Temozolomide
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Check Drug InteractionsTemozolomide Prescribing Information
Indications and Usage (
Temozolomidecapsules are indicated for the:
•adjuvant treatment of adults with newly diagnosed anaplastic astrocytoma;
•treatmentof adults with refractory anaplastic astrocytoma.
•adjuvant treatment of adults with newly diagnosed anaplastic astrocytoma;
•treatmentof adults with refractory anaplastic astrocytoma.
Dosage and Administration (
Prior to dosing, withhold temozolomide capsules until patients have an absolute neutrophil count (ANC) of 1.5 x 109/L or greater and a platelet count of 100 x 109/L or greater.
For concomitant radiotherapy, obtain a complete blood count prior to initiation of treatment and weekly during treatment.
For the 28-day treatment cycles, obtain a complete blood count prior to treatment on Day 1 and on Day 22 of each cycle. Perform complete blood counts weekly until recovery if the ANC falls below 1.5 x 109/L and the platelet count falls below 100 x 109/L.
For concomitant use with focal radiotherapy, obtain a complete blood count weekly and as clinically indicated.
Administertemozolomide capsules either orally or intravenously once daily for 42 to 49 consecutive days during the concomitant use phase withfocalradiotherapy, and then once daily on Days 1 to 5 of each 28-day cycle for 6 cycles during the maintenance use phase.
Provide
The recommended dosage of temozolomide capsules is 75 mg/m2either orally or intravenously once daily for 42 to 49 days in combination with focalradiotherapy. Focal radiotherapy includes the tumor bed or resection site with a 2 to 3 cm margin.
Otheradministration schedules have been used.
Obtaina complete blood count weekly. The recommended dosage modifications due to adverse reactions during concomitant use phase areprovided in
Provide
Pneumocystis
pneumonia (PCP) prophylaxis during the concomitant use phase and continue in patients who develop lymphopenia untilresolutionto Grade 1 or less[see Warnings and Precautions (5.3)]
.ConcomitantUse Phase:
The recommended dosage of temozolomide capsules is 75 mg/m2either orally or intravenously once daily for 42 to 49 days in combination with focalradiotherapy. Focal radiotherapy includes the tumor bed or resection site with a 2 to 3 cm margin.
Otheradministration schedules have been used.
Obtaina complete blood count weekly. The recommended dosage modifications due to adverse reactions during concomitant use phase areprovided in
Table 1
.TABLE 1:Dosage Modifications Due to Adverse Reactions During Concomitant Use Phase
AdverseReaction | Interruption | Discontinuation |
AbsoluteNeutrophil Count | Withhold temozolomide capsules if ANC is greater than or equal to 0.5 x 109/L and less than 1.5 x 109/L. Resume temozolomide capsules at the same dose when ANC is greater than or equal to 1.5 x 109/L. | Discontinue temozolomide capsules if ANC is less than 0.5 x 109/L. |
PlateletCount | Withhold temozolomide capsules if platelet count is greater than or equal to 10 x 109/L and less than 100 x 109/L. Resume temozolomide capsules at the same dose when platelet count is greater than or equal to 100 x 109/L. | Discontinue temozolomide capsules if platelet count is less than 10 x 109/L. |
Non-hematological Adverse Reaction (except for alopecia, nausea, vomiting) | Withhold temozolomide capsules if Grade 2 adverse reaction occurs. Resume temozolomide capsules at the same dose when resolution to Grade 1 or less. | Discontinue temozolomide capsules if Grade 3 or 4 adverse reaction occurs. |
Single Agent Maintenance Use Phase:
Beginning 4 weeks after concomitant use phase completion, administer temozolomide capsules either orally or intravenously once daily on Days 1 to5of each 28-day cycle for 6 cycles. The recommended dosage of temozolomide capsules in the maintenance use phase is:
•Cycle1: 150 mg/m2per day on days 1 to 5.
• Cycles2 to 6: May increase to 200 mg/m2per day on days 1 to 5 before starting Cycle 2 if no dosage interruptions or discontinuations arerequired (Table 1). If the dose is not escalated at the onset of Cycle 2,
do not
increase the dose for Cycles 3 to 6.Obtain a complete blood count on Day 22 and then weekly until the ANC is above 1.5 x 109/L and the platelet count is above 100 x 109/L. Do not start the next cycle until the ANC and platelet count exceed these levels.
