Long-term morbidity and mortality in 2-year hepatoblastoma survivors treated with SIOPEL risk-adapted strategies

被引:6
作者
Illiano, M. [1 ]
Colinard, M. [2 ]
Taque, S. [3 ]
Mallon, B. [1 ]
Larue, C. [1 ]
Laithier, V [4 ]
Verite-Goulard, C. [5 ]
Sudour-Bonnange, H. [6 ,7 ]
Faure-Conter, C. [8 ]
Coze, C. [9 ]
Aerts, I [10 ]
De Maricourt, C. Dumesnil [11 ]
Paillard, C. [12 ]
Branchereau, S. [13 ]
Brugieres, L. [1 ]
Fresneau, B. [1 ,14 ]
机构
[1] Univ Paris Saclay, Dept Pediat Oncol, Gustave Roussy, 114 Rue Edouard Vaillant, F-94805 Villejuif, France
[2] CHU Reims, Dept Pediat Oncol, Reims, France
[3] CHU Rennes, Dept Pediat, Rennes, France
[4] Hop Jean Minjoz, Dept Pediat Oncol, Besancon, France
[5] CHU Bordeaux, Dept Pediat Oncol, Bordeaux, France
[6] Ctr Oscar Lambret, Dept Pediat, Lille, France
[7] Ctr Oscar Lambret, AYA Unit, Lille, France
[8] Inst Pediat Hematol & Oncol IHOPe, Lyon, France
[9] Aix Marseille Univ, Hop Enfants La Timone, AP HM, Dept Pediat Oncohematol, Marseille, France
[10] Inst Curie, SIREDO Care Innovat & Res Children Adolescents &, Paris, France
[11] Hop Charles Nicolle, Dept Pediat Oncol, Rouen, France
[12] Hop Hautepierre, Dept Pediat Oncol, Strasbourg, France
[13] CHU Kremlin Bicetre, Dept Pediat Surg, Le Kremlin Bicetre, France
[14] Canc & Radiat, CESP, Unit 1018 INSERM, Villejuif, France
关键词
Late effects; Cisplatin; Carboplatin; Doxorubicin; Ototoxicity; Cirrhosis; Nephrotoxicity; Cardiotoxicity; Cavernoma; SMN; CHILDHOOD-CANCER; BILIARY COMPLICATIONS; INTERNATIONAL SOCIETY; CISPLATIN; DOXORUBICIN; CHILDREN; SURGERY; LIFE;
D O I
10.1007/s12072-021-10251-1
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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.
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收藏
页码:125 / 134
页数:10
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