Clinical and laboratory characteristics and prognosis of patients with hepatocellular carcinoma

Author(s):  
Hong Chuyen Nguyen Thi

Purpose: We investigated the influence of baseline characteristics of patients with hepatocellular carcinoma (HCC) on prognosis. Methods: A Retrospective descriptive study on patients with HCC was carry out at the Oncology Department of Hue University of Medicine and Pharmacy Hospital and Hue Central Hospital (HCH), Viet Nam, from Oct 2015 to Dec 2019. Demographic, laboratory, tumor characteristics, and performance status were determined before treatment. Predictors of survival were identified using the Kaplan - Meir test and the Cox model. Result: A total of 261 patients, 87.4% male; median age was 58.4; 80,1% of patients admitted to hospital because of right upper quadrant pain. 45.2% ECOG 0, 51.7% ECOG 1; AFP > 400 ng/mlhas 67.4%. The most robust predictors of survival were tumor size, ECOG, portal vein tumor thrombus, Barcelona Clinic Liver Cancer (BCLC), initial treatment. Overall survival in patients with HCC was 9.0 months. In a multivariate analysis: BCLC and initial treatment modalities were independent predictors of survival. Conclusions - Patients with HCC had a poor survival with a median of nine months. Five easily measurable clinical variables were significant predictors of survival in patients with HCC.

Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. 4637-4637
Author(s):  
Joshua Lukenbill ◽  
Paul Elson ◽  
Matt Kalaycio

Abstract Abstract 4637 Purine analogs, including fludarabine and pentostatin, are frequently used as first-line agents once therapy of CLL commences. However, as a result of such treatment, approximately 20% of patients become myelosuppressed to the extent that a full course of therapy cannot be given. Myelosuppression was defined as absolute neutrophil count < 1500/uL and/or platelets < 100,000 for two consecutive laboratory findings, occurring anytime from the initiation of purine analog chemotherapy until one month following last cycle of chemotherapy. We sought to determine the consequences of such myelosuppression by retrospective analysis of all patients with CLL undergoing initial treatment that included purine analogs between 2003 and 2008 at the Cleveland Clinic. We identified 45 patients meeting these criteria. The median age at treatment was 63 (range 41 to 82) and all met standard criteria for the diagnosis and treatment of CLL. Of these 45 patients, 19 could not complete all 6 cycles of planned treatment. Of these 45 patients, 9 (20% of the 45 patients analyzed) could not complete treatment due to persisting myelosuppression. The clinical characteristics of these 9 patients are compared to the other 36 patients in the table. N Median Age Rai 3-4 Performance Status CD38+ (≥20%) *Zap70+ (≥15%) Myelosuppressed 9 66 7 0.4 8 4 Other patients 36 61 17 0.6 21 10 * data available for only 7 myelosuppressed and 31 other patients We attempted to correlate CD38 and Zap-70 expression with pre-treatment risk factors (age, Rai stage, and performance status), but found no association, except in the case of CD38 positivity in relation to PS ≥ 1 (p = 0.04). Cytogenetics were unknown for a majority of patients and therefore were not analyzed. The 9 patients remained myelosuppressed for a median of 10 months (range 2 to 41), and 6 of these 9 patients were platelet transfusion dependent at some point (compared to 1 of 36 patients of the non-myelosuppressed group, p <0.001). Of the 9 myelosuppressed patients, 6 recovered hematopoiesis after a median of 11 months (range 7–41), 4 relapsed with CLL after a median of 29 months (range 12 – 51), and 4 died. Of the 4 who died, 2 died while remaining myelosuppressed. Our data corroborates the findings of others that approximately 20% of patients treated with purine analogs will experience enough myelosuppression to reduce the number of cycles that can be delivered. Although we could not identify many significant pre-treatment predictors of such myelosuppression, we did observe that some patients remained myelosuppressed for long periods of time, often with adverse consequences, including transfusion dependence, relapse, and death. Efforts to avoid prolonged myelosuppression by better patient selection and strict attention to recommendations for dose reductions, rather than dose delays, may lessen the incidence of such consequences. Disclosures: Kalaycio: Genzyme: Speakers Bureau; Genetech: Speakers Bureau; Cephalon: Speakers Bureau.


