Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Pixantrone
Drug ID BADD_D01786
Description Pixantrone is an aza-anthracenedione and DNA intercalator which inhibits topoisomerase II. It is similar in structure to anthracyclines such as mitoxantrone, but exerts fewer toxic effects on cardiac tissue. [2] The lower cardio-toxic effects of pixantrone may be explained, in part, by its redox inactivity [3]. Pixantrone does not bind iron and promotes the formation of reactive oxygen species to a lesser degree than other anthracyclines. It also inhibits doxorubicinol formation in human myocardium. [3] As a result, it is believed to be less cardiotoxic while still exerting efficacy. Pixantrone was designed to treat relapsed or refractory aggressive non-Hodgkin's lymphoma(NHL) in patients who have failed two prior lines of therapy. [2] For patients suffering from NHL, first line therapies consist of anthracycline containing multi-drug treatments which unfortunately are known to cause irreversible myocardial tissue damage. Patients refractory to treatment, or those who relapse, are discouraged from further anthracycline use due to cumulative cardiotoxicity. Pixantrone dimaleate, administered intravenously, was designed by Cell Therapeutics Incorporated as an alternative second line therapy in refractory or relapsed NHL. It is currently being tested in Phase III trials. [2] Although pixantrone has not yet received FDA approval in the United States, it has been granted conditional marketing approval by the European Union. Conditional approval was granted by the European Medicines Agency after a phase III EXTEND trial of patients with NHL showed that pixantrone was tolerable and that it resulted in significantly higher complete response rate and progression free survival in comparison to other single chemotherapy agents. However, it is notable that the EXTEND trial was stopped early, leaving the statistical significance of the results in question. Based on this uncertainty, in 2009, the FDA ultimately rejected Cell Therapeutic's initial application for accelerated approval for pixantrone use in relapsed or refractory NHL. Another phase III trial, PIX-R, is now ongoing to clarify pixantrones place in therapy. It will compare pixantrone efficacy to that of gemcitabine. [2]
Indications and Usage Pixantrone dimaleate has also been investigated as a treatment for acute myelogenous leukemia, diffuse large B-cell lymphoma, follicular lymphoma, metastatic breast cancer, low grade small lymphocytic lymphomas and general metastatic cancers.
Marketing Status Not Available
ATC Code L01DB11
DrugBank ID DB06193
KEGG ID D05522
MeSH ID C086548
PubChem ID 134019
TTD Drug ID D0Q4OW
NDC Product Code Not Available
Synonyms pixantrone | 5,8-bis(2-aminoethylamino)-2-azaanthracene-9,10-dione | 6,9-bis((2-aminoethyl)amino)benzo(g)isoquinoline-5,10-dione | 5,8-bis((2-aminoethyl)amino)-2-aza-anthracene-9,10-dione | 6,9-AEA-BIQDO | BBR 2778 | BBR2778 | BBR-2778
Chemical Information
Molecular Formula C17H19N5O2
CAS Registry Number 144510-96-3
SMILES C1=CC(=C2C(=C1NCCN)C(=O)C3=C(C2=O)C=NC=C3)NCCN
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Rhinorrhoea22.02.05.010--
Septic shock24.06.02.011; 11.01.11.004--Not Available
Sinus tachycardia02.03.03.010--
Skin discolouration23.03.03.005--Not Available
Skin disorder23.03.03.007--Not Available
Skin ulcer24.04.03.007; 23.07.03.003--
Sleep disorder19.02.04.001--Not Available
Somnolence19.02.05.003; 17.02.04.006--
Stomatitis07.05.06.005--
Tachycardia02.03.02.007--Not Available
Thrombocytopenia01.08.01.002--Not Available
Urethral disorder20.07.01.002--Not Available
Urinary tract disorder20.08.01.001--Not Available
Vein discolouration24.03.02.004--Not Available
Vein disorder24.03.02.015--Not Available
Vertigo17.02.12.002; 04.04.01.003--
Vomiting07.01.07.003--
Weight decreased13.15.01.005--
Cardiotoxicity12.03.01.007; 02.01.01.002--Not Available
Spontaneous penile erection21.03.01.010--Not Available
Left ventricular dysfunction02.04.02.011--
Injection site coldness12.07.03.023; 08.02.03.023--Not Available
Blood phosphorus increased13.11.01.016--Not Available
Ejection fraction decreased13.14.02.003--
Musculoskeletal chest pain15.03.04.012; 22.09.01.001--
Lymphatic disorder01.09.01.003--Not Available
Musculoskeletal stiffness15.03.01.005--Not Available
Protein urine present13.13.02.006--Not Available
Musculoskeletal discomfort15.03.04.001--Not Available
Paraesthesia oral17.02.06.008; 07.05.03.003--Not Available
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