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Tumor lysis syndrome

 
Oncology Encyclopedia: Tumor Lysis Syndrome

Key Terms: AFP, Beta-HCG, Biopsy, CA 15-3, CA 19-9, CA 27-29, CA 125, CEA, Prognosis, PSA, Sensitivity, Serial measurements, Specificity.

Description

Tumor lysis syndrome is a life-threatening metabolic emergency frequently associated with certain types of tumors (neoplasms). Concentrations of intracellular electrolytes, those that are within the cell, differ from extracellular electrolytes, or those that are outside the cell and in the bloodstream. In tumor lysis syndrome, tumor cells lyse, or break apart, releasing their contents into the blood stream. The result is a dangerous alteration in the normal balance of serum electrolytes—potassium, phosphate and uric acid levels are elevated, while calcium levels are decreased. The changes occur so quickly and can be so dramatic, that immediate death can result.

Causes

Many factors contribute to the development of tumor lysis syndrome. Most of the research performed to date revolves around high-grade non-Hodgkin's lymphoma cases, 40% of which demonstrate laboratory evidence of tumor lysis syndrome. (An estimated 6% demonstrate clinical evidence of the syndrome.) Tumors that carry the highest risk of the development of tumor lysis syndrome are those that are large and bulky, usually greater than eight to ten cm (3-4 in.), and comprised of rapidly dividing cells. In addition, tumors that respond well to treatment are associated with tumor lysis syndrome because treatment results in rupture of a large number of cells.

Most often, the syndrome is associated with blood-based (hematologic) tumors, such as non-Hodgkin's lymphoma, particularly Burkitt's lymphoma, and acute leukemia. Though less likely because of lower rates of cell division, tumor lysis syndrome can also occur in solid tumors such as breast cancer. The Washington Manual of Medical Therapeutics associates the following cancer types with tumor lysis syndrome:

  • Non-Hodgkin's lymphoma (NHL)
  • Acute lymphocytic leukemia (ALL)
  • Acute myelocytic leukemia (AML)
  • Chronic lymphocytic leukemia (CLL)
  • Chronic myelocytic leukemia (CML)
  • Breast cancer
  • Testicular cancer
  • Medulloblastoma
  • Merkel cell carcinoma
  • Neuroblastoma
  • Small cell carcinoma of the lung

Usually, tumor lysis syndrome develops after the administration of combination chemotherapy regimens, but it may also occur spontaneously or as a result of radiation or corticosteroid therapy. Lactic acid dehydrogenase (LDH) is an enzyme found in cells of body tissues. An increase in the LDH level is considered a marker of bulky disease that correlates with the risk of tumor lysis syndrome.

Patients with underlying kidney (renal) dysfunction and/or decreased urine output are at a higher risk of developing tumor lysis syndrome. Without optimal kidney functioning, waste products that build up cannot be excreted in the urine at a high enough rate. Patients with cancer may be predisposed to conditions that increase the risk of renal failure due to increased uric acid buildup. For example, a patient undergoing chemotherapy may experience nausea and vomiting, and may, as a result, be dehydrated, increasing the risk. The same patient may have decreased white blood cell counts, making him or her more susceptible to infections. Many antibiotics adversely affect the kidneys, also increasing the risk.

Treatments

Treatment is aimed at prevention and supportive care, with the main goals being to prevent renal failure and severe electrolyte imbalances. Patients at risk receive treatment on an inpatient basis to allow for close monitoring by medical personnel. At all times, patients should have reliable intravenous access. Prior to initiating treatment, a patient's hydration status and electrolyte levels are carefully evaluated. If there are abnormalities, a treatment delay may be considered, though this is not always an option.

Laboratory tests are done frequently to monitor levels of calcium, potassium, phosphate, magnesium and uric acid. A typical hospital protocol may require blood be drawn for these tests every two to six hours over the course of two to three days. Following are prevention and management strategies for each of the major electrolyte imbalances, hyperuricemia, hyperkalenia, hyperphosphatemia, and hypocalcemia.

Hyperuricemia is a medical term used to describe an abnormal increase of uric acid levels in the blood that can lead to acute renal failure. There are several methods employed to prevent kidney damage—aggressive hydration being a major focus. Intravenous (IV) hydration is started before treatment and continues throughout to maintain a urine output of 100 to 200 milliliters per hour (ml/hr). Medications called diuretics, such as furosemide or acetazolamide, are given to help increase urine output when necessary.

