Objectives: The complement component 5 (C5) inhibitor ravulizumab demonstrated non-inferiority to eculizumab following 26 weeks of treatment in complement inhibitor-naïve and complement inhibitor-experienced patients with paroxysmal nocturnal hemoglobinuria (PNH; studies 301 and 302, respectively). This study aims to describe the results of both studies from 27 weeks to 2 years. Methods: Patients (N = 441) continued to receive ravulizumab throughout the extension period. Efficacy endpoints included lactate dehydrogenase (LDH) normalization, transfusion avoidance and fatigue score (FACIT-F). Safety analyses were also performed. Results: From 27 weeks to 2 years, improvements in LDH levels were maintained in both study populations. Transfusion avoidance was maintained in 81.9% (study 301) and 85.6% (study 302) of patients, and FACIT-F scores remained stable. Ravulizumab was well tolerated, and the incidence of adverse events (AEs) were similar between patients of both studies. Incidence of serious AEs deemed related to ravulizumab treatment was low (<3%). Conclusions: This study reports, to date, the longest period of follow-up in over 400 patients with PNH treated with ravulizumab (662 patient-years). Long-term, ravulizumab demonstrated durable efficacy and was well tolerated, highlighting the importance of C5 inhibitors as the mainstay of PNH treatment.

Long-term safety and efficacy of ravulizumab in patients with paroxysmal nocturnal hemoglobinuria: 2-year results from two pivotal phase 3 studies / Kulasekararaj, A. G.; Griffin, M.; Langemeijer, S.; Usuki, K.; Kulagin, A.; Ogawa, M.; Yu, J.; Mujeebuddin, A.; Nishimura, J. -I.; Lee, J. W.; Peffault de Latour, R.; Latypova, A.; Barcellini, W.; Barraco, F.; Beam, D.; Bettelheim, P.; Borisenkova, E.; Brodsky, A.; Carnley, B.; Cermak, J.; Chen, T. -Y.; Chew, L. P.; Chew, T. K.; Choi, C. W.; Choi, Y.; Chung, J. S.; De Guibert, S.; Devos, T.; Dunaev, Y.; Dwilewicz-Trojaczek, J.; Edahiro, Y.; Elykomov, I.; Engelberger, M. I.; Pomponi, F.; Fuereder, W.; Fujii, N.; Fujiwara, S.; Galieni, P.; Gaya Valls, A.; Girault, S.; Gomez Almaguer, D.; Gonzalez Fernandez, F. A.; Gritsaev, S.; Gunduz, E.; Hantaweepant, C.; Harada, H.; Hoglund, M.; Huang, W. -H.; Husin, A.; Ikezoe, T.; Ishiyama, K.; Ito, Y.; Jang, J. H.; Jo, D. -Y.; Kang, K. -W.; Kennedy, J.; Kim, H. J.; Kim, J. -A.; Kim, J. S.; Kimura, F.; Kobune, M.; Kosugi, H.; Kulasekararaj, A.; Lai, K. -M.; Larratt, L.; Lee, G. -W.; Lee, J. H.; Lee, J. -H.; Lee, J. W.; Lin, C. -C.; Lukina, E.; Martynova, E.; Matsumura, I.; Meike, G.; Menosi Gualandro, S. F.; Minaeva, N.; Mori, Y.; Morita, K.; Morselli Ramalho, F. M.; Mun, Y. -C.; Muus, P.; Myasnikov, A.; Naito, K.; Ninomiya, H.; Nogami, A.; Notaro, R.; Ojeda Gutierrez, E.; Okada, M.; Okamoto, S.; Olkhovik, T.; Pane, F.; Paquette, R.; Park, J. S.; Peffault de la Tour, R.; Piatek, C.; Piekarska, A.; Pontes Reis, M. L.; Pospelova, T.; Ptushkin, V.; Roeth, A.; Rojnuckarin, P.; Rosa Pessoa, V. D. L.; Rossi, B.; Salleh, S.; Salvino de Araujo, M. A.; Samuel, D.; Saraeva, N.; Schrezenmeier, H.; Shatokhin, Y.; Shelekhova, T.; Sohn, S. K.; Steinerova, K.; Sunami, K.; Syed Abdul Kadir, S. S.; Tamura, S.; Theunissen, K.; Toh, S. G.; Tomita, A.; Torregrosa Diaz, J. M.; Ueda, Y.; Usuki, K.; Vannucchi, A. M.; Viboonjuntra, P.; Viigimaa, I.; Volkova, S.; Wang, M. -C.; Won, J. -H.; Wong, L. L. L.; Wong, V. F.; Yap, E. S.; Yeh, S. -P.; Yhim, H. -Y.; Yonemura, Y.; Yoon, S. -S.; Zhuravkov, A.. - In: EUROPEAN JOURNAL OF HAEMATOLOGY. - ISSN 0902-4441. - 109:3(2022), pp. 205-214. [10.1111/ejh.13783]

Long-term safety and efficacy of ravulizumab in patients with paroxysmal nocturnal hemoglobinuria: 2-year results from two pivotal phase 3 studies

