ANALYSIS OF THE RESULTS OF THE XELOX REGIMEN IN PREOPERATIVE CHEMORADIOTHERAPY FOR LOCALLY ADVANCED RECTAL CANCER
Keywords:
locally advanced rectal cancer, oxaliplatin, fluoropyrimidines, preoperative chemoradiotherapy, efficacy, toxicityAbstract
Summary. Objective: a comparative evaluation of the study
of the efficacy and clinical safety of neoadjuvant chemotherapy (NACT) for the use of the XELOX regimen or monochemotherapy with fluoropyrimidine preparations in patients with locally advanced rectal cancer (LARC). Object
and methods: a prospective, randomized, single-centered
study was started in the clinic of the National Cancer Institute. Patients with a clinically radiologic diagnosis were
randomized to a ratio of 1:1. Patients with the main (O)
group (n = 35) performed radiotherapy (RT) with a total
focal dose (TFD) of 50.4Gy (1.8 Gy × 28) and polychemotherapy in XELOX regimen. Patients in the comparison
group (C) (n = 34) performed TFD 50.4 Gy (1.8 Gy × 28)
and monochemotherapy based on preparations of fluoropyrimidine groups. The efficacy of NACT was determined by
QMRT data and by the level of treatment pathomorphism.
The manifestations of chemotherapy toxicity were recorded according to STCAE 4.03 criteria. All patients received
surgical interventions of various types. Results: both groups
achieved statistically identical (p > 0.05) high radicalism
of the operation, although the resection frequency R0 was
slightly higher in patients with the group O — 33 (97.1%)
vs 25 (93.5%) in the group P. R2 resection was not. In both
groups, the most common (58.1–79.4%) were gastrointestinal manifestations of chemotherapy toxicity (I–II degrees).
In the group O, the toxicity of the III and IVdegrees (35.3 vs
19.4%) was recorded more often than in the groupP: in particular, anemia was 2 (5.9%) and 1 (2.9%) vs 1(3.2%) and
1 (3.2%), anorexia — 4 (11.7%) and 0 (0%) vs 3 (9.7%)
and 0 (0%), neurotoxicity — 3 (8,8%) and 2 (5.9%) vs
1 (3.2%) and 0 (0%), respectively, but the differences are
not reliable (p=0.151). Conclusion: oxaliplatin-containing
NACRT (XELOX regimen) with LARC is a safe tactic provided patients are selected in specialized oncological centers.
References
Peng J, Lin J, Zeng Z, et al. Addition of oxaliplatin to
capecitabine-based preoperative chemoradiotherapy for locally advanced rectal cancer: long-term outcome of a phase II study. Oncol
Lett 2017; 14 (4): 4543–50. doi:10.3892/ol.2017.6764.
Singh K, Gupta MK, Seam RK, et al.A prospective randomized trial comparing capecitabine-based chemoradiotherapy with
-FU-based chemoradiotherapy in neoadjuvant setting in locally
advanced carcinoma rectum. Indian J Cancer 2017; 54 (1): 347–
doi: 10.4103/ijc.IJC_174_17.
Fernández-Martos C, Nogué M, Cejas P, et al. The role of
capecitabine in locally advanced rectal cancer treatment: an update.
Drugs 2012; 72(8): 1057–73. doi: 10.2165/11633870–000000000–00000.
Cividalli A, Ceciarelli F, Livdi E, et al. Radiosensitization by
oxaliplatin in a mouse adenocarcinoma: influence of treatment
schedule. Int J Radiat Oncol Biol Phys 2002; 52: 1092–8.
Rahbari N, Weitz J, Hohenberger W, et al. Definition and
grading of anastomotic leakage following anterior resection of the
rectum: a proposal by the International Study Group of Rectal
Cancer. Surgery 2010; 147 (3): 339–51.
Ryan R, Gibbons D, Hyland JMP, et al. Pathological response following long-course neoadjuvant chemoradiotherapy
for locally advanced rectal cancer. Histopatholge 2005; 47: 141–6.
Du D, Su Z, Wang D, et al. Optimal interval to surgery after neoadjuvant chemoradiotherapy in rectal cancer: a systematic review and meta-analysis. Clin Colorectal Cancer 2017; (15):
S1533–0028(17)30183–4.
Vendrely V, Terlizzi M, Huguet F, et al. How to manage a rectal
cancer with synchronous liver metastases? A question of strategy. Cancer Radiother 2017; 21 (6–7): 539–43. doi: 10.1016/j.canrad.2017.07.021.
Zheng J, Feng X, Hu W, et al. Systematic review and meta-analysis of preoperative chemoradiotherapy with or without oxaliplatin in locally advanced rectal cancer. Medicine (Baltimore) 2017; 96 (13): e6487.