Department of Radiotherapy, University Hospital, Verona, Italy.
Strahlenther Onkol. 2011 Oct;187(10):619-25. doi: 10.1007/s00066-011-2226-6. Epub 2011 Sep 19.
To evaluate the therapeutic effect of delivering regional hyperthermia (HT) plus chemoradiotherapy (CRT) in patients suffering from locally advanced unresectable pancreatic cancer (LAPC).
Between January 2000 and December 2008, 68 patients affected by primary (56/68) or recurrent (12/68) LAPC were treated either with CRT alone or CRT plus HT. Radiotherapy (RT) consisted of 3D conformal irradiation of tumor and regional lymph nodes (dose ranged from 30 Gy/10 fractions to 66 Gy/33 fractions). Chemotherapy (CT) consisted of gemcitabine (GEM) alone or in association with either oxaliplatin, cisplatin, or 5-FU. HT was delivered twice a week, concomitant with RT.
In the current study, 60 of the original 68 patients were included. Median overall survival (OS) was 15 months in the HT group versus 11 months in the control group (log-rank test: p = 0.025). HT did not increase CRT toxicity.
HT can be added safely to CRT in LAPC, thus, resulting in slightly prolonged survival in certain cases.
评估在局部晚期不可切除胰腺癌(LAPC)患者中实施区域高热(HT)联合放化疗(CRT)的治疗效果。
2000 年 1 月至 2008 年 12 月期间,68 例初治(56/68)或复发性(12/68)LAPC 患者分别接受 CRT 单独治疗或 CRT 联合 HT 治疗。放疗(RT)采用三维适形照射肿瘤和区域淋巴结(剂量范围为 30 Gy/10 个分次至 66 Gy/33 个分次)。化疗(CT)采用吉西他滨(GEM)单独或联合奥沙利铂、顺铂或 5-FU。HT 每周进行两次,与 RT 同时进行。
在本研究中,68 例患者中有 60 例纳入。HT 组的中位总生存期(OS)为 15 个月,对照组为 11 个月(对数秩检验:p=0.025)。HT 并未增加 CRT 的毒性。
HT 可安全地添加到 LAPC 的 CRT 中,从而在某些情况下略微延长生存时间。