All Cycles | |||||||
---|---|---|---|---|---|---|---|
Name | NC/NA, % | Grade 1, % | Grade 2, % | Grade 3, % | Grade 4, % | Grade 5, % | All grades, % |
Platelet count decreased | 85 | 5 | 5 | 0 | 5 | 0 | 15 |
Neutrophil count decreased | 57 | 0 | 5 | 24 | 14 | 0 | 43 |
Lymphocyte count decreased | 81 | 0 | 0 | 14 | 5 | 0 | 19 |
White blood cell decreased | 90 | 5 | 0 | 5 | 0 | 0 | 10 |
Anemia | 67 | 0 | 14 | 14 | 5 | 0 | 33 |
Headache | 95 | 0 | 0 | 5 | 0 | 0 | 5 |
Aspartate aminotransferase increased | 95 | 0 | 0 | 5 | 0 | 0 | 5 |
Alanine aminotransferase increased | 95 | 0 | 0 | 5 | 0 | 0 | 5 |
Gait disturbance | 95 | 0 | 0 | 5 | 0 | 0 | 5 |
Thromboembolic event | 90 | 0 | 10 | 0 | 0 | 0 | 10 |
Dysgeusia | 95 | 0 | 5 | 0 | 0 | 0 | 5 |
Fatigue | 86 | 0 | 14 | 0 | 0 | 0 | 14 |
Anorexia | 90 | 5 | 5 | 0 | 0 | 0 | 10 |
Diarrhea | 95 | 0 | 5 | 0 | 0 | 0 | 5 |
Rash maculopapular | 95 | 0 | 5 | 0 | 0 | 0 | 5 |
Cough | 95 | 5 | 0 | 0 | 0 | 0 | 5 |
Five patients required dose interruption and four patients required dose reduction to 100 mg of palbociclib because of thrombocytopenia and/or neutropenia. All nonhematologic toxicities were managed without modification of palbociclib dosage.
Abbreviation: NC/NA, no change from baseline/no adverse event.