计算卡方值。结果:255名参与者中,男性175人(68.6%),女性80人(31.3%)。与前测相比,所有13个项目的后测正确回答数都有所增加。其中有9项差异具有显著统计学意义(P≤0.0001),有2项差异具有显著统计学意义(P = 0.012, 0.005)。结论:本研究提供证据,证明海报可以作为门诊病人和护理人员之间癌症健康沟通的有效工具。
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引用次数: 0
A Retrospective analysis of biosimilar and reference trastuzumab in human epidermal growth factor receptor-2 positive early and/or locally advanced breast cancer patients treated with neoadjuvant-adjuvant setting: Safety and event-free survival outcomes 生物仿制药和参考曲妥珠单抗在人表皮生长因子受体-2阳性早期和/或局部晚期乳腺癌患者中应用新佐剂辅助治疗的回顾性分析:安全性和无事件生存结果
Pub Date : 2021-09-01 DOI: 10.4103/oji.oji_25_21
Rahul Kulkarni, S. Kulkarni, A. Pathan, S. Nag
Background: There is limited real-world evidence on the treatment outcomes with Trastuzumab, specifically with biosimilars. This analysis aims to evaluate the safety and effectiveness of Trastuzumab in early and/or locally advanced breast cancer patients treated with neoadjuvant-adjuvant treatment in the real world setting and to compare biosimilar with reference trastuzumab. Materials and Methods: We retrospectively analyzed the data of patients with human epidermal growth factor receptor-2 (HER-2)-positive breast cancers, who were treated with trastuzumab-based standard therapies. The survival curves were generated using the Kaplan–Meier method. Event-free survival (EFS) was calculated. All patients were assessed for toxicity as per CTCAE version 4.0. The subgroup analysis was carried out to compare the effectiveness of biosimilar with reference trastuzumab. Results: A total of 88 patients were evaluated from 2008 to 2018. EFS at 1, 2, and 5-year was 89.5%, 78%, and 44.2%, respectively. The median EFS was 43 months. In subgroup analysis, the 1, 2-, and 3-year EFS rates were 86.7%, 86.7%, and 57.8%, respectively, for reference Trastuzumab (n = 29) as compared to 91%, 74.4%, and 56.9%, respectively, for Biosimilar Trastuzumab (n = 59). Similarly, median EFS was 43 months and not reached, respectively. There was no significant difference in EFS between the two groups (P = 0.991). A significant asymptomatic decrease in the left ventricular ejection fraction (LVEF) of ≥10% to below the lower limit of normal was noted in only two patients (2.3%). There was no significant difference observed in reduction of LVEF to below the lower limit of normal between the two groups (P = 0.514). The common grade 3/4 adverse events (AEs) observed such as vomiting, diarrhea, pancytopenia, and anemia were mostly due to chemotherapy. These AEs were comparable in both groups. Conclusions: The EFS in our study is consistent with the historical data. Safety and effectiveness of biosimilars were comparable to the reference transtuzumab.
