RET in non-small cell lung cancer
2 EU-approved indications in non-small cell lung cancer need a RET result: sugemalimab (1st line, metastatic) and selpercatinib (advanced).
Line of therapy
| Drug | Biomarker requirement | Regimen | Setting | Conditions |
|---|---|---|---|---|
| RET fusion1 | ||||
Retsevmo | Monotherapy | Any line advanced | Not previously treated with a RET inhibitor | |
| EGFR/ALK/ROS1/RET negative1 | ||||
Cejemly | No sensitising EGFR mutations, or ALK, ROS1 or RET genomic tumour aberrations | + platinum-based chemotherapy | 1L metastatic | None |
Tumour-agnostic approvals1
Approved for any solid tumour that carries the alteration, wherever the tumour started.
| Drug | Biomarker requirement | Regimen | Setting | Conditions |
|---|---|---|---|---|
| RET fusion1 | ||||
Retsevmo | Monotherapy | Any line advanced | Treatment options not targeting RET provide limited clinical benefit, or have been exhausted; Aged 2 years and older | |
16 approvals for NSCLC need no biomarker and apply whatever the result. All approvals for NSCLC
See also
Label wording2
The sentence from section 4.1 of the SmPC that each indication above comes from.
- Sugemalimab (Cejemly)
Cejemly in combination with platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small-cell lung cancer (NSCLC) with no sensitising EGFR mutations, or ALK, ROS1 or RET genomic tumour aberrations.
- Selpercatinib (Retsevmo)
advanced RET fusion-positive non-small cell lung cancer (NSCLC) not previously treated with a RET inhibitor.