Conde Sofia, Borrego Margarida, Teixeira Tânia, Teixeira Rubina, Sá Anabela, Soares Paula
Radiotherapy Department, Hospitais da Universidade de Coimbra, Portugal.
Oncology Department, Hospitais da Universidade de Coimbra, Portugal.
Rep Pract Oncol Radiother. 2012 Aug 11;17(6):376-83. doi: 10.1016/j.rpor.2012.07.009. eCollection 2012.
To evaluate the differences in treatment response and the impact on survival with both oral agents (UFT and Capecitabine) as neoadjuvant chemotherapy administered concomitantly with radiotherapy.
There are still no studies comparing the use of neoadjuvant oral chemotherapy either with UFT plus Folinic acid or Capecitabine concomitant with radiotherapy in locally advanced rectal cancer (LARC).
A set of 112 patients with LARC were treated preoperatively. GROUP 1 - 61 patients underwent concomitant oral chemotherapy with Capecitabine (825 mg/m(2) twice daily). GROUP 2 - 51 patients submitted to concomitant oral chemotherapy with UFT (300 mg/m(2)/d) + Folinic acid (90 mg/d) and radiotherapy. 57.1% of patients were submitted to adjuvant chemotherapy.
GROUP 1: acute toxicity - 80.3%; pathological complete response (pCR) - 10.5%; tumor downstaging (TD) - 49.1%; nodal downstaging (ND) - 76.5%; loco-regional response (LRR) - 71.9%; toxicity to adjuvant chemotherapy - 75%. GROUP 2: acute toxicity - 80.4%; pCR - 28%; TD - 62%; ND - 75.6%; LRR - 78%; toxicity to adjuvant chemotherapy - 56%. There was no difference in survival nor loco-regional control between the groups.
Patients treated with neoadjuvant oral UFT + Folinic acid had a higher rate of pathologic complete response than patients treated with Capecitabine concomitant with radiotherapy. There were no differences in downstaging, LRR, toxicity, survival or loco-regional control between both groups. There was a trend to a higher rate of toxicity to adjuvant chemotherapy in the Capecitabine group.
评估口服药物(优福定和卡培他滨)作为新辅助化疗与放疗联合应用时治疗反应的差异及其对生存的影响。
目前仍没有关于在局部晚期直肠癌(LARC)中比较优福定加亚叶酸或卡培他滨与放疗联合应用新辅助口服化疗的研究。
一组112例LARC患者接受术前治疗。第1组-61例患者接受卡培他滨口服化疗(825mg/m²,每日两次)。第2组-51例患者接受优福定(300mg/m²/d)+亚叶酸(90mg/d)口服化疗及放疗。57.1%的患者接受辅助化疗。
第1组:急性毒性-80.3%;病理完全缓解(pCR)-10.5%;肿瘤降期(TD)-49.1%;淋巴结降期(ND)-76.5%;局部区域反应(LRR)-71.9%;辅助化疗毒性-75%。第2组:急性毒性-80.4%;pCR-28%;TD-62%;ND-75.6%;LRR-78%;辅助化疗毒性-56%。两组之间在生存及局部区域控制方面无差异。
新辅助口服优福定+亚叶酸治疗的患者比接受卡培他滨与放疗联合治疗的患者病理完全缓解率更高。两组在降期、LRR、毒性、生存或局部区域控制方面无差异。卡培他滨组辅助化疗毒性率有更高的趋势。