Doxobin

Doxobin Uses, Dosage, Side Effects, Food Interaction and all others data.

Doxobin is a cytotoxic anthracycline antibiotic. The cytotoxic action results from its binding to DNA and inhibition of nucleic acid synthesis. Doxobin has been shown to produce regression in a variety of disseminated malignancies.

Doxobin is an antineoplastic in the anthracycline class. General properties of drugs in this class include: interaction with DNA in a variety of different ways including intercalation (squeezing between the base pairs), DNA strand breakage and inhibition with the enzyme topoisomerase II. Most of these compounds have been isolated from natural sources and antibiotics. However, they lack the specificity of the antimicrobial antibiotics and thus produce significant toxicity. The anthracyclines are among the most important antitumor drugs available. Doxobin is widely used for the treatment of several solid tumors while daunorubicin and idarubicin are used exclusively for the treatment of leukemia. Doxobin may also inhibit polymerase activity, affect regulation of gene expression, and produce free radical damage to DNA. Doxobin possesses an antitumor effect against a wide spectrum of tumors, either grafted or spontaneous. The anthracyclines are cell cycle-nonspecific.

Trade Name Doxobin
Availability Prescription only
Generic Doxorubicin
Doxorubicin Other Names 14-hydroxydaunomycin, 14-hydroxydaunorubicine, Doxorubicin, Doxorubicina, Doxorubicine, Doxorubicinum, Hydroxydaunorubicin
Related Drugs prednisone, methotrexate, dexamethasone, Keytruda, Armour Thyroid, Arimidex, rituximab, carboplatin, pembrolizumab, fluorouracil
Weight 10mg, 50mg
Type Injection
Formula C27H29NO11
Weight Average: 543.5193
Monoisotopic: 543.174060775
Protein binding

Doxorubicin and its major metabolite, doxorubicinol, is 74-76% bound to plasma protein. The extent to binding is independent of plasma concentration up to 1.1 mcg/mL. Doxorubicin does not cross the blood brain barrier.

Groups Approved, Investigational
Therapeutic Class Cytotoxic Chemotherapy
Manufacturer Biological E Limited, Umair Associates
Available Country India, Pakistan
Last Updated: September 19, 2023 at 7:00 am
Doxobin
Doxobin

Uses

Doxobin is an anthracycline topoisomerase II inhibitor used for:

  • Ovarian cancer: After failure of platinum-based chemotherapy.
  • AIDS-related Kaposi’s Sarcoma: After failure of prior systemic chemotherapy or intolerance to such therapy.
  • Multiple Myeloma: In combination with bortezomib in patients who have not previously received bortezomib and have received at least one prior therapy.

Doxobin is also used to associated treatment for these conditions: Acute Lymphoblastic Leukaemias (ALL), Acute Myeloblastic Leukemia, Advanced Endometrial Cancer, Advanced Soft Tissue Sarcoma, Bladder transitional cell carcinoma, Carcinoma, Bronchogenic, Gastric Carcinoma, Kaposi's Sarcoma AIDS Related, Lymphoma, Hodgkins, Malignant Lymphomas, Metastatic Breast Cancer, Multiple Myeloma (MM), Mycosis Fungoides (MF), Neuroblastomas, Ovarian Cancer Metastatic, Ovarian Carcinoma, Sarcoma, Bone, Sezary Syndrome, Soft Tissue Sarcoma (STS), Thyroid Carcinoma, Waldenström's Macroglobulinemia (WM), Wilms' tumor, Advanced Thymoma, Advanced uterine sarcoma

How Doxobin works

Doxobin has antimitotic and cytotoxic activity through a number of proposed mechanisms of action: Doxobin forms complexes with DNA by intercalation between base pairs, and it inhibits topoisomerase II activity by stabilizing the DNA-topoisomerase II complex, preventing the religation portion of the ligation-religation reaction that topoisomerase II catalyzes.