Therecommended dosage modifications due to adverse reactions during the maintenance use phase are provided in
Table 2
.If temozolomide capsule is withheld, reduce the dose for the next cycle by 50 mg/m2per day. Permanently discontinue temozolomide capsules in patients who are unable to tolerate a dose of 100 mg/m2per day.
TABLE2: Dosage Modifications Due to Adverse Reactions During Maintenance and Adjuvant Treatment
Adverse Reactions | Interruption and Dose Reduction | Discontinuation |
AbsoluteNeutrophil Count | Withhold temozolomide capsules if ANC less than 1 x 109/L. When ANC is above 1.5 x 109/L, resume temozolomide capsules at reduced dose for the next cycle. | Discontinue temozolomide capsules if unable to tolerate a dose of 100 mg/m2per day. |
PlateletCount | Withhold temozolomide capsules if platelet less than 50 x 109/L. When platelet count is above 100 x 109/L, resume temozolomide capsules at reduced dose for the next cycle. | Discontinue temozolomide capsules if unable to tolerate a dose of 100 mg/m2per day. |
NonhematologicalAdverse Reactions (except for alopecia, nausea, vomiting) | Withhold temozolomide capsules if Grade 3 adverse reaction occurs. When resolved to Grade 1 or less, resume temozolomide capsules at reduced dose for the next cycle. | Discontinue temozolomide capsules if recurrent Grade 3 adverse reaction occurs after dose reduction, if Grade 4 adverse reaction occurs, or if unable to tolerate a dose of 100 mg/m2per day. |
Adjuvant Treatmentof Newly Diagnosed Anaplastic Astrocytoma
Beginning 4 weeks after the end of radiotherapy, administer temozolomide capsules orally in a single dose on days 1 to 5 of a 28-day cycle for 12 cycles. The recommended dosage of temozolomide capsules is: • Cycle 1: 150 mg/m2per day on days 1 to 5.
• Cycles 2 to 12: 200 mg/m2per day on days 1 to 5 if patient experienced no or minimal toxicity in Cycle 1. If the dose was not escalated at the onset of Cycle 2,
do not
increase the dose during Cycles 3 to 6.The recommended complete blood count testing and dosage modifications due to adverse reactions during adjuvant treatment are provided above and in Table 2
[see Dosage and Administration (2.2)]
.RefractoryAnaplastic Astrocytoma
The recommended initial dosage of temozolomide capsules is 150 mg/m2once daily on Days 1 to 5 of each 28-day cycle. Increase the temozolomide capsules dose to 200 mg/m2per day if the following conditions are met at the nadir and on Day 1 of the next cycle:
•ANC is greater than or equal to 1.5 x 109/L, and
• Platelet count is greater than or equal to 100 x 109/L.
Continue temozolomide capsules until disease progression or unacceptable toxicity.
Obtain a complete blood count on Day 22 and then weekly until the ANC is above 1.5 x 109/L and the platelet count is above 100 x 109/L. Do not start the next cycle until the ANC and platelet count exceed these levels.
If the ANC is less than 1 x 109/L or the platelet count is less than 50 x 109/L during any cycle, reduce the temozolomide capsules dose for the next cycle by 50 mg/m2per day. Permanently discontinue temozolomide capsules in patients who are unable to tolerate a dose of 100 mg/m2per day.
Temozolomidecapsules is a hazardous drug. Follow applicable special handling and disposal procedures.1
Take temozolomide capsules at the same time each day. Administer temozolomide capsules consistently with respect to food (fasting vs. nonfasting)
Swallow temozolomide capsules whole with water. Advise patients not to open, chew, or dissolve the contents of the capsules
If capsules are accidentally opened or damaged, take precautions to avoid inhalation or contact with the skin or mucous membranes. In case of powder contact, wash the affected area with water immediately.
Take temozolomide capsules at the same time each day. Administer temozolomide capsules consistently with respect to food (fasting vs. nonfasting)
[see Clinical Pharmacology (12.3)]
. To reduce nausea and vomiting, take temozolomide capsules on an empty stomach or at bedtime and consider antiemetic therapy prior to and following temozolomide capsules administration.Swallow temozolomide capsules whole with water. Advise patients not to open, chew, or dissolve the contents of the capsules
[see Warnings and Precautions (5.6)]
.If capsules are accidentally opened or damaged, take precautions to avoid inhalation or contact with the skin or mucous membranes. In case of powder contact, wash the affected area with water immediately.
