Evaluation of Response and Toxicity in Patients with Locally Advanced Rectal Cancer Treated with Neoadjuvant Chemoradiation

Dr. B. K. Shewalkar, Dr. Arpit A. Gite, Dr. Jitendra Patel, Dr. Punita Pant
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Abstract

Aims and Objective: To study response after giving neoadjuvant chemoradiation in patients with locally advanced rectal cancer with Cap capecitabine 825 mg/m2 daily PO Bid with radiation in dose of 45Gy/20#/4 weeks and to study to the clinical profile of different patients with locally advanced rectal cancer and to assess the toxicity of patients treated with neoadjuvant chemoradiation Materials and Methods: A prospective observational study was conducted in 60 patients from October 2018 to April 2020 with locally advanced Rectal carcinoma which were proven histopathologically. Neoadjuvant chemoradiation was planned with Capecitabine 825mg/m2 PO Bid with radiation to a dose of 45 Gy/20#/4 weeks. Radiological response assessed after 6 weeks of completion of treatment and then surgery was planned according to response. Results: Thirty-seven patients received definitive surgery. Pathological complete response was observed in 1 patient, near complete response in 7, partial response in 27 and poor or no response was seen in 2 patients. Among 37 patients who have undergone surgery ,30% of patients received sphincter preserving surgery. Radiation induced acute skin and acute lower gastrointestinal were seen. Capecitabine induced diarrhea, hematological toxicities and few patients of hand foot syndrome were seen. Conclusion: In locally advanced rectal cancer, preoperative radio chemotherapy with Capecitabine improves local control and reduces the risks of acute and late toxicity as compared to postoperative radio chemotherapy . Thus, preoperative radio chemotherapy with Capecitabine is safe and well-tolerated in locally advanced rectal cancer, especially in tumors of the lower and middle rectum. Keywords: Rectal Cancer, Capecitabine, Neoadjuvant Chemoradiation 
局部晚期直肠癌新辅助放化疗的疗效和毒性评价
目的与目的:研究局部晚期直肠癌患者应用卡培他滨825 mg/m2 / PO Bid, 45Gy/20#/4周新辅助放化疗后的疗效,研究不同局部晚期直肠癌患者的临床特点,评价新辅助放化疗患者的毒性。对2018年10月至2020年4月60例经组织病理学证实的局部晚期直肠癌患者进行前瞻性观察研究。计划使用卡培他滨825mg/m2 PO Bid进行新辅助放化疗,放疗剂量为45 Gy/20#/4周。治疗结束6周后评估放射学反应,然后根据反应计划手术。结果:37例患者接受了最终手术。病理完全缓解1例,接近完全缓解7例,部分缓解27例,不良或无缓解2例。在37例接受手术的患者中,30%的患者接受了保留括约肌手术。可见放射引起的急性皮肤和急性下胃肠道。卡培他滨引起腹泻、血液学毒性和少数手足综合征。结论:与术后放化疗相比,局部晚期直肠癌术前加卡培他滨放化疗可改善局部控制,降低急性和晚期毒性风险。因此,术前加卡培他滨放化疗对局部进展期直肠癌,尤其是直肠中下部肿瘤是安全且耐受性良好的。关键词:直肠癌,卡培他滨,新辅助放化疗
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