Dosage

Doxobin dosage

Administer Doxobin at an initial rate of 1 mg/min to minimize the risk of infusion reactions. If no infusion related reactions occur, increase rate of infusion to complete administration over 1 hour. Do not administer as bolus injection or undiluted solution.

  • Ovarian cancer: 50 mg/m2 IV every 4 weeks
  • AIDS-related Kaposi’s Sarcoma: 20 mg/m2 IV every 3 weeks
  • Multiple Myeloma: 30 mg/m2 IV on day 4 following bortezomib

Side Effects

Leucopenia, thrombocytopenia, nausea, vomiting, diarrhoea. Rarely facial flushing, rash, alopecia. Blurred vision, headache, seizures, paraesthesia, confusion, malaise, lethargy, skin pigmentation.

Toxicity

LD50=21800 ug/kg (rat, subcutaneous)

Precaution

Elderly, children, hepatic impairment. Monitor blood counts and ECG.

Interaction

Doxobin interacts with a number of other drugs e.g. antibiotics (aminoglycosides), steroids, aminophylline and propranolol.

Food Interaction

  • Avoid St. John's Wort. This herb induces CYP3A4 metabolism, which may reduce the serum concentration of doxorubicin.
  • Exercise caution with grapefruit products. Grapefruit inhibits CYP3A4 metabolism, which may increase the serum concentration of doxorubicin.

Volume of Distribution

The distributive half-life is 5 minutes, which suggests that doxorubicin is rapidly taken up by tissue. Steady state volume of distribution = 809 to 1214 L/m2

Half Life

Terminal half life = 20 - 48 hours.

Clearance

  • 324-809 mL/min/m2 [by metabolism and biliary excretion]
  • 1088 mL/min/m2 [Men]
  • 433 mL/min/m2 [Women]
  • 1540 mL/min/m2 [children greater than 2 years of age receiving administration of 10 to 75 mg/m2 doses]
  • 813 mL/min/m2 [infants younger than 2 years of age receiving administration of 10 to 75 mg/m2 doses]

Elimination Route

40% of the dose appears in bile in 5 days. 5-12% of the drug and its metabolites appears in urine during the same time period. <3% of the dose recovered in urine was doxorubicinol.

Pregnancy & Breastfeeding use

Category D: There is positive evidence of human foetal risk, but the benefits from use in pregnant women may be acceptable despite the risk (e.g., if the drug is needed in a life-threatening situation or for a serious disease for which safer drugs cannot be used or are ineffective).

Contraindication

Cardiac disease, neonates, pregnancy and lactation, prior irradiation to mediastinum. IM/SC admin. Severe myelosuppression due to previous treatment with antitumour agents or radiotherapy.

Special Warning

Hepatic Impairment-

serum-bilirubin: 12-30 mcg/ml: Half the normal dose;

serum-bilirubin: >30 mcg/ml: Quarter of the usual dose.

Acute Overdose

Acute overdosage may increase the toxic effects of mucositis, leukopenia and thrombocytopenia. Treatment includes hospitalisation of the severely myelosuppressed patient, antimicrobials, platelet transfusions and symptomatic treatment of mucositis. Use of haemopoietic growth factor (G-CSF, GM-CSF) may be considered. Cumulative dosage increases risk of cardiomyopathy and resultant congestive heart failure which may be managed with digitalis preparations, diuretics, and after load reducers such as ACE inhibitors.

Storage Condition

Powder for injection: Store at 15-30°C.

Solution for injection & liposomal formulations: Refrigerate at 2-8°C. Do not freeze.

Innovators Monograph

You find simplified version here Doxobin

Doxobin contains Doxorubicin see full prescribing information from innovator Doxobin Monograph, Doxobin MSDS, Doxobin FDA label

FAQ

What is Doxobin used for?

Doxobin is used in combination with other medications to treat certain types of bladder, breast, lung, stomach, and ovarian cancer; Hodgkin's lymphoma (Hodgkin's disease) and non-Hodgkin's lymphoma (cancer that begins in the cells of the immune system); and certain types of leukemia (cancer of the white blood cells). It is often used together with other chemotherapy agents.

