Hubungan Kadar Alpha Fetoprotein dengan Derajat Keparahan Karsinoma Hepatoseluler

Authors

  • Favian R. Fadillah Universitas Sam Ratulangi
  • Linda W. A. Rotty Universitas Sam Ratulangi
  • Cerelia E. C. Sugeng Universitas Sam Ratulangi

DOI:

https://doi.org/10.35790/msj.v7i1.54829

Abstract

Abstract: Hepatocellular carcinoma (HCC) is the most common primary liver tumor and ranks third as the highest cause of cancer-related mortality. Hepatitis B virus infection is a risk factor found in 50% of subjects, while the remaining 50% have non-hepatitis B and non-hepatitis C etiologies. Alpha-fetoprotein (AFP) and the Barcelona Clinic Liver Cancer (BCLC) are the most widely used biological marker and disease staging system. This study aimed to determine the relationship between AFP levels and BCLC stages in HCC patients at Prof. Dr. R. D. Kandou Hospital, Manado. This was a retrospective and analytical study with a cross-sectional approach using patient medical records as samples. The results showed a total of 56 HCC patients, consisting of 43 males and 13 females, obtained using consecutive sampling techniques. Each variable was categorized into two groups: ≤200 ng/ml and >200 ng/ml for AFP; and operable (BCLC 0/A) and non-operable (BCLC B/C/D) for BCLC staging. There were two patients (3.6%) in the operable category and 54 patients (96.4%) in the non-operable category. Fisher's exact test results showed no significant relationship between AFP levels and disease severity in HCC patients (p=0.228). In conclusion, there is no significant relationship between alpha-fetoprotein levels and disease severity in hepatocellular carcinoma patients.

Keywords: alpha-fetoprotein levels; hepatocellular carcinoma; BCLC staging

 

 Abstrak: Karsinoma hepatoseluler (KHS) merupakan tumor primer pada hati yang paling umum terjadi dan menyandang peringkat ke-3 sebagai penyumbang angka kematian tertinggi yang disebabkan oleh kanker. Infeksi virus hepatitis B merupakan faktor risiko yang ditemukan pada 50% subjek dan sisanya (50%) memiliki etiologi non hepatitis B dan non hepatitis C. Alpha fetoprotein (AFP) dan Barcelona Clinic Liver Cancer (BCLC) merupakan penanda biologis dan sistem pemeringkatan derajat penyakit yang paling banyak digunakan saat ini. Penelitian ini bertujuan untuk mengetahui hubungan antara kadar AFP dengan derajat BCLC pada subjek KHS di RSUP. Prof. Dr. R. D. Kandou Manado. Penelitian ini merupakan retrospektif analitik dengan pendekatan potong lintang yang menggunakan rekam medis pasien sebagai sampel penelitian. Hasil penelitian mendapatkan 56 pasien KHS terdiri dari 43 laki-laki dan 13 perempuan dengan menggunakan teknik consecutive sampling. Masing-masing variabel dikategorikan menjadi dua kelompok, yaitu ≤200 ng/ml dan >200 ng/ml untuk AFP, serta operable (BCLC 0/A) dan non-operable (BCLC B/C/D) untuk staging BCLC. Terdapat dua subjek (3,6%) untuk kategori operable dan 54 subjek (96,4%) untuk kategori non-operable. Hasil uji Fisher’s exact menunjukkan bahwa tidak terdapat hubungan bermakna antara kadar AFP dengan derajat keparahan penyakit pada pasien KHS (p=0,228). Simpulan penelitian ini ialah tidak terdapat hubungan bermakna antara kadar alpha fetoprotein dengan derajat keparahan penyakit pada pasien karsinoma hepatoseluler.