背景:关于曲妥珠单抗治疗结果的真实证据有限,特别是生物仿制药。该分析旨在评估曲妥珠单抗在早期和/或局部晚期乳腺癌患者中接受新辅助辅助治疗的安全性和有效性,并将生物仿制药与参考曲妥珠单抗进行比较。材料和方法:我们回顾性分析了接受基于曲妥珠单抗的标准治疗的人表皮生长因子受体-2 (HER-2)阳性乳腺癌患者的数据。生存曲线采用Kaplan-Meier法生成。计算无事件生存期(EFS)。所有患者均按照CTCAE 4.0版进行毒性评估。进行亚组分析以比较生物仿制药与参考曲妥珠单抗的有效性。结果:2008 - 2018年共评估88例患者。1、2和5年的EFS分别为89.5%、78%和44.2%。中位EFS为43个月。在亚组分析中,参考曲妥珠单抗(n = 29)的1年、2年和3年EFS发生率分别为86.7%、86.7%和57.8%,而生物类似药曲妥珠单抗(n = 59)的EFS发生率分别为91%、74.4%和56.9%。同样,中位EFS分别为43个月和未达到。两组患者EFS评分差异无统计学意义(P = 0.991)。左心室射血分数(LVEF)显著无症状下降≥10%至低于正常值下限的仅有2例(2.3%)。两组患者LVEF降至正常下限以下差异无统计学意义(P = 0.514)。常见的3/4级不良事件(ae)如呕吐、腹泻、全血细胞减少、贫血等主要由化疗引起。两组的ae具有可比性。结论:本研究的EFS与历史数据一致。生物仿制药的安全性和有效性与参考药物曲妥珠单抗相当。
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引用次数: 0
Epidemiological, clinical profile, and treatment outcome of stage iv nonsquamous nonsmall cell lung cancer patients presenting to tertiary care hospital in North India 印度北部三级医院非鳞状非小细胞肺癌患者的流行病学、临床特征和治疗结果
Pub Date : 2021-09-01 DOI: 10.4103/oji.oji_34_21
V. Koyyala, M. Sharma, P. Goyal, Varun Goel, S. Bommera, Mohit Agrawal, K. Domadia, Krushna Choudhary, S. Bothra, A. Jajodia, B. Amrith, S. Joga, S. Pasricha, U. Batra
Background: Better planning of limited resources in oncology is possible with more real-world data of lung cancer, one of the most common causes of cancer related mortality in India and Globe. Aim: This study aimed to evaluate the clinical profile and treatment outcomes in patients with Stage IV adenocarcinoma of lung at our center. Materials and Methods: One hundred and eighty-two patients with Stage IV adenocarcinoma of lung were prospectively screened and analyzed, of which 107 patients who met the inclusion criteria were included in the final analysis. Patients with epidermal growth factor receptor (EGFR) and echinodermal microtubule-associated protein-like 4-anaplastic lymphoma kinase (EML4-ALK) genomic alterations were treated with tyrosine kinase inhibitors and others were treated as per standard chemotherapy regimens. Response rates (RRs), progression-free survival (PFS), and overall survival (OS) were measured. Results: Median age of patients was 55.6 years (range, 26–82) with a male-to-female ratio of 1.23:1. Analyses for EGFR and EML4-ALK alterations were possible for 104 (96.3%) patients and were detected in 31.7% and 8.7% patients, respectively. The overall RR for the entire cohort was 51.4%, while median PFS and median OS were 6.9 and 13.7 months, respectively. Median PFS for the EGFR-mutated and ALK-rearranged group was 9.6 and 10.2 months, respectively, which was higher than non-EGFR non-ALK patients. Median OS for the whole cohort was 13.7 months, while median OS was not reached for EGFR and ALK altered groups. Conclusions: As patients with driver mutations like EGFR and ALK have better prognosis than those who do not, every patient diagnosed with advanced nonsmall cell lung cancer should be offered mutational analysis.
