Successful treatment of acute tumor lysis syndrome associated with transcatheter chemoembolization with large hepatocellular carcinomas: two case reports
Case Report

Successful treatment of acute tumor lysis syndrome associated with transcatheter chemoembolization with large hepatocellular carcinomas: two case reports

Hao Wang, Guang Chen, Haijun Gao, Zhengjia Yi

Department of Radiology, Tianjin First Center Hospital, Tianjin, China

Correspondence to: Guang Chen. Department of Radiology, Tianjin First Center Hospital, No. 24, Fukang Road, Tianjin, China. Email: cg7266@sina.com.

Abstract: Tumor lysis syndrome (TLS) is a potentially lethal complication of cancer therapy, and mostly in patients suffering from hematological disease. Acute TLS is a rare complication in the treatment of solid organ tumors, such as hepatocellular carcinoma (HCC), since the cancer cells of these organs are generally considered to be insensitive to tumor therapy. However, the mortality of acute TLS of solid organs is higher than that of malignant tumors of the blood system. One such reasons is due to the lack of understanding of TLS in solid organs. This study presents two cases of large HCC treated via conventional transarterial chemoembolization (cTACE) and drug-eluting beads transarterial chemoembolization (DEB-TACE), respectively, that developed TLS. The patient developed symptoms of high fever and renal insufficiency following TACE. The diagnosis was confirmed according to the Cairo-Bishop criteria. Fortunately, both patients recovered and were discharged with rehydration, diuresis and timely dialysis. The tumor necrosis rate was higher after DEB-TACE and as TLS may occur more frequently with the increasing application of DEB-TACE, clinicians should pay more attention to it. TLS is a very rare and easily neglected complication that may occur following TACE, which is easily confused with contrast-induced acute renal failure. Appropriate preventive measures should be given to the patient who with high risk factors for TLS. Furthermore, during treatment, the use of Fasturtec may have also played a certain role in the treatment’s efficacy. Dialysis should be carried out as soon as the patients were oliguric, which may serve as the most important factor in saving the patient’s life. Clinical practice has proven that early recognition and treatment can reduce mortality rates due to TLS. This study provides additional references for the management of complications that occur after TACE, thereby improving the clinical outcomes of patients.

Keywords: Hepatocellular carcinoma (HCC); transcatheter chemoembolization (TACE); tumor lysis syndrome (TLS); case report

Submitted Feb 23, 2020. Accepted for publication Aug 14, 2020.

doi: 10.21037/tcr-20-1158

Introduction

Hepatocellular carcinoma (HCC) was the sixth most commonly diagnosed cancer and the fourth leading cause of cancer deaths worldwide in 2018, with approximately 841,000 new cases and 782,000 deaths annually. In addition, the incidence and mortality rates were four times higher than those estimated among men in China (1). conventional transarterial chemoembolization (cTACE) and drug-eluting beads transarterial chemoembolization (DEB-TACE) have been widely accepted as options treatment for unresectable HCC (2).

The major complications after TACE are liver rupture, liver abscess, femoral artery pseudoaneurysm, cholecystitis, biloma, pulmonary embolism, cerebral lipiodol embolism, tumor lysis syndrome (TLS), partial intestinal obstruction, and gallbladder perforation (3). Among these major complications, TLS is easily neglected and may be fatal. It most commonly occurs after chemotherapy in high-grade, rapidly proliferating treatment-sensitive tumors, such as Burkitt’s lymphoma. Only several cases of TACE-associated TLS have been reported in literature to date. The two cases of TLS reported in the present study have their symptoms and treatment specifically introduced. We present the following article in accordance with the CARE reporting checklist (available at http://dx.doi.org/10.21037/tcr-20-1158).