Kata kunci: kadar alpha-fetoprotein; karsinoma hepatoseluler; BCLC staging

Author Biographies

Favian R. Fadillah, Universitas Sam Ratulangi

Program Studi Pendidikan Dokter Fakultas Kedokteran Universitas Sam Ratulangi, Manado, Indonesia

Linda W. A. Rotty, Universitas Sam Ratulangi

Bagian Ilmu Penyakit Dalam Fakultas Kedokteran Universitas Sam Ratulangi, Manado, Indonesia

Cerelia E. C. Sugeng, Universitas Sam Ratulangi

Bagian Ilmu Penyakit Dalam Fakultas Kedokteran Universitas Sam Ratulangi, Manado, Indonesia

References

Vogel A, Meyer T, Sapisochin G, Salem R, Saborowski A. Hepatocellular carcinoma. Lancet. 2022;400(10360):1345–62. Doi: 10.1016/S0140-6736(22)01200-4

Liu Z, Jiang Y, Yuan H, Fang Q, Cai N, Suo C, et al. The trends in incidence of primary liver cancer caused by specific etiologies: Results from the Global Burden of Disease Study 2016 and implications for liver cancer prevention. J Hepatol. 2019;70(4);674-83. Doi: 10.1016/j.jhep.2018.12.001

Torimura T, Iwamoto H. Treatment and the prognosis of hepatocellular carcinoma in Asia. Liver Int. 2022;42(9):2042–54. Doi: 10.1111/liv.15130

Tzartzeva K, Obi J, Rich NE, Parikh ND, Marrero JA, Yopp A, et al. Surveillance imaging and alpha fetoprotein for early detection of hepatocellular carcinoma in patients with cirrhosis: a meta-analysis. Gastroenterology. 2018;154(6):1706-18.e1. Doi: 10.1053/j.gastro.2018.01.064

Yang JD, Hainaut P, Gores GJ, Amadou A, Plymoth A, Roberts LR. A Global view of hepatocellular carcinoma: trends, risk, prevention and management. Nat Rev Gastroenterol Hepatol. 2019;16(10):589–604. Doi: 10.1038/s41575-019-0186-y

Akinyemiju T, Abera S, Ahmed M, Alam N, Alemayohu MA, Allen C. The burden of primary liver cancer and underlying etiologies from 1990 to 2015 at the global, regional, and national level. JAMA J Am Med Assoc. 2017;3(12):1683–91. Doi: 10.1001/jamaoncol.2017.3055

Kanwal F, Kramer J, Asch SM, Chayanupatkul M, Cao Y, El-Serag HB. Risk of hepatocellular cancer in HCV patients treated with direct-acting antiviral agents. Gastroenterology. 2017;153(4):996-1005.e1. Doi: http://dx.doi.org/10.1053/j.gastro.2017.06.012

Estes C, Razavi H, Loomba R, Younossi Z, Sanyal AJ. Modeling the epidemic of nonalcoholic fatty liver disease demonstrates an exponential increase in burden of disease. Hepatology. 2018;67(1):123–33. Doi: 10.1002/hep.29466

Liu C, Wu J, Chang Z. Trends and age-period-cohort effects on the prevalence, incidence and mortality of hepatocellular carcinoma from 2008 to 2017 in Tianjin, China. Int J Environ Res Public Health. 2021;18(11):1-14. Doi: 10.3390/ijerph18116034

Parikh ND, Mehta AS, Singal AG, Block T, Marrero JA, Lok AS. Biomarkers for the early detection of hepatocellular carcinoma. Cancer Epidemiol Biomarkers Prev. 2020;29(12):2495–503. Doi: 10.1158/1055-9965.EPI-20-0005

Jearth V, Patil PS, Mehta S, Sundaram S, Seth V, Goel M, et al. Correlation of clinicopathological profile, prognostic factors, and survival outcomes with baseline alpha-fetoprotein levels in patients with hepatocellular carcinoma: a biomarker that is bruised but not broken. J Clin Exp Hepatol. 2022;12(3):841–52. Doi: https://doi.org/10.1016/j.jceh.2021.11.006

