Reason for request

Inclusion on the list of medicines approved for use by hospitals in the extension of indication “treatment of patients with epidermal growth factor receptor (EGFR)-expressing, KRAS wild-type metastatic colorectal cancer: in combination with chemotherapy, and as a single agent in patients who have failed oxaliplatin and irinotecan based therapy and who are intolerant to irinotecan”.

Erbitux is indicated for the treatment of patients with epidermal growth factor receptor (EGFR)-expressing, KRAS wild-type metastatic colorectal cancer • in combination with chemotherapy,

  • as monotherapy in patients who have failed oxaliplatin- and irinotecan-based therapy and who are intolerant to irinotecan. Erbitux is indicated for the treatment of patients with squamous cell cancer of the head and neck
  • in combination with radiotherapy in the case of locally advanced disease,
  • in combination with platinum-based chemotherapy for recurrent and/or metastatic disease

Clinical Benefit

Substantial

As first-line treatment: Alternative drugs are available; The efficacy/adverse effects ratio is moderate; The actual benefit is susbtantial.

For second and further lines of treatment: There are very few alternative medications at this stage of the disease; The efficacy/ adverse effects ratio is moderate; The actual benefit is susbtantial.


Clinical Added Value

minor

Based on available data, the Transparency Committee considers that:

- as first- and second-line treatment, ERBITUX combined with standard chemotherapy does not improve actual benefit (level V) compared to usual management.

- as monotherapy after failure of irinotecan or oxaliplatin-based treatment, ERBITUX provides a minor improvement in actual benefit (level IV) compared to best supportive care alone.

no clinical added value

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