AFP-L3 as a Prognostic Predictor of Recurrence in Hepatoblastoma: A Pilot Study.


Journal

Journal of pediatric hematology/oncology
ISSN: 1536-3678
Titre abrégé: J Pediatr Hematol Oncol
Pays: United States
ID NLM: 9505928

Informations de publication

Date de publication:
01 2021
Historique:
pubmed: 24 10 2020
medline: 7 4 2021
entrez: 23 10 2020
Statut: ppublish

Résumé

The α-fetoprotein (AFP) level is a sensitive biomarker of active hepatoblastoma (HB). This study aimed to clarify whether the Lens culinaris agglutinin A-reactive fraction of AFP (AFP-L3) after complete resection is a prognostic predictor of HB recurrence. Fourteen HB patients who underwent complete resection of HB were divided into the recurrence group (RG, n=4) and the non-recurrence group (NRG, n=10). The AFP level and AFP-L3 before and after radical surgery were compared between the 2 groups. There was no significant difference in AFP levels in the early postoperative period between the 2 groups (P=0.54), and AFP was not an early prognostic factor for HB recurrence. At 2 months after surgery, the AFP-L3 fell below the detection limit only in the NRG (7/10 cases) (NRG=70.0% vs. RG=0%, P=0.03). In addition, there were some cases of recurrence in those whose AFP level decreased to the normal range, but none in those whose AFP-L3 fell below the detection limit. In conclusion, the AFP-L3 decreased earlier than did the AFP level; thus, the AFP-L3 after complete resection may be a predictor for HB recurrence.

Identifiants

pubmed: 33093349
doi: 10.1097/MPH.0000000000001971
pii: 00043426-202101000-00027
doi:

Substances chimiques

AFP protein, human 0
Biomarkers, Tumor 0
Plant Lectins 0
alpha-Fetoproteins 0
lentil lectin 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e76-e79

