Lakatos G, Petranyi A, Szűcs A, Nehéz L, Harsanyi L, Hegyi P, Bodoky G
Department of Oncology, St. Istvan and St. Laszlo Hospital and Out-Patient Department, 5-7 Albert Flórián street, Budapest, H-1097, Hungary.
First Department of Surgery, Semmelweis University, Budapest, Hungary.
Pathol Oncol Res. 2017 Oct;23(4):753-759. doi: 10.1007/s12253-016-0176-0. Epub 2017 Jan 6.
The management of locally advanced pancreatic cancer (LAPC) is a major challenge. Although new drugs are available for the treatment of metastatic disease, the optimal treatment of non-metastatic cases remains controversial. The role of neoadjuvant therapy is still a question of debate in this setting. The aim of the study was to prospectively collect and analyse data on efficacy and safety of a modified FOLFIRINOX regimen in LAPC patients treated in a single institution. Another major objective was to assess the capability of FOLFIRINOX to render primary non-resectable cancer to resectable. No bolus fluorouracil was given and a 20% dose reduction of oxaliplatin and irinotecan was applied. Primary G-CSF prophylaxis was applied to prevent febrile neutropenia. Thirty-two patients (mean age 60.2 years, range: 40-77 years) have been enrolled into the study. All patients had ECOG performance status of 0 or 1. Best response to therapy was stable disease (SD) or partial regression (PR) in 18 (56.2%) and 6 (18.8%) cases. Two patients (6.3%) underwent surgical resection (100% R0). The most frequent grade 3/4 adverse events were nausea (18.8%), fatigue (12.5%) and diarrhea (12.5%). The incidence of severe neutropenia was 28.1%, with only one documented case of febrile neutropenia. The probability of disease progression was 25% and 50% after 75 and 160 days with 88.4% of possibility of disease progression after 500 days. OS probability was 92.1, 71.5% and 49.5% at 180-, 365 and 540 days. Our data does not support the capability of FOLFIRINOX to render primary non-resectable cancer to resectable. However, due to the high disease control rate observed, FOLFRINOX might be recommended as first line option for the palliative treatment of LAPC. Despite reduced chemotherapy doses significant toxicity has been seen.
局部晚期胰腺癌(LAPC)的管理是一项重大挑战。尽管有新药可用于治疗转移性疾病,但非转移性病例的最佳治疗方法仍存在争议。在这种情况下,新辅助治疗的作用仍是一个有争议的问题。本研究的目的是前瞻性收集和分析在单一机构接受治疗的LAPC患者中改良FOLFIRINOX方案的疗效和安全性数据。另一个主要目标是评估FOLFIRINOX将原发性不可切除癌症转变为可切除癌症的能力。未给予推注氟尿嘧啶,奥沙利铂和伊立替康剂量降低20%。应用原发性粒细胞集落刺激因子(G-CSF)预防以防止发热性中性粒细胞减少。32例患者(平均年龄60.2岁,范围:40-77岁)入组本研究。所有患者的东部肿瘤协作组(ECOG)体能状态均为0或1。治疗的最佳反应为病情稳定(SD)或部分缓解(PR),分别有18例(56.2%)和6例(18.8%)。2例患者(6.3%)接受了手术切除(R0切除率100%)。最常见的3/4级不良事件为恶心(18.8%)、疲劳(12.5%)和腹泻(12.5%)。严重中性粒细胞减少的发生率为28.1%,仅有1例记录在案的发热性中性粒细胞减少病例。75天和160天后疾病进展的概率分别为25%和50%,500天后疾病进展的可能性为88.4%。180天、365天和540天时总生存期(OS)概率分别为92.1%、71.5%和49.5%。我们的数据不支持FOLFIRINOX将原发性不可切除癌症转变为可切除癌症的能力。然而,由于观察到较高的疾病控制率,FOLFRINOX可能被推荐作为LAPC姑息治疗的一线选择。尽管化疗剂量降低,但仍观察到显著的毒性。