Ibrance (palbociclib) vs Nerlynx (neratinib)

Ibrance (palbociclib) vs Nerlynx (neratinib)

Ibrance (palbociclib) is a CDK4/6 inhibitor used primarily in combination with hormonal therapy for the treatment of hormone receptor-positive, HER2-negative advanced or metastatic breast cancer. Nerlynx (neratinib), on the other hand, is a tyrosine kinase inhibitor indicated for the extended adjuvant treatment of adult patients with early-stage HER2-positive breast cancer, to follow adjuvant trastuzumab-based therapy. The choice between Ibrance and Nerlynx would largely depend on the specific subtype of breast cancer a patient has, as well as the stage of the disease, with Ibrance being more suitable for HR-positive, HER2-negative cases, and Nerlynx being tailored for patients who have HER2-positive breast cancer and have completed initial treatment with trastuzumab.

Difference between Ibrance and Nerlynx

Metric Ibrance (palbociclib) Nerlynx (neratinib)
Generic name Palbociclib Neratinib
Indications HR-positive, HER2-negative advanced or metastatic breast cancer Extended adjuvant treatment of HER2-positive early-stage breast cancer
Mechanism of action CDK4/6 inhibitor, halts cell cycle progression Tyrosine kinase inhibitor, blocks several enzymes that promote cell growth
Brand names Ibrance Nerlynx
Administrative route Oral Oral
Side effects Neutropenia, leukopenia, infections, fatigue Diarrhea, nausea, abdominal pain, fatigue
Contraindications Hypersensitivity to palbociclib or any of its components Hypersensitivity to neratinib or any of its components
Drug class Antineoplastic agent, kinase inhibitor Antineoplastic agent, kinase inhibitor
Manufacturer Pfizer Puma Biotechnology

Efficacy

Efficacy of Ibrance (Palbociclib) in Breast Cancer

Ibrance (palbociclib) is a targeted therapy known as a cyclin-dependent kinase (CDK) 4/6 inhibitor, which is used in the treatment of certain types of breast cancer. Specifically, it is indicated for hormone receptor-positive (HR+), human epidermal growth factor receptor 2-negative (HER2-) advanced or metastatic breast cancer. The efficacy of palbociclib has been demonstrated in multiple clinical trials, where it has been shown to significantly improve progression-free survival (PFS) when used in combination with hormonal therapies such as letrozole or fulvestrant. Patients receiving palbociclib in combination with these hormonal therapies were found to have a delay in disease progression compared to those receiving hormonal therapy alone.

In the PALOMA-2 trial, for example, palbociclib in combination with letrozole was evaluated in postmenopausal women with ER+/HER2- advanced breast cancer as a first-line treatment. The results indicated a substantial improvement in median PFS. Similarly, the PALOMA-3 trial demonstrated that palbociclib, when used with fulvestrant, significantly improved PFS in women with HR+/HER2- metastatic breast cancer who had relapsed or progressed during prior endocrine therapy.

Efficacy of Nerlynx (Neratinib) in Breast Cancer

Nerlynx (neratinib) is an oral tyrosine kinase inhibitor that specifically targets HER2-positive breast cancer. It is primarily used as an extended adjuvant treatment for early-stage HER2-positive breast cancer in patients who have previously completed adjuvant trastuzumab-based therapy. The efficacy of neratinib was established in the ExteNET trial, which included women with early-stage HER2-positive breast cancer. The study showed that neratinib, taken for one year after completing trastuzumab therapy, significantly reduced the risk of breast cancer recurrence or death compared to placebo.

Furthermore, the use of neratinib has been associated with a reduction in the risk of invasive disease recurrence and has shown a sustained benefit over time. It is important to note that the treatment with neratinib is associated with a risk of severe diarrhea, and therefore, antidiarrheal prophylaxis during the first cycles of treatment is recommended to manage this side effect. The decision to use neratinib should be based on an individual assessment of the benefits and risks for each patient.

Regulatory Agency Approvals

Ibrance
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)
Nerlynx
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia

Access Ibrance or Nerlynx today

If Ibrance or Nerlynx are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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