Abstract

Objective: comparison of the effectiveness of the results of neoadjuvant chemoradiotherapy in patients with locally advanced rectal cancer using classical and hypofractionated schedule of radiation therapy.Materials and methods. This study is based on a retrospective analysis of a database of patients with locally advanced rectal cancer (T3C–D, positive circumferential resection margin or T4) who underwent a prolonged course of neoadjuvant chemoradiotherapy followed by surgery. The patients were divided into two groups: the first (main) group, 71 patients who received a course of chemoradiotherapy in hypofractionation schedule as part of neoadjuvant treatment (4 Gy × 40 Gy, 3 fractions per week) in combination with chemotherapy with capecitabine 1650 mg / m2 in two doses on weekdays. The second group (control group) included 79 patients who treated with long-course chemoradiotherapy in the classic fractionation mode (2 Gy × 50–58 Gy, 5 fractions per week) in combination with chemotherapy with capecitabine 1650 mg / m2 in two doses on weekdays. In the preoperative period, along with chemoradiotherapy, 4–8 courses of the systemic chemotherapy in the CapOx mode was used. The primary endpoint of this study was pathological complete response. Secondary endpoints included the seve rity of early radiation and hematological toxicity, the incidence of local recurrence, distant metastases, overall and disease-free survival. Results. The study included 150 patients. The overall frequency of acute radiation toxicity of grade III–IV was 5.6 % in the main group and 8.9 % in the control group (p = 0.658), from them hematological toxicity – 2.82 % and 7.6 %, respectively (p = 0.350), skin and pelvic organ toxicity – 2.82 % and 1.3 %, respectively (p = 0.926). Complete pathological response of III degree in the groups achieved 22.5 % and 19 %, respectively (p = 0.593), grade IV – 18.3 % and 15.2 %, respectively (p = 0.829). In the main and control groups, 4.2 % and 3.8 % of local recurrence were registered, respectively (p = 0.954; hazard ratio (HR) 1.05; 95 % confidence interval (CI) 0.21–5.22). The median time of disease-free survival was 39.4 months. The three-year disease-free survival in the main group was 73.2 % and in the control group 64.6 %, respectively (p = 0.353; HR 0.79; 95 % CI 0.42–1.35). The three-year overall survival in the main and control groups were 84.5 % and 82.3 %, respectively (p = 0.743; HR 0.87; 95 % CI 0.39–1.92). Conclusions. The hypofractionation schedule can be considered as an alternative and not inferior to the standard dose fractionation regimen in a prolonged course of neoadjuvant chemoradiotherapy in patients with locally advanced rectal cancer.

Highlights

  • Цель исследования – сравнение эффективности результатов неоадъювантной химиолучевой терапии больных местно-распространенным раком прямой кишки при использовании классического и гипофракционного режима лучевой терапии

  • This study is based on a retrospective analysis of a database of patients with locally advanced rectal cancer (T3C–D, positive circumferential resection margin or T4) who underwent a prolonged course of neoadjuvant chemoradiotherapy followed by surgery

  • The patients were divided into two groups: the first group, 71 patients who received a course of chemoradiotherapy in hypofractio­ nation schedule as part of neoadjuvant treatment (4 Gy × 40 Gy, 3 fractions per week) in combination with chemotherapy with capecitabine 1650 mg / m2 in two doses on weekdays

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Summary

Тазовая хирургия и онкология Pelvic Surgery and Oncology

Результаты неоадъювантной химиолучевой терапии больных местно-распространенным раком прямой кишки. Цель исследования – сравнение эффективности результатов неоадъювантной химиолучевой терапии больных местно-распространенным раком прямой кишки при использовании классического и гипофракционного режима лучевой терапии. Работа основана на ретроспективном анализе базы данных больных местно-распространенным раком прямой кишки (T3C–D, положительный циркулярный край резекции либо T4), которым был проведен пролонгированный курс неоадъювантной химиолучевой терапии с последующим оперативным вмешательством. Во 2‐ю (контрольную) группу было включено 79 пациентов, которым был проведен курс химиолучевой терапии в режиме классического фракционирования (разовая очаговая доза 2 Гр, суммарная очаговая доза 50–58 Гр, 5 фракций в неделю) в комбинации с химиотерапией капецитабином 1650 мг / м2 в 2 приема в будние дни. Objective: comparison of the effectiveness of the results of neoadjuvant chemoradiotherapy in patients with locally advanced rectal cancer using classical and hypofractionated schedule of radiation therapy

Materials and methods
Группа группа контроля p
Всего Total
Experimental group
Тромбоцитопения Thrombocytopenia
Степень регресса Основная
Findings
Grade IV
Full Text
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