Brodsky A.;Choi Y.;Pane F.;
2022

Abstract

Objectives: The complement component 5 (C5) inhibitor ravulizumab demonstrated non-inferiority to eculizumab following 26 weeks of treatment in complement inhibitor-naïve and complement inhibitor-experienced patients with paroxysmal nocturnal hemoglobinuria (PNH; studies 301 and 302, respectively). This study aims to describe the results of both studies from 27 weeks to 2 years. Methods: Patients (N = 441) continued to receive ravulizumab throughout the extension period. Efficacy endpoints included lactate dehydrogenase (LDH) normalization, transfusion avoidance and fatigue score (FACIT-F). Safety analyses were also performed. Results: From 27 weeks to 2 years, improvements in LDH levels were maintained in both study populations. Transfusion avoidance was maintained in 81.9% (study 301) and 85.6% (study 302) of patients, and FACIT-F scores remained stable. Ravulizumab was well tolerated, and the incidence of adverse events (AEs) were similar between patients of both studies. Incidence of serious AEs deemed related to ravulizumab treatment was low (<3%). Conclusions: This study reports, to date, the longest period of follow-up in over 400 patients with PNH treated with ravulizumab (662 patient-years). Long-term, ravulizumab demonstrated durable efficacy and was well tolerated, highlighting the importance of C5 inhibitors as the mainstay of PNH treatment.
2022
Long-term safety and efficacy of ravulizumab in patients with paroxysmal nocturnal hemoglobinuria: 2-year results from two pivotal phase 3 studies / Kulasekararaj, A. G.; Griffin, M.; Langemeijer, S.; Usuki, K.; Kulagin, A.; Ogawa, M.; Yu, J.; Mujeebuddin, A.; Nishimura, J. -I.; Lee, J. W.; Peffault de Latour, R.; Latypova, A.; Barcellini, W.; Barraco, F.; Beam, D.; Bettelheim, P.; Borisenkova, E.; Brodsky, A.; Carnley, B.; Cermak, J.; Chen, T. -Y.; Chew, L. P.; Chew, T. K.; Choi, C. W.; Choi, Y.; Chung, J. S.; De Guibert, S.; Devos, T.; Dunaev, Y.; Dwilewicz-Trojaczek, J.; Edahiro, Y.; Elykomov, I.; Engelberger, M. I.; Pomponi, F.; Fuereder, W.; Fujii, N.; Fujiwara, S.; Galieni, P.; Gaya Valls, A.; Girault, S.; Gomez Almaguer, D.; Gonzalez Fernandez, F. A.; Gritsaev, S.; Gunduz, E.; Hantaweepant, C.; Harada, H.; Hoglund, M.; Huang, W. -H.; Husin, A.; Ikezoe, T.; Ishiyama, K.; Ito, Y.; Jang, J. H.; Jo, D. -Y.; Kang, K. -W.; Kennedy, J.; Kim, H. J.; Kim, J. -A.; Kim, J. S.; Kimura, F.; Kobune, M.; Kosugi, H.; Kulasekararaj, A.; Lai, K. -M.; Larratt, L.; Lee, G. -W.; Lee, J. H.; Lee, J. -H.; Lee, J. W.; Lin, C. -C.; Lukina, E.; Martynova, E.; Matsumura, I.; Meike, G.; Menosi Gualandro, S. F.; Minaeva, N.; Mori, Y.; Morita, K.; Morselli Ramalho, F. M.; Mun, Y. -C.; Muus, P.; Myasnikov, A.; Naito, K.; Ninomiya, H.; Nogami, A.; Notaro, R.; Ojeda Gutierrez, E.; Okada, M.; Okamoto, S.; Olkhovik, T.; Pane, F.; Paquette, R.; Park, J. S.; Peffault de la Tour, R.; Piatek, C.; Piekarska, A.; Pontes Reis, M. L.; Pospelova, T.; Ptushkin, V.; Roeth, A.; Rojnuckarin, P.; Rosa Pessoa, V. D. L.; Rossi, B.; Salleh, S.; Salvino de Araujo, M. A.; Samuel, D.; Saraeva, N.; Schrezenmeier, H.; Shatokhin, Y.; Shelekhova, T.; Sohn, S. K.; Steinerova, K.; Sunami, K.; Syed Abdul Kadir, S. S.; Tamura, S.; Theunissen, K.; Toh, S. G.; Tomita, A.; Torregrosa Diaz, J. M.; Ueda, Y.; Usuki, K.; Vannucchi, A. M.; Viboonjuntra, P.; Viigimaa, I.; Volkova, S.; Wang, M. -C.; Won, J. -H.; Wong, L. L. L.; Wong, V. F.; Yap, E. S.; Yeh, S. -P.; Yhim, H. -Y.; Yonemura, Y.; Yoon, S. -S.; Zhuravkov, A.. - In: EUROPEAN JOURNAL OF HAEMATOLOGY. - ISSN 0902-4441. - 109:3(2022), pp. 205-214. [10.1111/ejh.13783]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/994256
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