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.
| Originalsprache | Englisch |
|---|---|
| Zeitschrift | Journal of Cancer Research and Clinical Oncology |
| Jahrgang | 146 |
| Ausgabenummer | 7 |
| Seiten (von - bis) | 1883-1890 |
| Seitenumfang | 8 |
| ISSN | 0171-5216 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 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.
| Träger | Trägernummer |
|---|---|
| University Center for Tumor Diseases/Transmed Fellowship of the Johannes Gutenberg University Mainz Medical Center | |
| Bayer HealthCare Frankreich |
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Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
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SDG 3 – Gesundheit und Wohlergehen
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Strategische Forschungsbereiche und Zentren
- Forschungsschwerpunkt: Biomedizintechnik
- Profilbereich: Lübeck Integrated Oncology Network (LION)
DFG-Fachsystematik
- 2.22-30 Radiologie
- 2.22-14 Hämatologie, Onkologie
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