2016 ◽  
Vol 34 (4_suppl) ◽  
pp. 305-305
Author(s):  
Feng JIN Zhang ◽  
JUN ZHI Shu ◽  
YI CHUN Xie ◽  
QI LI ◽  
Hong XI Jin ◽  
...  

305 Background: Many liver staging systems that include the tumor stage and the extent of liver function have been developed. However, Prognosis assessment for hepatocellular carcinoma (HCC) remains controversial. In this study, the performances of 7 staging systems were compared in a cohort of patients with HCC who underwent non-surgical treatment. Methods: A total of 196 consecutive patients with HCC who underwent non-surgical treatment seen between January 1, 2004, and December 31, 2007, were included. Performances of TNM sixth edition, Okuda, Barcelona Clinic Liver Cancer (BCLC), Cancer of the Liver Italian Program (CLIP), Chinese University Prognostic Index (CUPI), Japan Integrated Staging (JIS), and China integrated score (CIS) have been compared and ranked using concordance index (c-index). Predictors of survival were identified using univariate and multivariate Cox model analyses. Results: The median survival time for the cohort was 7.6 months (95% CI 5.6-9.7). The independent predictors of survival were performance status (P <.001), serum sodium (P <.001), alkaline phosphatase (P <.001), tumor diameter greater than 5 cm (P =.001), portal vein invasion (P <.001), lymph node metastasis (P =.025), distant metastasis (P =.004). CUPI staging system had the best independent predictive power for survival when compared with the other six prognostic systems. Performance status and serum sodium improved the discriminatory ability of CUPI. Conclusions: In our selected patient population whose main etiology is hepatitis B, CUPI was the most suitable staging systems in predicting survival in patients with unresectable HCC. BCLC was the second top-ranking staging system. CLIP, JIS, CIS, and TNM sixth edition were not helpful in predicting survival outcome, and their use is not supported by our data. Clinical trial information: 1103-10.


2015 ◽  
Vol 49 (10) ◽  
pp. 878-884 ◽  
Author(s):  
Chia-Yang Hsu ◽  
Po-Hong Liu ◽  
Yun-Hsuan Lee ◽  
Cheng-Yuan Hsia ◽  
Yi-Hsiang Huang ◽  
...  

2020 ◽  
Vol 38 (4_suppl) ◽  
pp. 319-319
Author(s):  
Haydee Cristina Verduzco-Aguirre ◽  
Mónica Isabel Meneses Medina ◽  
Ana Karen Valenzuela ◽  
Vanessa Rosas Camargo ◽  
Luis Guillermo Anaya Sánchez ◽  
...  

319 Background: gastric cancer is common in Mexico. Evaluation of treatment strategies is greatly important in early gastric cancer. National institutions rarely report their outcomes, limiting feedback and policy improvements. Methods: single-center retrospective review of patients with histologically confirmed localized gastric cancer diagnosed from Jan 2005 to Dec 2017. Overall survival (OS) and recurrence-free survival (RFS) were estimated by Kaplan-Meier curves and compared with log-rank rest. A p value < 0.05 was significant. Results: we included 78 cases, median age 63 years, 52.6% men. Surgery was the initial treatment in 46 patients (59%) and 87% achieved R0 resection. Adjuvant treatment was administered to 63% of patients. 29 patients (37.2%) started perioperative chemotherapy with 86.2% of them being resected, and 75.9% having R0 resection. 13 patients (44.8%) also received postoperative chemotherapy. Better performance status (p=0.036) and lower albumin levels (p=0.039) were found in patients with initial surgery vs those with perioperative chemotherapy. At the time of surgery, most patients had stage III disease in both groups but 5 patients had M1 disease despite negative initial laparoscopy in the chemotherapy group and 5 patients did not require aduvant tx given early stage in the surgery first group. Median OS and RFS are reported in table. Conclusions: Most patients in our center undergo initial surgery. We report a differential survival according to initial treatment. More advanced disease in chemotherapy first group may explain differences. Given non-random assignment, we could not show survival benefit of chemotherapy treated patients. [Table: see text]


1998 ◽  
Vol 16 (3) ◽  
pp. 864-871 ◽  
Author(s):  
J Y Blay ◽  
T Conroy ◽  
C Chevreau ◽  
A Thyss ◽  
N Quesnel ◽  
...  

