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Response and survival in unresectable in-transit metastatic melanoma according to treatment strategy.

Cato Boreel ,
Jessie de Ruijter ,
Olivier van Not ,
Manja Bloem ,
Lukas Been ,
Maureen Aarts ,
Franchette van den Berkmortel ,
Christian Blank ,
Marye Boers-Sonderen ,
Han Bonenkamp ,
Jan-Willem de Groot ,
Dirk Grünhagen ,
John Haanen ,
M Hilde Jalving ,
Djura Piersma ,
Bart Rikhof ,
Marion Stevense-den Boer ,
Astrid van der Veldt ,
Lieke Simkens ,
Michel Wouters ,
Ellen Kapiteijn ,
Fons van den Eertwegh ,
Karijn Suijkerbuijk

Abstract

METHODS

Using data from the nationwide Dutch Melanoma Treatment Registry, all patients receiving systemic treatment from 2012 to July 2025 for unresectable ITM, with or without lymph node metastases (LNM) (stage III-IVM1a), were analysed for overall response rate (ORR), progression-free survival (PFS), overall survival (OS), and melanoma-specific survival (MSS). A multivariable Cox model adjusted for age, sex, ECOG PS, LDH, and LNM.

CONCLUSIONS

For ITM unresectable melanoma, first-line anti-PD1, T-VEC, and BRAF(/MEK)i can induce clinically meaningful and durable responses. The optimal treatment choice depends on patient and disease characteristics and preferences.

RESULTS

In total, 530 patients were identified: 213 received first-line anti-PD1, 182 T-VEC, 67 BRAF(/MEK)i, 37 ipilimumab (IPI), and 31 ipilimumab + nivolumab (IPI+NIVO). Patients receiving T-VEC had more favorable baseline characteristics, including less often stage IV disease, less often LNM, and lower LDH. ORR were comparable between treatments: anti-PD1 53.1%, T-VEC 52.2%, BRAF(/MEK)i 62.7%. Median PFS was significantly shorter for T-VEC (5.6months; 95%CI 4.2-8.1) than for anti-PD1 (8.1months; 95%CI 5.9-13.8) and BRAF(/MEK)i (9.2months; 95%CI 6.9-14.3). Median OS favored T-VEC (not reached (NR); 95%CI 61.5-NR) over anti-PD1 (37.2months; 95%CI 32.3-64.7) and BRAF(/MEK)i (24.7months; 95%CI 18.0-62.1), but this difference between T-VEC and anti-PD1 disappeared after adjusting for confounders and no differences were observed in MSS. In the ITM-only subgroup, T-VEC-treated patients demonstrated longer observed OS than anti-PD1 and BRAF(/MEK)i, while in patients with ITM and LNM, anti-PD1 showed longer PFS but similar OS compared with T-VEC.

BACKGROUND

Currently, no comprehensive overview exists of response and survival outcomes for first-line immune checkpoint inhibition, BRAF/BRAF + MEK inhibition (BRAF(/MEK)i), and talimogene laherparepvec (T-VEC) in melanoma patients with unresectable in-transit metastases (ITM). This study aims to provide a real-world overview of these outcomes.

More about this publication

European journal of cancer (Oxford, England : 1990)

Volume 244
Pages 116889
Publication date 21-06-2026

Full text links

Publisher website (DOI) 10.1016/j.ejca.2026.116889
Europe PubMed Central 42335571
Pubmed 42335571

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