背景:肺癌是印度和全球癌症相关死亡的最常见原因之一,有了更多的真实数据,更好地规划有限的肿瘤学资源是可能的。目的:本研究旨在评估本中心IV期肺腺癌患者的临床概况和治疗结果。材料与方法:对182例IV期肺腺癌患者进行前瞻性筛选分析,其中符合纳入标准的107例患者纳入最终分析。表皮生长因子受体(EGFR)和棘皮微管相关蛋白样4-间变性淋巴瘤激酶(EML4-ALK)基因组改变的患者使用酪氨酸激酶抑制剂治疗,其他患者按标准化疗方案治疗。测量缓解率(rr)、无进展生存期(PFS)和总生存期(OS)。结果:患者中位年龄为55.6岁(范围26-82岁),男女比例为1.23:1。104例(96.3%)患者可以分析EGFR和EML4-ALK的改变,分别在31.7%和8.7%的患者中检测到。整个队列的总RR为51.4%,而中位PFS和中位OS分别为6.9和13.7个月。egfr突变组和alk重排组的中位PFS分别为9.6个月和10.2个月,高于非egfr非alk患者。整个队列的中位生存期为13.7个月,而EGFR和ALK改变组的中位生存期未达到。结论:由于EGFR、ALK等驱动突变的患者预后优于无驱动突变的患者,因此每一位诊断为晚期非小细胞肺癌的患者都应进行突变分析。
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引用次数: 0
Indian subset analysis of a phase iiib open-label study of afatinib in epidermal growth factor receptor tyrosine kinase inhibitor-naïve patients with epidermal growth factor receptor mutation positive non-small cell lung cancer 印度对表皮生长因子受体酪氨酸激酶inhibitor-naïve表皮生长因子受体突变阳性非小细胞肺癌患者的iiib期开放标签研究的亚群分析
Pub Date : 2021-09-01 DOI: 10.4103/oji.oji_40_21
S. Rajappa, B. Srinivasa, S. Bondarde, P. Gokhale, Pankaj Sonone, Arun Dahiya
Aims: The study aimed to evaluate the safety and efficacy of afatinib in locally advanced or metastatic nonsmall cell lung cancer (NSCLC) harboring epidermal growth factor receptor (EGFR) mutations, in Indian subset of a Phase IIIB open-label study. Methods: A multicenter, open-label, Phase IIIB study was conducted to evaluate afatinib in EGFR tyrosine kinase inhibitor-naïve patients with locally advanced/metastatic EGFRm + NSCLC across five countries (34 sites; China, Hong Kong, India, Singapore, and Taiwan). A total 541 patients were recruited, out of which 50 patients were from India. In this article, we have evaluated the safety and tolerability of afatinib in Indian subset of patients (n = 50). Treatment with afatinib was continued until lack of clinical benefit as determined by the investigator. Primary endpoint was safety in terms of patients with serious adverse events (SAEs). Secondary endpoints included number of patients with drug-related AEs, time to symptomatic progression (TTSP), and progression-free survival (PFS). Results: Forty-six out of 50 patients experienced at least one AE. As in the overall study, diarrhea was the most common drug-related AE in Indian patients. In majority (85%) of cases, severity of diarrhea was of grade 1 or 2. No new safety concern was identified in the study. Median TTSP and PFS were 13.43 months (95% confidence interval [CI]: 8.51, 18.33) and 10.08 months (95% CI: 7.32, 14.75), respectively, in Indian subset. Conclusions: Safety and tolerability of afatinib were consistent with overall study and previously reported data. Most of the AEs were manageable without any need of treatment discontinuation.
目的:该研究旨在评估阿法替尼在印度IIIB期开放标签研究中治疗表皮生长因子受体(EGFR)突变的局部晚期或转移性非小细胞肺癌(NSCLC)的安全性和有效性。方法:进行了一项多中心、开放标签、iii期ib研究,以评估阿法替尼对EGFR酪氨酸激酶inhibitor-naïve在5个国家(34个地点;中国、香港、印度、新加坡和台湾)。总共招募了541名患者,其中50名患者来自印度。在这篇文章中,我们评估了阿法替尼在印度亚组患者(n = 50)中的安全性和耐受性。继续使用阿法替尼治疗,直到研究者确定缺乏临床获益。主要终点是严重不良事件(SAEs)患者的安全性。次要终点包括药物相关ae患者数量、症状进展时间(TTSP)和无进展生存期(PFS)。结果:50例患者中有46例至少发生一次AE。在整个研究中,腹泻是印度患者中最常见的药物相关AE。在大多数(85%)病例中,腹泻的严重程度为1级或2级。研究中没有发现新的安全隐患。印度患者的中位TTSP和PFS分别为13.43个月(95%可信区间[CI]: 8.51, 18.33)和10.08个月(95% CI: 7.32, 14.75)。结论:阿法替尼的安全性和耐受性与整体研究和先前报道的数据一致。大多数不良反应是可控的,不需要停止治疗。
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引用次数: 1
Ifosfamide induced encephalopathy: A rare case presentation and management with review of the literature 异环磷酰胺引起的脑病:一例罕见病例的表现和处理,并复习文献
Pub Date : 2021-09-01 DOI: 10.4103/oji.oji_32_21
