da Rocha Lino Aline, Abrahão Carina Meira, Brandão Raphael Moreira, Gomes Jessica Ribeiro, Ferrian Andrea Malta, Machado Marcel Cerqueira César, Buzaid Antonio Carlos, Maluf Fernando Cotait, Peixoto Renata D'Alpino
Centro Oncológico Antônio Ermírio de Moraes, Beneficência Portuguesa de São Paulo, São Paulo, Brazil.
J Gastrointest Oncol. 2015 Oct;6(5):511-5. doi: 10.3978/j.issn.2078-6891.2015.041.
Cancer of the exocrine pancreas is a highly lethal malignancy. Surgical resection is the only potentially curative treatment. Unfortunately, because of the late presentation, the majority have either locally advanced cancer at initial diagnosis. Systemic chemotherapy provides benefit to patients with advanced pancreatic cancer, improving disease-related symptoms and survival when compared to best supportive care alone. Based on fase III study, FOLFIRINOX regimen became the standard first-line treatment. But, the optimal management strategy for patients who fail initial FOLFIRINOX is undefined. Despite the lack of clinical trials that report the real benefit of gemcitabine in patients with advanced exocrine pancreatic cancer as second line treatment. We aim at reporting our experience with this regimen.
Patients with advanced exocrine pancreatic cancer who received gemcitabine (1.000 mg/m(2) on days 1, 8 and 15 every 4 weeks) until disease progression, as second-line therapy at our institution were retrospectively evaluated. Progression-free survival (PFS) and overall survival (OS) were estimated by the Kaplan-Meier method.
A total of 20 patients were reviewed. Median age was 57 years (range, 43-74 years), and 55% were older than 60 years. Most patients were male (80%), had metastatic disease (60%), and ECOG performance status of 0 or 1 (65%). PFS and OS were 2.0 (95% CI, 1.2-2.8) and 5.7 months (95% CI, 3.9-7.4), respectively. There were no deaths due to the treatment.
In this study, gemcitabine was a reasonable second-line treatment option for patients with advanced pancreatic adenocarcinoma and good ECOG performance status. Phase III trials are urgently needed comparing gemcitabine versus best supportive of care (BSC) can evaluate the real benefit of this chemotherapy after progression on FOLFIRINOX.
胰腺外分泌癌是一种高度致命的恶性肿瘤。手术切除是唯一可能治愈的治疗方法。不幸的是,由于就诊时病情较晚,大多数患者在初诊时就已出现局部晚期癌症。全身化疗对晚期胰腺癌患者有益,与单纯最佳支持治疗相比,可改善与疾病相关的症状并延长生存期。基于III期研究,FOLFIRINOX方案成为标准的一线治疗方案。但是,初始FOLFIRINOX治疗失败的患者的最佳管理策略尚不明确。尽管缺乏临床试验报告吉西他滨作为晚期胰腺外分泌癌二线治疗的实际益处,但我们旨在报告我们使用该方案的经验。
回顾性评估在我们机构接受吉西他滨(每4周第1、8和15天1000mg/m²)直至疾病进展的晚期胰腺外分泌癌患者作为二线治疗的情况。采用Kaplan-Meier方法估计无进展生存期(PFS)和总生存期(OS)。
共审查了20例患者。中位年龄为57岁(范围43 - 74岁),55%的患者年龄大于60岁。大多数患者为男性(80%),有转移性疾病(60%),东部肿瘤协作组(ECOG)体能状态为0或1(65%)。PFS和OS分别为2.0个月(95%CI,1.2 - 2.8)和5.7个月(95%CI,3.9 - 7.4)。没有因治疗导致的死亡。
在本研究中,吉西他滨对于晚期胰腺腺癌且ECOG体能状态良好的患者是一种合理的二线治疗选择。迫切需要进行III期试验比较吉西他滨与最佳支持治疗(BSC),以评估FOLFIRINOX方案进展后这种化疗的实际益处。