Darmadi D, Ruslie RH. Association between prothrombin induced by vitamin K absence-II (PIVKA- II) and Barcelona Clinic Liver Cancer (BCLC) stage, tumor size, portal venous thrombosis in hepatocellular carcinoma patients. Sains Malaysiana. 2021;50(2):475–80. Doi: 10.17576/jsm-2021-5002-18

Petrick JL, Florio AA, Znaor A, Ruggieri D, Laversanne M, Alvarez CS, et al. International trends in hepatocellular carcinoma incidence, 1978–2012. Int J Cancer. 2020;147(2):317–30. Doi: 10.1002/ijc.32723

Galle PR, Foerster F, Kudo M, Chan SL, Llovet JM, Qin S, et al. Biology and significance of alpha ‐ fetoprotein in hepatocellular carcinoma. 2019;39(12):2214–29. Doi: 10.1111/liv.14223

Liang T, He Y, Mo S, Chen Z, Liao X, Zhou X, et al. Gender disparity in hepatocellular carcinoma recurrence after curative hepatectomy. Ann Hepatol. 2022;27(3):100695. Doi: https://doi.org/ 10.1016/j.aohep.2022.100695

Nevola R, Tortorella G, Rosato V, Rinaldi L, Imbriani S, Perillo P, et al. Gender differences in the pathogenesis and risk factors of hepatocellular carcinoma. Biology (Basel). 2023;12(7):1–25. Doi: 10.3390/biology12070984

Prenner S, Kulik L. 46 - Hepatocellular carcinoma. Zakim and Boyer’s Hepatology (7th ed). Elsevier Inc. 2023. p. 668-92.e9. Doi: http://dx.doi.org/10.1016/B978-0-323-37591-7.00046-X

Oh JH, Lee J, Yoon EL, Jeong SW, Kim SS, Chon YE, et al. Regular alpha-fetoprotein tests boost curative treatment and survival for hepatocellular carcinoma patients in an endemic area. Cancers (Basel). 2024;16(1):150. Doi: 10.3390/cancers16010150

Hamayun A, Gardezi SAA, Niazi NK, Tirmizi SH, Rafique I Sadiq R. Evaluation of co-relation between BCLC stage of HCC and alpha-fetoprotein levels. 2022;16(08):104–6. Doi: 10.53350/pjmhs22168104

Nursriyanti D, Kartini A, Mutmainnah. Analysis of alfa-fetoprotein as a staging determiner of hepatocellular carcinoma progresivity. Indonesian Journal of Clinical Pathology and Medical Laboratory. 2023;29(3):268–71. Doi: 10.24293/ijcpml.v29i3.2044

Chen X, Wong STC. Cancer Theranostics. United States: Elsevier; 2014. Doi: 10.1016/B978-0-12-407722-5.00001-3

Kojima K, Takata A, Vadnais C, Otsuka M, Yoshikawa T, Akanuma M, et al. MicroRNA122 is a key regulator of α-fetoprotein expression and influences the aggressiveness of hepatocellular carcinoma. Nat Commun. 2011;2(1). Doi: 10.1038/ncomms1345

Soresi M, Magliarisi C, Campagna P, Leto G, Bonfissuto G, Riili A. Usefulness of alpha-fetoprotein in the diagnosis of hepatocellular carcinoma. Anticancer Res. 2003;23(2C):1747–53. Available from: https://pubmed.ncbi.nlm.nih.gov/12820452/

Aprilicia G, Bantas K, Syarif S, Kalista KF. Evaluasi Perbandingan Serum Alfa-Fetoprotein pada Pasien Karsinoma Hepatoseluler dengan Etiologi Non-Viral. J Penyakit Dalam Indones. 2021;8(1):37. Doi: 10.7454/jpdi.v8i1.566

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Published

2024-06-23

How to Cite

Fadillah, F. R., Rotty, L. W. A., & Sugeng, C. E. C. (2024). Hubungan Kadar Alpha Fetoprotein dengan Derajat Keparahan Karsinoma Hepatoseluler . Medical Scope Journal, 7(1), 74–79. https://doi.org/10.35790/msj.v7i1.54829

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