| Literature DB >> 34871232 |
Jinpeng Li1, Congcong Shi2, Jutian Shi1, Jinlong Song1, Nan Wang3.
Abstract
ABSTRACT: This study was to identify risk factors affecting postembolization fever (PEF) of CalliSpheres drug-eluting bead transarterial chemoembolization (DEB-TACE) in the treatment of primary hepatocellular carcinoma (HCC).One hundred eighty-eight consecutive patients with HCC who underwent DEB-TACE with fever between June 2017 and May 2019 were included in this retrospective study. The patients were divided into 4 groups based on the severity of posttransarterial chemoembolization (TACE) fever according to the degrees of body temperature. Univariate analysis and multivariate logistics regression were performed to identify potential risk factors for post-TACE fever.In the stepwise multiple regression analysis, pre-TACE blood urea, small particle size and Cental liqefction (P < .05) were independent risk factors of severe post-TACE fever (P < .05, respectively). Portal vein thrombosis (P < .01), Child-Pugh stage (P < .01), and cycles of DEB-TACE (P < .05) were independent risk factors for clinical death, PEF was not associated with clinical death (P = .754) and 6-month survival (P = .524) in the univariate analysis. Moreover, multivariate Cox regression was performed, and Child-Pugh stage (B vs A) (P = .040) and portal vein thrombosis (yes vs no) (P = .033) were independent factors predicting unfavorable overall survival in HCC patients.Pre-TACE blood urea, small particle size, and Cental liqefction were significantly correlated with the occurrence fever after DEB-TACE. Therefore, these factors should be taken into full consideration for the relief of fever. However, PEF after D-TACE was not associated with clinical death and 6-month survival rate.Entities:
Mesh:
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Year: 2021 PMID: 34871232 PMCID: PMC8568383 DOI: 10.1097/MD.0000000000027636
Source DB: PubMed Journal: Medicine (Baltimore) ISSN: 0025-7974 Impact factor: 1.817
The demographic and laboratorial characteristics of all patients.
| Characteristics | |
| Age (yrs) | 54.62 ± 11.25 |
| Gender (male/female) | 118/70 (62.7%/37.3%) |
| Child-Pugh class (A/B) | 145/43 (77.1%/22.9%) |
| ECOG status (0/1) | 157/31 (83.5%/16.5%) |
| Underlying liver disease (HBV/HCV/ none) | 128/12/48 (68.1%/6.3%/25.6%) |
| Dose of epirubicin administrated (mg) | 60 (IQR 60–80) |
| Size of DEB (100–300 μm/300–500 μm/500–700 μm) | 48/135/5 (25.5%/71.8%/2.7%) |
| History of hepatectomy (presence/ absence) | 15/173 (7.9%/92.1%) |
| Albumin (g/L) | 35.3 (IQR 30.4–36.0) |
| Alpha-fetoprotein (>400 μg/L/≤400 μg/L) | 87/101 (46.3%/53.7%) |
| Total serum bilirubin (μmol/L) | 18.6 (IQR 11.5–24.4) |
| PVTT (presence/absence) | 80/108 (42.6%/57.4%) |
| Superselective chemoembolization (presence/absence) | 95/93 (50.5%/49.5%) |
DEB = drug-eluting bead, ECOG = Eastern Cooperative Oncology Group.
Follow-up results based on the mRECIST criteria.
| Groups | n | CR | PR | SD |
| Group A | 46 | 0 | 19 | 10 |
| Group B | 78 | 4 | 37 | 14 |
| Group C | 48 | 18 | 26 | 5 |
| Group D | 16 | 4 | 8 | 1 |
CR = complete remission, mRECIST = modified response evaluation criteria in solid tumors, PR = partial remission, SD = stable disease.
Figure 1Male, 54 years old, HCC, BCLC A stage, refused surgical treatment and received D-TACE. (A) The specimens showed a 7.0 cm × 8.5 cm tumor at the right liver with significant enhancement in the arterial phase. (B) The patient developed chills and fever with a maximum temperature of 39.5°C 2 days after D-TACE, and was treated with anti-inflammatory, hepatoprotective and rehydration fluids for symptomatic management and resolved. Discharged after 6 days of hospitalization for observation. CT shows extensive liquefied necrosis within the tumor with a small amount of gas. (C) CT showed complete necrosis of the tumor in the right lobe of the liver at 1 month postoperative follow-up, mRECIST: CR. BCLC = Barcelona Clinic Liver Cancer, CR = complete remission, HCC = hepatocellular carcinoma, mRECIST = modified response evaluation criteria in solid tumors.
