The following adverse reactions are discussed in greater detail in other sections of the label:
Clinical Trials Experience
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
In clinical trials, KADCYLA has been evaluated as single-agent in 884 patients with HER2positive metastatic breast cancer. The most common (frequency ≥ 25%) adverse drug reactions (ADRs) seen in 884 patients treated with KADCYLA were fatigue, nausea, musculoskeletal pain, hemorrhage, thrombocytopenia, headache, increased transaminases, constipation and epistaxis.
The ADRs described in Table 6 were identified in patients with HER2-positive metastatic breast cancer treated in a randomized trial (Study 1) [see Clinical Studies]. Patients were randomized to receive KADCYLA or lapatinib plus capecitabine. The median duration of study treatment was 7.6 months for patients in the KADCYLA-treated group and 5.5 months and 5.3 months for patients treated with lapatinib and capecitabine, respectively. Two hundred and eleven (43.1%) patients experienced ≥ Grade 3 adverse events in the KADCYLA-treated group compared with 289 (59.2%) patients in the lapatinib plus capecitabine-treated group. Dose adjustments for KADCYLA were permitted [see DOSAGE AND ADMINISTRATION]. Thirty-two patients (6.5%) discontinued KADCYLA due to an adverse event, compared with 41 patients (8.4%) who discontinued lapatinib, and 51 patients (10.5%) who discontinued capecitabine due to an adverse event. The most common adverse events leading to KADCYLA withdrawal were thrombocytopenia and increased transaminases. Eighty patients (16.3%) treated with KADCYLA had adverse events leading to dose reductions. The most frequent adverse events leading to dose reduction of KADCYLA (in ≥ 1% of patients) included thrombocytopenia, increased transaminases, and peripheral neuropathy. Adverse events that led to dose delays occurred in 116 (23.7%) of KADCYLA treated patients. The most frequent adverse events leading to a dose delay of KADCYLA (in ≥ 1% of patients) were neutropenia, thrombocytopenia, leukopenia, fatigue, increased transaminases and pyrexia.
Table 6 reports the ADRs that occurred in patients in the KADCYLA-treated group (n=490) of the randomized trial (Study 1). Selected laboratory abnormalities are shown in Table 7. The most common ADRs seen with KADCYLA in the randomized trial (frequency > 25%) were nausea, fatigue, musculoskeletal pain, hemorrhage, thrombocytopenia, increased transaminases, headache, and constipation. The most common NCI-CTCAE (version 3) ≥ Grade 3 ADRs (frequency > 2%) were thrombocytopenia, increased transaminases, anemia, hypokalemia, peripheral neuropathy and fatigue.
Table 6 : Summary of Adverse Drug Reactions Occurring in Patients on the KADCYLA Treatment Arm in the Randomized Trial (Study 1)
| Adverse Drug Reactions |
(MedDRA) System Organ Class
| KADCYLA (3.6 mg/kg) |
Frequency rate %
| Lapatinib (1250 mg) + Capecitabine (2000 mg/m²) |
Frequency rate %
|All grades (%)||Grade 3 - 4 (%)||All grades (%)||Grade 3 - 4 (%)|
|Blood and Lymphatic System Disorders|
|Left ventricular dysfunction||1.8||0.2||3.3||0.4|
|General Disorders and Administration|
|Nodular regenerative hyperplasia||0.4||ND||0||0|
|Immune System Disorders|
|Injury, Poisoning, and Procedural|
|Infections and Infestations|
|Urinary tract infection||9.4||0.6||3.9||0|
|Blood alkaline phosphatase increased||4.7||0.4||3.7||0.4|
|Metabolism and Nutrition Disorders|
|Musculoskeletal and Connective Tissue Disorders|
|Nervous System Disorders|
|Respiratory, Thoracic, and Mediastinal Disorders|
|Skin and Subcutaneous Tissue Disorders|
| Nodular Regenerative Hyperplasia and Portal Hypertension occurred in the same patient. |
ND = Not determined
Table 7 : Selected Laboratory Abnormalities
|Parameter||KADCYLA (3.6 mg/kg)||Lapatinib (1250 mg) + Capecitabine (2000 mg/m²)|
|All Grade %||Grade 3 %||Grade 4 %||All Grade %||Grade 3 %||Grade 4 %|
|Increased bilirubin||17||< 1||0||57||2||0|
|Increased AST||98||7||< 1||65||3||0|
|Increased ALT||82||5||< 1||54||3||0|
|Decreased platelet count||83||14||3||21||< 1||< 1|
|Decreased hemoglobin||60||4||1||64||3||< 1|
|Decreased neutrophils||39||3||< 1||38||6||2|
|Decreased potassium||33||3||0||31||6||< 1|
Hepatic failure has been observed in two patients (0.2%) with HER2-positive metastatic breast cancer in clinical trials (n=884) with KADCYLA as single-agent.
As with all therapeutic proteins, there is the potential for an immune response to KADCYLA. A total of 836 patients from six clinical studies were tested at multiple time points for anti-therapeutic antibody (ATA) responses to KADCYLA. Following KADCYLA dosing, 5.3% (44/836) of patients tested positive for anti-KADCYLA antibodies at one or more post-dose time points. The presence of KADCYLA in patient serum at the time of ATA sampling may interfere with the ability of this assay to detect anti-KADCYLA antibodies. As a result, data may not accurately reflect the true incidence of anti-KADCYLA antibody development. In addition, neutralizing activity of anti-KADCYLA antibodies has not been assessed.
Immunogenicity data are highly dependent on the sensitivity and specificity of the test methods used. Additionally, the observed incidence of a positive result in a test method may be influenced by several factors, including sample handling, timing of sample collection, drug interference, concomitant medication and the underlying disease. Therefore, comparison of the incidence of antibodies to KADCYLA with the incidence of antibodies to other products may be misleading. Clinical significance of anti-KADCYLA antibodies is not yet known.
Read the entire FDA prescribing information for Kadcyla (Ado-trastuzumab Emtansine Injection for IV Use)
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