Literature DB >> 28683459

Natural History of T1N0M0 Hepatocellular Carcinoma: Large-Scale Study in the United States.

Humaid O Al-Shamsi1, Reham Abdel-Wahab, Manal M Hassan, Ahmed S Shalaby, Ibrahim Dahbour, Sahin Lacin, Armeen Mahvash, Bruno C Odisio, Ravi Murthy, Rony Avritscher, Mohamed E Abdelsalam, Asif Rashid, Jean-Nicolas Vauthey, Thomas A Aloia, Claudius Conrad, Yun Shin Chun, Sunil Krishnan, Prajnan Das, Eugene J Koay, Hesham M Amin, James C Yao, Ahmed O Kaseb.   

Abstract

BACKGROUND: Hepatocellular carcinoma (HCC) prognosis depends on clinicopathological features in addition to the treatment provided. We aimed to assess the natural history of TNM stage I HCC tumors which received different treatment over a period of 20 years.
METHODS: Between 1992 and 2011, a total of 397 stage I HCC patients were included. Detailed information was retrieved from MD Anderson Cancer Center patients' medical records. The Kaplan-Meier method was used to calculate patients' overall survival (OS). Cox regression analysis was used to calculate the estimated hazard ratio and 95% confidence interval of different prognostic factors.
RESULTS: Out of 397 patients, 67.5% were males, 42.8% had hepatitis-related HCC, and 59.7% had underlying cirrhosis. After adjustment for confounding factors, we found that all therapeutic modalities were associated with a significant mortality rate reduction with an OS of 63, 42.03, 34.3, and 22.1 months among patients treated with surgery, ablation, local, and systemic therapy, respectively. A restricted analysis of cirrhotic and noncirrhotic patients showed that ablative and local therapy were significantly associated with a longer OS compared to systemic therapy.
CONCLUSION: TNM stage I HCC patients have a favorable prognosis regardless of the type of treatment. Notably, ablative and local therapy significantly improved OS compared to systemic therapy.
© 2017 S. Karger AG, Basel.

Entities:  

Keywords:  Hepatocellular carcinoma; Stage I; TNM

Mesh:

Substances:

Year:  2017        PMID: 28683459      PMCID: PMC6743737          DOI: 10.1159/000455957

Source DB:  PubMed          Journal:  Oncology        ISSN: 0030-2414            Impact factor:   2.935


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