Vogl T J, Zangos S, Heller M, Hammerstingl R M, Böcher E, Jacob U, Bauer R W
Institut für Diagnostische und Interventionelle Radiologie, J. W. Goethe-Universität Frankfurt, Frankfurt.
Rofo. 2007 Nov;179(11):1181-8. doi: 10.1055/s-2007-963568.
The purpose of this study was to evaluate local transarterial chemoperfusion (TACP) in locally recurrent pancreatic carcinoma and advanced tumor stages which did not respond to prior systemic chemotherapy. The tumor response, survival, and pain response were retrospectively analyzed.
Forty outpatients (median age 62 years, range 36-79) were treated with a minimum of 3 (mean 6, range 3-12) applications per patient in four-week intervals. Twenty-eight patients were in advanced tumor stages, and 12 patients had locally recurrent tumors. Gemcitabine (1,000 mg/m(2)) and mitomycin C (8.5 mg/m(2)) were administered within 1 hour through a celiac trunk catheter. The tumor response (diameter, volume) was measured using MRI or CT and classified according to RECIST. The pain response was defined as a reduction of pain intensity of more than 50% on a visual analog scale, or a reduction of more than 50% in analgesics consumption, or a switch to a less potent analgesic agent.
The treatment was tolerated well by all patients. No clinically relevant problems or grade III or IV toxicity according to CTC (Common Toxicity Criteria) were observed. Tumor-related pain was relieved in 20/32 (62.5%) cases. Radiologically, "complete response" was found in 3/40 (7.5%), "partial response" in 9/40 (22.5%), "stable disease" in 16/40 (40%), and "progressive disease" in 12/40 (30%) of the patients. The median survival period since initial diagnosis and first TACP was 16.4 months and 8.1 months, respectively. Locally recurrent tumors showed better, but still not significant results regarding tumor response (41.7% vs. 25%) as well as survival (14.4 vs. 7 months) compared to advanced tumor stages. Responders (CR+PR) showed a significant survival advantage compared to patients with tumor progression (13.0 vs. 6.0 months; p=0.013).
TACP is a minimally invasive outpatient treatment for therapy-resistant locally recurrent pancreatic carcinoma and advanced tumor stages. It may be considered as an important aspect in palliative symptomatic pain-relieving treatment, or may even result in improved survival by achieving tumor response.
本研究旨在评估局部经动脉化疗灌注(TACP)在局部复发胰腺癌及对既往全身化疗无反应的晚期肿瘤阶段的应用效果。对肿瘤反应、生存率和疼痛反应进行回顾性分析。
40例门诊患者(中位年龄62岁,范围36 - 79岁)接受治疗,每位患者至少接受3次(平均6次,范围3 - 12次)治疗,间隔四周。28例患者处于晚期肿瘤阶段,12例患者有局部复发性肿瘤。吉西他滨(1000 mg/m²)和丝裂霉素C(8.5 mg/m²)通过腹腔干导管在1小时内给药。使用MRI或CT测量肿瘤反应(直径、体积)并根据RECIST进行分类。疼痛反应定义为视觉模拟量表上疼痛强度降低超过50%,或镇痛药消耗量减少超过50%,或改用效力较低的镇痛药。
所有患者对治疗耐受性良好。未观察到根据常见毒性标准(CTC)出现的临床相关问题或III级或IV级毒性。20/32(62.5%)的病例中肿瘤相关疼痛得到缓解。影像学上,3/40(7.5%)的患者出现“完全缓解”,9/40(22.5%)出现“部分缓解”,16/40(40%)出现“疾病稳定”,12/40(30%)出现“疾病进展”。自初次诊断和首次TACP以来的中位生存期分别为16.4个月和8.1个月。与晚期肿瘤阶段相比,局部复发性肿瘤在肿瘤反应(41.7%对25%)以及生存率(14.4对7个月)方面显示出较好但仍无显著差异的结果。反应者(CR + PR)与肿瘤进展患者相比显示出显著的生存优势(13.0对6.0个月;p = 0.013)。
TACP是一种针对治疗抵抗的局部复发性胰腺癌和晚期肿瘤阶段的微创门诊治疗方法。它可被视为姑息性对症止痛治疗的一个重要方面,甚至可能通过实现肿瘤反应而提高生存率。