Contraindications (
Temozolomideis contraindicated in patients with a history of serious hypersensitivity reactions to:
•temozolomideor any other ingredients in temozolomide capsules; and
• dacarbazine, since both temozolomide and dacarbazine are metabolized to the same active metabolite 5-(3-methyltriazen-1-yl)-imidazole-4-carboxamide.
Reactions to temozolomide have included anaphylaxis
•temozolomideor any other ingredients in temozolomide capsules; and
• dacarbazine, since both temozolomide and dacarbazine are metabolized to the same active metabolite 5-(3-methyltriazen-1-yl)-imidazole-4-carboxamide.
Reactions to temozolomide have included anaphylaxis
[see Adverse Reactions (6.2)]
.• History of serious hypersensitivity to temozolomide or any other ingredients in temozolomide capsules and dacarbazine.
Warnings and Precautions (
Myelosuppression, including pancytopenia, leukopenia, and anemia, some with fatal outcomes, have occurred with temozolomide
In MK-7365-006, myelosuppression usually occurred during the first few cycles of therapy and was generally not cumulative. The median nadirs occurred at 26 days for platelets (range: 21 to 40 days) and 28 days for neutrophils (range: 1 to 44 days). Approximately 10% of patients required hospitalization, blood transfusion, or discontinuation of therapy due to myelosuppression. Geriatric patients and women have been shown in clinical trials to have a higher risk of developing myelosuppression.
Obtain a complete blood count and monitor ANC and platelet counts before initiation of treatment and as clinically indicated during treatment. When temozolomide is used in combination with radiotherapy, obtain a complete blood count prior to initiation of treatment, weekly during treatment, and as clinically indicated
For severe myelosuppression, withhold temozolomide and then resume at same or reduced dose, or permanently discontinue, based on occurrence
[see Adverse Reactions (6.1, 6.2)]
.In MK-7365-006, myelosuppression usually occurred during the first few cycles of therapy and was generally not cumulative. The median nadirs occurred at 26 days for platelets (range: 21 to 40 days) and 28 days for neutrophils (range: 1 to 44 days). Approximately 10% of patients required hospitalization, blood transfusion, or discontinuation of therapy due to myelosuppression. Geriatric patients and women have been shown in clinical trials to have a higher risk of developing myelosuppression.
Obtain a complete blood count and monitor ANC and platelet counts before initiation of treatment and as clinically indicated during treatment. When temozolomide is used in combination with radiotherapy, obtain a complete blood count prior to initiation of treatment, weekly during treatment, and as clinically indicated
[see Dosage and Administration (2.1, 2.2, 2.3)]
.For severe myelosuppression, withhold temozolomide and then resume at same or reduced dose, or permanently discontinue, based on occurrence
[see Dosage and Administration (2.1, 2.2, 2.3)]
.Fataland severe hepatotoxicity have been reported in patients receiving temozolomide. Perform liver tests at baseline, midway through the first cycle, prior to each subsequent cycle, and approximately two to four weeks after the last dose of temozolomide.
Theincidence of secondary malignancies is increased in patients treated with temozolomide -containing regimens. Cases of myelodysplastic syndrome and secondary malignancies, including myeloid leukemia, have been observed following temozolomide administration.
Based on findings from animal studies and its mechanism of action, temozolomide can cause fetal harm when administered to a pregnant woman. Adverse developmental outcomes have been reported in both pregnant patients and pregnant partners of male patients. Oral administration of temozolomide to rats and rabbits during the period of organogenesis resulted in embryolethality and polymalformations at doses less than the maximum human dose based on body surface area.