Namratha Bijivemula, N. Vaddeboina, P. Dattatreya, A. Suresh, C. Vamsy
Ifosfamide-induced encephalopathy (IIE) is a rare adverse event and is usually transient and reversible. However, it may cause permanent neurological dysfunction and even death if not addressed early. The use of aprepitant and presence of acute kidney injury may precipitate IIE. In this report, a 55-year-old female presented with a 3-month history of abdominal mass and bleeding per vagina and was diagnosed as locally advanced high-grade uterine leiomyosarcoma. She underwent surgery followed by adjuvant radiotherapy and combination chemotherapy with doxorubicin plus ifosfamide regimen. During her third cycle chemotherapy, despite dose adjustment of ifosfamide according to patient's creatinine clearance, the patient became aphasic, disoriented, and landed in a stuporous state. After complete evaluation and ruling out other causes, she was diagnosed with IIE for which she was treated with methylene blue and thiamine. This patient showed dramatic response within 8 h of methylene blue administration and complete recovery within 24 h. Our report focuses on the risk factors for the development of IIE and the persistent risk despite ifosfamide dose adjustment according to creatinine clearance.
异环磷酰胺诱导的脑病(IIE)是一种罕见的不良事件,通常是短暂的和可逆的。然而,如果不及早处理,它可能导致永久性神经功能障碍甚至死亡。阿瑞吡坦的使用和急性肾损伤可能导致IIE的发生。在本报告中,一名55岁女性表现为3个月的腹部肿块和阴道出血史,被诊断为局部晚期高级别子宫平滑肌肉瘤。术后行辅助放疗和阿霉素+异环磷酰胺联合化疗。在第三周期化疗中,尽管根据患者肌酐清除率调整异环磷酰胺剂量,但患者出现失语、定向障碍、昏迷状态。经过全面评估并排除其他原因后,她被诊断为IIE,并接受亚甲基蓝和硫胺素治疗。该患者在亚甲基蓝给药后8小时内出现显著反应,24小时内完全恢复。我们的报告重点关注IIE发生的危险因素,以及根据肌酐清除率调整异环磷酰胺剂量后的持续风险。
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引用次数: 0
Primary tracheal cancer: A regional cancer center experience 原发性气管癌:区域性癌症中心经验
Pub Date : 2021-09-01 DOI: 10.4103/oji.oji_35_21
P. Babbar, A. Rudresha, D. Lokanatha, R. Arjunan, L. Jacob, M. Babu, K. Lokesh, L. Rajeev, S. Saldanha, G. Abhilash, Amit Pandey
Background: Primary tracheal cancers (PTC) are uncommon, and the treatment methods vary considerably. Aim: The aim of the present study was to explore the clinical features, management, and prognosis of PTC in an Indian context. Methods: Nineteen patients of PTC were retrieved from the medical records over a period from January 2013 to December 2019. The clinical profile, histological features, and treatment details were recorded and outcomes are analyzed in terms of progression-free survival (PFS) and overall survival (OS). Results: Histological distribution for the cases were squamous cell carcinoma (SCC) (n = 12), adenoid cystic carcinoma (ACC) (n = 6) and small cell carcinoma (n = 1). All the patients were symptomatic. SCC was located more (7 out of 12 cases; 58.33%) in the lower third of the trachea than ACC (2 out of 6 cases; 33.33%). At initial diagnosis, five patients had metastatic disease and all the cases were of SCC histology (4 cases treated with palliative chemotherapy and 1 case received best supportive care). Among nonmetastatic cases (n = 14), 4 patients (SCC: 2; ACC: 2) were considered for primary surgery and the rest were considered unresectable and treated with other modalities except one case of ACC who did not come for treatment after diagnosis. The median PFS for ACC patients was higher than SCC (32 months vs. 10 months; P = 0.013). The median OS for ACC was higher than SCC cases (34.5 months vs. 11.2 months; P = 0.009). Conclusions: SCC followed by ACC are the most common histology types for PTC. ACC has a better prognosis compared to SCC.
