Savene 20 mg/ml powder for concentrate and diluent for solution for infusion.
Each vial contains 500 mg dexrazoxane (589 mg dexrazoxane hydrochloride). Each ml contains 20 mg of dexrazoxane after reconstitution with 25 ml of Savene diluent. Excipients with known effects: Diluent bottle: Potassium 98 mg/500 ml or 5.0 mmol/l Sodium 1.61 g/500 ml or 140 mmol/l For the full list of excipients, see section 6.1.
Powder for concentrate and diluent for solution for infusion. Powder vial: White to off-white lyophilisate. Diluent bottle: Clear isotonic solution (295 mOsml/l, pH approx. 7.4).
Savene is indicated in adults for the treatment of anthracycline extravasation.
Savene must be administered under the supervision of a physician experienced in the use of anti- cancer medicinal products.
Posology
Treatment should be given once daily for 3 consecutive days. The recommended dose is: Day 1: 1000 mg/m2 Day 2: 1000 mg/m2 Day 3: 500 mg/m2 The first infusion should be initiated as soon as possible, within the first six hours after the accident. Treatment Day 2 and Day 3 should start at the same hour (+/- 3 hours) as Day 1. There is no experience with dose reduction/increase or modification of the schedule in the treatment of extravasation. For patients with a body surface area of more than 2 m2 the single dose should not exceed 2000 mg.
Renal impairment
No studies have been performed in patients with impaired renal function and treatment use in such patients is not recommended (see section 4.4). Decreased renal function may lead to decreased rate of elimination and prolonged systemic exposure.
Hepatic impairment
Dexrazoxane has not been studied in patients with impaired hepatic function and its use in such patients is not recommended (see section 4.4).
Elderly
Safety and efficacy have not been evaluated in the elderly and the use of dexrazoxane in such patients is not recommended.
Paediatric population
The safety and efficacy of Savene in children below the age of 18 years has not been established and no data are available.
Method of administration
For intravenous use after reconstitution and dilution. For instructions on the reconstitution and dilution of Savene before administration, see section 6.6. The indicated dose should be administered as an intravenous infusion over 1-2 hours into a large vein of an extremity or area other than the one affected by the extravasation. Cooling procedures such as ice packs should have been removed from the area at least 15 min before the Savene administration in order to allow sufficient blood flow.
Hypersensitivity to the active substance or to any of the excipients.
Women of childbearing potential not using contraceptive measures (see section 4.6).
Breast-feeding (see section 4.6).
Concomitant vaccination with yellow fever vaccine (see section 4.5).
Continuous monitoring
Local examination should be performed on a regular basis after treatment until resolution. If t here i s suspicion o f e xtravasation by vesicant c ompounds ot her t han a nthracyclines t hrough t he same I V a ccess, e.g. v incristine, mitomycin, an d v inorelbine, S avene wo uld n ot b e ef fective ag ainst the effects from these compounds. Since Savene will be administered to patients undergoing cytotoxic therapy with anthracyclines its cytotoxic potential (especially resulting in reversible haematological toxicity with a nadir occurring on days 11-12) will therefore add to that of the other chemotherapy administered. Haematological monitoring should therefore be undertaken regularly.
Hepatic and renal-function monitoring
Since liver dysfunction (increases in transaminases and bilirubin) may occur (especially after doses of above 1 000 mg/m2 dexrazoxane), it is recommended that routine liver function tests be performed before each administration of dexrazoxane in patients with known liver function disorders. Since renal dysfunction may decrease the rate of elimination of dexrazoxane, patients with initial impaired renal function should be monitored for signs of haematological toxicity.
Potassium and sodium contents
Savene diluent contains potassium (98 mg/500 ml). This must be taken into consideration by patients with reduced kidney function or patients on a controlled potassium diet. Plasma potassium level must be closely monitored in patients at risk of hyperkalaemia. It also contains sodium (1.61 g/500 ml) which may be harmful to patients on a controlled sodium diet.
Concomitant use contraindicated: Yellow fever vaccine: Risk of fatal generalised vaccinial disease (see section 4.3). Concomitant use not recommended:
Other live attenuated vaccines: risk of systemic, possible fatal disease. This risk is increased in subjects who are already immunosuppressed by their underlying disease. Use an inactivated vaccine where this exists (poliomyelitis) (see section 4.4).
Dimethylsulfoxide (DMSO) should not be used in patients who are administered dexrazoxane to treat anthracycline extravasation (see section 5.3)
Phenytoin: cytotoxic agents may reduce the absorption of phenytoin leading to an exacerbation of convulsions. Dexrazoxane is not recommended in combination with phenytoin.
