Efficacy and safety of erdafitinib in patients with locally advanced or metastatic urothelial carcinoma: long-term follow-up of a phase 2 study. Issue 2 (February 2022)
- Record Type:
- Journal Article
- Title:
- Efficacy and safety of erdafitinib in patients with locally advanced or metastatic urothelial carcinoma: long-term follow-up of a phase 2 study. Issue 2 (February 2022)
- Main Title:
- Efficacy and safety of erdafitinib in patients with locally advanced or metastatic urothelial carcinoma: long-term follow-up of a phase 2 study
- Authors:
- Siefker-Radtke, Arlene O
Necchi, Andrea
Park, Se Hoon
García-Donas, Jesús
Huddart, Robert A
Burgess, Earle F
Fleming, Mark T
Rezazadeh Kalebasty, Arash
Mellado, Begoña
Varlamov, Sergei
Joshi, Monika
Duran, Ignacio
Tagawa, Scott T
Zakharia, Yousef
Akapame, Sydney
Santiago-Walker, Ademi E
Monga, Manish
O'Hagan, Anne
Loriot, Yohann
Necchi, Andrea
Loriot, Yohann
Park, Se Hoon
Tagawa, Scott
Flechon, Aude
Alexeev, Boris
Varlamov, Sergey
Huddart, Robert
Burgess, Earle
Rezazadeh, Arash
Siefker-Radtke, Arlene
Vano, Yann
Gasparro, Donatello
Hamzaj, Alketa
Kopyltsov, Eugeniy
Gracia Donas, Jesus
Mellado, Begona
Parikh, Omi
Schatteman, Peter
Culine, Stephane
Houédé, Nadine
Zanetta, Sylvie
Facchini, Gaetano
Scagliotti, Giorgio
Schinzari, Giovanni
Lee, Jae Lyun
Shkolnik, Mikhail
Fleming, Mark
Joshi, Monica
O'Donnell, Peter
Stöger, Herbert
Decaestecker, Karel
Dirix, Luc
Machiels, Jean Pascal
Borchiellini, Dephine
Delva, Remy
Rolland, Frederic
Hadaschik, Boris
Retz, Margitta
Rosenbaum, Eli
Basso, Umberto
Mosca, Alessandra
Lee, Hyo Jin
Shin, Dong Bok
Cebotaru, Cristina
Duran, Ignacio
Moreno, Victor
Perez Gracia, Jose Luis
Pinto, Alvaro
Su, Wen-Pin
Wang, Shian-Shiang
Hainsworth, John
Schnadig, Ian
Srinivas, Sandhya
Vogelzang, Nicholas
Loidl, Wolfgang
Meran, Johannes
Gross Goupil, Marine
Joly, Florence
Imkamp, Florian
Klotz, Theodor
Krege, Susanne
May, Matthias
Schultze-Seemann, Wolfgang
Strauss, Arne
Zimmermann, Uwe
Keizman, Daniel
Peer, Avivit
Sella, Avishai
Berardi, Rossana
De Giorgi, Ugo
Sternberg, Cora Nanette
Rha, Sun Young
Bulat, Iurie
Izmailov, Adel
Matveev, Vsevolod
Vladimirov, Vladimir
Carles, Joan
Font, Albert
Saez, Maribel
Syndikus, Isabel
Tarver, Kathryn
Appleman, Leonard
Burke, John
Dawson, Nancy
Jain, Sharad
Zakharia, Yousef
… (more) - Abstract:
- Summary: Background: Erdafitinib, a pan-fibroblast growth factor receptor (FGFR) tyrosine kinase inhibitor, was shown to be clinically active and tolerable in patients with advanced urothelial carcinoma and prespecified FGFR alterations in the primary analysis of the BLC2001 study at median 11 months of follow-up. We aimed to assess the long-term efficacy and safety of the selected regimen of erdafitinib determined in the initial part of the study. Methods: The open-label, non-comparator, phase 2, BLC2001 study was done at 126 medical centres in 14 countries across Asia, Europe, and North America. Eligible patients were aged 18 years or older with locally advanced and unresectable or metastatic urothelial carcinoma, at least one prespecified FGFR alteration, an Eastern Cooperative Oncology Group performance status of 0–2, and progressive disease after receiving at least one systemic chemotherapy or within 12 months of neoadjuvant or adjuvant chemotherapy or were ineligible for cisplatin. The selected regimen determined in the initial part of the study was continuous once daily 8 mg/day oral erdafitinib in 28-day cycles, with provision for pharmacodynamically guided uptitration to 9 mg/day (8 mg/day UpT). The primary endpoint was investigator-assessed confirmed objective response rate according to Response Evaluation Criteria In Solid Tumors version 1.1. Efficacy