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IMPORTANT SAFETY INFORMATION including BOXED WARNING

WARNING
The incidence of treatment-related mortality associated with Taxotere® therapy is increased in patients with abnormal liver function, in patients receiving higher doses, and in patients with non-small cell lung carcinoma and a history of prior treatment with platinum-based chemotherapy who receive Taxotere® as a single agent at a dose of 100 mg/m2 (see WARNINGS section of the prescribing information)

Continued below

Taxotere® (docetaxel) Injection Concentrate: Dosing for early-stage breast cancer and metastatic
breast cancer1,2

In combination with doxorubicin and cyclophosphamide for the adjuvant treatment of patients with operable, node-positive breast cancer

  • Doxorubicin 50 mg/m2 and cyclophosphamide 500 mg/m2 followed by Taxotere® 75 mg/m2 IV infusion over 1 hour every 3 weeks for 6 cycles (or 18 weeks)
  • Taxotere® in combination with doxorubicin and cyclophosphamide should be administered when the neutrophil count is ≥1500 cells/mm3
Side Effects With TACa Regimen Dose Adjustment Other
Interventions
Taxotere® Doxorubicinb Cyclophophamideb
Febrile neutropenia
First episode      
  • Use G-CSF for all subsequent cyclesc
Second episode
  • Reduce dose to 60 mg/m2c
  • Reduce dose to 40 mg/m2
  • Reduce dose to 400 mg/m2
  • Maintain G-CSF therapyc
Grade 3/4 stomatitis
First episode
  • Reduce dose to 60 mg/m2
      
Second episode  
  • Reduce dose to 40 mg/m2
    
Second or cumulative cutaneous reactions
First episode
  • Reduce dose to 60 mg/m2
      
Second episode Discontinue      
Moderate neurosensory signs and/or symptoms
First episode
  • Reduce dose to 60 mg/m2
      
Second episode Discontinue      
a Taxotere® 75 mg/m2, doxorubicin 50 mg/m2, cyclophophamide 500 mg/m2.
b Additional guidelines used in registration study TAX 316.
c Prophylactic G-CSF may be used to mitigate the risk of hematologic toxicities.

Taxotere® (docetaxel) Injection Concentrate: Dosing for metastatic breast cancer1

For patients with locally advanced or metastatic breast cancer after failure of prior chemotherapy

  • Taxotere® 60 mg/m2, 75 mg/m2, or 100 mg/m2 IV infusion over 1 hour, administered every 3 weeks
Side Effect Taxotere® Dose Adjustment
Patients initially dosed at 100mg/m2
Febrile neutropenia, or ANC <500 cells/mm3 >7 days, or severe/cumulative cutaneous reactions
First episode Reduce dose to 75 mg/m2
Second episode Reduce dose to 55 mg/m2 or discontinue therapy
Patients initially dosed at 60 mg/m2
No febrile neutropenia, or ANC <500 cells/mm3 >7 days, or severe/cumulative cutaneous reactions
  Consider increasing dose
Patients initially dosed at 60-100 mg/m2
Grade 3/4 peripheral neurotherapy
First episode Discontinue

a One can estimate which dose may be appropriate for a patient based on that patient’s characteristics and the goal of therapy. For instance, lower doses may be more suitable for patients who have comorbidities or certain side-effect concerns.

IMPORTANT SAFETY INFORMATION

WARNINGS:

