Division of Surgical Oncology, Department of Surgery, University of Colorado, Anschutz Medical Campus, Aurora.
Amsterdam UMC, University of Amsterdam, Department of Surgery, Amsterdam, the Netherlands.
JAMA Netw Open. 2024 Jun 3;7(6):e2417625. doi: 10.1001/jamanetworkopen.2024.17625.
Preoperative chemo(radio)therapy is increasingly used in patients with localized pancreatic adenocarcinoma, leading to pathological complete response (pCR) in a small subset of patients. However, multicenter studies with in-depth data about pCR are lacking.
To investigate the incidence, outcome, and risk factors of pCR after preoperative chemo(radio)therapy.
DESIGN, SETTING, AND PARTICIPANTS: This observational, international, multicenter cohort study assessed all consecutive patients with pathology-proven localized pancreatic adenocarcinoma who underwent resection after 2 or more cycles of chemotherapy (with or without radiotherapy) in 19 centers from 8 countries (January 1, 2010, to December 31, 2018). Data collection was performed from February 1, 2020, to April 30, 2022, and analyses from January 1, 2022, to December 31, 2023. Median follow-up was 19 months.
Preoperative chemotherapy (with or without radiotherapy) followed by resection.
The incidence of pCR (defined as absence of vital tumor cells in the sampled pancreas specimen after resection), its association with OS from surgery, and factors associated with pCR. Factors associated with overall survival (OS) and pCR were investigated with Cox proportional hazards and logistic regression models, respectively.
Overall, 1758 patients (mean [SD] age, 64 [9] years; 879 [50.0%] male) were studied. The rate of pCR was 4.8% (n = 85), and pCR was associated with OS (hazard ratio, 0.46; 95% CI, 0.26-0.83). The 1-, 3-, and 5-year OS rates were 95%, 82%, and 63% in patients with pCR vs 80%, 46%, and 30% in patients without pCR, respectively (P < .001). Factors associated with pCR included preoperative multiagent chemotherapy other than (m)FOLFIRINOX ([modified] leucovorin calcium [folinic acid], fluorouracil, irinotecan hydrochloride, and oxaliplatin) (odds ratio [OR], 0.48; 95% CI, 0.26-0.87), preoperative conventional radiotherapy (OR, 2.03; 95% CI, 1.00-4.10), preoperative stereotactic body radiotherapy (OR, 8.91; 95% CI, 4.17-19.05), radiologic response (OR, 13.00; 95% CI, 7.02-24.08), and normal(ized) serum carbohydrate antigen 19-9 after preoperative therapy (OR, 3.76; 95% CI, 1.79-7.89).
This international, retrospective cohort study found that pCR occurred in 4.8% of patients with resected localized pancreatic adenocarcinoma after preoperative chemo(radio)therapy. Although pCR does not reflect cure, it is associated with improved OS, with a doubled 5-year OS of 63% compared with 30% in patients without pCR. Factors associated with pCR related to preoperative chemo(radio)therapy regimens and anatomical and biological disease response features may have implications for treatment strategies that require validation in prospective studies because they may not universally apply to all patients with pancreatic adenocarcinoma.
术前化疗(放化疗)在局部胰腺腺癌患者中的应用日益增多,导致一小部分患者出现病理完全缓解(pCR)。然而,缺乏关于 pCR 的多中心研究,且这些研究提供了深入的数据。
调查术前化疗(放化疗)后 pCR 的发生率、结果和危险因素。
设计、地点和参与者:本观察性、国际、多中心队列研究评估了来自 8 个国家 19 个中心的所有病理证实为局限性胰腺腺癌患者,这些患者在 19 个中心接受了 2 个或更多周期的化疗(联合或不联合放疗)后进行了手术(2010 年 1 月 1 日至 2018 年 12 月 31 日)。数据收集于 2020 年 2 月 1 日至 2022 年 4 月 30 日进行,分析于 2022 年 1 月 1 日至 2022 年 12 月 31 日进行。中位随访时间为 19 个月。
术前化疗(联合或不联合放疗)后行切除术。
pCR 的发生率(定义为手术后取样胰腺标本中无存活肿瘤细胞)、其与手术总生存(OS)的关系,以及与 pCR 相关的因素。分别使用 Cox 比例风险和 logistic 回归模型调查与 OS 和 pCR 相关的因素。
共纳入 1758 例患者(平均[标准差]年龄 64[9]岁;879[50.0%]为男性)。pCR 发生率为 4.8%(n=85),pCR 与 OS 相关(风险比,0.46;95%CI,0.26-0.83)。pCR 患者的 1 年、3 年和 5 年 OS 率分别为 95%、82%和 63%,无 pCR 患者分别为 80%、46%和 30%(P<0.001)。与 pCR 相关的因素包括术前多药化疗(m)FOLFIRINOX(改良亚叶酸钙[叶酸]、氟尿嘧啶、盐酸伊立替康和奥沙利铂)(OR,0.48;95%CI,0.26-0.87)、术前常规放疗(OR,2.03;95%CI,1.00-4.10)、术前立体定向体部放疗(OR,8.91;95%CI,4.17-19.05)、影像学反应(OR,13.00;95%CI,7.02-24.08)和术前治疗后正常(化)血清碳水化合物抗原 19-9(OR,3.76;95%CI,1.79-7.89)。
本国际回顾性队列研究发现,局部胰腺腺癌患者在接受术前化疗(放化疗)后,有 4.8%发生 pCR。尽管 pCR 并不能反映治愈,但它与 OS 改善相关,与无 pCR 的患者相比,5 年 OS 提高了一倍,达到 63%。与 pCR 相关的因素与术前化疗(放化疗)方案以及解剖学和生物学疾病反应特征有关,这可能对需要在前瞻性研究中验证的治疗策略具有重要意义,因为这些因素可能并不普遍适用于所有胰腺腺癌患者。