Références

Meyers RL. Tumors of the liver in children. Surg Oncol. 2007;16:195–203.
Ng K, Mogul DB. Pediatric liver tumors. Clin Liver Dis. 2018;22:753–772.
Lovvorn HN III, Ayers D, Zhao Z, et al. Defining hepatoblastoma responsiveness to induction therapy as measured by tumor volume and serum alpha-fetoprotein kinetics. J Pediatr Surg. 2010;45:121–128.
Kinoshita Y, Tajiri T, Souzaki R, et al. Diagnostic value of lectin reactive alpha-fetoprotein for neoinfantile hepatic tumors and malignant germ cell tumors. J Pediatr Hematol Oncol. 2008;30:447–450.
Tsuchida Y, Kaneko M, Fukui M, et al. Three different types of alpha-fetoprotein in the diagnosis of malignant solid tumors: use of a sensitive lectin-affinity immunoelectrophoresis. J Pediatr Surg. 1989;24:350–355.
Li D, Mallory T, Satomura S. AFP-L3: a new generation of tumor marker for hepatocellular carcinoma. Clin Chim Acta. 2001;313:15–19.
Aoyagi Y, Suzuki Y, Isemura M, et al. The fucosylation index of alpha-fetoprotein and its usefulness in the early diagnosis of hepatocellular carcinoma. Cancer. 1988;61:769–774.
Taketa K, Endo Y, Sekiya C, et al. A collaborative study for the evaluation of lectin-reactive α-fetoproteins in early detection of hepatocellular carcinoma. Cancer Res. 1993;53:5419–5423.
Kobayashi M, Hosaka T, Ikeda K, et al. Highly sensitive AFP-L3% assay is useful for predicting recurrence of hepatocellular carcinoma after curative treatment pre- and postoperatively. Hepatol Res. 2011;41:1036–1045.
Lai Q, Melandro F, Pinheiro RS, et al. Alpha-fetoprotein and novel tumor biomarkers as predictors of hepatocellular carcinoma recurrence after surgery: a brilliant star raises again. Int J Hepatol. 2012;2012:893103.
Park SJ, Jang JY, Jeong SW, et al. Usefulness of AFP, AFP-L3, and PIVKA-II, and their combinations in diagnosing hepatocellular carcinoma. Medicine. 2017;96:e5811.
Kumada T, Nakano S, Takeda I, et al. Clinical utility of Lens culinaris agglutinin-reactive alpha-fetoprotein in small hepatocellular carcinoma: special reference to imaging diagnosis. J Hepatol. 1999;30:125–130.
Yamashiki N, Seki T, Wakabayashi M, et al. Usefulness of Lens culinaris agglutinin A-reactive fraction of alpha-fetoprotein (AFP-L3) as a marker of distant metastasis from hepatocellular carcinoma. Oncol Rep. 1999;6:1229–1232.
Kudo M, Izumi N, Kokudo N, et al. Management of hepatocellular carcinoma in Japan: consensus-based clinical practice guidelines proposed by the Japan Society of Hepatology (JSH) 2010 updated version. Dig Dis. 2011;29:339–364.
Sasaki F, Matsunaga T, Iwafuchi M, et al. Outcome of hepatoblastoma treated with the JPLT-1 (Japanese Study Group for Pediatric Liver Tumor) Protocol-1: a report from the Japanese Study Group for Pediatric Liver Tumor. J Pediatr Surg. 2002;37:851–856.
Hishiki T, Matsunaga T, Sasaki F, et al. Outcome of hepatoblastomas treated using the Japanese Study Group for Pediatric Liver Tumor (JPLT) protocol-2: report from the JPLT. Pediatr Surg Int. 2011;27:1–8.
Fukuzawa H, Urushihara N, Fukumoto K, et al. Can we predict the prognosis of resectable hepatoblastoma from serum alpha-fetoprotein response during preoperative chemotherapy? Pediatr Surg Int. 2012;28:887–891.
Koh KN, Park M, Kim BE, et al. Prognostic implications of serum alpha-fetoprotein response during treatment of hepatoblastoma. Pediatr Blood Cancer. 2011;57:554–560.
Van Tornout JM, Buckley JD, Quinn JJ, et al. Timing and magnitude of decline in alpha-fetoprotein levels in treated children with unresectable or metastatic hepatoblastoma are predictors of outcome: a report from the Children’s Cancer Group. J Clin Oncol. 1997;15:1190–1197.
Kondo R, Kato S, Kaneko K. Congenital hepatoblastoma treated by combination of chemotherapy and resection of the right lobe and caudate lobe. J Jpn Pediatr Soc. 2016;52:982–986.

Auteurs

Insu Kawahara (I)

Department of Pediatric Surgery, Kobe Children's Hospital.

Hiroaki Fukuzawa (H)

Department of Pediatric Surgery, Kobe Children's Hospital.
Department of Surgery, Division of Pediatric Surgery, Kobe University Graduate School of Medicine.

Naoto Urushihara (N)

Department of Pediatric Surgery, Shizuoka Children's Hospital, Shizuoka, Japan.

Yoshiyuki Kosaka (Y)

Department of Hematology and Oncology, Hyogo Prefectural Kobe Children's Hospital, Kobe.

Yasuhiro Kuroda (Y)

Department of Pediatric Surgery, Kobe Children's Hospital.

Yuki Fujieda (Y)

Department of Pediatric Surgery, Kobe Children's Hospital.

Yuki Takeuchi (Y)

Department of Pediatric Surgery, Kobe Children's Hospital.

Kotaro Uemura (K)

Department of Pediatric Surgery, Kobe Children's Hospital.

Tamaki Iwade (T)

Department of Pediatric Surgery, Kobe Children's Hospital.

Yoshitomo Samejima (Y)

Department of Pediatric Surgery, Kobe Children's Hospital.

Keiichi Morita (K)

Department of Pediatric Surgery, Kobe Children's Hospital.

Kosaku Maeda (K)

Department of Pediatric Surgery, Kobe Children's Hospital.
Department of Surgery, Division of Pediatric Surgery, Kobe University Graduate School of Medicine.

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