Yasmeen Samia, Arshad Farah, Shaukat Sabah, Badar Farhana, Kazmi Syed Ather Saeed, Ahmad Usman
Department of Medical Oncology, Prince Faisal Cancer Center, Buraidah, Kingdom of Saudi Arabia.
Department of Internal Medicine, Shalamar Institute of Health Sciences, Lahore, Pakistan.
J Cancer Allied Spec. 2021 May 31;7(2):e409. doi: 10.37029/jcas.v7i2.409. eCollection 2021.
To report response rates, progression-free survival (PFS) and overall survival (OS) in patients with advanced pancreatic cancer treated with different available chemotherapeutic regimens over 10 years.
This is a retrospective observational study. All patients with locally advanced and metastatic pancreatic cancer (MPC) at Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, Pakistan, from January 2008 to December 2017 were studied. Data were collected from the hospital information system. The characteristics and outcomes of all the patients were analysed. PFS and OS were also estimated. Kaplan-Meier curves and log-rank test were applied, and SPSS version 20 was used for data analysis.
Eighty-seven subjects with a median age of 56 years (range 21-76) were included. Sixty-two (71%) subjects were male. The most common tumour location was the head of the pancreas in 46 (53%) of all the subjects. Sixty-three (72%) subjects had elevated carbohydrate antigen-19.9 values. About 47 (54%) subjects had locally advanced pancreatic cancer (LAPC), and 40 (46%) subjects had MPC. Chemotherapy regimens used were FOLFIRINOX in 23 (26%), gemcitabine (GEM) based in 66 (65%) and capecitabine (CAP) based in 8 (9%) of the subjects. One (1%) subject had a complete response, 12 (14%) had a partial response, 10 (11%) had stable disease and 59 (68%) of the subjects had progressive disease. The objective response rate (ORR) was 15% and the disease control rate (DCR) was 26%. In MPC, the ORR was 10%, DCR was 18% and tumour progression was seen in 72% of the patients, while in LAPC, the ORR was 19.1, DCR 34% and tumour progression was documented in 64% of the patients, respectively. The FOLFIRINOX chemotherapy regimen had better ORR, DCR and lesser number of progressions as compared to GEM- and CAP-based chemotherapy regimens. The median PFS of the whole group was 32 weeks, and the median OS was 54 weeks. The PFS was significantly higher for LAPC (39 weeks) as compared to the MPC group (25 weeks) ( = 0.028). There was no statistically significant difference between the OS of these two groups ( = 0.451). In addition, PFS was significantly higher with FOLFIRINOX chemotherapy as compared to the other chemotherapy regimens. Regarding OS, there was no statistically significant difference among all chemotherapy regimen groups ( = 0.267).
Based on our results, FOLFIRINOX remained the most effective chemotherapy regimen despite the dose modifications and toxicities in all groups, indicating that modified FOLFIRINOX could be considered as a first-line regimen in Southeast Asian population.
报告10年间接受不同可用化疗方案治疗的晚期胰腺癌患者的缓解率、无进展生存期(PFS)和总生存期(OS)。
这是一项回顾性观察研究。对2008年1月至2017年12月在巴基斯坦拉合尔的沙卡特汗姆纪念癌症医院和研究中心的所有局部晚期和转移性胰腺癌(MPC)患者进行了研究。数据从医院信息系统收集。分析了所有患者的特征和结局。还估算了PFS和OS。应用了Kaplan-Meier曲线和对数秩检验,并使用SPSS 20版进行数据分析。
纳入了87名中位年龄为56岁(范围21 - 76岁)的受试者。62名(71%)受试者为男性。最常见的肿瘤部位是胰腺头部,占所有受试者的46名(53%)。63名(72%)受试者的糖类抗原19.9值升高。约47名(54%)受试者患有局部晚期胰腺癌(LAPC),40名(46%)受试者患有MPC。所使用的化疗方案中,23名(26%)受试者采用FOLFIRINOX,66名(65%)基于吉西他滨(GEM),8名(9%)基于卡培他滨(CAP)。1名(1%)受试者完全缓解,12名(14%)部分缓解,10名(11%)病情稳定,59名(68%)受试者病情进展。客观缓解率(ORR)为15%,疾病控制率(DCR)为26%。在MPC中,ORR为10%,DCR为18%,72%的患者出现肿瘤进展;而在LAPC中,ORR为19.1%,DCR为34%,分别有64%的患者记录有肿瘤进展。与基于GEM和CAP的化疗方案相比,FOLFIRINOX化疗方案具有更好的ORR、DCR且进展次数更少。整个组的中位PFS为32周,中位OS为54周。LAPC的PFS(39周)显著高于MPC组(25周)(P = 0.028)。这两组的OS之间无统计学显著差异(P = 0.451)。此外,与其他化疗方案相比,FOLFIRINOX化疗的PFS显著更高。关于OS,所有化疗方案组之间无统计学显著差异(P = 0.267)。
基于我们的结果,尽管所有组中都有剂量调整和毒性,但FOLFIRINOX仍然是最有效的化疗方案,这表明改良的FOLFIRINOX可被视为东南亚人群的一线方案。