Department of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, 6-5-1, Kashiwanoha, Kashiwa, Chiba, 277-8577, Japan.
Department of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, Tokyo, Japan.
BMC Cancer. 2020 Oct 1;20(1):946. doi: 10.1186/s12885-020-07462-4.
Undifferentiated carcinoma (UC) of the pancreas is a rare subtype of pancreatic cancer. Although UC has been considered a highly aggressive malignancy, no clinical studies have addressed the efficacy of chemotherapy for unresectable UC. Therefore, we conducted multicenter retrospective study to investigate the efficacy of chemotherapy in patients with UC of the pancreas.
This multicenter retrospective cohort study was conducted at 17 institutions in Japan between January 2007 and December 2017. A total of 50 patients treated with chemotherapy were analyzed.
The median overall survival (OS) in UC patients treated with chemotherapy was 4.08 months. The details of first-line chemotherapy were as follows: gemcitabine (n = 24), S-1 (n = 12), gemcitabine plus nab-paclitaxel (n = 6), and other treatment (n = 8). The median progression-free survival (PFS) was 1.61 months in the gemcitabine group, 2.96 months in the S-1 group, and 4.60 months in the gemcitabine plus nab-paclitaxel group. Gemcitabine plus nab-paclitaxel significantly improved PFS compared with gemcitabine (p = 0.014). The objective response rate (ORR) was 4.2% in the gemcitabine group, 0.0% in the S-1 group, and 33.3% in the gemcitabine plus nab-paclitaxel group. Gemcitabine plus nab-paclitaxel also showed a significantly higher ORR compared with both gemcitabine and S-1 (gemcitabine plus nab-paclitaxel vs. gemcitabine: p = 0.033; gemcitabine plus nab-paclitaxel vs. S-1: p = 0.034). A paclitaxel-containing first-line regimen significantly improved OS compared with a non-paclitaxel-containing regimen (6.94 months vs. 3.75 months, respectively; p = 0.041). After adjustment, use of a paclitaxel-containing regimen in any line was still an independent predictor of OS (hazard ratio for OS, 0.221; 95% confidence interval, 0.076-0.647; p = 0.006) in multiple imputation by chained equation.
The results of the present study indicate that a paclitaxel-containing regimen would offer relatively longer survival, and it is considered a reasonable option for treating patients with unresectable UC.
胰腺未分化癌(UC)是一种罕见的胰腺癌亚型。尽管 UC 被认为是一种高度侵袭性的恶性肿瘤,但尚无临床研究探讨不可切除 UC 的化疗疗效。因此,我们进行了多中心回顾性研究,以调查化疗在胰腺 UC 患者中的疗效。
这项多中心回顾性队列研究于 2007 年 1 月至 2017 年 12 月在日本的 17 家机构进行。共分析了 50 例接受化疗的患者。
接受化疗的 UC 患者的中位总生存期(OS)为 4.08 个月。一线化疗的详细信息如下:吉西他滨(n=24)、替吉奥(S-1)(n=12)、吉西他滨加 nab-紫杉醇(n=6)和其他治疗(n=8)。吉西他滨组的中位无进展生存期(PFS)为 1.61 个月,S-1 组为 2.96 个月,吉西他滨加 nab-紫杉醇组为 4.60 个月。吉西他滨加 nab-紫杉醇组的 PFS 明显优于吉西他滨组(p=0.014)。吉西他滨组的客观缓解率(ORR)为 4.2%,S-1 组为 0.0%,吉西他滨加 nab-紫杉醇组为 33.3%。吉西他滨加 nab-紫杉醇组的 ORR 也明显高于吉西他滨组和 S-1 组(吉西他滨加 nab-紫杉醇与吉西他滨:p=0.033;吉西他滨加 nab-紫杉醇与 S-1:p=0.034)。一线含紫杉醇方案与不含紫杉醇方案相比,OS 明显改善(分别为 6.94 个月和 3.75 个月;p=0.041)。在多变量 Cox 比例风险回归分析中,调整混杂因素后,任何线治疗中使用含紫杉醇方案仍然是 OS 的独立预测因素(OS 的风险比为 0.221;95%置信区间为 0.076-0.647;p=0.006)。
本研究结果表明,含紫杉醇方案可能会带来更长的生存时间,对于治疗不可切除的 UC 患者,这是一种合理的选择。