PURPOSE The impact of treatment options on survival and late neurologic toxicity was investigated in a series of patients with primary cerebral lymphoma (PCL) and no known cause of immunosuppression. PATIENTS AND METHODS Prognostic factors for survival and treatment-induced late neurotoxicity were investigated in a retrospective series of 226 patients with PCL. RESULTS With a median follow-up of 76 months, the median overall survival was 16 months and 5-year survival was 19%. In a univariate analysis, age greater than 60 years, performance status, CSF protein level greater than 0.6 g/L, involvement of corpus callosum or subcortical grey structures, detectable lymphoma cells in CSF, increased serum lactate dehydrogenase (LDH), but not histological subtype, were significantly correlated with a poor survival. Treatment with chemotherapy versus radiotherapy alone (P = .05), high-dose methotrexate (HDMTX; P = .0007), and cytarabine (P = .04) correlated with a better survival in univariate analysis. Using the Cox model, age, performance status, and CSF protein were independently correlated with survival. After adjustment of these factors, treatment with an HDMTX-containing regimen remained the only treatment-related factor independently correlated with survival (P = .01). The projected incidence of treatment-induced late neurotoxicity was 26% at 6 years in this series, with a median survival from the diagnosis of late neurotoxicity of 12 months. Treatment with radiotherapy followed by chemotherapy was the only parameter correlated with late neurotoxicity in multivariate analysis (relative risk, 11.5; P = .0007). CONCLUSION Patients with PCL treated with regimens that included HDMTX followed by radiotherapy have an improved survival, but not a higher risk of late neurotoxicity as compared with other treatment modalities in this series.


2021 ◽  
Author(s):  
Mahmoud Aryan ◽  
Ellery Altshuler ◽  
Xia Qian ◽  
Wei Zhang

Hepatocellular Carcinoma (HCC) is the fifth most common cancer and represents the fourth most common cause of cancer related death worldwide. Treatment of HCC is dictated based upon cancer stage, with the most universally accepted staging system being the Barcelona Clinic Liver Cancer (BCLC) staging system. This system takes into account tumor burden, active liver function, and patient performance status. BCLC stage C HCC is deemed advanced disease, which is often characterized by preserved liver function (Child-Pugh A or B) with potential portal invasion, extrahepatic spread, cancer related symptoms, or decreased performance status. Sorafenib has been the standard treatment for advanced HCC over the past decade; however, its use is limited by low response rates, decreased tolerance, and limited survival benefit. Researchers and clinicians have been investigating effective treatment modalities for HCC over the past several years with a focus on systemic regimens, locoregional therapy, and invasive approaches. In this systemic review, we discuss the management of advanced HCC as well as the ongoing research on various treatment opportunities for these patients.


2016 ◽  
Vol 29 (2) ◽  
pp. 139 ◽  
Author(s):  
Adélia Simão ◽  
Raquel Silva ◽  
Lurdes Correia ◽  
Filipe Caseiro Alves ◽  
Armando Carvalho ◽  
...  

Sorafenib is a multi-targeted tyrosine kinase inhibitor, with antiangiogenic and antiproliferative properties, approved for the treatment of advanced hepatocellular carcinoma. It induces a significant increase in the median overall survival, despite a complete response to treatment being rare. We report a clinical case of a 60-year-old male with hepatic cirrhosis, Child-Pugh class A and performance status 0, and advanced hepatocellular carcinoma. The primary tumor measured 17 x 8 cm and had diffuse intrahepatic metastization, extensive lung and left adrenal invasion, as well as thrombosis of inferior vena cava, with projection to the right atrium. This patient showed a rapid and complete response to sorafenib, evaluated by mRECIST (modified Response Evaluation Criteria in Solid Tumors), that remains after three years of treatment.


2020 ◽  
Vol 38 (15_suppl) ◽  
pp. 4090-4090
Author(s):  
Christos Stelios Karapetis ◽  
Heshan Liu ◽  
Michael Sorich ◽  
Jack Fiskum ◽  
Axel Grothey ◽  
...  

