Weekly carboplatin plus paclitaxel chemotherapy in advanced melanoma patients resistant to anti-PD-1 inhibitors: a retrospective, monocentric experience
Francesca Romana Di Pietro,
Daniele Marinelli,
Sofia Verkhovskaia,
Giulia Poti,
Rosa Falcone,
Maria Luigia Carbone,
Maria Francesca Morelli,
Albina Rita Zappalà,
Zorika Christiana Di Rocco,
Roberto Morese,
Gabriele Piesco,
Paolo Chesi,
Paolo Marchetti,
Cristina Maria Failla,
Federica De Galitiis
Affiliations
Francesca Romana Di Pietro
Department of Oncology and Dermatological Oncology, IDI-IRCCS
Daniele Marinelli
Department of Experimental Medicine, Sapienza University
Sofia Verkhovskaia
Department of Oncology and Dermatological Oncology, IDI-IRCCS
Giulia Poti
Department of Oncology and Dermatological Oncology, IDI-IRCCS
Rosa Falcone
Department of Oncology and Dermatological Oncology, IDI-IRCCS
Maria Luigia Carbone
Clinical Trial Center, IDI-IRCCS
Maria Francesca Morelli
Department of Oncology and Dermatological Oncology, IDI-IRCCS
Albina Rita Zappalà
Department of Oncology and Dermatological Oncology, IDI-IRCCS
Zorika Christiana Di Rocco
Department of Oncology and Dermatological Oncology, IDI-IRCCS
Roberto Morese
Department of Oncology and Dermatological Oncology, IDI-IRCCS
Gabriele Piesco
Department of Oncology and Dermatological Oncology, IDI-IRCCS
Paolo Chesi
Department of Oncology and Dermatological Oncology, IDI-IRCCS
Paolo Marchetti
Department of Oncology and Dermatological Oncology, IDI-IRCCS
Cristina Maria Failla
Experimental Immunology Laboratory, IDI-IRCCS
Federica De Galitiis
Department of Oncology and Dermatological Oncology, IDI-IRCCS
Abstract Immunotherapy with anti-PD-1 antibodies significantly improved the prognosis in advanced melanoma patients, but most of them develop primary or secondary resistance to the treatment. In this study, we evaluated efficacy and safety of a chemotherapy regimen with weekly carboplatin plus paclitaxel (wCP) in patients previously treated with anti-PD-1 antibodies. We retrospectively identified 30 patients with advanced melanoma treated at our Institute over the last eight years with wCP. The co-primary endpoints of the study were overall survival (OS) and progression-free survival (PFS). In addition, we evaluated treatment tolerability. For this patient cohort, median PFS and OS were 3.25 and 7.69 months, respectively. All included patients had previously received anti-PD-1 immunotherapy, most of them had ECOG PS 0–1, and only 5 patients had a BRAF V600 mutation. In univariable analysis, we observed shorter OS in patients with > 2 involved metastatic sites, superficial spreading histology, and serum lactate dehydrogenase (LDH) values above the median. Liver metastases were associated with worse outcomes, while radiotherapy treatment of brain metastases was associated with improved OS. However, in a multivariable Cox regression model, only LDH above the median, superficial spreading histology, and female sex were significantly associated with worse OS. We reported grade 3 and 4 treatment-related toxicities in 4 and 0 patients, respectively. In conclusion, chemotherapy with wCP is a valid palliative treatment in advanced melanoma who progressed with anti-PD-1 antibodies.