Treatment outcomes and prognostic factors in children with hepatoblastoma using a risk‐stratified approach

Author:

Srinivasan Shyam1ORCID,Prasad Maya1ORCID,Parambil Badira C.1ORCID,Shrimal Anurag2ORCID,Gollamudi Venkata Rama Mohan1,Subramani Vignesh1,Ramadwar Mukta3,Khanna Nehal4,Baheti Akshay D5,Gala Kunal5,Patil Vasundhara5,Laskar Siddhartha4ORCID,Qureshi Sajid6ORCID,Chinnaswamy Girish1

Affiliation:

1. Division of Pediatric Oncology Tata Memorial Centre Homi Bhabha National Institute Mumbai Maharashtra India

2. Institute of Liver Pancreas & Intestine Transplantation Dr Balabhai Nanavati Hospital Mumbai Maharashtra India

3. Department of Pathology Tata Memorial Centre Homi Bhabha National Institute Mumbai Maharashtra India

4. Department of Radiation Oncology Tata Memorial Centre Homi Bhabha National Institute Mumbai Maharashtra India

5. Department of Radiodiagnosis Tata Memorial Centre Homi Bhabha National Institute Mumbai Maharashtra India

6. Department of Pediatric Surgery Tata Memorial Centre Homi Bhabha National Institute Mumbai Maharashtra India

Abstract

AbstractBackgroundNot all the significant progress made in the management of children with hepatoblastoma (HB) has translated into improved outcomes in limited‐resource settings. There are limited data on outcomes in children with HB from India.MethodsAll patients diagnosed with HB between July 2013 and December 2020 were risk‐stratified and treated as per International Liver Tumor Strategy Group (SIOPEL). Patients with standard‐risk HB received cisplatin monotherapy and those with high‐risk HB received alternating cycles of cisplatin and the combination of carboplatin plus doxorubicin. Data regarding demographic details, chemotherapy, surgery, liver transplantation, outcomes, prognostic factors, and toxicity were collected.ResultsOf 157 patients with HB, 117 (74%) were high risk, 31 (20%) were standard risk, and nine (6%) unknown. Patients with standard‐risk disease had excellent outcomes, with 3‐year event‐free survival (EFS) and overall survival (OS) of 96% and 100%, respectively. Among high‐risk HB, six underwent orthotopic liver transplantation of which four were alive at last follow‐up. The 3‐year EFS and OS of patients with high‐risk disease was 56% and 66%, respectively. Outcomes of patients with PRETEXT IV (3‐year EFS: 42%, 3‐year OS: 50%) and metastatic disease (3‐year EFS: 30%, 3‐year OS: 50%) were dismal. Patients with serum alpha‐fetoprotein (AFP) reduction greater than 90% following two courses of chemotherapy had favorable outcomes; 3‐year EFS: 80% versus 58% (p = .013) and 3‐year OS: 95% vs. 68% (p < .01). Only two (6%) of 31 patients with relapse/refractory HB were alive at a median follow‐up of 36 months, and both had received salvage chemotherapy and surgery.ConclusionsWhile children with standard‐risk HB had excellent outcomes, those with high‐risk disease continue to do poorly. Serial monitoring of serum AFP values is a cost‐effective and reliable predictor of outcomes. Orthotopic liver transplantation remains a viable option for inoperable disease in resource‐limited settings as well.

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

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