Macchia Gabriella, Valentini Vincenzo, Mattiucci Gian Carlo, Mantini Giovanna, Alfieri Sergio, Digesù Cinzia, Deodato Francesco, Trodella Lucio, Doglietto Gian Battista, Cellini Numa, Morganti Alessio Giuseppe
Unità Operativa di Radioterapia, Universitti Cattolica del S. Cuore, Campobasso.
Tumori. 2007 Jan-Feb;93(1):53-60. doi: 10.1177/030089160709300110.
In recent years, preoperative chemoradiation has received growing interest for the treatment of locally advanced pancreatic cancer. In an attempt to improve resectability and disease control, we used preoperative radiation therapy and concomitant 5-fluorouracil in a combined modality therapy protocol. The aim of the study was to evaluate definitive results in terms of toxicity, response and clinical outcome.
Twenty-eight patients with unresectable (cT4, 19 patients) or resectable (cT3, 9 patients) nonmetastatic pancreatic tumors received radiotherapy (39.6 Gy) plus 5-fluorouracil (continuous infusion, days 1-4 at 1000 mg/m(2)/day). After 4 weeks, patients were evaluated for surgical resection. In 9 resected patients, electron-beam intra-operative radiotherapy (10 Gy) was given before reconstruction. Thereafter, in resected patients, adjuvant chemotherapy was prescribed.
During chemoradiation, 1 patient (3.6%) developed grade 3 acute gastrointestinal toxicity and 2 patients (7.1%) developed grade 3 hematological toxicity. Three of 19 patients with unresectable tumors had tumor downstaging (15.8%). Two patients showed partial response (response rate, 7.1%; 95% CI, 0.2-25.3) and 4 patients (14.3%) had minimal tumor response. Four patients (14.3%) showed progressive disease after chemoradiation. One postoperative death was recorded. The median survival time was 11.3 months (20.5 and 9.0 months in resected and unresected patients, respectively). Only one local failure was recorded in 8 patients resected with negative margins.
Although the response rate is still low, our preliminary results suggest that preoperative 5-fluorouracil chemoradiation is well tolerated and may result in tumor downstaging. Delivery of intra-operative radiotherapy seems to be associated with a low rate of local recurrences.
近年来,术前放化疗在局部晚期胰腺癌的治疗中越来越受到关注。为了提高可切除性和疾病控制效果,我们在联合治疗方案中采用了术前放射治疗及同步5-氟尿嘧啶治疗。本研究的目的是评估在毒性、反应及临床结局方面的确切结果。
28例不可切除(cT4,19例)或可切除(cT3,9例)的非转移性胰腺肿瘤患者接受了放射治疗(39.6 Gy)加5-氟尿嘧啶(持续输注,第1 - 4天,1000 mg/m²/天)。4周后,对患者进行手术切除评估。在9例接受切除的患者中,术中电子束放疗(10 Gy)在重建前进行。此后,对接受切除的患者进行辅助化疗。
在放化疗期间,1例患者(3.6%)出现3级急性胃肠道毒性,2例患者(7.1%)出现3级血液学毒性。19例不可切除肿瘤患者中有3例肿瘤降期(15.8%)。2例患者显示部分缓解(缓解率7.1%;95%可信区间,0.2 - 25.3),4例患者(14.3%)有最小肿瘤反应。4例患者(14.3%)在放化疗后出现疾病进展。记录到1例术后死亡。中位生存时间为11.3个月(接受切除和未接受切除的患者分别为20.5个月和9.0个月)。在切缘阴性的8例接受切除的患者中仅记录到1例局部复发。
尽管缓解率仍然较低,但我们的初步结果表明术前5-氟尿嘧啶放化疗耐受性良好,可能导致肿瘤降期。术中放疗的应用似乎与较低的局部复发率相关。