OPDIVO/YERVOY (nivolumab/ipilimumab) - Cancer bronchique non à petites cellules (CBNPC)

Opinions on drugs - Posted on Oct 07 2021

Reason for request

New indication

Key points

Favourable opinion for reimbursement in combination with 2 cycles of platinum-based chemotherapy for the first-line treatment of metastatic non-small cell lung cancer in adults whose tumours have no sensitising EGFR mutation or ALK translocation.

What therapeutic improvement?

Therapeutic improvement compared to chemotherapy.

Role in the care pathway?

The current management for metastatic non-small cell lung cancer (NSCLC) in first line-treatment, in the absence of molecular abnormalities (EGFR mutations, or ALK or ROS-1 rearrangements), is based on immunotherapy, for eligible patients.

Pembrolizumab (anti-PDL1 immunotherapy) is a first-line treatment:

  • as monotherapy, in PD-L1 ≥ 50% patients, and
  • in combination with chemotherapy, irrespective of PD-L1 expression:
    • in combination with pemetrexed and platinum chemotherapy, in non-squamous NSCLC,
    • in combination with carboplatin and paclitaxel (or nab-paclitaxel) chemotherapy, in squamous NSCLC.

In the event of contraindication to immunotherapy, or to one of the chemotherapy drugs combined with pembrolizumab, chemotherapy is indicated. This involves dual therapy combining a platinum (cisplatin or carboplatin) with one of the following substances: vinorelbine, gemcitabine, docetaxel, paclitaxel or pemetrexed (only in non-squamous NSCLC for the latter). In non-squamous NSCLC, in the absence of contraindications, bevacizumab can be added to the dual chemotherapy regimen; and atezolizumab can be combined with bevacizumab + paclitaxel + carboplatin.

Role of the medicinal product in the care pathway

Combination of OPDIVO/YERVOY (nivolumab/ipilimumab) and 2 cycles of platinum-based chemotherapy is an alternative in the first-line treatment of metastatic non-small cell lung cancer in adults whose tumours have no sensitising EGFR mutation or ALK translocation.

However, the Committee regrets the absence of data enabling the role of the OPDIVO/YERVOY (nivolumab/ipilimumab) combination to be positioned compared to current standard of care therapies: pembrolizumab as monotherapy, only if PD-L1 ≥ 50%, as well as the pembrolizumab + chemotherapy combination, irrespective of PD-L1 expression.

Considering these elements, the role of the nivolumab/ipilimumab combination plus 2 cycles chemotherapy compared to these different protocols is not known therefore. The Committee considers that the therapeutic decision should be taken after a documented proposal resulting from a multidisciplinary team meeting. This choice should take into account the efficacy and safety results of each protocol, along with the patient’s general condition and preferences. The Committee highlights the fact that patients with an ECOG score > 1 were not included in the study.


Clinical Benefit

Moderate

The Committee considers that the clinical benefit of the OPDIVO/YERVOY (nivolumab/ipilimumab) combination is moderate in the MA indication.


Clinical Added Value

minor

Considering:

  • demonstration of the superiority of nivolumab/ipilimumab in combination with 2 chemotherapy cycles, compared to chemotherapy, in terms of overall survival (HR=0.69 [CI95%: 0.56-0.86], with an individual estimate of an absolute improvement of 3.4 months, deemed clinically relevant), in an open-label, randomised phase 3 study;

and despite:

  • a comparator that is not optimal on the date of the assessment;
  • the absence of data making it possible to differentiate between the proportion attributable (efficacy and toxicity) to each immunotherapy (nivolumab/ipilimumab), and hence the specific value of the combination of these two drugs compared to monotherapy (nivolumab or ipilimumab);
  • a higher toxicity, with the occurrence of grade ≥ 3 adverse events in 47% of patients, in particular immunological (with an increased frequency compared to single-agent immunotherapy), and permanent discontinuation of treatment due to an adverse event in 28% of patients;
  • the lack of demonstrated impact on quality of life;

the Transparency Committee considers that combination of OPDIVO/YERVOY (nivolumab/ipilimumab) and 2 cycles of platinum-based chemotherapy provides a minor clinical added value (CAV IV) compared to chemotherapy in the first-line treatment of metastatic non-small cell lung cancer in adults whose tumours have no sensitising EGFR mutation or ALK translocation.

 

 

 


Contact Us

Évaluation des médicaments