Urine may be alkalized to prevent uric acid buildup. Alkalization can be accomplished by adding sodium bicarbonate to the patient's IV fluid. For example, the basic maintenance IV fluid may consist of 5% dextrose in 0.25 normal saline, to which sodium bicarbonate, in amounts ranging from 50 to 200 milliequivalents (mEq—the total number of charges of electrolytes in solution), may be added. Urine pH is routinely tested, and the sodium bicarbonate is periodically increased or decreased to maintain a pH level between 7 and 8.

Urine alkalinization is somewhat controversial. If urine is too alkaline, calcium phosphate crystal formation may occur, increasing the likelihood of renal failure. However, it is generally believed that if urine output levels are appropriately maintained, calcium phosphate will be diluted, and the possibility of crystal formation will diminish.

Patients at risk for tumor lysis syndrome may also be given allopurinol prophylactically. One dose of 600 milligrams (mg) may be given the day before treatment, followed by 300 mg once a day for the remainder of treatment days. Allopurinol is effective because it inhibits the formation of uric acid. In 2004, a new drug called rasburicase became available in the United States. It prevents the damaging effects of tumor lysis syndrome with fewer side effects.

Hyperkalemia is a medical term used to describe an abnormal increase of potassium levels in the blood that can cause dangerous abnormalities in heart rhythms, heart attack, and muscle weakness. Frequent monitoring with electrocardiography (EKG) is recommended in patients at risk for tumor lysis syndrome so that alterations in the electrical activity of the heart can be caught early. Potassium-rich foods may also be restricted to prevent already elevated levels from increasing. Sometimes, medications such as Kayexalate are administered to help reduce potassium levels.

Hyperphosphatemia is a medical term used to describe an abnormal increase on phosphate levels in the blood that can cause neuromuscular irritability and worsen kidney function. Malignant cells may contain up to four times as much phosphate as non-malignant cells. Patients experiencing acute tumor lysis syndrome may be instructed to reduce their dietary intake of phosphate. In addition, they may be given medications that bind to phosphate, thereby inhibiting its absorption in the intestines.

Hypocalcemia is a medical term used to describe an abnormal decrease in calcium levels in the blood that can cause muscle spasms (tetany), muscle cramps, and seizures. A calcium supplement may be required.

Dialysis is a procedure used to normalize electrolyte imbalances through the diffusion and ultrafiltration of fluid. Potassium, for example, can be separated and filtered from fluid, bringing levels back to a safer range. Hemodialysis is a procedure that removes waste products through the blood. Dialysis can alternatively be performed through the peritoneum, the tissue that lines the abdominal area and surrounds the organs in what is called peritoneal dialysis. Because peritoneal dialysis does not clear phosphate and urate as efficiently, and because it is not feasible in patients with abdominal tumors, hemodialysis is the preferred method. A doctor who specializes in nephrology will generally examine a high-risk patient before cancer treatment begins, to prepare for the possibility of dialysis treatment. In some cases, dialysis is started as a preventive measure, either before or during chemotherapy treatment.

Resources

Books

Abeloff, A. Clinical Oncology. 2nd ed. New York: Churchill Livingstone, Inc., 2000.

Goldman, L. Cecil Textbook of Medicine. 21st ed. St Louis, MO: W.B. Saunders Company, 2000.

Lee, G., et al., editors. Wintrobe's Clinical Hematology. Baltimore, MD: Williams & Wilkins Publishing, 1999.

Periodicals

Meyer, M. "Renal Replacement Therapies." Critical Care Clinics January 2000: 29-58.

"Rasburicase Mitigates the Nephropathic Effects of Tumor Lysis Syndrome." Cancer Weekly June 29, 2004: 229.

—Tamara Brown, R.N.; Teresa G. Odle

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Medical Dictionary: tumor lysis syndrome
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n.

A syndrome characterized by abnormally high levels of phosphates, potassium, and uric acid and by abnormally low levels of calcium in the blood following induction chemotherapy of malignant tumors, possibly caused by the release of intracellular products by cell lysis.

