Grose Derek, McIntosh David, Jamieson Nigel, Carter Ross, Dickson Euan, Chang David, Marashi Husam, Wilson Christina, Alfayez Mohammed, Kerr Ashleigh, O'Donoghue Roisin, Haskins Lea, Duthie Fraser, McKay Colin J, Graham Janet
Beatson West of Scotland Cancer Centre, Glasgow, UK.
J Gastrointest Oncol. 2017 Aug;8(4):683-695. doi: 10.21037/jgo.2017.04.01.
Despite being relatively rare pancreatic cancer is one of the highest causes of death. Even within the potentially resectable group outcomes are poor. We present our initial experiences utilising a neoadjuvant approach to localised pancreatic cancer, evaluating survival, response rates and tolerability.
This was a retrospective analysis of a prospectively maintained database. Patients from 2012 to 2015 referred to a busy regional Hepato-Pancreatic Biliary (HPB) MDT were included. Patients were classified according to respectability criteria (utilising NCCN guidelines) and a treatment plan agreed. Systemic therapy with either FOLFIRINOX or Gem/Cap was delivered followed by chemoradiotherapy if disease remained localised. Toxicity, response, pathological outcomes and survival were all recorded.
A total of 85 patients were included in the study: 45 had initially resectable disease; 19 required a response for resection and 21 had locally advanced inoperable disease; 34 patients underwent resection. The median survival for the potentially resectable group was 22.2 months while for those undergoing resection it was 37 months.
We have demonstrated that a neoadjuvant approach is deliverable and tolerable. In addition we have demonstrated impressive survival results in patients undergoing resection with no detriment in outcome for those not proceeding to surgery.
尽管胰腺癌相对少见,但却是导致死亡的主要原因之一。即使在潜在可切除组中,预后也很差。我们介绍了我们采用新辅助方法治疗局限性胰腺癌的初步经验,评估了生存率、缓解率和耐受性。
这是一项对前瞻性维护数据库的回顾性分析。纳入了2012年至2015年转诊至繁忙的地区肝胆胰(HPB)多学科诊疗团队的患者。根据可切除性标准(采用美国国立综合癌症网络指南)对患者进行分类,并商定治疗方案。给予FOLFIRINOX或吉西他滨/卡培他滨全身治疗,如果疾病仍局限,则随后进行放化疗。记录毒性、缓解情况、病理结果和生存率。
共有85例患者纳入研究:45例最初为可切除疾病;19例需要缓解后进行切除,21例为局部晚期不可切除疾病;34例患者接受了切除。潜在可切除组的中位生存期为22.2个月,而接受切除的患者为37个月。
我们已经证明新辅助方法是可行且可耐受的。此外,我们已经证明接受切除的患者生存率令人印象深刻,对于未进行手术的患者,其预后没有损害。