  • The incidence of treatment-related mortality associated with Taxotere® therapy is increased in patients with abnormal liver function, in patients receiving higher doses, and in patients with non-small cell lung carcinoma and a history of prior treatment with platinum-based chemotherapy who receive Taxotere® as a single agent at a dose of 100 mg/m2
  • Taxotere® should not be given to patients with bilirubin >upper limit of normal (ULN), or to patients with AST and/or ALT>1.5 X ULN concomitant with alkaline phosphatase >2.5 X ULN
    • Patients with elevations of bilirubin or abnormalities of transaminase concurrent with alkaline phosphatase are at increased risk for the development of grade 4 neutropenia, febrile neutropenia, infections, severe thrombocytopenia, severe stomatitis, severe skin toxicity, and toxic death
    • Patients with isolated elevations of transaminase >1.5 X ULN also had a higher rate of febrile neutropenia grade 4 but did not have an increased incidence of toxic death
    • Bilirubin, AST or ALT, and alkaline phosphatase values should be obtained prior to each cycle of Taxotere® therapy
  • Taxotere® therapy should not be given to patients with neutrophil counts of <1500 cells/mm3
    • In order to monitor the occurrence of neutropenia, which may be severe and result in infection, frequent blood cell counts should be performed on all patients receiving Taxotere®
  • Severe hypersensitivity reactions characterized by generalized rash/erythema, hypotension and/or bronchospasm, or very rarely fatal anaphylaxis, have been reported in patients who received the recommended 3-day dexamethasone premedication
    • Hypersensitivity reactions require immediate discontinuation of Taxotere® infusion and administration of appropriate therapy
  • Taxotere® must not be given to patients who have a history of severe hypersensitivity reactions to Taxotere® or to other drugs formulated with polysorbate 80
  • Severe fluid retention occurred in 6.5% (6/92) of patients despite use of a 3-day dexamethasone premedication regimen. It was characterized by one or more of the following events: poorly tolerated peripheral edema, generalized edema, pleural effusion requiring urgent drainage, dyspnea at rest, cardiac tamponade, or pronounced abdominal distention (due to ascites)
  • Neutropenia (<2,000 neutrophils/mm3) occurs in virtually all patients given 60-100 mg/m2 of Taxotere® and grade 4 neutropenia (<500 cells/mm3) occurs in 85% of patients given 100 mg/m2 and 75% of patients given
    60 mg/m2
  • Patients should be premedicated with oral corticosteroids prior to each Taxotere® administration to reduce the incidence and severity of fluid retention. Patients with pre-existing effusions should be closely monitored from the first dose for possible exacerbation of the effusions
  • Treatment-related acute myeloid leukemia (AML) or myelodysplasia has occurred in patients given anthracyclines and/or cyclophosphamide, including use with Taxotere® in adjuvant therapy of breast cancer
  • Localized erythema of the extremities with edema followed by desquamation has been observed
    • In case of severe skin toxicity, an adjustment in dosage is recommended
  • Severe neurosensory symptoms (paresthesia, dysesthesia, pain) were observed in 5.5% (53/965) of metastatic breast cancer patients, and resulted in treatment discontinuation in 6.1%
    • When these symptoms occur, dosage must be adjusted; if symptoms persist, treatment should be discontinued
  • Severe asthenia was reported in 14.9% (144/965) of metastatic breast cancer patients, but led to treatment discontinuation in only 1.8%
    • Symptoms of fatigue and weakness may last a few days up to several weeks and may be associated with deterioration of performance status in patients with progressive disease
  • Taxotere® can cause fetal harm when administered to pregnant women. Women of childbearing potential should be advised to avoid becoming pregnant during therapy with Taxotere®
  • The most common adverse reactions across all Taxotere® indications are infections, neutropenia, anemia, febrile neutropenia, hypersensitivity, thrombocytopenia, neuropathy, dysgeusia, dyspnea, constipation, anorexia, nail disorders, fluid retention, asthenia, pain, nausea, diarrhea, vomiting, mucositis, alopecia, skin reactions and myalgia
  • In patients treated with TCF for gastric cancer, the incidence of serious adverse events was higher in patients ≥65 years than in younger patients. Adverse events (all grades) occurring at rates ≥10% higher in elderly patients included lethargy, stomatitis, diarrhea, dizziness, edema, and febrile neutropenia/neutropenic infection.
  • Taxotere® should be administered in a facility equipped to manage possible complications (e.g. anaphylaxis)

Please click here for Taxotere full prescribing information, including boxed WARNING.

Taxotere® (docetaxel) Injection Concentrate Indications

Breast Cancer
TAXOTERE® is indicated for the treatment of patients with locally advanced or metastatic breast cancer after failure of prior chemotherapy
TAXOTERE® in combination with doxorubicin and cyclophosphamide is indicated for the adjuvant treatment of patients with operable node-positive breast cancer

Advanced Non-Small Cell Lung Cancer
TAXOTERE®, as a single agent, is indicated for the treatment of patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) after failure of prior platinum-based chemotherapy
TAXOTERE® in combination with cisplatin is indicated for the treatment of patients with unresectable, locally advanced or metastatic NSCLC who have not previously received chemotherapy for this condition.

Metastatic Androgen-Independent Prostate Cancer
TAXOTERE® in combination with prednisone is indicated for the treatment of patients with androgen-independent (hormone-refractory) metastatic prostate cancer.

Advanced Gastric/GE Junction Cancer
TAXOTERE® in combination with cisplatin and fluorouracil is indicated for the treatment of patients with advanced gastric adenocarcinoma, including adenocarcinoma of the gastroesophageal junction, who have not received prior chemotherapy for advanced disease.

Locally Advanced Head and Neck Cancer
TAXOTERE® in combination with cisplatin and fluorouracil is indicated for the induction treatment of patients with locally advanced squamous cell carcinoma of the head and neck (SCCHN).



References

  1. Taxotere® Prescribing Information. Bridgewater, NJ: sanofi-aventis U.S. LLC; August 2010.
  2. Data on file. Final study report. A multicenter phase III randomized trial comparing docetaxel in combination with doxorubicin and cyclophosphamide (TAC) versus 5-fluorouracil in combination with doxorubicin and cyclophosphamide (FAC) as adjuvant treatment of operable breast cancer patients with positive axillary lymph nodes. Protocol RP56976V-316. Aventis Pharmaceuticals Inc., November 3, 2003.
  3. Harvey V, Mouridsen H, Semiglazov V, et al. Phase III trial comparing three doses of docetaxel for second-line treatment of advanced breast cancer. J Clin Oncol. 2006;24(31):4963–4970.
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US.DOC.10.05.002  Last update:  June 2010