Advise pregnant women and females of reproductive potential of the potential risk to a fetus. Advise females of reproductive potential to use effective contraception during treatment with temozolomide and for 6 months after the last dose. Because of potential risk of genotoxic effects on sperm, advise male patients with female partners of reproductive potential to use condoms during treatment with temozolomide and for 3 months after the last dose. Advise male patients not to donate semen during treatment with temozolomide and for 3 months after the last dose
Advise pregnant women and females of reproductive potential of the potential risk to a fetus. Advise females of reproductive potential to use effective contraception during treatment with temozolomide and for 6 months after the last dose. Because of potential risk of genotoxic effects on sperm, advise male patients with female partners of reproductive potential to use condoms during treatment with temozolomide and for 3 months after the last dose. Advise male patients not to donate semen during treatment with temozolomide and for 3 months after the last dose
[see Use in Specific Populations (8.1, 8.3)]
.Advisepatients not to open, chew or dissolve the contents of the temozolomide capsules. Swallow capsules whole with a glass of water. If a capsule becomes damaged, avoid contact of the powder contents with skin or mucous membranes. In case of powder contact, wash affected area with water immediately
[see Dosage and Administration (2.4)]
. If temozolomide capsules must be opened or the contents must be dissolved, this should be done by a professional trained in safe handling of hazardous drugs using appropriate equipment and safety procedures.Temozolomide capsule is an alkylating drug indicated for the treatment of adults with:
• Newly diagnosed glioblastoma concomitantly with radiotherapy and then as maintenance treatment. (
Temozolomide capsules are indicated for the treatment of adults with newly diagnosed glioblastoma, concomitantly with radiotherapy and then as maintenance treatment.
• Anaplastic astrocytoma. (
Temozolomidecapsules are indicated for the:
•adjuvant treatment of adults with newly diagnosed anaplastic astrocytoma;
•treatmentof adults with refractory anaplastic astrocytoma.
•adjuvant treatment of adults with newly diagnosed anaplastic astrocytoma;
•treatmentof adults with refractory anaplastic astrocytoma.
o Adjuvant treatment of adults with newly diagnosed anaplastic astrocytoma. (
Temozolomidecapsules are indicated for the:
•adjuvant treatment of adults with newly diagnosed anaplastic astrocytoma;
•treatmentof adults with refractory anaplastic astrocytoma.
•adjuvant treatment of adults with newly diagnosed anaplastic astrocytoma;
•treatmentof adults with refractory anaplastic astrocytoma.
o Treatment of adults with refractory anaplastic astrocytoma. (
Temozolomidecapsules are indicated for the:
•adjuvant treatment of adults with newly diagnosed anaplastic astrocytoma;
•treatmentof adults with refractory anaplastic astrocytoma.
•adjuvant treatment of adults with newly diagnosed anaplastic astrocytoma;
•treatmentof adults with refractory anaplastic astrocytoma.
•
Newly Diagnosed Glioblastoma:
o 75 mg/m
2once daily for 42 to 49 days concomitant with focal radiotherapy followed by initial maintenance dose of 150 mg/m
2once daily for Days 1 to 5 of each 28-day cycle for 6 cycles. May increase maintenance dose to 200 mg/m
2for Cycles 2 to 6 based on toxicity. (
Prior to dosing, withhold temozolomide capsules until patients have an absolute neutrophil count (ANC) of 1.5 x 109/L or greater and a platelet count of 100 x 109/L or greater.
For concomitant radiotherapy, obtain a complete blood count prior to initiation of treatment and weekly during treatment.
For the 28-day treatment cycles, obtain a complete blood count prior to treatment on Day 1 and on Day 22 of each cycle. Perform complete blood counts weekly until recovery if the ANC falls below 1.5 x 109/L and the platelet count falls below 100 x 109/L.
For concomitant use with focal radiotherapy, obtain a complete blood count weekly and as clinically indicated.
o Provide
Pneumocystis
pneumonia (PCP) prophylaxis during concomitant phase and continue in patients who develop lymphopenia until resolution to Grade 1 or less. (Prior to dosing, withhold temozolomide capsules until patients have an absolute neutrophil count (ANC) of 1.5 x 109/L or greater and a platelet count of 100 x 109/L or greater.
For concomitant radiotherapy, obtain a complete blood count prior to initiation of treatment and weekly during treatment.
For the 28-day treatment cycles, obtain a complete blood count prior to treatment on Day 1 and on Day 22 of each cycle. Perform complete blood counts weekly until recovery if the ANC falls below 1.5 x 109/L and the platelet count falls below 100 x 109/L.