Concomitant use to assess carefully: Ciclosporine, tacrolimus: Excessive immunosuppression with risk of lymphoproliferative disease. Interactions common to all cytotoxics: Due to an increased thrombotic risk in patients with malignant diseases, the use of anticoagulants treatment is frequent. Patients treated with anticoagulants should be monitored more frequently as cytotoxic agents may interact with oral anticoagulants. Dexrazoxane may add to the toxicity induced by the chemotherapy cycle during which the accident took place, requiring careful monitoring of haematological parameters (see section 4.4). Interaction specific to dexrazoxane: When tested in five major cytochrome P450 isoenzymes CYP1A, CYP2C9, CYP2C19, CYP2D6 and CYP3A4, none of these were inhibited by dexrazoxane.
Women of childbearing potential/Contraception in males and females
Women of childbearing potential must use contraceptive measures during treatment and must inform their doctor immediately if they become pregnant (see section 4.3). Since dexrazoxane possesses mutagenic activity, men being treated with dexrazoxane are advised not to father a child during and up to three months after treatment and/or should use contraceptives for the same time period.
Pregnancy
There are no data from the use of dexrazoxane in pregnant women. Dexrazoxane may cause foetal harm when administered to pregnant women. Few pre-clinical data are available with respect to reproductive toxicity (see section 5.3). Dexrazoxane should not be administered to pregnant women unless clearly necessary.
Breast-feeding
It is not known whether dexrazoxane is excreted in human milk. Because of the potential for serious adverse reactions in breast-fed infants exposed to dexrazoxane, mothers must discontinue breast- feeding during Savene therapy (see section 4.3).
Dizziness, somnolence and syncope have been reported in a few patients included in Savene studies TT01 and TT02 (see section 4.8). Dexrazoxane is considered to have a limited influence on the ability to drive and use machines.
A number of published reports comprising more than 1000 patients have demonstrated a uniform pattern of dose dependent adverse reactions. Most common adverse reactions are nausea/vomiting, bone marrow suppression (neutropenia, thrombocytopenia), injection site reactions, diarrhoea, stomatitis and increase in hepatic transaminases (ALT/AST). All adverse reactions have been rapidly reversible. The following information is based on two clinical studies, TT01 and TT02, of Savene administered to extravasation patients already receiving cycles of chemotherapeutic agents. The adverse reactions were those typically seen with standard chemotherapy and also with dexrazoxane: Nausea/vomiting in about one third of the patients, neutropenia and thrombocytopenia in about half of the patients, more rarely increased concentration of liver enzymes (ALT/AST). Adverse reactions observed in the two studies are listed below.
Incidence of adverse reactions (MedDRA) in studies TT01 and TT02 (n=80 patients)
(Note that numbers for Blood and Lymphatic System Disorders are described in a separate table of laboratory examinations) Adverse reactions reported are listed according to the following frequency: Very common (>=1/10) Common (>=1/100 to <1/10) Uncommon (>=1/1,000 to <1/100) Rare (>=1/10,000 to <1/1,000) Very rare (<1/10,000)
| System Organ Classes (SOC) | Frequency | Adverse reactions |
| Infections and infestations | Very common | Postoperative infection |
| Common | Infection | |
| Neutropenic infection | ||
| Metabolism and nutrition disorders | Common | Decreased appetite |
| Nervous system disorders | Common | Dizziness |
| Sensory loss | ||
| Syncope | ||
| Tremor | ||
| Vascular disorders | Common | Phlebitis |
| Superficial thrombophlebitis | ||
| Venous thrombosis limb | ||
| Respiratory, thoracic and mediastinal disorders | Common | Dyspnoea |
| Pneumonia | ||
| Gastrointestinal disorders | Very common | Nausea |
| Common | Vomiting | |
| Diarrhoea | ||
| Stomatitis | ||
| Dry mouth | ||
| Skin and subcutaneous tissue disorders | Common | Alopecia |
| Pruritus | ||
| Musculoskeletal and connective tissue disorders | Common | Myalgia |
| Reproductive system and breast disorders | Common | Vaginal haemorrhage |
| General disorders and administration site conditions | Very common | Injection site pain |
| Common | Pyrexia | |
| Injection site phlebitis | ||
| Injection site erythema | ||
| Fatigue | ||
| Injection site induration | ||
| Injection site swelling | ||
| Oedema peripheral | ||
| Somnolence | ||
| Investigations | Common | Weight decreased |
| Injury, poisoning and procedural complications | Common | Wound complication |
Incidence of laboratory abnormalities in TT01 and TT02 (n=80 patients)
| Lab test | No of patients with post baseline value | CTC grade 3-4 | |
| N | % | ||
| Haemoglobin | 80 | 2 | 2.5% |
| WBC | 80 | 36 | 45.0% |
| Neutrophils | 78 | 36 | 46.2% |
| Platelets | 80 | 17 | 21.3% |
| Sodium (Hypo) | 79 | 5 | 6.3% |
| Potassium (Hypo) | 79 | 2 | 2.5% |
| Potassium (Hyper) | 79 | 0 | 0.0% |
| Alkaline Phosphatase | 77 | 0 | 0.0% |
| Bilirubin | 77 | 1 | 1.3% |
| AST | 57 | 2 | 3.5% |
| ALT | 71 | 3 | 3.9% |
| Creatinine | 76 | 2 | 2.6% |
| LDH | 78 | 0 | 0.0% |
| Calcium Total (Hypo) | 28 | 2 | 7.1% |
Signs and symptoms of overdosage are likely to consist of leucopenia, thrombocytopenia, nausea, vomiting, diarrhoea, skin reactions and alopecia. Treatment should be symptomatic.
