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Preoperative hyperthermia combined with radiochemotherapy in locally advanced rectal cancer: a phase II clinical trial.

机译:术前热疗联合放化疗治疗局部晚期直肠癌:II期临床试验。

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摘要

OBJECTIVE: A prospective phase II study was performed to determine the feasibility and efficacy in terms of response rate, resectability, and morbidity in patients with locally advanced rectal cancer who received preoperative regional hyperthermia combined with radiochemotherapy (HRCT). SUMMARY BACKGROUND DATA: Recent studies suggest that preoperative radiochemotherapy in locally advanced rectal cancer can induce downstaging, but after resection the incidence of local recurrences remains high. Hyperthermia (HT) may add tumoricidal effects and improve the efficacy of radiochemotherapy in a trimodal approach. PATIENTS AND METHODS: Thirty-seven patients with histologically proven rectal cancer and T3 or T4 lesions, as determined by endorectal ultrasound and computed tomography, entered the trial. 5-Fluorouracil (300-350 mg/m2) and leucovorin (50 mg) were administered on days 1 to 5 and 22 to 26. Regional HT using the SIGMA 60 applicator (BSD-2000) was given once a week before radiotherapy (45 Gy with 1.8-Gy fractions for 5 weeks). Surgery followed 4 to 6 weeks after completion of HRCT. RESULTS: Preoperative treatment was generally well tolerated, with 16% of patients developing grade III toxicity. No grade IV complications were observed. The overall resectability rate was 32 of 36 patients (89%), and 31 resection specimens had negative margins (R0). One patient refused surgery. In 5 patients (14%), the histopathologic report confirmed no evidence of residual tumor (pCR). A partial remission (PR) was observed in 17 patients (46%). The survival rate after 38 months was 86%. In none of the patients was local recurrence detected after R0(L), but five patients developed distant metastases. CONCLUSION: Preoperative HRCT is feasible and effective and may contribute to locoregional tumor control of advanced rectal cancer, which is to be proven in an ongoing phase III trial.
机译:目的:进行了一项前瞻性II期研究,以确定在术前局部热疗联合放化疗(HRCT)的局部晚期直肠癌患者中,在反应率,可切除性和发病率方面的可行性和有效性。摘要背景资料:近期研究表明,局部晚期直肠癌的术前放化疗可引起肿瘤分期降低,但切除后局部复发的发生率仍然很高。热疗(HT)可能会增加肿瘤作用,并以三峰方式提高放化疗的疗效。患者和方法:37例经直肠内超声和计算机断层扫描确定的经组织学证实为直肠癌且T3或T4病变的患者进入试验。在第1至5天和22至26天使用5-氟尿嘧啶(300-350 mg / m2)和亚叶酸(50 mg)。每周一次使用SIGMA 60涂药器(BSD-2000)进行局部HT放疗(45)以1.8-Gy分数进行Gy治疗5周)。 HRCT完成后的4至6周进行手术。结果:术前治疗一般耐受良好,有16%的患者发展为III级毒性。没有观察到IV级并发症。总体可切除率为36例患者中的32例(89%),并且31个切除标本的切缘阴性(R0)。一名患者拒绝手术。在5例患者中(14%),组织病理学报告证实没有残留肿瘤(pCR)的证据。在17例患者中观察到部分缓解(PR)(46%)。 38个月后的存活率为86%。 R0(L)后未发现局部复发,但5例发生远处转移。结论:术前HRCT是可行和有效的,并且可能有助于晚期直肠癌的局部肿瘤控制,这一点将在正在进行的III期临床试验中得到证实。

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