How safe is Doxobin?

Doxobin effects help patients achieve lengthy and good quality of life remission and survival times for many types of malignancies. Although Doxobin poses significant risks in administration and toxicity, it is one of the most effective chemotherapeutic agents in veterinary medicine.

What is the mechanism of action of Doxobin?

Doxobin has antimitotic and cytotoxic activity through a number of proposed mechanisms of action: Doxobin forms complexes with DNA by intercalation between base pairs, and it inhibits topoisomerase II activity by stabilizing the DNA-topoisomerase II complex, preventing the religation portion of the ligation-religation reaction that topoisomerase II catalyzes.

What are the common side effects of Doxobin?

Common side effects of Doxobin are include:

  • Atazanavir
  • Boceprevir
  • Cobicistat
  • Lopinavir
  • Measles Virus Vaccine, Live
  • Mumps Virus Vaccine, Live
  • Nelfinavir
  • Rotavirus Vaccine, Live
  • Rubella Virus Vaccine, Live
  • Saquinavir
  • Tasonermin
  • Telaprevir
  • Varicella Virus Vaccine, Live
  • Zoster Vaccine, Live

Is Doxobin safe during pregnancy?

Cyclophosphamide and Doxobin are pregnancy category D agents; however, potential benefits may warrant treatment with these agents during pregnancy under special circumstances.

Is Doxobin safe during breastfeeding?

Most sources consider breastfeeding to be contraindicated during maternal antineoplastic Doxobin therapy, especially anthracyclines such as Doxobin. 

Can I drink alcohol with Doxobin?

The drinking of alcohol does not appear to affect the safety or usefulness of pegylated liposomal Doxobin.

How often do I take Doxobin?

Doxobin is usually given once every 21 to 28 days.

How long does Doxobin take to work?

Doxobin is a light red liquid that you have through a drip (infusion) into your bloodstream. It usually takes between 30 to 90 minutes each time you have it.

How long is Doxobin treatment?

You usually have liposomal Doxobin every 2 to 4 weeks. Your treatment plan will depend on the type of cancer you have.

What is the half life of Doxobin?

The initial distribution half-life of approximately 5 minutes suggests rapid tissue uptake of doxorubicin, while its slow elimination from tissues is reflected by a terminal half-life of 20 to 48 hours.

What happens if I miss a dose?

Call your doctor for instructions if you miss an appointment for your Doxobin injection.

What happens if I overdose?

Since this medication is given by a healthcare professional in a medical setting, an overdose is unlikely to occur.

Who should not take Doxobin?

You should not use Doxobin if you have severe liver disease, severe heart problems, very low blood cell counts caused by prior chemotherapy, or if you recently had a heart attack. You should not use this medicine if you are allergic to Doxobin or similar medications or if you have:

very low blood cell counts caused by chemotherapy you received in the past; severe liver disease; severe heart problems; or if you have recently had a heart attack.

Will Doxobin affect my fertility?

We know that certain chemotherapy medicines are more likely than others to cause infertility, including Doxobin.

Can Doxobin affects my heart?

Doxobin is well recognized that Doxobin may cause damage to the heart in some individuals.

Can Doxobin affect my kidneys?

Researches have shown that Doxobin chemotherapy could generate severe tissue injury in heart and kidney and the symptoms of renal damage like hematuresis and proteinuria are especially evident.

Can Doxobin affects my liver?

While hepatotoxicity from Doxobin, epirubicin or idarubicin may be rare, it is likely due to direct toxic injury to the liver. Doxobin and its analogues are metabolized in the liver via microsomal enzymes, and production of a toxic or immunogenic intermediate may trigger liver injury.

What happen If I stop taking Doxobin?

If you decide to stop chemotherapy, be sure you're still getting relief from symptoms such as pain, constipation, and nausea. This is called palliative care, and it's meant to improve your quality of life

*** Taking medicines without doctor's advice can cause long-term problems.
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