Potential risk factors for post-TACE fever.
| Characteristics | Group A (n = 46) | Group B (n = 78) | Group C (n = 48) | Group D (n = 16) | Univariate | Multivariate |
| Age (yrs) | 55.38 ± 10.45 | 53.78 ± 11.23 | 54.98 ± 10.79 | 53.05 ± 11.27 | .328 | .19 |
| Gender (male/female) | 40/6 (86.9%/13.1%) | 68/10 (87.2%/12.8%) | 43/5 (89.6%/10.4%) | 12/4 (75.0%/25.0%) | .519 | – |
| Child-Pugh class (A/B) | 38/8 (82.6%/17.4%) | 59/19 (75.6%/24.4%) | 38/10 (79.2%/20.8%) | 10/6 (62.5%/37.5%) | .402 | – |
| ECOG status 0/1 | 37/9 (80.4%/19.6%) | 62/16 (79.5%/20.5%) | 41/7 (85.4%/14.6%) | 14/2 (87.5%/12.5%) | .774 | – |
| Underlying liver disease HBV/HCV/none | 30/2/14 (65.2%/4.3%/30.5%) | 60/2/16 (76.9%/2.6%/20.5%) | 28/6/14 (58.3%/12.5%/29.2%) | 10/2/4 (62.5%/12.5/25.0%) | .175 | – |
| PVTT (presence/absence) | 10/36 (21.7%/78.3%) | 36/42 (32.1%/67.9%) | 23/25 (37.5%/62.5%) | 11/5 (31.2%/68.8%) | .003 | – |
| pre-TACE blood urea (mmol/L) | 6.65 ± 5.68 | 5.23 ± 1.79 | 4.54 ± 1.38 | 4.60 ± 1.26 | .025 | |
| Largest tumor size (cm) | 5.8 (IQR 3.8–9.7) | 7.3 (IQR 4.8–11.4) | 6.6 (IQR4.8–10.7) | 6.5 (IQR 4.3–10.5) |
| – |
| Tumor near liver capsule (presence/absence) | 14/32 (30.4%/69.6%) | 28/50 (35.9%/64.1%) | 20/28 (41.7%/58.3%) | 7/9 (43.7%/56.3%) | .648 | – |
| AFP > 400 μg/L/≤400 μg/L | 18/28 (39.1%/60.9%) | 38/40 (48.7%/51.3%) | 25/23 (52.1%/47.9%) | 6/10 (37.5%/62.5%) | .517 | – |
| Albumin (g/L) | 35.6 (IQR 30.1–37.0) | 33.1 (IQR 29.7–35.4) | 32.3 (IQR29.6–34.8) | 31.5 (IQR 28.8–33.7) | .412 | – |
| Total bilirubin (μmol/L) | 17.2 (IQR 11.0–23.2) | 18.3 (IQR 12.5–27.4) | 18.7 (IQR14.0–23.0) | 19.1 (IQR 14.0–23.0) | .376 | – |
| Tumor involved scope (left/right/bilobar) | 3/37/6 (6.5%/80.4%/13.1%) | 12/58/8 (15.4%/74.3%/10.3%) | 8/36/4 (16.7%/75.0%/8.3%) | 3/9/4 (18.7%/56.3%/25.0%) | .370 | – |
| Number of lesions 1/2–3/>3 | 9/20/17 (19.5%/43.5%/37.0%) | 26/30/22 (33.3%/38.5%/28.2%) | 10/25/13 (20.8%/52.1%/27.1%) | 4/8/4 (25.0%/50.0%/25.0%) | .503 | – |
| Dose of epirubicin (mg) | 60 (IQR 60–80) | 60 (IQR 60–80) | 70 (IQR 60–80) | 80 (IQR 60–80) | .676 | – |
| Size of DEB (μm) 100–300/300–500/500–700 | 8/35/3 (17.3%/76.1%/6.6%) | 40/28/10 (51.2%/35.9%/12.9%) | 22/18/8 (45.8%/37.5%/16.7%) | 9/4/3 (56.2%/25.0%/18.8%) | .001 | – |
| Superselective TACE (absence/presence) | 18/28 (39.1%/60.9%) | 40/38 (51.3%/48.7%) | 25/23 (52.1%/47.9%) | 10/6 (62.5%/37.5%) | .349 | – |
| Increase of ALT value after TACE (presence/absence) | 10/36 (21.7%/78.3%) | 58/20 (74.4%/25.6%) | 36/12 (75.0%/25.0%) | 14/2 (87.5%/12.5%) | .001 | – |
AFP = alpha-fetoprotein, ALT = alanine aminotransferase, DEB = drug-eluting bead, ECOG = Eastern Cooperative Oncology Group, TACE = transarterial chemoembolization.
Figure 2Comparison of OS between fever group and no fever group. OS = overall survival.
Multivariate analysis for postembolization fever and clinical death after D-TACE.
| Variables | HR | 95%CI | |
| Multivariate analysis∗ | |||
| pre-TACE blood urea | 3.477 | 1.172–10.319 | .025 |
| Size of DEB | 4.374 | 1.339–14.286 | .015 |
| Univariate analysis† | |||
| Portal vein thrombosis | 2.673 | 1.773–4.034 | <.01 |
| Number of lesions | 3.242 | 1.029–10.215 | .045 |
| Child-Pugh stage (B vs A) | 1.555 | 1.261–1.923 | .006 |
| Cycles of DEB-TACE (≥2 vs 1) | 0.273 | 0.081–0.918 | .036 |
| Multivariate analysis‡ | |||
| Portal vein thrombosis (yes vs no) | 2.490 | 1.078–5.751 | .033 |
| Child-Pugh stage (B vs A) | 2.420 | 1.040–5.629 | .040 |
DEB-TACE = drug-eluting bead transarterial chemoembolization, HR = hazard ratio, TACE = transarterial chemoembolization.
Predictors for postembolization fever.
Risk factors for clinical death.
Predictors for clinical death.