背景:原发性气管癌(PTC)并不常见,治疗方法也各不相同。目的:本研究的目的是探讨PTC的临床特点,管理和预后在印度的背景下。方法:从2013年1月至2019年12月的医疗记录中检索19例PTC患者。记录临床资料、组织学特征和治疗细节,并根据无进展生存期(PFS)和总生存期(OS)分析结果。结果:本组病例的组织学分布为鳞状细胞癌(SCC) (n = 12)、腺样囊性癌(ACC) (n = 6)和小细胞癌(n = 1),均有症状。SCC的位置较多(7 / 12;58.33%)在气管下三分之一处较ACC(6例中2例;33.33%)。初诊时,5例患者有转移性疾病,所有病例均为鳞状细胞癌组织学(4例接受姑息性化疗,1例接受最佳支持治疗)。在非转移性病例(n = 14)中,4例患者(SCC: 2;ACC: 2例)考虑进行初始手术,其余患者认为不可切除,除1例ACC诊断后未来治疗外,其余患者采用其他方式治疗。ACC患者的中位PFS高于SCC(32个月vs 10个月;P = 0.013)。ACC的中位生存期高于SCC(34.5个月vs 11.2个月;P = 0.009)。结论:SCC其次是ACC是PTC最常见的组织学类型。ACC与SCC相比预后更好。
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引用次数: 0
Primary ureteral mucinous adenocarcinoma with xanthogranulomatous pyelonephritis masquerading as a giant renal mass 原发性输尿管粘液腺癌伴黄色肉芽肿性肾盂肾炎,伪装成巨大的肾脏肿块
Pub Date : 2021-09-01 DOI: 10.4103/oji.oji_53_20
A. Kanbur, Atul Mokashi, S. Dutta, A. Hase
Primary ureteral carcinoma is rare among all urogenital malignancies, with transitional cell carcinoma being the most common histology followed by squamous cell carcinoma. Adenocarcinoma is extremely rare. Herein, we report a case of primary mucin secreting adenocarcinoma of the right lower ureter in a 67-year-old male. Contrast-enhanced computed tomography (CECT) scan showed a large cystic mass occupying the whole abdomen along with a mass in the lower third of the right ureter mimicking as a giant renal mass. Ureteroscopy followed by laparotomy including right nephroureterectomy with bladder cuff excision was performed. On histopathological examination, the CECT scan-based suspected giant renal mass revealed to be xanthogranulomatous pyelonephritis of the kidney along with primary mucin secreting adenocarcinoma of the ureter.
原发性输尿管癌在所有泌尿生殖系统恶性肿瘤中是罕见的,移行细胞癌是最常见的组织学,其次是鳞状细胞癌。腺癌极为罕见。在此,我们报告一例67岁男性右输尿管下段原发性粘液分泌腺癌。增强计算机断层扫描(CECT)显示一个巨大的囊性肿块占据整个腹部,并在右输尿管下三分之一处有一个肿块,酷似巨大的肾肿块。输尿管镜检查后进行剖腹手术,包括右肾输尿管切除术和膀胱袖切除术。组织病理学检查,基于CECT扫描的疑似巨大肾脏肿块显示为肾脏黄色肉芽肿性肾盂肾炎并输尿管原发性粘液分泌腺癌。
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引用次数: 0
Prevalence of breakthrough chemotherapy-induced nausea vomiting in patients on highly emetogenic chemotherapy: A Single-center observational study 突破性化疗引起的恶心呕吐在高致吐性化疗患者中的发生率:一项单中心观察性研究
Pub Date : 2021-09-01 DOI: 10.4103/oji.oji_22_21
P. Lokkur, N. Mahanta, N. Kalita, Hitesh Deka, Niharika Kutum, A. Ray
Introduction: Chemotherapy-induced nausea and vomiting (CINV) is a distressing side-effect of cancer chemotherapy which may lead to noncompliance with treatment or delay in treatment. Breakthrough nausea and vomiting is the current unmet need in the management in of CINV. Objectives: The present study was planned to determine the prevalence of breakthrough CINV in patients on highly emetogenic chemotherapy (HEC) and to evaluate the need for rescue medications in them. Materials and Methods: The present observational study was conducted on chemotherapy-naive patients, who were scheduled to receive HEC. The patients who received at least 2 cycles of HEC over a 1-year study period enrolled as a study sample. All patients were subjected to a questionnaire which consists of the demographic details, details of disease and prescribed chemotherapy, and probable risk factors for CINV. The severity of nausea vomiting was calculated using the Multinational Association of Supportive Care in Cancer antiemetic tool. The incidence of breakthrough nausea vomiting was assessed and accordingly the rescue medication was used. Results: A total of 100 patients received at least 2 