Case presentation

Case 1

A 41-year-old man suffered from dull pain for about 3 months, for which an abdominal computed tomography (CT) showed a 17-cm hepatic tumor in the right lobe with contrast enhancement in the arterial phase and washout in the venous phase without evidence of portal vein thrombosis was noted. Preoperative portal venous embolization (PVE) plus TACE were planned to decrease the tumor burden and promote liver remnant hypertrophy. He was categorized as Child Class A (Child-Pugh score =6). One day after TACE, the patient developed acute renal insufficiency and liver dysfunction. Contrast-induced acute renal failure was suspected in the beginning, however, his symptoms did not improve following adequate resuscitation. Three days after TACE, the patient developed symptoms of high fever and oliguria with elevations of laboratory investigations aminotransferase, bilirubin, uric acid, creatinine, and lactic dehydrogenase levels were noted (Table 1). TLS with acute kidney injury was subsequently diagnosed. The patient’s renal and liver functions gradually improved after hemodialysis (4th day after TACE, for 25 days) and adequate hydration (3,000 mL/m2/d). The patient made a satisfactory recovery on day 40 after TACE, though left lobe hypertrophy after PVE was observed. He was then discharged after undergoing hepatectomy.

Table 1

Serial laboratory data before and after TACE

Laboratory investigation Reference range Baseline After TACE
3 d 5 d 7 d 9 d 12 d 15 d 40 d
ALT 9–50 U/L 52.7 905.7 491.7 312.3 185.6 44.2 25.3 15.4
AST 15–40 U/L 78.2 192.1 102.5 62.2 44.6 65.0 25.1 19.0
TBIL 0–26 μmol/L 8.76 34.48 25.95 25.93 24.62 22.05 21.45 16.86
Cr 59–104 μmol/L 79.8 1,318.9 1,029.4 848.9 848.9 687.2 412.6 98.6
K 3.5–5.3 mmol/L 4.25 7.34 6.42 5.17 4.73 4.68 4.23 4.05
Ca 2.11–2.52 mmol/L 2.26 1.78 1.89 2.09 2.21 2.22 2.20 2.31
Ua 208–428 μmol/L 482.2 1411.5 921.9 734.3 630.5 587.7 498.8 343.3

ALT, alanine aminotransferase; AST, aspartate aminotransferase; TBIL, total bilirubin; Cr, creatinine; K, potassium; Ca, calcium; Ua, uric acid; TACE, transarterial chemoembolization.

Case 2

A 57-year-old man was admitted to our hospital via outpatient clinic after presenting with abdominal dull pain and decreased appetite. On admission, a CT scan of the abdomen found a large tumor palpable in the upper abdomen (largest 17.3 cm × 18.4 cm). Laboratory investigations showed an alanine aminotransferase (ALT) of 11.7 IU/L, total bilirubin of 1.0 mg/dL, creatinine of 66 ng/mL, uric acid of 301.2 ng/mL and alpha-fetoprotein of 334 ng/mL. He was categorized as Child Class A (Child-Pugh score =6). DEB-TACE was suggested as the treatment of choice after discussion with the hepatobiliary team, and 300–500 µm DC Beads (Biocompatibles, Farnham, United Kingdom) were selected and loaded with the chemotherapy drug, epirubicin, which was followed by gelatin sponge particles in order to completely embolize the tumor vessels. The team’s previous experience gave clues into encountering TLS in such a situation, which encompassed performing complex treatment such as adequate hydration, alkalization of urine as well as zyloprim in preventing TLS. Unfortunately, the patient developed symptoms of high fever and renal insufficiency 2 days after TACE. His laboratory profile was checked for TLS immediately. Hyperuricemia (1,041.4 µmol/L), potassium (6.39 mmol/L) and hypocalcemia (2.01 mmol/L) were subsequently noted, and TLS was diagnosed. The patient’s vital signs (heart rate, blood pressure, respiratory rate, urine volume), blood electrolyte level (sodium, potassium, calcium, phosphorus), renal function and blood uric acid level were monitored every 6 hours in the first 24 hours of developing TLS, and was then monitored every day. After treatment using rasburicase (0.2 mg/kg, ivgtt, for 11 days), adequate hydration (3,000 mL/m2/d), diuresis (maintaining urine volume ≥100 mL/m2/h) and correcting the electrolyte disorder (hyperkalemia, hyperphosphatemia and hypocalcemia), the patient’s symptoms improved dramatically. Finally, he was discharged 16 days after TACE without any other complications.

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee(s) and with the Helsinki Declaration (as revised in 2013). Written informed consent was obtained from the patient.

