A Prospective, Multicenter, Observational Registry (ReCoRD) on Demography, Molecular Profile, Clinical Features, and Treatment Outcomes in Individuals undergoing Treatment for Metastatic Colorectal Cancer

Sunil Kumar Yadav Y, Rohit Desai, Pranav Sopory, Femina Dawer, Rajan Mittal, Kumar Gaurav, Rahul Rathod, Akhila Paspulate
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Abstract

Objective: Out of all newly diagnosed colorectal cancer cases globally, 20% of the patients present with metastasis, and 25% develop metastasis later. The 5-year survival rate after diagnosis for mCRC patients is <20%. Although many studies using population-based cancer registries from India are available on various cancers, data on mCRC in India is scarce. Therefore, the purpose of the ReCoRD registry is to obtain real world data on demographics, treatment pattern and outcomes in Indian patients with mCRC. Methods: This is a prospective, multicenter, observational study on 1000 participants with mCRC, who are enrolled in the registry in up to 15 centers for 2 years. The recruitment will be stopped 2 years following the first patient enrollment. A minimum follow-up of 12–18 months is being carried out post-enrollment in the registry. Data on the demography, clinical features, molecular profile, treatment options, and outcomes of treatment for these patients is being collected from the study sites by investigators. The Kaplan-Meier Plot will be utilized to examine the survival data, and the median time computed by the Kaplan-Meier technique will be presented with a confidence interval of 95%.Conclusion: Although mCRC remains incurable in most cases, survival rates have improved with the advent of newer cytotoxic chemotherapeutic drugs and targeted agents. The ReCoRD registry will collect details of the demography, tumor characteristics, molecular aspects, treatment, and treatment outcomes in individuals with mCRC, which can guide the clinicians in decision making and treatment based on Indian patient data.
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关于接受转移性结直肠癌治疗者的人口统计学、分子特征、临床特征和治疗结果的前瞻性多中心观察登记(ReCoRD)
目的:在全球所有新确诊的结直肠癌病例中,20%的患者会出现转移,25%的患者会在后期出现转移。mCRC患者确诊后的5年生存率低于20%。虽然印度有许多关于各种癌症的人群癌症登记研究,但关于印度 mCRC 的数据却很少。因此,ReCoRD 登记的目的是获取有关印度 mCRC 患者的人口统计学、治疗模式和预后的真实数据。方法:这是一项前瞻性、多中心、观察性研究,研究对象为1000名mCRC患者,他们将在最多15个中心登记,为期2年。首例患者入组 2 年后停止招募。注册后将进行至少 12-18 个月的随访。研究人员将从研究地点收集有关这些患者的人口统计学、临床特征、分子特征、治疗方案和治疗结果的数据。研究人员将利用卡普兰-梅耶图(Kaplan-Meier Plot)来检验生存数据,并将列出卡普兰-梅耶技术计算出的中位生存时间以及 95% 的置信区间:结论:虽然大多数 mCRC 仍无法治愈,但随着新型细胞毒性化疗药物和靶向药物的出现,生存率已有所提高。ReCoRD 登记将收集 mCRC 患者的人口统计学、肿瘤特征、分子方面、治疗和治疗结果等详细信息,从而指导临床医生根据印度患者的数据做出决策和进行治疗。
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