and safety were analysed in all treated patients who received at least one dose of erdafitinib. This is the finalSummary: Background: Erdafitinib, a pan-fibroblast growth factor receptor (FGFR) tyrosine kinase inhibitor, was shown to be clinically active and tolerable in patients with advanced urothelial carcinoma and prespecified FGFR alterations in the primary analysis of the BLC2001 study at median 11 months of follow-up. We aimed to assess the long-term efficacy and safety of the selected regimen of erdafitinib determined in the initial part of the study. Methods: The open-label, non-comparator, phase 2, BLC2001 study was done at 126 medical centres in 14 countries across Asia, Europe, and North America. Eligible patients were aged 18 years or older with locally advanced and unresectable or metastatic urothelial carcinoma, at least one prespecified FGFR alteration, an Eastern Cooperative Oncology Group performance status of 0–2, and progressive disease after receiving at least one systemic chemotherapy or within 12 months of neoadjuvant or adjuvant chemotherapy or were ineligible for cisplatin. The selected regimen determined in the initial part of the study was continuous once daily 8 mg/day oral erdafitinib in 28-day cycles, with provision for pharmacodynamically guided uptitration to 9 mg/day (8 mg/day UpT). The primary endpoint was investigator-assessed confirmed objective response rate according to Response Evaluation Criteria In Solid Tumors version 1.1. Efficacy and safety were analysed in all treated patients who received at least one dose of erdafitinib. This is the final analysis of this study. This study is registered with ClinicalTrials.gov, NCT02365597 . Findings: Between May 25, 2015, and Aug 9, 2018, 2328 patients were screened, of whom 212 were enrolled and 101 were treated with the selected erdafitinib 8 mg/day UpT regimen. The data cutoff date for this analysis was Aug 9, 2019. Median efficacy follow-up was 24·0 months (IQR 22·7–26·6). The investigator-assessed objective response rate for patients treated with the selected erdafitinib regimen was 40 (40%; 95% CI 30–49) of 101 patients. The safety profile remained similar to that in the primary analysis, with no new safety signals reported with longer follow-up. Grade 3–4 treatment-emergent adverse events of any causality occurred in 72 (71%) of 101 patients. The most common grade 3–4 treatment-emergent adverse events of any cause were stomatitis (in 14 [14%] of 101 patients) and hyponatraemia (in 11 [11%]). There were no treatment-related deaths. Interpretation: With longer follow-up, treatment with the selected regimen of erdafitinib showed consistent activity and a manageable safety profile in patients with locally advanced or metastatic urothelial carcinoma and prespecified FGFR alterations. Funding: Janssen Research & Development. … (more)
- Is Part Of:
- Lancet oncology. Volume 23:Issue 2(2022)
- Journal:
- Lancet oncology
- Issue:
- Volume 23:Issue 2(2022)
- Issue Display:
- Volume 23, Issue 2 (2022)
- Year:
- 2022
- Volume:
- 23
- Issue:
- 2
- Issue Sort Value:
- 2022-0023-0002-0000
- Page Start:
- 248
- Page End:
- 258
- Publication Date:
- 2022-02
- Subjects:
- Oncology -- Periodicals
Neoplasms -- Periodicals
Cancérologie -- Périodiques
Oncologie
Oncology
Periodicals
Electronic journals
616.994005 - Journal URLs:
- http://www.sciencedirect.com/science/journal/14702045 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/S1470-2045(21)00660-4 ↗
- Languages:
- English
- ISSNs:
- 1470-2045
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5146.090000
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British Library STI - ELD Digital store - Ingest File:
- 20691.xml