Ren Jiaqiang, Wu Shuai, Su Tong, Ding Jiachun, Chen Fan, Li Jie, Wang Zheng, Han Liang, Wu Zheng
Department of Hepatobiliary Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
School of Public Health, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, China.
Cancer Med. 2024 May;13(9):e7229. doi: 10.1002/cam4.7229.
To investigate the relationship between chemoresistance in pancreatic cancer patients receiving postoperative gemcitabine adjuvant therapy and specific clinical/pathological characteristics, as well as its impact on patient prognosis.
From June 2018 to June 2021, clinical and pathological data of 148 pancreatic cancer patients were collected, and 101 patients were followed up for tumor recurrence/metastasis and survival status. The correlation between chemoresistance and specific clinical/pathological characteristics or patient prognosis was retrospectively analyzed.
Of the 148 patients, 78 were in the chemoresistance group and 70 in the non-chemoresistance group. Univariate analysis showed that the development of chemoresistance may be related to patient age, combined diabetes, preoperative CA19-9 level, tumor size, AJCC stage, vascular invasion, and positive lymph node ratio. Furthermore, subsequent multivariate analysis incorporating these variables indicated that tumor size may be a key factor influencing chemoresistance (p < 0.001, OR = 1.584). Log-rank test showed patients in the chemoresistance group had worse overall survival (OS) (HR = 2.102, p = 0.018) and progression free survival (PFS) (HR = 3.208, p = 0.002) than patients in the non-chemoresistance group; and patients with smaller size tumors (diameter ≤3 cm) had significantly better OS (HR = 2.923, p < 0.001) and PFS (HR = 2.930, p = 0.003) than those with larger size tumors (diameter >3 cm).
Patients with pancreatic cancer receiving postoperative gemcitabine adjuvant therapy are more likely to develop chemoresistance when their tumor sizes are larger (diameter >3 cm). Development of chemoresistance exacerbates the prognosis of patients with pancreatic cancer, and larger tumor size is also a risk factor for poor prognosis in these patients.
探讨接受术后吉西他滨辅助治疗的胰腺癌患者化疗耐药与特定临床/病理特征之间的关系,及其对患者预后的影响。
收集2018年6月至2021年6月期间148例胰腺癌患者的临床和病理资料,对其中101例患者进行肿瘤复发/转移及生存状态随访。回顾性分析化疗耐药与特定临床/病理特征或患者预后之间的相关性。
148例患者中,化疗耐药组78例,非化疗耐药组70例。单因素分析显示,化疗耐药的发生可能与患者年龄、合并糖尿病、术前CA19-9水平、肿瘤大小、美国癌症联合委员会(AJCC)分期、血管侵犯及阳性淋巴结比例有关。此外,纳入这些变量的后续多因素分析表明,肿瘤大小可能是影响化疗耐药的关键因素(p < 0.001,OR = 1.584)。对数秩检验显示,化疗耐药组患者的总生存期(OS)(HR = 2.102,p = 0.018)和无进展生存期(PFS)(HR = 3.208,p = 0.002)均较非化疗耐药组患者差;肿瘤较小(直径≤3 cm)的患者的OS(HR = 2.923,p < 0.001)和PFS(HR = 2.930,p = 0.003)显著优于肿瘤较大(直径>3 cm)的患者。
接受术后吉西他滨辅助治疗的胰腺癌患者,肿瘤较大(直径>3 cm)时更易发生化疗耐药。化疗耐药的发生会使胰腺癌患者的预后恶化,且肿瘤较大也是这些患者预后不良的危险因素。