Wikipedia: Tumor lysis syndrome
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Tumor lysis syndrome
Classification and external resources
ICD-9 277.8, 995.29
DiseasesDB 32051
eMedicine med/2327
MeSH [1]

In medicine (oncology and hematology), tumor lysis syndrome (TLS) is a group of metabolic complications that can occur after treatment of cancer,[1] usually lymphomas and leukemias, and sometimes even without treatment. These complications are caused by the break-down products of dying cancer cells and include hyperkalemia, hyperphosphatemia, hyperuricemia and hyperuricosuria, hypocalcemia, and consequent acute uric acid nephropathy and acute renal failure.

Contents

Cause and risk factors

The most common tumors associated with this syndrome are poorly differentiated lymphomas, such as Burkitt's lymphoma, and leukemias, such as acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML). Other cancers (such as melanoma) have also been associated with TLS but are less common.

Usually, the precipitating medication regimen includes combination chemotherapy, but those patients with lymphoma and ALL can be affected with steroid treatment alone, and sometimes without any treatment—in this case the condition is referred to as "spontaneous tumor lysis syndrome".

Symptoms and pathogenesis

Hyperkalemia. Potassium is mainly an intracellular ion. High turnover of tumor cells leads to spill of potassium into the blood. Symptoms usually do not manifest until levels are high (> 7 mmol/dL) [normal 3.5-5.0 mmol/dL] and they include

  • cardiac conduction abnormalities (can be fatal)
  • severe muscle weakness or paralysis

Hyperphosphatemia. Like potassium, phosphates are also predominantly intracellular. Hyperphosphatemia causes acute renal failure in tumor lysis syndrome, because of deposition of calcium phosphate crystals in the renal parenchyma.

Hypocalcemia. Because of the hyperphosphatemia, calcium is precipitated to form calcium phosphate, leading to hypocalcemia. Symptoms of hypocalcemia include (but are not limited to):

  • tetany
  • seizures
  • mental retardation / dementia
  • parkinsonian (extrapyramidal) movement disorders
  • papilledema
  • emotional instability / agitation / anxiety
  • myopathy

Hyperuricemia[2] and Hyperuricosuria. Acute uric acid nephropathy (AUAN) due to hyperuricosuria has been a dominant cause of acute renal failure but with the advent of effective treatments for hyperuricosuria, AUAN has become a less common cause than hyperphosphatemia. Two common conditions related to excess uric acid, gout and uric acid nephrolithiasis, are not features of tumor lysis syndrome.

Pretreatment spontaneous tumor lysis syndrome. This entity is associated with acute renal failure due to uric acid nephropathy prior to the institution of chemotherapy and is largely associated with lymphomas and leukemias. The important distinction between this syndrome and the post-chemotherapy syndrome is that spontaneous TLS is not associated with hyperphosphatemia. One suggestion for the reason of this is that the high cell turnover rate leads to high uric acid levels through nucleobase turnover but the tumor reuses the released phosphate for growth of new tumor cells. In post-chemotherapy TLS, tumor cells are destroyed and no new tumor cells are being synthesized.

Diagnosis

TLS should be suspected in patients with large tumor burden who develop acute renal failure along with hyperuricemia (> 15 mg/dL) or hyperphosphatemia (> 8 mg/dL). (Most other acute renal failure occurs with uric acid < 12 mg/dL and phosphate < 6 mg/dL). Acute uric acid nephropathy is associated with little or no urine output. The urinalysis may show uric acid crystals or amorphous urates. The hypersecretion of uric acid can be detected with a high urine uric acid - creatinine ratio > 1.0, compared to a value of 0.6-0.7 for most other causes of acute renal failure.

Cairo-Bishop Definition

In 2004, Cairo and Bishop defined a classification system for tumor lysis syndrome.[3]

  • Laboratory tumor lysis syndrome: abnormalitiy in two or more of the following and occurs within 3 days before or 7 days after chemotherapy.
    • uric acid > 8 mg/dL or 25% increase
    • potassium > 6 meq/L or 25% increase
    • phosphate > 4.5 mg/dL or 25% increase
    • calcium < 7 mg/dL or 25% decrease
  • Clinical tumor lysis syndrome: laboratory tumor lysis syndrome plus one or more of the following:
    • increase serum creatinine (1.5 times upper limit of normal)
    • cardiac arrhythmia or sudden death
    • seizure

A grading scale (0-5) is used depending on the presence of lab TLS, serum creatinine, arrhythmias, or seizures.