Discussion

TLS was first reported in 1929 and is due to a series of complications caused by the rapid release of intracellular contents and their metabolites into the blood following the rapid dissolution of tumor cells, essentially manifested by electrolyte disorders and metabolic abnormalities. It is characterized by the development of acute kidney injury and other metabolic abnormalities including hyperuricemia, hyperkalemia, hypocalcemia and hyperphosphatemia after effective treatment (4). Hyperuricemia is caused by purine degradation and can lead to precipitation of uric acid crystals in the kidneys’ collecting tubules, resulting in obstructive nephropathy. Moreover, hyperkalemia following potassium effusion from the cytoplasm, may lead to cardiac arrhythmias and arrest. Therefore, TLS can lead to acute kidney failure and is life-threatening. TLS occurs mostly in patients with blood-borne malignancies such as Burkitt’s lymphoma acute lymphocytic leukemia and high-grade non-Hodgkin’s lymphoma following chemotherapy. In addition, TLS can also occur in certain metastatic solid tumors, such as breast cancer, gastrointestinal cancer, neuroblastoma and small cell lung cancer, though its incidence is relatively low. The main factors leading to TLS include: (I) tumor size, growth rate and sensitivity to chemotherapy; and (II) the basic condition of patients, such as dehydration and renal insufficiency, which may lead to a reduction in the clearance rate of cell metabolites (5). TLS is a rare complication of solid organ tumor treatment as these cancers are generally resistant to cytotoxic therapies. Furthermore, the mortality rate in such patients is higher due to delayed diagnosis (6,7).

TACE has been widely accepted as a choice of treatment for advanced HCC and hepatic metastases and has been considered to be an effective treatment modality compared to other methods (2,3). However, TACE possesses various complications, including liver dysfunction, liver abscess, liver rupture, biliary tract injury, renal failure, necrotizing pancreatitis, cerebral lipiodol embolism, and hepatic encephalopathy (8). Besides, TLS is a very rare and easily neglected complication that may occur following TACE. Since 1998, after treatment of HCC, 25 cases of TLS after treatment have been reported in English literature (Table 2), which consist of 15 cases that occurred following TACE/transcatheter arterial embolization (TAE), of which the mortality rate was 40% (6/15) (8-15). The most common cause for acute renal insufficiency is radiocontrast-induced. It is much more common than that induced by TLS, but it also an early clinical sign of TLS. According to the Cairo-Bishop classification (Table 3), the diagnostic criteria of TLS are mainly based on laboratory investigations (16). For high-risk cases after TACE, once the patient has developed acute renal insufficiency, laboratory tests should be promptly performed in order to diagnose TLS and encompass levels of serum potassium, uric acid, calcium, phosphate, lactate dehydrogenase and renal function.

Table 2

Cases of TLS after HCC treatment since 1998

Author, year Age (years) Diagnosis Tumor size (cm) Therapeutic method Clinical outcome
Burney IA, 1998 44 HCC >5 TACE Die
Burney IA, 1998 46 HCC 14×12.3 TACE Recover
Vaisban E, 2003 72 HCC >5 Unknown Die
Lehner SG, 2005 64 HCC 3.2 RFA Die
Lee CC, 2006 62 HCC 8 Thalidomide Recover
Sakamoto N, 2007 55 HCC 17×13×21 TACE Die
Shiba H, 2008 77 HCC >10 TACE Recover
Huang WS, 2009 55 HCC >12 TACE Die
Hsieh PM, 2009 76 HCC >10 TACE Die
Hsieh PM, 2009 56 HCC >5 TACE Recover
Finch MR, 2009 62 HCC Unknown TACE Unknown
Choi DH, 2010 71 HCC 3.5 RFA Recover
Wang K, 2010 54 HCC 15×12×11 TACE Recover
Tsai WL, 2012 51 HCC 17 TACE Recover
Chao CT, 2012 51 HCC 17 TACE Recover
Kekre N, 2012 76 HCC 19×11×8 Unknown Die
Katiman D, 2012 55 HCC 15 TACE Die
Liu PH, 2014 70 HCC >10 TAE Die
Mehrzad R, 2014 70 HCC 3.6×3×3 Unknown Recover
Lin HH, 2014 65 HCC 8.2 TACE Recover
Kim HY, 2014 55 HCC Unknown Sorafenib Unknown
Chieko Kudo, 2015 70 HCC >10 Sorafenib Renal dysfunction
Nishida H, 2013 70 HCC >10 TACE Recover
Jianfei Tu, 2016 58 HCC Unknown Sorafenib Recover
Sardar Zakariya Imam, 2018 49 HCC 11.3×10.1 Sorafenib Die

TLS, tumor lysis syndrome; HCC, hepatocellular carcinoma; TACE, transarterial chemoembolization; RFA, radiofrequency ablation; TAE, transcatheter arterial embolization.