For concomitant use with focal radiotherapy, obtain a complete blood count weekly and as clinically indicated.
•
Adjuvant Treatment of Newly Diagnosed Anaplastic Astrocytoma:
Beginning 4 weeks after the end of radiotherapy, administer temozolomide capsules orally in a single dose on days 1 to 5 of a 28-day cycle for 12 cycles. The recommended dosage for Cycle 1 is 150 mg/m2per day and for Cycles 2 to 12 is 200 mg/m
2if patient experienced no or minimal toxicity in Cycle 1. (
Administertemozolomide capsules either orally or intravenously once daily for 42 to 49 consecutive days during the concomitant use phase withfocalradiotherapy, and then once daily on Days 1 to 5 of each 28-day cycle for 6 cycles during the maintenance use phase.
Provide
The recommended dosage of temozolomide capsules is 75 mg/m2either orally or intravenously once daily for 42 to 49 days in combination with focalradiotherapy. Focal radiotherapy includes the tumor bed or resection site with a 2 to 3 cm margin.
Otheradministration schedules have been used.
Obtaina complete blood count weekly. The recommended dosage modifications due to adverse reactions during concomitant use phase areprovided in
Provide
Pneumocystis
pneumonia (PCP) prophylaxis during the concomitant use phase and continue in patients who develop lymphopenia untilresolutionto Grade 1 or less[see Warnings and Precautions (5.3)]
.ConcomitantUse Phase:
The recommended dosage of temozolomide capsules is 75 mg/m2either orally or intravenously once daily for 42 to 49 days in combination with focalradiotherapy. Focal radiotherapy includes the tumor bed or resection site with a 2 to 3 cm margin.
Otheradministration schedules have been used.
Obtaina complete blood count weekly. The recommended dosage modifications due to adverse reactions during concomitant use phase areprovided in
Table 1
.TABLE 1:Dosage Modifications Due to Adverse Reactions During Concomitant Use Phase
AdverseReaction | Interruption | Discontinuation |
AbsoluteNeutrophil Count | Withhold temozolomide capsules if ANC is greater than or equal to 0.5 x 109/L and less than 1.5 x 109/L. Resume temozolomide capsules at the same dose when ANC is greater than or equal to 1.5 x 109/L. | Discontinue temozolomide capsules if ANC is less than 0.5 x 109/L. |
PlateletCount | Withhold temozolomide capsules if platelet count is greater than or equal to 10 x 109/L and less than 100 x 109/L. Resume temozolomide capsules at the same dose when platelet count is greater than or equal to 100 x 109/L. | Discontinue temozolomide capsules if platelet count is less than 10 x 109/L. |
Non-hematological Adverse Reaction (except for alopecia, nausea, vomiting) | Withhold temozolomide capsules if Grade 2 adverse reaction occurs. Resume temozolomide capsules at the same dose when resolution to Grade 1 or less. | Discontinue temozolomide capsules if Grade 3 or 4 adverse reaction occurs. |
Single Agent Maintenance Use Phase:
Beginning 4 weeks after concomitant use phase completion, administer temozolomide capsules either orally or intravenously once daily on Days 1 to5of each 28-day cycle for 6 cycles. The recommended dosage of temozolomide capsules in the maintenance use phase is:
•Cycle1: 150 mg/m2per day on days 1 to 5.
• Cycles2 to 6: May increase to 200 mg/m2per day on days 1 to 5 before starting Cycle 2 if no dosage interruptions or discontinuations arerequired (Table 1). If the dose is not escalated at the onset of Cycle 2,
do not
increase the dose for Cycles 3 to 6.Obtain a complete blood count on Day 22 and then weekly until the ANC is above 1.5 x 109/L and the platelet count is above 100 x 109/L. Do not start the next cycle until the ANC and platelet count exceed these levels.
Therecommended dosage modifications due to adverse reactions during the maintenance use phase are provided in
Table 2
.If temozolomide capsule is withheld, reduce the dose for the next cycle by 50 mg/m2per day. Permanently discontinue temozolomide capsules in patients who are unable to tolerate a dose of 100 mg/m2per day.
