Zur Hauptnavigation wechseln Zur Suche wechseln Zum Hauptinhalt wechseln

Survival prediction for patients with non-resectable intrahepatic cholangiocarcinoma undergoing chemotherapy: a retrospective analysis comparing the tumor marker CA 19-9 with cross-sectional imaging

Felix Hahn, Lukas Müller, Florian Jungmann, Aline Mähringer-Kunz, Yasemin Tanyildizi, Christoph Düber, Peter R. Galle, Arndt Weinmann, Roman Kloeckner*

*Korrespondierende/r Autor/-in für diese Arbeit

Abstract

Purpose: Carbohydrate antigen (CA) 19-9 has been established as the main serum marker for patients with intrahepatic cholangiocarcinoma (ICC). The aim of this study was to compare the prognostic value of CA 19-9 changes versus response determined by imaging in patients with ICC undergoing chemotherapy. Methods: Between 2003 and 2018, 151 patients with histopathologically confirmed ICC underwent chemotherapy at our tertiary care center for non-resectable or recurrent ICC, of whom 121 were included in this study. Serum CA 19-9 levels and imaging were retrospectively evaluated during chemotherapy. Log-rank testing and optimal stratification were used to classify patients into risk groups. Results: Prior to chemotherapy, baseline serum CA 19-9 levels above the previously published cut-off of 37 U/ml were associated with poor survival (median OS 8.7 vs. 12.4 months, p = 0.003). After the beginning of chemotherapy, an increase in CA 19-9 of more than 40 U/ml resulted in impaired residual survival (median OS 5.0 vs. 12.1 months, p < 0.001). However, progressive disease at the first follow-up imaging proved the strongest predictor for poor outcome (median OS 4.6 vs. 15.5 months, p < 0.001). In contrast to prior studies, our data did not show statistically relevant differences in survival time with respect to absolute or relative decreases in serum CA 19-9 levels. Conclusion: In our study, the disease control rate—that is, the absence of progressive disease—was the strongest predictor of prolonged residual OS. To this end, both CA 19-9 changes and progressive disease on initial follow-up showed remarkable discriminatory power, with the latter slightly outperforming the former. Therefore, imaging should remain the mainstay of patient evaluation during follow-up.

OriginalspracheEnglisch
ZeitschriftJournal of Cancer Research and Clinical Oncology
Jahrgang146
Ausgabenummer7
Seiten (von - bis)1883-1890
Seitenumfang8
ISSN0171-5216
DOIs
PublikationsstatusVeröffentlicht - 01.07.2020

Fördermittel

PRG has received grants and personal fees from Bayer and personal fees from Bristol-Myers Squibb, MSD Sharp & Dohme, Lilly, Sillajen, SIRTEX, and AstraZeneca. AW has received speaker fees and travel grants from Bayer. RK has received speaker fees from BTG, Guerbet, and SIRTEX and personal fees from Boston Scientific, Bristol-Myers Squibb, Guerbet, and SIRTEX. None of these companies supported this study, and none of the authors reports a conflict of interest. Open Access funding provided by Projekt DEAL. FH was granted protected research time by a University Center for Tumor Diseases/Transmed Fellowship of the Johannes Gutenberg University Mainz Medical Center.

TrägerTrägernummer
University Center for Tumor Diseases/Transmed Fellowship of the Johannes Gutenberg University Mainz Medical Center
Bayer HealthCare Frankreich

    UN SDGs

    Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

    1. SDG 3 – Gesundheit und Wohlergehen
      SDG 3 – Gesundheit und Wohlergehen
    2. SDG 9 – Industrie, Innovation und Infrastruktur
      SDG 9 – Industrie, Innovation und Infrastruktur

    Strategische Forschungsbereiche und Zentren

    • Forschungsschwerpunkt: Biomedizintechnik
    • Profilbereich: Lübeck Integrated Oncology Network (LION)

    DFG-Fachsystematik

    • 2.22-30 Radiologie
    • 2.22-14 Hämatologie, Onkologie

    Fingerprint

    Untersuchen Sie die Forschungsthemen von „Survival prediction for patients with non-resectable intrahepatic cholangiocarcinoma undergoing chemotherapy: a retrospective analysis comparing the tumor marker CA 19-9 with cross-sectional imaging“. Zusammen bilden sie einen einzigartigen Fingerprint.

    Zitieren