4090 Background: EGFR mAbs have become incorporated into clinical practice for the management of mCRC over the last decade. KRAS and NRAS mutations are used as predictive biomarkers and BRAF V600E mutations are associated with an adverse prognosis. The observed TE within biomarker subpopulations has varied between studies. Methods: IPD from randomized trials with head-to-head comparison between EGFR mAb versus no EGFR mAb (chemotherapy alone or BSC) in mCRC, across all lines of therapy (first, second and later), were pooled. Biomarker subpopulations are defined in the table. Overall survival (OS) and progression-free survival (PFS) were compared between groups by Cox model, stratified by studies and adjusted by age, gender, and performance status. TEs were estimated by adjusted hazard ratio (HRadj) and 95% confidence interval (CI). Within each biomarker subgroup, EGFR mAb efficacy was explored according to multiple exploratory factors, including line of therapy, type of backbone chemo, gender, sidedness and site of metastasis. Interaction tests were performed. P-values < 0.01 were considered statistically significant to account for multiple comparisons. Results: 5729 pts from 8 studies with data available for ≥ 1 biomarker were analysed. PFS benefits (median 9.2 mos in EGFR mAbs, 8.0 mos in no EGFR mAbs) were confirmed in triple-WT pts, but not for OS (refer to table). No OS/PFS benefits were observed for pts with any of the MT tumors. Exploratory analyses showed a potential detrimental TE of EGFR mAbs in KRAS MT mCRC with liver metastasis (OS: HRadj 1.22, p = .003, pinteraction .0056; PFS: HRadj 1.24, p = .0009, pinteraction .0008). These results were confirmed within the subgroup of pts with all 3 biomarkers available. Conclusions: This is the largest IPD analysis to explore the predictive value of RAS/BRAF biomarkers in mCRC. Our findings demonstrate that there is no evidence of efficacy of EGFR mAbs in KRAS, BRAF and/or NRAS MT mCRC. EGFR mAbs might have a detrimental effect in KRAS MT mCRC with liver metastases. [Table: see text]


2014 ◽  
Vol 53 (02) ◽  
pp. 46-53 ◽  
Author(s):  
S. Ezziddin ◽  
K. Wilhelm ◽  
R. Fimmers ◽  
U. Spengler ◽  
H. Palmedo ◽  
...  

SummaryThis study investigated the efficacy of 131iod- ine-labeled lipiodol (1311-lipiodol) as a palliative therapy, evaluated overall survival (OS) across Barcelona Clinic Liver Cancer (BCLC) stages, and determined the main prognostic factors influencing OS in patients with hepatocellular carcinoma (HCC). Patients, methods: We retrospectively analyzed 57 (44 men; mean age, 65.7 years; mean activity per session, 1.6 GBq; mean cumulative activity in patients with >1 sessions, 3.9 GBq) HCC patients who underwent 1311-lipiodol therapy. A majority of patients exhibited Child-Pugh class B (53.6%) disease and a good Eastern Cooperative Oncology Group performance status (0-1; 72%). Multinodular disease was observed in 87.7% patients, bilobar disease in 73%, and portal vein occlusion (PVO) in 54%. Furthermore, 21.1% patients were staged as BCLC B and 59.6 % as BCLC C. All patients were followed until death. Results: The median OS was 6.4 months, which varied significantly with disease stage (median OS for BCLC A, B, C, and D was 29.4, 12.0, 4.6, and 2.7 months, respectively; p = 0.009); Child-Pugh score and class; presence of ascites, PVO, or extrahepatic disease; largest lesion size; favourable treatment response; international normalized ratio, baseline albumin and alpha-fetopro- tein levels. Patients with a Child-Pugh A liver disease had a longer OS. Conclusion: Currently, different treatment modalities for HCC include radioembolization, transarterial chemoemboliz- ation, and systemic therapy with sorafenib; however, 1311-lipiodol therapy remains a feasible alternative for patients without a favourable response to other therapies, particularly for patients with Child-Pugh A liver cirrhosis.


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