Erschienen in:
10.09.2021 | Original Article
Long-term morbidity and mortality in 2-year hepatoblastoma survivors treated with SIOPEL risk-adapted strategies
verfasst von:
M. Illiano, M. Colinard, S. Taque, B. Mallon, C. Larue, V. Laithier, C. Vérité-Goulard, H. Sudour-Bonnange, C. Faure-Conter, C. Coze, I. Aerts, C. Dumesnil De Maricourt, C. Paillard, S. Branchereau, L. Brugières, B. Fresneau
Erschienen in:
Hepatology International
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Ausgabe 1/2022
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Abstract
Background and aims
Prognosis of hepatoblastoma patients has increased with cisplatin-based chemotherapy and high-quality resection including liver transplant. Consequently current risk-adapted therapeutic strategy aims to reduce long-term side effects in patients with standard risk disease.
Methods
We report long-term mortality and morbidity data concerning 151 2-year hepatoblastoma survivors treated with SIOPEL risk-adapted strategies (sex-ratio M/F = 1.6, median age at diagnosis = 2.6 years [range 0–17.7], median year at diagnosis = 2008 [1994–2017]). Fifty-three patients had loco-regional risk factors VPEFR, 12 were PRETEXT-IV and 30 were metastatic. All received cisplatin and 84 anthracyclines. Twelve had liver transplant. To assess hearing, renal and cardiac functions, audiograms were performed in 116/151 patients (76.8%), glomerular filtration rate in 113/151 (74.8%) and cardiac ultrasound in 65/84 (77.4%) anthracycline-exposed patients.
Results
With a median follow-up of 9.4 years (range 2.1–25.8), four late relapses, one second malignancy (Acute Myeloid Leukemia AML-M5) and two deaths (one from hepatoblastoma, one from AML) occurred. The 10-years event free survival and overall survival probabilities were 95.5% (95% CI 91.9–99.1) and 98.7% (95% CI 96.8–100), respectively. Sixty-eight non-oncologic health-events included 57 cases of hearing loss (including 25 Brock 3–4), three liver cirrhosis, three pre-operative portal cavernoma, two focal nodular hyperplasia, two grade-1 chronic kidney diseases and one asymptomatic cardiac dysfunction were reported. Ototoxicity was significantly associated with cisplatin cumulative dose (OR = 2.07, 95% CI 1.32–3.24, p = 0.001) and carboplatin exposure (OR = 3.14, 95% CI 1.30–7.58, p = 0.01) in multivariable analysis adjusted for sex and age at diagnosis.
Conclusions
With current risk-adapted strategies, hepatoblastoma is a highly curable disease, with very rare relapses, and few late effects except hearing loss which remains a serious condition in these very young patients.