Management of Fibroblast Growth Factor Inhibitor Treatment- emergent Adverse Events of Interest in Patients with Locally Advanced or Metastatic Urothelial Carcinoma

被引:7
|
作者
Siefker-Radtke, Arlene O. [1 ]
Necchi, Andrea [2 ]
Park, Se Hoon [3 ]
Garcia-Donas, Jesus [4 ]
Huddart, Robert A. [5 ,6 ]
Burgess, Earle F. [7 ]
Fleming, Mark T. [8 ]
Kalebasty, Arash Rezazadeh [9 ]
Mellado, Begona [10 ]
Varlamov, Sergei [11 ]
Joshi, Monika [12 ]
Duran, Ignacio [13 ]
Tagawa, Scott T. [14 ]
Zakharia, Yousef [15 ]
Qi, Keqin [16 ]
Akapame, Sydney [17 ]
Triantos, Spyros [17 ]
O'Hagan, Anne [17 ]
Loriot, Yohann [18 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Houston, TX USA
[2] Univ Vita Salute San Raffaele, IRCCS San Raffaele Hosp, Dept Med Oncol, Milan, Italy
[3] Sungkyunkwan Univ, Samsung Med Ctr, Sch Med,Dept Med, Div Hematol Oncol, Seoul, South Korea
[4] Fdn Hosp Madrid, Madrid, Spain
[5] Inst Canc Res, London, England
[6] Royal Marsden NHS Fdn Trust, London, England
[7] Atrium Hlth, Levine Canc Inst, Charlotte, NC USA
[8] US Oncol Res, Virginia Oncol Associates, Norfolk, VA USA
[9] Univ Calif Irvine, Irvine, CA USA
[10] Univ Barcelona, Hosp Clin Inst Invest Biomed August Pi I Sunyer, Barcelona, Spain
[11] Altai Reg Canc Ctr, Barnaul, Russia
[12] Penn State Canc Inst, Hershey, PA USA
[13] Hosp Univ Marques Valdecilla, Dept Med Oncol, IDIVAL, Santander, Spain
[14] Weill Cornell Med Coll, New York, NY USA
[15] Univ Iowa, Iowa City, IA USA
[16] Janssen Res & Dev, Titusville, NJ USA
[17] Janssen Res & Dev, Spring House, PA USA
[18] Inst Gustave Roussy, Villejuif, France
来源
关键词
Erdafitinib; Fibroblast growth factor; inhibitor; Toxicity; Urothelial carcinoma; BGJ398;
D O I
10.1016/j.euros.2022.12.019
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Erdafitinib is indicated for the treatment of adults with locally advanced/metastatic urothelial carcinoma and susceptible FGFR3/2 alterations pro-gressing 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 uptitra-tion 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 hyper-phosphatemia (78%; 2.0%), stomatitis (59%; 14%), nail events (59%; 15%), non-cen-tral 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 deter-mine 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. (c) 2023 The Authors. Published by Elsevier B.V. on behalf of European Association of Urology. This is an open access article under the CC BY-NC-ND license (http://creative-commons.org/licenses/by-nc-nd/4.0/).
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页码:1 / 9
页数:9
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