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Management of Fibroblast Growth Factor Inhibitor Treatment-emergent Adverse Events of Interest in Patients with Locally Advanced or Metastatic Urothelial Carcinoma.
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; Qi, Keqin; Akapame, Sydney; Triantos, Spyros; O'Hagan, Anne; Loriot, Yohann.
Afiliação
  • Siefker-Radtke AO; Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Necchi A; Department of Medical Oncology, IRCCS San Raffaele Hospital, Vita-Salute San Raffaele University, Milan, Italy.
  • Park SH; Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
  • García-Donas J; Fundacion Hospital de Madrid, Madrid, Spain.
  • Huddart RA; Institute of Cancer Research and The Royal Marsden NHS Foundation Trust, Sutton, London, UK.
  • Burgess EF; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Fleming MT; Virginia Oncology Associates, US Oncology Research, Norfolk, VA, USA.
  • Rezazadeh Kalebasty A; University of California Irvine, Irvine, CA, USA.
  • Mellado B; Hosptial Clinic Insitut d'Investigacions Biomèdiques August Pi I Sunyer, University of Barcelona, Barcelona, Spain.
  • Varlamov S; Altai Regional Cancer Center, Barnaul, Russia.
  • Joshi M; Penn State Cancer Institute, Hershey, PA, USA.
  • Duran I; Department of Medical Oncology, Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain.
  • Tagawa ST; Weill Cornell Medical College, New York, NY, USA.
  • Zakharia Y; University of Iowa, Iowa City, IA, USA.
  • Qi K; Janssen Research & Development, Titusville, NJ, USA.
  • Akapame S; Janssen Research & Development, Spring House, PA, USA.
  • Triantos S; Janssen Research & Development, Spring House, PA, USA.
  • O'Hagan A; Janssen Research & Development, Spring House, PA, USA.
  • Loriot Y; Institut Gustave Roussy, Villejuif, France.
Eur Urol Open Sci ; 50: 1-9, 2023 Apr.
Article em En | MEDLINE | ID: mdl-37101768
ABSTRACT

Background:

Erdafitinib is indicated for the treatment of adults with locally advanced/metastatic urothelial carcinoma and susceptible FGFR3/2 alterations progressing on/after one or more lines of prior platinum-based chemotherapy.

Objective:

To better understand the frequency and management of select treatment-emergent adverse events (TEAEs) to enable optimal fibroblast growth factor receptor inhibitor (FGFRi) treatment. Design setting and

participants:

Longer-term efficacy and safety results of the BLC2001 (NCT02365597) trial in patients with locally advanced and unresectable or metastatic urothelial carcinoma were studied. Intervention Erdafitinib schedule of 8 mg/d continuous in 28-d cycles, with uptitration to 9 mg/d if serum phosphate level was <5.5 mg/dl and no significant TEAEs occurred. Outcome measurements and statistical

analysis:

Adverse events were graded using National Cancer Institute Common Terminology Criteria for Adverse Events version 4.0. The Kaplan-Meier methodology was used for the cumulative incidence of the first onset of TEAEs by grade. Time to resolution of TEAEs was summarized descriptively. Results and

limitations:

At data cutoff, the median treatment duration was 5.4 mo among 101 patients receiving erdafitinib. Select TEAEs (total; grade 3) were hyperphosphatemia (78%; 2.0%), stomatitis (59%; 14%), nail events (59%; 15%), non-central serous retinopathy (non-CSR) eye disorders (56%; 5.0%), skin events (55%; 7.9%), diarrhea (55%; 4.0%), and CSR (27%; 4.0%). Select TEAEs were mostly of grade 1 or 2, and were managed effectively with dose modifications, including dose reductions or interruptions, and/or supportive concomitant therapies, resulting in few events leading to treatment discontinuation. Further work is needed to determine whether management is generalizable to the nonprotocol/general population.

Conclusions:

Identification of select TEAEs and appropriate management with dose modification and/or concomitant therapies resulted in improvement or resolution of most TEAEs in patients, allowing for continuation of FGFRi treatment to ensure maximum benefit. Patient

summary:

Early identification and proactive management are warranted to mitigate or possibly prevent erdafitinib side effects to allow for maximum drug benefit in patients with locally advanced or metastatic bladder cancer.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Eur Urol Open Sci Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Eur Urol Open Sci Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos
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