cycles of HEC which consisted of breast carcinomas (n = 74), ovarian carcinoma (n = 13), lung carcinoma (n = 2), periampullary carcinoma (n = 3), sarcoma (n = 4), lymphoma (n = 3), and seminoma (n = 1). Anthracycline-cyclophosphamide combination for breast cancer was the most prescribed chemotherapy regimen. Forty-six patients developed breakthrough nausea/vomiting. Domperidone followed by olanzapine was the preferred rescue medications used. History of CINV in previous cycle and young age (<50 years) were the risk factors associated with breakthrough nausea vomiting in our study. Conclusion: Breakthrough nausea vomiting is a major challenge in patients receiving HEC regimen.
化疗引起的恶心和呕吐(CINV)是癌症化疗的一个令人痛苦的副作用,可能导致治疗不依从性或延迟治疗。突破恶心呕吐是目前CINV治疗中尚未满足的需求。目的:本研究旨在确定高致吐性化疗(HEC)患者中突破性CINV的患病率,并评估这些患者对抢救药物的需求。材料与方法:本观察性研究在计划接受HEC化疗的首次化疗患者中进行。在1年的研究期内接受至少2个周期HEC治疗的患者被纳入研究样本。所有患者都接受了一份调查问卷,其中包括人口统计细节、疾病细节和处方化疗以及CINV的可能危险因素。恶心呕吐的严重程度使用多国癌症支持护理协会止吐工具计算。评估突破性恶心呕吐的发生率,并给予相应的抢救用药。结果:100例患者接受了至少2个周期的HEC治疗,包括乳腺癌(74例)、卵巢癌(13例)、肺癌(2例)、壶腹周围癌(3例)、肉瘤(4例)、淋巴瘤(3例)和精原细胞瘤(1例)。蒽环类药物-环磷酰胺联合治疗乳腺癌是最常用的化疗方案。46例患者出现突破性恶心/呕吐。多潘立酮和奥氮平是首选的抢救药物。在我们的研究中,前一个周期的CINV病史和年轻(<50岁)是突破性恶心呕吐的危险因素。结论:突破性恶心呕吐是HEC方案患者的主要挑战。
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引用次数: 1
Histomorphological spectrum of incidentally detected fallopian tube lesions in patients operated for various clinical conditions and detection of precursor lesion by applying sectioning and extensively examining the fimbriated end sampling protocol 不同临床条件下手术患者偶然发现的输卵管病变的组织形态学谱,并通过切片和广泛检查纤维端取样方案检测前体病变
Pub Date : 2021-09-01 DOI: 10.4103/oji.oji_7_21
Neha Singh, I. Dhal, Aneesha Mohanpuria, S. Saxena
Background: Fallopian tube specimens are studied either in conjunction with ovaries, uterus, and cervix or alone. However, there is less knowledge about the spectrum of histopathological changes in these specimens due to paucity of data. Aim: This study aims to describe the spectrum of histopathological changes with frequency observed in the resected fallopian tube specimens, especially to detect the malignant precursor lesions and malignancy rate. Materials and Methods: Four hundred and ninety-four patients of resected fallopian tubes either separately or along with other female genital tract organs were retrospectively reviewed for histopathological findings. Hematoxylin- and eosin-stained histopathology slides were retrieved and re-examined. The distal fimbriated end was longitudinally sectioned for examination of fimbrial epithelium. The “sectioning and extensively examining the fimbriated end” (SEE-FIM) sampling protocol was used. Results: Out of 494 resected specimens, 247 patients (50%) had some kind of fallopian tube pathology. Fibrosis was the most common lesion observed in 59 cases followed by hematosalpinx (33 cases). Primary neoplasm was seen in 3 (0.6%) of specimens and all were of serous adenocarcinoma histology. Whereas, secondary malignancies were seen in 2 cases (0.4%), with primary being ovary. Four cases of serous tubal intraepithelial carcinoma (STIC) (0.8%) were detected using SEE-FIM protocol. Conclusion: A thorough histopathological examination including SEE-FIM protocols should be followed for detection of various fallopian tube lesions, which will eventually help in appropriate patient workup and treatment. Early detection of precursor lesions such as STIC and prompt treatment intervention may help in the prevention of ovarian malignancies.