Table 3

Cairo-Bishop criteria for laboratory tumor lysis syndrome

At least two metabolites met within 3 days before the start of the intervention or 7 days afterward as below: Laboratory TLS plus one clinical manifestation as below:
Hyperuricemia: ≥476 mmol/L or 25% increase from baseline Renal injury
Hyperkalemia: ≥6 mmol/L or 25% increase from baseline Cardiac dysrhythmia
Hyperphosphatemia: ≥1.45 mmol/L or 25% increase from baseline Seizures
Hypocalcemia: ≤1.75 mmol/L or 25% decrease from baseline –

TLS, tumor lysis syndrome.

The early stratification of patients for TLS is critical in its effective prevention and treatment. In 2010, an expert consensus panel on TLS developed guidelines for risk stratification and associated TLS prophylaxis recommendations (17). Factors included tumor bulk and stage, large area of tumor necrosis after therapy, renal dysfunction prior to therapy, exposure to nephrotoxic agents, as well as baseline elevations in phosphorus, potassium, and uric acid (18), as well as the two present cases regarding TACE-induced TLS, the patients had large HCC (>5 cm in size) tumor sizes and baseline renal functions within normal limits. The main principles in treating TLS include hydration, correction of metabolic abnormalities, and treatment of acute renal failure (5).

Early recognition and treatment can reduce the mortality rates of TLS. Hemodialysis should be actively used when medications fail to correct metabolic abnormalities, renal insufficiency with associated oliguria/hyperhydration, or uremia (19). The mortality of TLS after TACE is very high (40%), however, the two patients in this study were successfully treated, achieving satisfactory results. Clinical outcomes depended on the cooperation of our team, timely diagnosis and timely treatment. Particularly, for the first patient, dialysis was carried out as soon as the patient was oliguric, which served as the most important factor in the patient’s eventual recovery. Following 40 days of treatment, the patient was finally discharged. Certain limitations exist in the treatment of the two patients. Partial embolization may have prevented TLS; due to our inadequate understanding of TLS, the first patient was not given adequate preventive measures during the perioperative period. The second patient received DEB-TACE since the tumor necrosis rate may have been higher compared to cTACE. Additionally, high-risk factors were present for TLS, such as the tumor size being larger than 5 cm. Due to the clinicians’ experience with the first patient, appropriate preventive measures were given to the second patient. Consequently, after a short period of treatment, the patient recovered. Furthermore, during treatment, the use of Fasturtec may have also played a certain role in the treatment’s efficacy.

Conclusions

TLS may have developed after TACE in the presently reported high-risk patients. Measures should be taken to prevent TLS prior to performing TACE. Laboratory indexes should be examined in a timely manner. Once the TLS is diagnosed, prompt treatment of metabolic abnormalities, including administration of allopurinol and sodium bicarbonate along with adequate hydration should be performed.

Acknowledgments

Funding: None.

Footnote

Reporting Checklist: The authors have completed the CARE reporting checklist. Available at http://dx.doi.org/10.21037/tcr-20-1158

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tcr-20-1158). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work were appropriately investigated and resolved. All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee(s) and with the Helsinki Declaration (as revised in 2013). Written informed consent was obtained from the patient.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.