Pharmacotherapeutic group: Detoxifying agents for antineoplastic agents, ATC code: V03AF02 Two pharmacodynamic properties of dexrazoxane are described in the literature:
Prevention of anthracycline cardiotoxicity, and
Antineoplastic action
Mechanism of action
Dexrazoxane has two major mechanisms of action:
Chelation of iron, especially through its ring-opened metabolite thus reducing the iron-dependent oxidative stress causing anthracycline-induced cardiotoxicity.
Inhibition of topoisomerase II.
It is not known to what extent each of these mechanisms contributes to the preventive effect on tissue destruction following anthracycline extravasation. The chelating property is probably also responsible for an increased urinary excretion of iron and zinc and a decreased serum concentration of calcium as described in a few studies.
The following efficacy data relate to Savene used as treatment of anthracycline extravasation:
The clinical programme for Savene (dexrazoxane) included two open, single-arm, multicentre studies. The overall purpose of each trial was to investigate the efficacy of intravenous Savene in preventing tissue damage from accidentally extravasated anthracycline, and thus preventing the patients from undergoing the routinely used surgical excision of the affected tissue. Due to the rarity of the condition only historical data could be used for comparison (demonstrating surgical rates of 35-50 %, in one country 100% in biopsy proven cases) In both studies the dosage regimen was the same. Treatment with Savene had to be started within 6 hours from the incident and was repeated after 24 and 48 hours. The first and second doses were 1000 mg/m2 and the third was 500 mg/m2. A requirement for inclusion in the efficacy part of the study was that the anthracycline extravasation was proven by fluorescence microscopy of one or more biopsies. For study purposes, patients with extravasations from a central venous access device (CVAD) were not included in the efficacy evaluation. Patients with neutropenia and thrombocytopenia > CTC grade 1 (Common Toxicity Criteria) have not been included in the clinical studies. In study TT01, 23 patients were entered and received treatment with Savene. Eighteen were evaluable for efficacy and safety and a further five patients were evaluable for toxicity only. None of the patients required surgical intervention. In study TT02, 57 patients entered the study and received the first dose of Savene. 36 patients were evaluable for efficacy. Only one of the 36 patients required surgery. In both studies all patients had received anthracycline. Overall, the most commonly received anthracycline was epirubicin (56 % of the patients). In both studies dexrazoxane treatment prevented the development of necrosis, allowed cancer treatment to continue as scheduled in the majority of patients (70.4 %), and reduced the occurrence of sequelae (only few and mild long-term sequelae were observed).
