Clinical outcome and treatment sequences of patients with advanced pancreatic cancer treated with contemporary chemotherapy protocols

被引:1
|
作者
Roehrle, Julius [1 ,10 ]
Kasper, Stefan [1 ,7 ]
Treckmann, Juergen-Walter [2 ]
Markus, Peter [3 ]
Schumacher, Brigitte [4 ]
Albers, David [4 ]
Wendling, Johanna [1 ]
Ting, Saskia [5 ]
Mende, Bastian [6 ]
Massmann, Marlene [1 ]
Markus, Maximilian [1 ]
Virchow, Isabel [1 ]
Rosery, Vivian [1 ]
Laue, Katharina [1 ]
Zaun, Gregor [1 ]
Kostbade, Karina [1 ]
Pogorzelski, Michael [1 ]
Reissig, Timm M. [1 ,7 ,8 ,9 ]
Liffers, Sven-Thorsten [1 ,7 ,8 ,9 ]
Schmid, Kurt [5 ,7 ]
Schildhaus, Hans-Ulrich [5 ,7 ]
Schuler, Martin [1 ,7 ]
Siveke, Jens T. [1 ,7 ,8 ,9 ]
Wiesweg, Marcel [1 ]
机构
[1] Univ Hosp Essen, West German Canc Ctr, Dept Med Oncol, Essen, Germany
[2] Univ Hosp Essen, West German Canc Ctr, Dept Gen Visceral & Transplant Surg, Essen, Germany
[3] Elisabeth Hosp Essen, Dept Gen Surg & Traumatol, Essen, Germany
[4] Elisabeth Hosp Essen, Dept Gastroenterol, Essen, Germany
[5] Univ Hosp Essen, Inst Pathol Essen, West German Canc Ctr, Essen, Germany
[6] Univ Hosp Essen, Cent Pharm, Essen, Germany
[7] Univ Hosp Essen, German Canc Consortium DKTK, Partner Site, Essen, Germany
[8] Univ Hosp Essen, Bridge Inst Expt Tumor Therapy, West German Canc Ctr, Essen, Germany
[9] German Canc Res Ctr, German Canc Consortium DKTK, Div Solid Tumor Translat Oncol, Heidelberg, Germany
[10] Univ Hosp Essen, Dept Med Oncol, Hufelandstr 55, D-45147 Essen, Germany
关键词
GEMCITABINE; PACLITAXEL; FOLFIRINOX; IMMUNOTHERAPY; MULTICENTER; LYMPHOCYTE; SURVIVAL; THERAPY; RATIO;
D O I
10.1159/000529452
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
IntroductionSystemic therapy is firmly established in patients with advanced or metastatic pancreatic ductal adenocarcinoma (PDAC). Clinical efficacy is still modest and options are limited. Combination therapy protocols such as FOLFIRINOX and gemcitabine/nab-paclitaxel (Gem/NP) define standard-of-care. Patients may receive a sequence of both regimens as first- and second-line palliative treatment. However, there is no guidance regarding a preferred order. MethodsRetrospective analysis of clinical characteristics, treatment trajectories and outcomes of patients with advanced PDAC treated at the West German Cancer Center Essen from 2014 to 2020 to inform treatment decisions with respect to predictive factors, impact of chemotherapy regimen sequence and maintenance treatment. ResultsWe identified 170 patients with available follow-up. Of those, 160 (94.1%) pts received palliative CTX for primary metastatic, locally advanced or recurrent PDAC. Median PFS upon first palliative chemotherapy was 4.1 (3.1 - 5.9) months. First-line FOLFIRINOX associated with superior PFS (median 6.3 months) and OS (9.7 months, HR 0.7, p=0.03) as compared to gemcitabine/nab-paclitaxel or other regimens (PFS 3.0, OS 6.9 months). However, OS benefit of first-line FOLFIRINOX was lost in patients who received at least two treatment lines (median OS 12.1 vs. 13.1 months, p=0.43). A landmark analysis of patients with clinical benefit (defined at CR/PR/SD for at least 20 weeks) upon first-line therapy revealed improved OS (HR 0.53, p=0.02) for patients receiving continued deescalated maintenance therapy. Second-line regimens resulted in similar PFS (overall log-rank p=0.92, median PFS2 2.3 (1.8-2.9), per-regimen median between 1.8 and 3.9 months). A previously established systemic inflammation score proved to be strongly prognostic and allowed identification of a patient subgroup with dismal prognosis (OS 2.9 vs. 11.4 months, HR 5.23, p<0.001), independent of other prognostic factors and with no relevant interaction with the choice of first-line regimen. ConclusionIn this real world population of PDAC patients treated with contemporary combination chemotherapies, a positive impact of first line FOLFIRINOX was only observed when no second or further line treatment was administered. Intensity-reduced maintenance therapy may lead to superior survival.
引用
收藏
页码:140 / 150
页数:11
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