背景:输卵管标本可以与卵巢、子宫和子宫颈一起研究,也可以单独研究。然而,由于缺乏数据,对这些标本的组织病理学变化谱的了解较少。目的:本研究旨在描述切除输卵管标本中组织病理学变化的频谱,特别是恶性前体病变和恶性率的检测。材料与方法:回顾性分析494例输卵管单独切除或与其他女性生殖道器官一起切除的患者的组织病理学结果。取苏木精和伊红染色的组织病理学切片并重新检查。对远端毛缘纵向切片,检查毛缘上皮。采用“纤维端切片和广泛检查”(SEE-FIM)取样方案。结果:在494例切除标本中,247例(50%)患者出现不同程度的输卵管病变。纤维化是59例中最常见的病变,其次是输卵管积血(33例)。原发肿瘤3例(0.6%),组织学均为浆液性腺癌。继发性恶性肿瘤2例(0.4%),原发肿瘤为卵巢。采用SEE-FIM方法检测浆液性输卵管上皮内癌(STIC) 4例(0.8%)。结论:对输卵管病变进行全面的组织病理学检查,包括SEE-FIM检查,有助于发现各种输卵管病变,最终帮助患者进行适当的检查和治疗。早期发现前驱病变,如STIC和及时的治疗干预可能有助于预防卵巢恶性肿瘤。
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引用次数: 1
A rare presentation of myelomatous pleural effusion in immunoglobulin g subtype of multiple myeloma 免疫球蛋白g亚型多发性骨髓瘤少见的骨髓瘤性胸腔积液
Pub Date : 2021-05-01 DOI: 10.4103/oji.oji_32_20
Yawar Yaseen, P. Shah, B. Mir, Saika Amreen
Myeloma is a disease of neoplastic plasma cells that synthesize an abnormal amount of immunoglobulins (Igs) or Ig fragments. Multiple myeloma is associated with many complications such as impaired hematopoiesis resulting in anemia and other cytopenias, osteolytic bone lesions, hypercalcemia, and renal dysfunction. However, myelomatous pleural effusion is a rare complication of multiple myeloma, particularly at initial presentation. Herein, we report such a rare complication of myelomatous pleural effusion as initial presentation in a 65-year-old female with IgG type of myeloma.
骨髓瘤是一种肿瘤浆细胞合成异常数量的免疫球蛋白(igg)或igg片段的疾病。多发性骨髓瘤与许多并发症相关,如造血功能受损导致贫血和其他细胞减少、溶骨性骨病变、高钙血症和肾功能障碍。然而,骨髓瘤性胸腔积液是多发性骨髓瘤的罕见并发症,特别是在最初的表现。在此,我们报告一例罕见的骨髓瘤性胸腔积液的并发症,作为65岁女性IgG型骨髓瘤的初始表现。
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Oncology Journal of India
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