Jakobsen Anders, Mortensen John Pløen, Bisgaard Claus, Lindebjerg Jan, Rafaelsen Søren Rafael, Bendtsen Vagn Ove
Department of Oncology, Danish Colorectal Cancer Group South, Vejle Hospital, University of Southern Denmark, Vejle, Denmark.
Int J Colorectal Dis. 2008 Mar;23(3):251-5. doi: 10.1007/s00384-007-0407-7. Epub 2007 Dec 7.
The aim of this study was to investigate the possible effect of a COX-2 inhibitor in addition to chemoradiation of locally advanced rectal cancer.
The study included 35 patients with rectal adenocarcinoma. All patients had a tumor localised <or=10 cm from the anal verge and a circumferential margin <or=5 mm on a magnetic resonance scan. The patients were scheduled to receive external radiation with a tumor dose of 60 Gy supplemented with an endorectal boost of 5 Gy. Concurrent with radiation, the patients received uracil-tegafur 300 mg/m(2) daily. Celexocib was scheduled throughout the radiation period in a dose of 400 mg x 2 daily.
A macular papular rash was seen in 17 (49%) of the patients leading to stop of medication with celecoxib. Thirty-three patients were operated, and all patients responded to treatment. Complete pathological remission was found in 21% of the patients and further 24% had only microscopic residual tumor cells. The results did not suggest any difference according to the accomplishment of the COX-2 medication.
The addition of a COX-2 inhibitor to chemotherapy-enhanced radiation treatment of rectal cancer was not feasible due to a high incidence of rash in the present study.
本研究旨在探讨环氧化酶-2(COX-2)抑制剂联合放化疗对局部晚期直肠癌的可能疗效。
本研究纳入35例直肠腺癌患者。所有患者肿瘤距肛缘≤10 cm,磁共振扫描显示环周切缘≤5 mm。患者计划接受外照射,肿瘤剂量为60 Gy,直肠内追加剂量5 Gy。放疗期间,患者每天接受尿嘧啶替加氟300 mg/m²。塞来昔布在整个放疗期间按每日400 mg×2的剂量给药。
17例(49%)患者出现斑丘疹,导致塞来昔布停药。33例患者接受了手术,所有患者对治疗均有反应。21%的患者达到完全病理缓解,另有24%的患者仅存在微小残留肿瘤细胞。结果未显示COX-2用药情况存在差异。
在本研究中,由于皮疹发生率高,COX-2抑制剂联合化疗强化放疗治疗直肠癌不可行。