Savene must only be administered intravenously. Bibliographical data demonstrate that serum kinetics of dexrazoxane after intravenous administration follow an open two-compartment model independent of schedule and dose. The apparent volumes of distribution are 0.13-1.3 l/kg (median 0.49 l/kg). Volume of distribution is independent of dose. AUCs were dose-proportional. Tissue distribution is rapid, with the highest levels of unchanged parent compound and hydrolysed product appearing in liver and kidneys. About 2% of dexrazoxane is protein-bound. Biotransformation: Dexrazoxane undergoes intracellular hydrolysis first to its two one-ring open intermediates (B and C) and then to the two-ring opened form (ADR-925) which has a structure similar to EDTA and is a strong chelator of iron and divalent cations as calcium ions. Elimination: Dexrazoxane displays biphasic elimination kinetics. Initial elimination half lives (alpha) are 0.18-1 h (median 0.34 h) and terminal elimination half lives 1.9-9.1 h (median 2.8 h). Total urinary recovery of unchanged dexrazoxane is 34-60 %. Systemic clearance is independent of dose. The pharmacokinetics of the metabolites is derived from a single study with five patients. The mean elimination half-lives of the one-ring opened metabolite B and metabolite C are 0.9-3.9 h (n=5) and 0.5-0.8 h (n=3), respectively. The elimination half-life of the two-ring opened metabolite ADR-925 is not given in literature. ADR-925 is reported to increase three-fold within 15 min after infusion of 1500 mg/m2 and remain relatively constant on a plateau for 4 hours and then decreased to about half at 24 hours. Clearance may be reduced in patients with low creatinine clearance. In-vitro studies on dexrazoxane in human microsomes have shown high stability of dexrazoxane indicating that major metabolism via cytochrome P450 is unlikely. There is insufficient data available to draw any definite conclusions regarding intrinsic pharmaco- kinetic factors such as age, gender, race and weight. Inter- and intra-individual pharmacokinetic variabilities have not been studied systematically. Based on a limited number of patients, inter- individual variability calculated as the coefficient of variation (CV %) was estimated to be approximately 30 % for the main pharmacokinetic parameters.
Dexrazoxane has been shown to possess mutagenic activity. The carcinogenic potential of dexrazoxane has not been investigated, however, razoxane (the racemic mixture of dexrazoxane and levrazoxane) has been reported to be associated with the development of secondary malignancies in mice (lymphoid neoplasms) and rats (uterine carcinomas) after administration for a prolonged period of time. Both of these effects are expected for this class of compound. Repeat-dose toxicity studies have shown that primary target organs were tissues that undergo rapid cell division: bone marrow, lymphoid tissue, testes and digestive tract. Myelosuppression is thus common. The apparent effects were greater during chronic than acute administration. The toxicity in combination with doxorubicin was additive and not synergistic. The related razoxane has been demonstrated to be embryotoxic in mice, rats and rabbits and teratogenic in rats and mice. When mice with experimental daunorubicin extravasation were treated with dexrazoxane systemically combined with topical treatment with DMSO on the daunorubicin-affected skin area, 67 % of the mice developed small skin wounds, whereas dexrazoxane treatment alone completely prevented the daunorubicin-induced skin necrosis in another group of mice. Thus, dimethylsulfoxide (DMSO) should not be used in patients who are administered dexrazoxane to treat anthracycline extravasation.
Powder vial
none
Diluent bottle
Sodium chloride Potassium chloride
Magnesium chloride hexahydrate Sodium acetate trihydrate Sodium gluconate Sodium hydroxide Water for injections
In the absence of compatibility studies, this medicinal product must not be mixed with other medicinal products.
Powder and diluent: 3 years. After reconstitution and dilution: Chemical and physical in-use stability has been demonstrated for 4 hours when stored at 2 to 8 degC. From a microbiological point of view the product should be used immediately. If not used immediately, in-use storage times and conditions prior to use are the responsibility of the user and would normally not be longer than 4 hours at 2 to 8 degC.
Store below 25 degC. Keep the vials and bottles in the outer carton in order to protect from light. For storage conditions after reconstitution and dilution of the medicinal product, see section 6.3.
Savene powder: Amber-coloured, 36-ml, glass type I vial with stopper made of chlorobutyl rubber and a flip-off or tear-off cap. Savene diluent: 500 ml solution in bottles made of Type-I (Ph.Eur.) glass. Pack sizes: Savene is available as an emergency kit consisting of 10 vials of Savene powder and 3 bottles of Savene diluent.
Before infusion, Savene powder must be reconstituted with 25 ml Savene diluent to give a concentration of 20 mg dexrazoxane per ml. The concentrate is slightly yellow. The concentrate should then be diluted further in the remaining Savene diluent. Caution must be exercised during reconstitution and dilution and the normal procedures for proper handling of cytotoxic medicinal products should be adopted. If the powder or solution contacts the skin or mucous membranes, wash immediately and thoroughly with water. Any unused product or waste material should be disposed of in accordance with local requirements.
Norgine B.V. Hogehilweg 7 1101 CA Amsterdam ZO The Netherlands
EU/1/06/350/001
Date of first authorisation 28/07/2006 Date of latest renewal 28/07/2011
Detailed information on this product is available on the website of the European Medicines Agency http://www.ema.europa.eu