TABLE2: Dosage Modifications Due to Adverse Reactions During Maintenance and Adjuvant Treatment
Adverse Reactions | Interruption and Dose Reduction | Discontinuation |
AbsoluteNeutrophil Count | Withhold temozolomide capsules if ANC less than 1 x 109/L. When ANC is above 1.5 x 109/L, resume temozolomide capsules at reduced dose for the next cycle. | Discontinue temozolomide capsules if unable to tolerate a dose of 100 mg/m2per day. |
PlateletCount | Withhold temozolomide capsules if platelet less than 50 x 109/L. When platelet count is above 100 x 109/L, resume temozolomide capsules at reduced dose for the next cycle. | Discontinue temozolomide capsules if unable to tolerate a dose of 100 mg/m2per day. |
NonhematologicalAdverse Reactions (except for alopecia, nausea, vomiting) | Withhold temozolomide capsules if Grade 3 adverse reaction occurs. When resolved to Grade 1 or less, resume temozolomide capsules at reduced dose for the next cycle. | Discontinue temozolomide capsules if recurrent Grade 3 adverse reaction occurs after dose reduction, if Grade 4 adverse reaction occurs, or if unable to tolerate a dose of 100 mg/m2per day. |
•
Refractory Anaplastic Astrocytoma:
Initial dose of 150 mg/m2once daily on Days 1 to 5 of each 28-day cycle. (
Administertemozolomide capsules either orally or intravenously once daily for 42 to 49 consecutive days during the concomitant use phase withfocalradiotherapy, and then once daily on Days 1 to 5 of each 28-day cycle for 6 cycles during the maintenance use phase.
Provide
The recommended dosage of temozolomide capsules is 75 mg/m2either orally or intravenously once daily for 42 to 49 days in combination with focalradiotherapy. Focal radiotherapy includes the tumor bed or resection site with a 2 to 3 cm margin.
Otheradministration schedules have been used.
Obtaina complete blood count weekly. The recommended dosage modifications due to adverse reactions during concomitant use phase areprovided in
Provide
Pneumocystis
pneumonia (PCP) prophylaxis during the concomitant use phase and continue in patients who develop lymphopenia untilresolutionto Grade 1 or less[see Warnings and Precautions (5.3)]
.ConcomitantUse Phase:
The recommended dosage of temozolomide capsules is 75 mg/m2either orally or intravenously once daily for 42 to 49 days in combination with focalradiotherapy. Focal radiotherapy includes the tumor bed or resection site with a 2 to 3 cm margin.
Otheradministration schedules have been used.
Obtaina complete blood count weekly. The recommended dosage modifications due to adverse reactions during concomitant use phase areprovided in
Table 1
.TABLE 1:Dosage Modifications Due to Adverse Reactions During Concomitant Use Phase
AdverseReaction | Interruption | Discontinuation |
AbsoluteNeutrophil Count | Withhold temozolomide capsules if ANC is greater than or equal to 0.5 x 109/L and less than 1.5 x 109/L. Resume temozolomide capsules at the same dose when ANC is greater than or equal to 1.5 x 109/L. | Discontinue temozolomide capsules if ANC is less than 0.5 x 109/L. |
PlateletCount | Withhold temozolomide capsules if platelet count is greater than or equal to 10 x 109/L and less than 100 x 109/L. Resume temozolomide capsules at the same dose when platelet count is greater than or equal to 100 x 109/L. | Discontinue temozolomide capsules if platelet count is less than 10 x 109/L. |
Non-hematological Adverse Reaction (except for alopecia, nausea, vomiting) | Withhold temozolomide capsules if Grade 2 adverse reaction occurs. Resume temozolomide capsules at the same dose when resolution to Grade 1 or less. | Discontinue temozolomide capsules if Grade 3 or 4 adverse reaction occurs. |
Single Agent Maintenance Use Phase:
Beginning 4 weeks after concomitant use phase completion, administer temozolomide capsules either orally or intravenously once daily on Days 1 to5of each 28-day cycle for 6 cycles. The recommended dosage of temozolomide capsules in the maintenance use phase is:
•Cycle1: 150 mg/m2per day on days 1 to 5.
