视网膜母细胞瘤——印度东部一家三级医疗中心5年护理模式和促成因素的经验教训

Debjit Ghosh, Bidyut Mondal, A. Basu, Janmenjoy Mondal, S. Gangopadhyay
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引用次数: 2

摘要

目的:视网膜母细胞瘤是世界范围内儿童最常见的眼内恶性肿瘤。尽管关于视网膜母细胞瘤在西方人群中的流行病学有足够的数据,但来自印度等发展中国家的报告却很少。在这项回顾性研究中,我们旨在描述视网膜母细胞瘤的流行病学模式、生存特征和预后因素。材料与方法:回顾性分析2013年1月至2017年12月在我院诊断为视网膜母细胞瘤的68例患儿的病历资料。收集性别、宗教、侧发、诊断年龄、表现体征、家族史、治疗滞后时间、肿瘤滞后时间及肿瘤扩散原因、治疗方式、生存时间等资料。结果:中位发病年龄22±19.73个月(范围2 ~ 92个月)。单侧病例发病年龄中位数为23±20.6个月,双侧病例发病年龄中位数为21±16.2个月。中位总生存期为28.1±2.2个月。单侧病例为30.1±2.5个月,双侧病例为19.7±2.9个月。总无进展生存期(PFS)为22.2±2.3个月。单侧病例为24.18±2.7个月,双侧病例为13.9±2.9个月。本文报告家族性视网膜母细胞瘤4例。在13例双侧病例中,发现3例也有松果体母细胞瘤。Cox回归分析发现,发病年龄小于36个月、诊断延迟小于5个月、诊断后开始治疗延迟小于2个月对OS有显著影响。发现前两者对PFS有显著影响,而后者无显著影响(p1)。结论:几乎81%的患者出现在疾病的晚期,其原因是由于许多原因导致的诊断和治疗延迟,主要原因是由看似非暴力但无效的替代医学实践所避免的。尽管遵循了与国际准则相同的制度协议,但分析显示,与发达国家相比,这项研究的存活率要低得多。原因可能是在疾病的晚期才出现病例。
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Retinoblastoma – Lessons Learned about Patterns of Care and Contributory Factors from 5 Years’ Experience in a Tertiary Care Center in Eastern India
Objectives: Retinoblastoma is the most common intraocular malignancy afflicting children worldwide. Even though there are enough data about the epidemiology of retinoblastoma in western population, there are only few reports from developing countries like India. In this retrospective study, we aimed to describe the epidemiological patterns, survival characteristics and prognostic factors of retinoblastoma. Materials and Methods: From medical records, we retrospectively analyzed the data of 68 children diagnosed in our hospital between January 2013 and December 2017 as having retinoblastoma. Data on sex, religion, laterality, age at diagnosis, presenting signs, family history, lag time for treatment, cause of such lag time and spread of tumor, treatment mode, and survival time were collected. Results: The median age of onset was 22 ± 19.73 months (range 2-92 months).The median  patient age of onset of  the unilateral cases was 23 ± 20.6 months, and that of the bilateral cases was 21 ±16.2 months. The median overall survival was 28.1±2.2 months. For unilateral cases, it was 30.1±2.5 months and for bilateral cases it was 19.7±2.9 months. The overall progression free survival (PFS) was 22.2±2.3 months. For unilateral cases, it was 24.18±2.7 months and for bilateral cases it was 13.9±2.9 months. 4 cases of familial retinoblastoma were reported. Among the 13 bilateral cases, 3 were found to have pinealoblastoma too. On Cox regression analysis, age of onset below 36 months, diagnostic delay of less than 5 months and delay of treatment initiation (after diagnosis) less than 2 months were found to have significant effect on OS. The former two were found to have significant effect on PFS but not the latter (p<0.05 and HR>1). Conclusions: Almost 81% of patients presented at an advanced stage of the disease, the reason being accounted by diagnostic and therapeutic delay by virtue of a number of causes, the major one being eluded by apparently nonviolent yet ineffective alternative medicine practices. In spite of following the institutional protocols which are at par to the international guidelines, analysis shows much poorer survival in this study compared to those of developed countries. The cause might be such late presentation of the cases in already advanced stages of the disease.
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