TENIPOSIDE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
Epipodophyllotoxin, 4'-demethyl-,9-(4,6-O-2-thenylidene-beta-D-glucopyranoside) 4'-Demethyl-epipodophyllotoxin-beta-D-thenylidene-glucoside VM-26 NSC-122819 CAS 29767-20-2
IDENTIFIERS
USES/FORMS/SOURCES
In combination with other antineoplastic agents, teniposide is used for induction therapy in patients with refractory childhood acute lymphoblastic leukemia (Prod Info teniposide intravenous injection, 2015).
Teniposide is available in 50 mg/5 mL (10 mg/mL) ampules for injection. Each mL contains 10 mg teniposide, 30 mg benzyl alcohol, 60 mg N,N-dimethylacetamide, 500 mg purified polyoxyl 35 castor oil and 42.7% (v/v) dehydrated alcohol (Prod Info teniposide intravenous injection, 2015).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- USES: Teniposide, a phase-specific cytotoxic agent, is used in combination with other antineoplastic agents for induction therapy in patients with refractory childhood acute lymphoblastic leukemia.
- PHARMACOLOGY: Teniposide acts at the premitotic stage of cell division to prevent cells from entering mitosis by causing dose-dependent single- and double-stranded breaks in DNA and DNA-protein cross-links. It does not intercalate into or bind strongly to DNA. It is cell phase–specific, acting in the late S or early G2 phase of cell division.
- TOXICOLOGY: Teniposide is a semi-synthetic derivative of podophyllotoxin. Overdose effects are likely to occur in rapidly dividing cells (ie, bone marrow, gastrointestinal tract).
- EPIDEMIOLOGY: Teniposide is intended for children only; limited reports of exposure.
OVERDOSE: Severe myelosuppression is anticipated following overdose. Hypotension, metabolic acidosis and somnolence have been reported after 3 to 5 times the usual therapeutic dose. MILD TO MODERATE TOXICITY: Events are anticipated to be similar to adverse effects reported with therapy. Hematologic toxicity includes: myelosuppression, leukopenia, neutropenia, thrombocytopenia and anemia. Gastrointestinal effects include: mucositis, diarrhea and nausea/vomiting. SEVERE TOXICITY: Severe myelosuppression may produce bleeding and infection. Hypersensitivity reactions including anaphylaxis-like symptoms may develop.
ADVERSE EFFECTS: FREQUENT: Myelosuppression is the dose-limiting toxicity. Other adverse effects that may commonly occur include nausea, vomiting, mucositis, and diarrhea. RARE: Hypersensitivity reactions, consisting of chills, fever, tachycardia, flushing, bronchospasm, dyspnea, and blood pressure changes (hypotension or hypertension). Transient hypotension following rapid intravenous administration have been infrequently reported in pediatric patients and may be due to the ethanol content of the formulation.
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
-RANGE OF TOXICITY
MAXIMUM TOLERATED EXPOSURE
- Three children who received doses of 567 mg/m(2), 614 mg/m(2), and 893 mg/m(2) developed hypotension, somnolence and metabolic acidosis, but recovered (McLeod et al, 1991). Effects were believed to be related, at least in part, to the ethanol content of the formulation.
- Based on therapeutic use, dose-limiting bone marrow suppression is the most significant toxicity associated with teniposide (Prod Info teniposide intravenous injection, 2015).
- Carcinogenicity Ratings for CAS29767-20-2 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed EPA (U.S. Environmental Protection Agency, 2011): Not Listed IARC (International Agency for Research on Cancer (IARC), 2016; International Agency for Research on Cancer, 2015; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010a; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2008; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2007; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2006; IARC, 2004): 2A ; Listed as: Teniposide 2A : The agent (mixture) is probably carcinogenic to humans. The exposure circumstance entails exposures that are probably carcinogenic to humans. This category is used when there is limited evidence of carcinogenicity in humans and sufficient evidence of carcinogenicity in experimental animals. In some cases, an agent (mixture) may be classified in this category when there is inadequate evidence of carcinogenicity in humans and sufficient evidence of carcinogenicity in experimental animals and strong evidence that the carcinogenesis is mediated by a mechanism that also operates in humans. Exceptionally, an agent, mixture or exposure circumstance may be classified in this category solely on the basis of limited evidence of carcinogenicity in humans.
NIOSH (National Institute for Occupational Safety and Health, 2007): Not Listed MAK (DFG, 2002): Not Listed NTP (U.S. Department of Health and Human Services, Public Health Service, National Toxicology Project ): Not Listed
TOXICITY AND RISK ASSESSMENT VALUES
- EPA Risk Assessment Values for CAS29767-20-2 (U.S. Environmental Protection Agency, 2011):
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS29767-20-2 (American Conference of Governmental Industrial Hygienists, 2010):
- AIHA WEEL Values for CAS29767-20-2 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS29767-20-2 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS29767-20-2 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS29767-20-2 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS29767-20-2 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS29767-20-2 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS29767-20-2 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS29767-20-2 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS29767-20-2 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS29767-20-2 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS29767-20-2 (EPA, 2005):
LABELS
- NFPA Hazard Ratings for CAS29767-20-2 (NFPA, 2002):
-PERSONAL PROTECTION
SUMMARY
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 29767-20-2.
-PHYSICAL HAZARDS
FIRE HAZARD
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS29767-20-2 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
- NFPA Extinguishing Methods for CAS29767-20-2 (NFPA, 2002):
EVACUATION PROCEDURES
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
- AIHA ERPG Values for CAS29767-20-2 (AIHA, 2006):
- DOE TEEL Values for CAS29767-20-2 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS29767-20-2 (National Research Council, 2010; National Research Council, 2009; National Research Council, 2008; National Research Council, 2007; NRC, 2001; NRC, 2002; NRC, 2003; NRC, 2004; NRC, 2004; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; 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National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; 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62 FR 58840, 1997; 65 FR 14186, 2000; 65 FR 39264, 2000; 65 FR 77866, 2000; 66 FR 21940, 2001; 67 FR 7164, 2002; 68 FR 42710, 2003; 69 FR 54144, 2004):
- NIOSH IDLH Values for CAS29767-20-2 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
- 656.66 (Prod Info teniposide intravenous injection, 2015)
DESCRIPTION/PHYSICAL STATE
- Teniposide is a white to off-white crystalline powder that is insoluble in water and ether, slightly soluble in methanol, and very soluble in acetone and dimethylformamide (Prod Info teniposide intravenous injection, 2015).
PH
- Adjusted to approximately 5 (Prod Info teniposide intravenous injection, 2015)
OCTANOL/WATER PARTITION COEFFICIENT
- Lipophilic agent with a partition coefficient value (octanol/water) of approximately 100 (Prod Info teniposide intravenous injection, 2015).
-REFERENCES
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