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العنوان
Survival Benefit from Total Neo-adjuvant Therapy in Locally Advanced Rectal cancer Patients/
المؤلف
Ahmed,Hager Reda Mohammed
هيئة الاعداد
باحث / هاجر رضا محمد أحمد
مشرف / على محمد عزمى
مشرف / نسرين أحمد مسلم
مشرف / محمد ياسين مصطفى
مشرف / محمد عصام صالح
تاريخ النشر
2024
عدد الصفحات
236.p:
اللغة
الإنجليزية
الدرجة
الدكتوراه
التخصص
الطب
تاريخ الإجازة
1/1/2024
مكان الإجازة
جامعة عين شمس - كلية الطب - Clinical Oncology & Nuclear Medicine
الفهرس
Only 14 pages are availabe for public view

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from 235

Abstract

Background: Preoperative chemoradiation in patients with locally advanced rectal cancer has no impact on overall survival (OS) and distant recurrences. The aim of the study was to evaluate local downstaging, toxicity, patient compliance and long-term outcome (2 year OS and DFS) in patients with locally advanced rectal cancer after induction chemotherapy with 12 weeks of 5 fluorouracil based chemotherapy followed by radiotherapy concomitant with capecitabine before total mesorectal excision (TME).
Patients and methods: Between January 2018, and December 2019, we enrolled eligible patients with poor-risk rectal cancer defined by high-resolution MRI (Any cT3 and T4 stage, T2 low lying tumor at or below the levators and node positive tumor) and without metastatic disease
Patients were planned for 12 weeks of neoadjuvant capecitabine and oxaliplatin (oxaliplatin 130 mg/m² on day 1 with capecitabine 1000 mg/m² twice daily for 14 days every 3 weeks) followed by chemoradiotherapy (50.4 Gy in a conventional fractionation) with capecitabine (825 mg/m² twice daily), then total mesorectal excision (TME) was carried out 6 weeks after the completion of CRT.
Results: Of 70 consecutively admitted patients starting induction chemotherapy, 55 patients underwent surgery. R0 resection was seen in 92.7% and pathological downstaging in 72.7%. In the intention-to-treat group, Objective response rates after neoadjuvant chemotherapy and chemoradiotherapy were 51.4% and 48.6%, respectively. Pathological complete response was seen in 15.7 %. Two-year disease-free survival (DFS) and OS were 62.5% and 82.6%, respectively. Grade 3/4 toxicity was seen in 20 %, and only one case died within 2 months of therapy.
Conclusion: Intensification of systemic therapy with neoadjuvant combination chemotherapy before standard treatment is feasible in poor-risk potentially operable rectal cancer, with acceptable safety and promising long-term outcomes. Future development of this multidisciplinary treatment strategy in randomized trials is warranted.