A Case Study on Complete Pathological Response in Advanced Rectal Cancer Patient with Oxaliplatin-based Chemotherapy without Cumulative Neurotoxicity.

IF 1.6 Q4 ONCOLOGY
Rehab A M Jawad, Bahir Abdul-Razzaq Mshimesh, Qasim S Al-Mayah, Fawaz Al-Alloosh
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引用次数: 0

Abstract

Background: The pathological response in rectal cancer treatment provides insight into the molecular mechanisms, including genetic alterations and signaling pathways that influence tumor behavior and resistance to treatment.

Case presentation: This report describes a 34-year-old Iraqi male diagnosed with stage III rectal cancer who achieved a complete pathological response following treatment with oxaliplatin-based chemotherapy. Notably, this outcome was achieved without the administration of chemoradiotherapy or the occurrence of neurotoxicity despite the efficacious cumulative‑dose administration (1700 mg/m2) of oxaliplatin. Genomic analysis revealed the presence of a heterozygous (Ile/Val) genotype in the GSTP1 gene, which may have contributed to the observed treatment response.

Conclusions: Genetic biomarkers play a crucial role in refining treatment strategies by enabling a more precise selection of patients who may safely forgo radiotherapy, thereby minimizing its associated toxicities. Additionally, molecular profiling can help predict susceptibility to oxaliplatin-induced neurotoxicity, facilitating dose adjustments or alternative therapeutic approaches to enhance treatment tolerance and long-term quality of life. Our findings highlight the importance of molecular profiling in optimizing treatment strategies while minimizing toxicity, especially in situations where radiological assessments suggest residual disease or produce unclear results.

晚期直肠癌奥沙利铂化疗无累积神经毒性的完全病理反应病例研究。
背景:直肠癌治疗中的病理反应提供了对分子机制的深入了解,包括影响肿瘤行为和治疗耐药性的遗传改变和信号通路。病例介绍:本报告描述了一名34岁的伊拉克男性,被诊断为III期直肠癌,在接受奥沙利铂为基础的化疗后取得了完全的病理反应。值得注意的是,尽管奥沙利铂的有效累积剂量(1700 mg/m2),但该结果是在没有进行放化疗或发生神经毒性的情况下实现的。基因组分析显示GSTP1基因存在杂合(Ile/Val)基因型,这可能有助于观察到的治疗反应。结论:遗传生物标志物在完善治疗策略中发挥着至关重要的作用,可以更精确地选择可能安全放弃放疗的患者,从而最大限度地减少其相关毒性。此外,分子谱分析可以帮助预测对奥沙利铂诱导的神经毒性的易感性,促进剂量调整或替代治疗方法,以提高治疗耐受性和长期生活质量。我们的研究结果强调了分子谱分析在优化治疗策略的同时最小化毒性的重要性,特别是在放射评估提示残留疾病或产生不明确结果的情况下。
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来源期刊
CiteScore
3.80
自引率
0.00%
发文量
121
期刊介绍: The Journal of Gastrointestinal Cancer is a multidisciplinary medium for the publication of novel research pertaining to cancers arising from the gastrointestinal tract.The journal is dedicated to the most rapid publication possible.The journal publishes papers in all relevant fields, emphasizing those studies that are helpful in understanding and treating cancers affecting the esophagus, stomach, liver, gallbladder and biliary tree, pancreas, small bowel, large bowel, rectum, and anus. In addition, the Journal of Gastrointestinal Cancer publishes basic and translational scientific information from studies providing insight into the etiology and progression of cancers affecting these organs. New insights are provided from diverse areas of research such as studies exploring pre-neoplastic states, risk factors, epidemiology, genetics, preclinical therapeutics, surgery, radiation therapy, novel medical therapeutics, clinical trials, and outcome studies.In addition to reports of original clinical and experimental studies, the journal also publishes: case reports, state-of-the-art reviews on topics of immediate interest or importance; invited articles analyzing particular areas of pancreatic research and knowledge; perspectives in which critical evaluation and conflicting opinions about current topics may be expressed; meeting highlights that summarize important points presented at recent meetings; abstracts of symposia and conferences; book reviews; hypotheses; Letters to the Editors; and other items of special interest, including:Complex Cases in GI Oncology:  This is a new initiative to provide a forum to review and discuss the history and management of complex and involved gastrointestinal oncology cases. The format will be similar to a teaching case conference where a case vignette is presented and is followed by a series of questions and discussion points. A brief reference list supporting the points made in discussion would be expected.
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