• Cycles2 to 6: May increase to 200 mg/m2per day on days 1 to 5 before starting Cycle 2 if no dosage interruptions or discontinuations arerequired (Table 1). If the dose is not escalated at the onset of Cycle 2,
do not
increase the dose for Cycles 3 to 6.Obtain a complete blood count on Day 22 and then weekly until the ANC is above 1.5 x 109/L and the platelet count is above 100 x 109/L. Do not start the next cycle until the ANC and platelet count exceed these levels.
Therecommended dosage modifications due to adverse reactions during the maintenance use phase are provided in
Table 2
.If temozolomide capsule is withheld, reduce the dose for the next cycle by 50 mg/m2per day. Permanently discontinue temozolomide capsules in patients who are unable to tolerate a dose of 100 mg/m2per day.
TABLE2: Dosage Modifications Due to Adverse Reactions During Maintenance and Adjuvant Treatment
Adverse Reactions | Interruption and Dose Reduction | Discontinuation |
AbsoluteNeutrophil Count | Withhold temozolomide capsules if ANC less than 1 x 109/L. When ANC is above 1.5 x 109/L, resume temozolomide capsules at reduced dose for the next cycle. | Discontinue temozolomide capsules if unable to tolerate a dose of 100 mg/m2per day. |
PlateletCount | Withhold temozolomide capsules if platelet less than 50 x 109/L. When platelet count is above 100 x 109/L, resume temozolomide capsules at reduced dose for the next cycle. | Discontinue temozolomide capsules if unable to tolerate a dose of 100 mg/m2per day. |
NonhematologicalAdverse Reactions (except for alopecia, nausea, vomiting) | Withhold temozolomide capsules if Grade 3 adverse reaction occurs. When resolved to Grade 1 or less, resume temozolomide capsules at reduced dose for the next cycle. | Discontinue temozolomide capsules if recurrent Grade 3 adverse reaction occurs after dose reduction, if Grade 4 adverse reaction occurs, or if unable to tolerate a dose of 100 mg/m2per day. |
Temozolomide capsules, USP are available in 5 mg, 20 mg, 100 mg, 140 mg, 180 mg, and 250 mg strengths. The capsules contain a white capsule body with a color cap, and the colors vary based on the dosage strength.
5 mg: Opaque green cap and opaque white body, hard gelatin capsules imprinted with ‘13’ on cap and ‘H’ on body, filled with off-white to pink or tan color granular powder.
20 mg: Opaque yellow cap and opaque white body, hard gelatin capsules imprinted with ‘14’ on cap and ‘H’ on body, filled with off-white to pink or tan color granular powder.
100 mg: Opaque pink cap and opaque white body, hard gelatin capsules imprinted with ‘15’ on cap and ‘H’ on body, filled with off-white to pink or tan color granular powder.
140 mg: Opaque blue cap and opaque white body, hard gelatin capsules imprinted with ‘16’ on cap and ‘H’ on body, filled with off-white to pink or tan color granular powder.
180 mg: Opaque orange cap and opaque white body, hard gelatin capsules imprinted with ‘17’ on cap and ‘H’ on body, filled with off-white to pink or tan color granular powder.
250 mg: Opaque white cap and opaque white body, hard gelatin capsules imprinted with ‘18’ on cap and ‘H’ on body, filled with off-white to pink or tan color granular powder.
• Lactation: Advise not to breastfeed. (
There are no data on the presence of temozolomide or its metabolites in human milk, the effects on a breastfed child, or the effects on milk production. Because of the potential for serious adverse reactions, including myelosuppression from temozolomide in the breastfed children, advise women not to breastfeed during treatment with temozolomide and for 1 week after the last dose.
Temozolomideis contraindicated in patients with a history of serious hypersensitivity reactions to:
•temozolomideor any other ingredients in temozolomide capsules; and
• dacarbazine, since both temozolomide and dacarbazine are metabolized to the same active metabolite 5-(3-methyltriazen-1-yl)-imidazole-4-carboxamide.
Reactions to temozolomide have included anaphylaxis
•temozolomideor any other ingredients in temozolomide capsules; and
• dacarbazine, since both temozolomide and dacarbazine are metabolized to the same active metabolite 5-(3-methyltriazen-1-yl)-imidazole-4-carboxamide.
Reactions to temozolomide have included anaphylaxis
[see Adverse Reactions (6.2)]
.We receive information directly from the FDA and PrescriberPoint is updated as frequently as changes are made available