| Literature DB >> 28407686 |
Jian-Hong Zhong1,2, Ning-Fu Peng1,2, Xue-Mei You1,2, Liang Ma1,2, Xiao Xiang1, Yan-Yan Wang1, Wen-Feng Gong1,2, Fei-Xiang Wu1,2, Bang-De Xiang1,2, Le-Qun Li1,2.
Abstract
The current clinical reality of tumor stages and primary treatments of hepatocellular carcinoma (HCC) is poorly understood. This study reviewed the distribution of tumor stages and primary treatment modalities among a large population of patients with primary HCC. Medical records of patients treated between January 2003 and October 2013 for primary HCC at our tertiary hospital in China were retrospectively reviewed. A total of 6241 patients were analyzed. The distribution of Barcelona Clinic Liver Cancer (BCLC) stages was as follows: stage 0/A, 28.9%; stage B, 16.2%; stage C, 53.6%; stage D, 1.3%. The distribution of Hong Kong Liver Cancer (HKLC) stages was as follows: stage I, 8.4%; stage IIa, 1.5%; stage IIb, 29.0%; stage IIIa, 10.0%; stage IIIb, 33.6%; stage IVa, 3.4%; stage IVb, 2.5%; stage Va, 0.2%; stage Vb, 11.4%. The most frequent therapy was hepatic resection for patients with BCLC-0/A/B disease, and transarterial chemoembolization for patients with BCLC-C disease. Both these treatments were the most frequent for patients with HKLC I to IIIb disease, while systemic chemotherapy was the most frequent first-line therapy for patients with HKLC IVa or IVb disease. The most frequent treatment for patients with HKLC Va/Vb disease was traditional Chinese medicine. In conclusion, Prevalences of BCLC-B and -C disease, and of HKLC I to IIIb disease, were relatively high in our patient population. Hepatic resection and transarterial chemoembolization were frequent first-line therapies.Entities:
Keywords: hepatic resection; hepatocellular carcinoma; transarterial chemoembolization; treatment selection; tumor stage
Mesh:
Year: 2017 PMID: 28407686 PMCID: PMC5392328 DOI: 10.18632/oncotarget.15433
Source DB: PubMed Journal: Oncotarget ISSN: 1949-2553
Figure 1Frequencies of different primary treatments among patients with primary hepatocellular carcinoma A. without stratification or B-C. with stratification, based on the (B) Barcelona Clinic Liver Cancer system or (C) Hong Kong Liver Cancer system
BSC, best supportive care; NT, no active treatment; RFA, radiofrequency ablation; RT, radiotherapy; SC, systemic chemotherapy; TACE, transarterial chemoembolization; TCM, traditional Chinese medicine.
Barcelona Clinic Liver Cancer staging system [39]
| Stage | Tumor features | Child-Pugh grade | ECOG performance status |
|---|---|---|---|
| BCLC-A | Single tumor or 2-3 tumors ≤3 cm | A or B | 0 |
| BCLC-B | 2-3 tumors with a maximum diameter >3 cm or >3 tumors of any diameter | A or B | 0 |
| BCLC-C | Concomitant or isolated portal vein, hepatic vein, or vena cava tumor thrombus; bile duct tumor thrombi; preoperative tumor rupture; tumor metastasis to the lymph nodes; distant metastases | A or B | 1-2 |
| BCLC-D | Any | C | 3-4 |
ECOG, Eastern Cooperative Oncology Group.
Figure 2Distribution of primary treatments among patients with hepatocellular carcinoma in different stages of the Barcelona Clinic Liver Cancer (BCLC) system: (A) stage A (n = 1805), (B) stage B (n = 1012), (C) stage C (n = 3348), (D) stage D (n = 76)
BSC, best supportive care; NT, no active treatment; RFA, radiofrequency ablation; RT, radiotherapy; SC, systemic chemotherapy; TCM, traditional Chinese medicine; TACE, transarterial chemoembolization.
Hong Kong Liver Cancer staging system [40]
| Stage | Prognostic factor | |||
|---|---|---|---|---|
| ECOG PS | Child-Pugh grade | Tumor status | EVM | |
| I | 0 | A | Early | No |
| IIa | 1a | Ba | Early | No |
| IIb | 0-1 | A | Intermediate | No |
| IIIa | 0-1 | B | Intermediate | No |
| IIIb | 0-1 | A/B | Locally advanced | No |
| IVa | 0-1 | A | Any | Yes |
| IVb | 0-1 | B | Any | Yes |
| Va | 2-4b | Cb | Early | No |
| Vb | 2-4b | Cb | Intermediate or locally advancedc | Yesc |
ECOG PS, Eastern Cooperative Oncology Group performance status; EVM, extrahepatic vascular invasion/metastasis.
a ECOG PS 1 and/or Child-Pugh B.
b ECOG PS 2-4 and/or Child-Pugh C.
c Intermediate/locally advanced tumor or EVM.