Clinical Outcome and Treatment Sequences of Patients with Advanced Pancreatic Cancer Treated with Contemporary Chemotherapy Protocols.


Journal

Oncology research and treatment
ISSN: 2296-5262
Titre abrégé: Oncol Res Treat
Pays: Switzerland
ID NLM: 101627692

Informations de publication

Date de publication:
2023
Historique:
received: 15 08 2022
accepted: 11 01 2023
medline: 13 4 2023
pubmed: 1 2 2023
entrez: 31 1 2023
Statut: ppublish

Résumé

Systemic 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. This is a retrospective 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. We identified 170 patients with available follow-up. Of those, 160 (94.1%) patients received palliative CTX for primary metastatic, locally advanced, or recurrent PDAC. Median progression-free survival (PFS) upon first palliative chemotherapy was 4.1 (3.1-5.9) months. First-line FOLFIRINOX was associated with superior PFS (median 6.3 months) and OS (9.7 months, HR 0.7, p = 0.03) as compared to Gem/NP 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 as 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 PFS upon second-line therapy 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. In 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.

Identifiants

pubmed: 36720216
pii: 000529452
doi: 10.1159/000529452
doi:

Substances chimiques

Gemcitabine 0
Deoxycytidine 0W860991D6
Paclitaxel P88XT4IS4D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

140-150

Informations de copyright

© 2023 S. Karger AG, Basel.

Auteurs

Julius Roehrle (J)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.

Stefan Kasper (S)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.
German Cancer Consortium (DKTK), Partner Site University Hospital Essen, Essen, Germany.

Jürgen-Walter Treckmann (JW)

Department of General, Visceral and Transplant Surgery, West German Cancer Center, University Hospital Essen, Essen, Germany.

Peter Markus (P)

Department of General Surgery and TraumatologyElisabeth Hospital Essen, Essen, Germany.

Brigitte Schumacher (B)

Department of Gastroenterology, Elisabeth Hospital Essen, Essen, Germany.

David Albers (D)

Department of Gastroenterology, Elisabeth Hospital Essen, Essen, Germany.

Johanna Wendling (J)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.

Saskia Ting (S)

West German Cancer Center, Institute of Pathology Essen, University Hospital Essen, Essen, Germany.

Bastian Mende (B)

Central Pharmacy, University Hospital Essen, Essen, Germany.

Marlene Maßmann (M)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.

Maximilian Markus (M)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.

Isabel Virchow (I)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.

Vivian Rosery (V)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.

Katharina Laue (K)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.

Gregor Zaun (G)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.

Karina Kostbade (K)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.

Michael Pogorzelski (M)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.

Timm M Reissig (TM)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.
German Cancer Consortium (DKTK), Partner Site University Hospital Essen, Essen, Germany.
Bridge Institute of Experimental Tumor Therapy, West German Cancer Center, University Hospital Essen, Essen, Germany.
Division of Solid Tumor Translational Oncology, German Cancer Consortium (DKTK), German Cancer Research Center (DKFZ), Heidelberg, Germany.

Sven-Thorsten Liffers (ST)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.
German Cancer Consortium (DKTK), Partner Site University Hospital Essen, Essen, Germany.
Bridge Institute of Experimental Tumor Therapy, West German Cancer Center, University Hospital Essen, Essen, Germany.
Division of Solid Tumor Translational Oncology, German Cancer Consortium (DKTK), German Cancer Research Center (DKFZ), Heidelberg, Germany.

Kurt Schmid (K)

German Cancer Consortium (DKTK), Partner Site University Hospital Essen, Essen, Germany.
West German Cancer Center, Institute of Pathology Essen, University Hospital Essen, Essen, Germany.

Hans-Ulrich Schildhaus (HU)

German Cancer Consortium (DKTK), Partner Site University Hospital Essen, Essen, Germany.
West German Cancer Center, Institute of Pathology Essen, University Hospital Essen, Essen, Germany.

Martin Schuler (M)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.
German Cancer Consortium (DKTK), Partner Site University Hospital Essen, Essen, Germany.

Jens T Siveke (JT)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.
German Cancer Consortium (DKTK), Partner Site University Hospital Essen, Essen, Germany.
Bridge Institute of Experimental Tumor Therapy, West German Cancer Center, University Hospital Essen, Essen, Germany.
Division of Solid Tumor Translational Oncology, German Cancer Consortium (DKTK), German Cancer Research Center (DKFZ), Heidelberg, Germany.

Marcel Wiesweg (M)

Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.

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