First-line chemotherapy with selective internal radiation therapy for intrahepatic cholangiocarcinoma: The French ACABi GERCOR PRONOBIL cohort

Selective internal radiation therapy (SIRT) is a promising option for liver-only unresectable intrahepatic cholangiocarcinoma (iCCA). The Real-SIRTCCA study retrospectively assessed the benefit of adding SIRT to chemotherapy in this setting within the French nationwide observational cohort ACABi-GER...

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Veröffentlicht in:JHEP reports 2025-02, Vol.7 (2), p.101279, Article 101279
Hauptverfasser: Adamus, Nicolas, Edeline, Julien, Henriques, Julie, Fares, Nadim, Lecomte, Thierry, Turpin, Anthony, Vernerey, Dewi, Vincens, Mathilde, Chanez, Brice, Tougeron, David, Tournigand, Christophe, Assenat, Eric, Delaye, Matthieu, Manfredi, Sylvain, Bouché, Olivier, Williet, Nicolas, Vienot, Angelique, Blaise, Lorraine, Mas, Léo, Neuzillet, Cindy, Boilève, Alice, Roth, Gaël S.
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Sprache:eng
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Zusammenfassung:Selective internal radiation therapy (SIRT) is a promising option for liver-only unresectable intrahepatic cholangiocarcinoma (iCCA). The Real-SIRTCCA study retrospectively assessed the benefit of adding SIRT to chemotherapy in this setting within the French nationwide observational cohort ACABi-GERCOR-PRONOBIL. Inclusion criteria were advanced iCCA with limited or no extrahepatic disease, treated with first-line gemcitabine plus platinum chemotherapy +/- concurrent SIRT. All patients treated with chemotherapy and concurrent SIRT were included. To ensure groups’ similarity, a rigorous selection was applied to the chemo-only group, with exclusion of patients with liver involvement >50% and extrahepatic metastases. The primary outcome was progression-free survival (PFS). Secondary outcomes were overall survival (OS), objective response rate (ORR) and tumor resection rate. Propensity score and inverse probability of treatment weighting (IPTW) propensity approaches were used to address confounding factors between groups. Between July 2007 and December 2023, 277 patients met the Real-SIRTCCA inclusion criteria, with 88 in the chemo-SIRT group and 189 in chemo-only group. Chemo-SIRT was associated with longer PFS (median = 10.8 vs. 5.5 months, hazard ratio [HR] 0.54, 95% CI 0.41-0.71, p
ISSN:2589-5559
2589-5559
DOI:10.1016/j.jhepr.2024.101279