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DOI 10.1200/jco-24-02595

Медицинская библиотека · Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2025

BO-112 Plus Pembrolizumab for Patients With Anti-PD-1-Resistant Advanced Melanoma: Phase II Clinical Trial SPOTLIGHT-203.

Márquez-Rodas Iván, Dutriaux Caroline, Saiag Philippe, de la Cruz Merino Luis, Castañón Álvarez Eduardo, Robert Caroline, Rodríguez-Moreno Juan F, Arance Ana, Cerezuela-Fuentes Pablo, Montaudié Henri, Sanmamed Miguel F, González-Cao María, Charles Julie, López Criado María Pilar, Berrocal Alfonso, de Miguel Enrique, Funck-Brentano Elisa, Prey Sorilla, Álamo de la Gala Mᵃ Carmen, Melero Ignacio, Avilés-Izquierdo Jose Antonio, Roman Ruth, Garcia-Pelaez Beatriz, Rodriguez Sonia, Trnkova Zuzana Jirakova, Quintero Marisol, Maciá Sonia, Chaney Marya F, Dalle Stephane

СтатьяКлиническое исследование II фазыМногоцентровое исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

PURPOSE: Patients with anti-PD-1-resistant melanoma (MEL) have no well-defined standard of care. BO-112 is a synthetic, double-stranded RNA (poly I:C) nanoplexed with polyethylenimine that when administered intratumorally has showed in patients with solid tumors potential to revert this resistance. We report efficacy and safety of the phase II clinical trial of intratumoral BO-112 plus intravenous pembrolizumab for patients with anti-PD-1-resistant MEL (ClinicalTrials.gov identifier: NCT04570332).

METHODS

Forty-two patients were treated with intratumoral BO-112 once every week for 7 weeks and then once every 3 weeks (up to 2 mg and up to eight lesions per treatment) combined with 200 mg pembrolizumab once every 3 weeks until progressive disease, unacceptable toxicity, death, or up to 1 year. Primary end point was RECIST 1.1 objective response rate (ORR) by independent central radiology review in modified intention-to-treat population (mITT; patients evaluable for response) with 20% ORR positivity threshold. Secondary key end points were progression-free survival (PFS), overall survival (OS), duration of response (DOR), and safety.

RESULTS

For mITT, there were 40 patients and the ORR was 25%, with 10% complete, 15% partial, and 40% stable disease, with nonachieved (NA) median DOR (95% CI, 8.3 to NA). For ITT, there were 42 patients, and the median PFS and OS were 3.7 months (95% CI, 2.2 to 9.2) and NA (95% CI, 9.9 to NA), respectively, with 54% patients alive at 24 months. The combination was well tolerated: 16 patients (38.1%) experiencing ≥G3-4 adverse events, four (9.5%) drug-related, and no deaths related to treatment.

CONCLUSION

The clinical trial has met its primary end point (ORR) making BO-112 with pembrolizumab a potential strategy to revert anti-PD-1 resistance in patients with MEL. PFS results are in line with other clinical trials in anti-PD-1-resistant scenario, with promising OS data.

Для цитирования: Márquez-Rodas Iván, Dutriaux Caroline, Saiag Philippe, de la Cruz Merino Luis, Castañón Álvarez Eduardo, Robert Caroline, Rodríguez-Moreno Juan F, Arance Ana, Cerezuela-Fuentes Pablo, Montaudié Henri, Sanmamed Miguel F, González-Cao María, Charles Julie, López Criado María Pilar, Berrocal Alfonso, de Miguel Enrique, Funck-Brentano Elisa, Prey Sorilla, Álamo de la Gala Mᵃ Carmen, Melero Ignacio, Avilés-Izquierdo Jose Antonio, Roman Ruth, Garcia-Pelaez Beatriz, Rodriguez Sonia, Trnkova Zuzana Jirakova, Quintero Marisol, Maciá Sonia, Chaney Marya F, Dalle Stephane. BO-112 Plus Pembrolizumab for Patients With Anti-PD-1-Resistant Advanced Melanoma: Phase II Clinical Trial SPOTLIGHT-203.. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 2025. DOI: 10.1200/jco-24-02595.

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