References

  1. Bray F, Ferlay J, Soerjomataram I, et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2018;68:394-424. Erratum in: CA Cancer J Clin 2020;70:313. [Crossref] [PubMed]
  2. Facciorusso A, Di Maso M, Muscatiello N. Drug-eluting beads versus conventional chemoembolization for the treatment of unresectable hepatocellular carcinoma: A meta-analysis. Dig Liver Dis 2016;48:571-7. [Crossref] [PubMed]
  3. Tu J, Jia Z, Ying X, et al. The incidence and outcome of major complication following conventional TAE/TACE for hepatocellular carcinoma. Medicine (Baltimore) 2016;95:e5606. [Crossref] [PubMed]
  4. Howard SC, Jones DP, Pui CH. The tumor lysis syndrome. N Engl J Med 2011;364:1844-54. Erratum in: N Engl J Med 2018;379:1094. [Crossref] [PubMed]
  5. McBride A, Westervelt P. Recognizing and managing the expanded risk of tumor lysis syndrome in hematologic and solid malignancies. J Hematol Oncol 2012;5:75. P. [Crossref] [PubMed]
  6. Baeksgaard L, Sørensen JB. Acute tumor lysis syndrome in solid tumors--a case report and review of the literature. Cancer Chemother Pharmacol 2003;51:187-92. [Crossref] [PubMed]
  7. Chu HJ, Lee CW, Yeh SJ, et al. Cerebral Lipiodol Embolism in Hepatocellular Carcinoma Patients Treated with Transarterial Embolization/Chemoembolization. PLoS One 2015;10:e0129367. [Crossref] [PubMed]
  8. Vaisban E, Braester A, Mosenzon O, et al. Spontaneous tumor lysis syndrome in solid tumors: really a rare condition?. Am J Med Sci 2003;325:38-40. [Crossref] [PubMed]
  9. Lehner SG, Gould JE, Saad WE, et al. Tumor lysis syndrome after radiofrequency ablation of hepatocellular carcinoma. AJR Am J Roentgenol 2005;185:1307-9. [Crossref] [PubMed]
  10. Lee CC, Wu YH, Chung SH, et al. Acute tumor lysis syndrome after thalidomide therapy in advanced hepatocellular carcinoma. Oncologist 2006;11:87-9. [Crossref] [PubMed]
  11. Sakamoto N, Monzawa S, Nagano H, et al. Acute tumor lysis syndrome caused by transcatheter oily chemoembolization in a patient with a large hepatocellular carcinoma. Cardiovasc Intervent Radiol 2007;30:508-11. [Crossref] [PubMed]
  12. Choi DH, Lee HS. A case of gouty arthritis following percutaneous radiofrequency ablation for hepatocellular carcinoma. World J Gastroenterol 2010;16:778-81. [Crossref] [PubMed]
  13. Wang K, Chen Z. Acute tumor lysis syndrome after transarterial chemoembolization for well-differentiated hepatocellular carcinoma with neuroendocrine features. Onkologie 2010;33:532-5. [Crossref] [PubMed]
  14. Kekre N, Djordjevic B, Touchie C. Spontaneous tumour lysis syndrome. CMAJ 2012;184:913-6. [Crossref] [PubMed]
  15. Katiman D, Manikam J, Goh KL, et al. Tumour Lysis Syndrome: a Rare Complication of Trans-Arterial Chemo-Embolisation with Doxorubicin Beads for Hepatocellular Carcinoma. J Gastrointest Cancer 2012;43:S187-90. [Crossref] [PubMed]
  16. Cairo MS, Bishop M. Tumour lysis syndrome: new therapeutic strategies and classification. Br J Haematol 2004;127:3-11. [Crossref] [PubMed]
  17. Cairo MS, Coiffier B, Reiter A, et al. Recommendations for the evaluation of risk and prophylaxis of tumour lysis syndrome (TLS) in adults and children with malignant diseases: an expert TLS panel consensus. Br J Haematol 2010;149:578-86. [Crossref] [PubMed]
  18. Wilson FP, Berns JS. Onco-nephrology: tumor lysis syndrome. Clin J Am Soc Nephrol 2012;7:1730-9. [Crossref] [PubMed]
  19. Nakamura M, Oda S, Sadahiro T, et al. The role of hypercytokinemia in the pathophysiology of tumor lysis syndrome (TLS) and the treatment with continuous hemodiafiltration using a polymethylmethacrylate membrane hemofilter (PMMA-CHDF). Transfus Apher Sci 2009;40:41-7. [Crossref] [PubMed]
Cite this article as: Wang H, Chen G, Gao H, Yi Z. Successful treatment of acute tumor lysis syndrome associated with transcatheter chemoembolization with large hepatocellular carcinomas: two case reports. Transl Cancer Res 2020;9(10):6516-6521. doi: 10.21037/tcr-20-1158

Article Options

Download Citation

Share