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Adjuvant selpercatinib verlengt overleving zonder ziekteprogressie bij vroeg RET-fusiepositief longkanker

Een fase 3-randomisatieonderzoek onder 151 patiënten met vroeg stadium (IB-IIIA) RET-fusiepositief niet-kleincellig longkanker toonde aan dat adjuvant selpercatinib effectiever is dan placebo. Na twee jaar was de overleving zonder ziekteprogressie bij patiënten met stadium II of IIIA 92 procent versus 61 procent (HR 0,17; 95%-BI 0,06 tot 0,51; p < 0,001).

Het veiligheidsprofiel was acceptabel met voornamelijk graden 3-4 transaminaseverhogingen en geen behandelgerelateerde sterfgevallen. Deze resultaten ondersteunen de opname van adjuvant selpercatinib als nieuwe behandelstandaard voor deze specifieke longkankersubgroep.

Abstract (original)

BACKGROUND: Selpercatinib, a highly selective, potent, and central nervous system-penetrant rearranged during transfection (RET) inhibitor, is approved for RET fusion-positive advanced or metastatic non-small-cell lung cancer (NSCLC). The efficacy and safety of selpercatinib in early-stage NSCLC are unknown. METHODS: We conducted a phase 3, double-blind trial involving patients with RET fusion-positive NSCLC who had received definitive therapy with curative intent (surgery or radiotherapy with adjuvant systemic anticancer therapy, if applicable). Patients were randomly assigned to receive adjuvant selpercatinib or placebo for up to 3 years. The primary end point was investigator-assessed event-free survival in patients with stage II or IIIA disease. Secondary end points were investigator-assessed event-free survival in patients with stage IB, II, or IIIA disease; event-free survival as assessed by blinded independent central review; overall survival; and safety. RESULTS: A total of 151 patients were assigned to receive selpercatinib (75 patients) or placebo (76 patients). Median follow-up was 24 months and 27 months in the respective groups. Among 109 patients with stage II or IIIA disease, 2-year investigator-assessed event-free survival was 92% with selpercatinib and 61% with placebo (hazard ratio for disease recurrence, progression, or death, 0.17; 95% confidence interval [CI], 0.06 to 0.51; P<0.001). Event-free survival as assessed by blinded independent central review was consistent with investigator-assessed event-free survival. Among the 151 patients with stage IB, II, or IIIA NSCLC, investigator-assessed event-free survival at 2 years was 94% with selpercatinib and 70% with placebo (hazard ratio for disease recurrence, progression, or death, 0.17; 95% CI, 0.06 to 0.49; P<0.001). The most common adverse events during the treatment period were increased levels of alanine aminotransferase and aspartate aminotransferase (grade ≥3 in 17% and 19% of patients, respectively, in the selpercatinib group). Three deaths occurred, all in the placebo group, owing to disease progression. CONCLUSIONS: Among patients with stage II or IIIA RET fusion-positive NSCLC, event-free survival was significantly longer with adjuvant selpercatinib than with placebo. (Funded by Lilly; LIBRETTO-432 ClinicalTrials.gov number, NCT04819100.).

Dit artikel is een samenvatting van een publicatie in The New England journal of medicine. Voor het volledige artikel, alle details en referenties verwijzen wij u naar de oorspronkelijke bron.

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DOI: 10.1056/NEJMoa2602628