Prevention

Patients about to receive chemotherapy for a cancer with high cell turnover rate, especially lymphomas and leukemias, should receive prophylactic oral or IV allopurinol (a xanthine oxidase inhibitor, which inhibits uric acid production) as well as adequate IV hydration to maintain a high urine output (> 2.5 L/day).

Rasburicase (Uricase) is an alternative to allopurinol[4][5] and is reserved for patients who are high-risk in developing TLS. It is a synthetic urate oxidase enzyme and acts by degrading uric acid.[6]

Alkalinization of the urine with acetazolamide or sodium bicarbonate is controversial. Routine alkalinization of urine above pH of 7.0 is not recommended. Alkalinization is also not required if uricase is used.

Treatment

Treatment is first targeted at the specific metabolic disorder.

Acute renal failure prior to chemotherapy. Since the major cause of acute renal failure in this setting is uric acid build-up, therapy consists of rasburicase to wash out excessive uric acid crystals as well as a loop diuretic and fluids. Sodium bicarbonate should not be given at this time. If the patient does not respond, hemodialysis may be instituted, which is very efficient in removing uric acid, with plasma uric acid levels falling about 50% with each six hour treatment.

Acute renal failure after chemotherapy. The major cause of acute renal failure in this setting is hyperphosphatemia, and the main therapeutic means is hemodialysis. Forms of hemodialysis used include continuous arteriovenous hemodialysis (CAVHD), continuous venovenous hemofiltration (CVVH), or continuous venovenous hemodialysis (CVVHD).

References

  1. ^ Davidson MB, Thakkar S, Hix JK, Bhandarkar ND, Wong A, Schreiber MJ (April 2004). "Pathophysiology, clinical consequences, and treatment of tumor lysis syndrome". Am. J. Med. 116 (8): 546–54. doi:10.1016/j.amjmed.2003.09.045. PMID 15063817. http://linkinghub.elsevier.com/retrieve/pii/S0002934303007253. 
  2. ^ Rampello E, Fricia T, Malaguarnera M (August 2006). "The management of tumor lysis syndrome". Nat Clin Pract Oncol 3 (8): 438–47. doi:10.1038/ncponc0581. PMID 16894389. http://dx.doi.org/10.1038/ncponc0581. 
  3. ^ Cairo MS, Bishop M (October 2004). "Tumour lysis syndrome: new therapeutic strategies and classification". Br. J. Haematol. 127 (1): 3–11. doi:10.1111/j.1365-2141.2004.05094.x. PMID 15384972. http://dx.doi.org/10.1111/j.1365-2141.2004.05094.x. 
  4. ^ Mayne N, Keady S, Thacker M (February 2008). "Rasburicase in the prevention and treatment of tumour lysis syndrome". Intensive Crit Care Nurs 24 (1): 59–62. doi:10.1016/j.iccn.2007.06.002. PMID 17698360. http://linkinghub.elsevier.com/retrieve/pii/S0964-3397(07)00055-9. 
  5. ^ Coiffier B, Mounier N, Bologna S, et al. (December 2003). "Efficacy and safety of rasburicase (recombinant urate oxidase) for the prevention and treatment of hyperuricemia during induction chemotherapy of aggressive non-Hodgkin's lymphoma: results of the GRAAL1 (Groupe d'Etude des Lymphomes de l'Adulte Trial on Rasburicase Activity in Adult Lymphoma) study". J. Clin. Oncol. 21 (23): 4402–6. doi:10.1200/JCO.2003.04.115. PMID 14581437. http://www.jco.org/cgi/pmidlookup?view=long&pmid=14581437. 
  6. ^ Cammalleri L, Malaguarnera M (2007). "Rasburicase represents a new tool for hyperuricemia in tumor lysis syndrome and in gout". Int J Med Sci 4 (2): 83–93. PMID 17396159. PMC: 1838823. http://www.medsci.org/v04p0083.htm. 

 
 

 

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Oncology Encyclopedia. Gale Encyclopedia of Cancer. Copyright © 2006 by The Gale Group, Inc. All rights reserved.  Read more
Medical Dictionary. The American Heritage® Stedman's Medical Dictionary Copyright © 2002, 2001, 1995 by Houghton Mifflin Company Read more
Wikipedia. This article is licensed under the Creative Commons Attribution/Share-Alike License. It uses material from the Wikipedia article "Tumor lysis syndrome" Read more