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Activity and safety of topical pimecrolimus in patients with early stage mycosis fungoides (PimTo-MF): a single-arm, multicentre, phase 2 trial

Abstract: Background: The calcineurin pathway is often activated in mycosis fungoides. We aimed to assess the activity and safety of topical pimecrolimus, a calcineurin inhibitor, in patients with early mycosis fungoides. Methods: PimTo-MF was a single-arm, multicentre, phase 2 trial done at six medical centres in Spain. Patients (aged ?18 years) had histologically confirmed early mycosis fungoides (stages IA-IIA) and an Eastern Cooperative Oncology Group performance status of 0-1. Key exclusion criteria included the use of concurrent treatments for mycosis fungoides, including sunbathing, topical or systemic corticosteroids, and other calcineurin inhibitors. Patients applied topical pimecrolimus 1% cream on their skin lesions twice daily for 16 weeks (1 g per 2% of body surface), with subsequent follow-up of 12 months. Dosage modifications were not allowed. To evaluate adherence to the treatment, patients were instructed to return all empty tubes to the hospital (as per drug accountability protocols). The primary endpoint was the overall response ratein the intention-to-treat population. PimTo-MF is registered with EudraCT, 2014-001377-14, and is complete. Findings: Between March 1, 2015, and Sept 30, 2016, 39 patients were enrolled. All patients were assessable, with a median age of 51·5 years (IQR 45-62), and the population was predominantly male (24 male [62%], 15 female [38%]). Median follow-up after baseline was 5·7 years (IQR 5·7-6·2). 22 (56%) of 39 patients had an overall response (one complete response, 21 partial responses). Responses were observed across IA (14 [54%] of 26 patients) and IB (eight [73%] of 11 patients) clinical stages, but not IIA. Topical pimecrolimus was well tolerated and no patient required a dose reduction or discontinued treatment because of unacceptable drug-related toxicity. No patients were lost to follow-up or discontinued treatment. 13 (33%) of 39 patients reported adverse events; transitory mild burning or pruritus (grade 1) was the most common, seen in eight (21%) patients. In three (8%) of these patients, the burning or pruritus was considered related to treatment. No grade 4 or 5 adverse events were observed. Interpretation: Pimecrolimus 1% cream seems active and safe in patients with early stage mycosis fungoides. Our findings should be taken with caution until long-term follow-up data are obtained that confirm the safety of this treatment. Further controlled clinical trials are warranted to confirm these results.

 Autoría: Ortiz-Romero P.L., Maroñas Jiménez L., Muniesa C., Estrach T., Servitje O., Fernández-de-Misa R., Gallardo F., Sanmartín O., Riveiro-Falkenbach E., García-Díaz N., Vega R., Lora D., Postigo C., Jiménez B., Sánchez-Beato M., Pedro Vaqué J., Rodríguez Peralto J.L., de la Cámara A.G., de la Cruz J., Piris Pinilla M.Á.,

 Fuente: Lancet Haematol . 2022 Jun;9(6):e425-e433

 Año de publicación: 2022

Nº de páginas: 9

Tipo de publicación: Artículo de Revista

 DOI: 10.1016/S2352-3026(22)00107-7

ISSN: 2352-3026

Url de la publicación: https://www.doi.org/10.1016/S2352-3026(22)00107-7

Autoría

ORTIZ-ROMERO, PABLO L

MAROÑAS JIMÉNEZ, LIDIA

MUNIESA, CRISTINA

ESTRACH, TERESA

SERVITJE, OCTAVIO

FERNÁNDEZ-DE-MISA, RICARDO

GALLARDO, FERNANDO

SANMARTÍN, ONOFRE

RIVEIRO-FALKENBACH, ERICA

GARCÍA-DÍAZ, NURIA

VEGA, ROSA

LORA, DAVID

POSTIGO, CONCEPCIÓN

JIMÉNEZ, BLANCA

SÁNCHEZ-BEATO, MARGARITA

RODRÍGUEZ PERALTO, JOSÉ LUIS

DE LA CÁMARA, AGUSTÍN GÓMEZ

DE LA CRUZ, JAVIER

PIRIS PINILLA, MIGUEL ÁNGEL