RSS-Feed abonnieren

DOI: 10.1055/s-0044-1782235
Comparison of PSA Response to Generic Versus Innovator (Zytiga) Formulations of Abiraterone in Metastatic CRPC: A Retrospective Analysis
Funding None.

Abstract
Introduction Abiraterone acetate has been shown to enhance overall survival and radiographic progression-free survival (rPFS) in men with metastatic castration-resistant prostate cancer (mCRPC). Presently, multiple generic brands of abiraterone are accessible in India. Nevertheless, evidence supporting the clinical equivalence of these generics when compared to the innovator has not been established, and thus, questions regarding their quality persist.
Objectives This retrospective analysis aimed to compare the prostate-specific antigen (PSA) response in patients receiving generic or innovator (Zytiga) abiraterone for mCRPC.
Materials and Methods This was a single-center, retrospective, comparative study. All relevant data from selected cases were collected from the hospital's electronic medical record (EMR). Patients with mCRPC, treated with either innovator or generic abiraterone from 2010 to 2019 and followed up until disease progression/death, were included. Patients who switched between generic and reference brands and vice versa were excluded. Patients in both arms were matched for prior treatment with docetaxel (yes/no), age at cancer diagnosis (>60, ≤60 years), and total Gleason's score (≥8, <8), in a ratio of 1:5. The primary outcome was to assess the difference in PSA nadir between the two study groups. Data were analyzed using Statistical Package for Social Sciences (SPSS) v.21 and GraphPad Prism 8.0.2.
Results Out of the 114 patients enrolled, 10 patients received Zytiga (innovator), and the remaining received generic abiraterone. No statistically significant difference was observed in the median PSA nadir between the generic and innovator arms: 20.5 versus 88.5 ng/mL (p = 0.293). Patients in the generic group exhibited a similar median rPFS compared to the innovator group: 9.0 months (95% confidence interval [CI]: 6.68–11.31 months) versus 9.0 months (95% CI: 0–18.6 months), respectively (p = 0.539). The median time to PSA nadir was similar (3 months) between the two groups. The proportion of patients showing a PSA response at day 90 did not significantly differ between the two groups, with p = 0.38. The number of adverse events of any grade was comparable between the study groups, although grade 3/4 events were numerically higher in the generic group.
Conclusion Generic abiraterone demonstrates a clinical response similar to that of Zytiga. Our findings strongly support the use of generic abiraterone in patients with mCRPC. The potential economic benefits of this substitution are substantial.
Data Availability Statement
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
Author's Contributions
Conception or design of the work was done by V.G., V.N., K.P. and A.J. Data collection was done by A.T., D.V., S.P., and S.K. Data analysis and interpretation were done by S.K. and S.P. S.K. drafted the article. Critical revision of the article was done by V.G., V.N., K.P. and A.J. Final approval of the version to be published was approved by V.G., A.J., D.V., S.P., A.T. and S.K. Accountability for all aspects of the work lies with V.G.
* These authors contributed equally to this work and should be considered as first authors.
Publikationsverlauf
Artikel online veröffentlicht:
20. Februar 2025
© 2025. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)
Thieme Medical and Scientific Publishers Pvt. Ltd.
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India
-
References
- 1 Wang L, Lu B, He M, Wang Y, Wang Z, Du L. Prostate cancer incidence and mortality: global status and temporal trends in 89 countries from 2000 to 2019. Front Public Health 2022; 10: 811044
- 2 Sung H, Ferlay J, Siegel RL. et al. Global Cancer Statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2021; 71 (03) 209-249
- 3 PDQ Adult Treatment Editorial Board. Prostate Cancer Treatment (PDQ®): Health Professional Version. In: PDQ Cancer Information Summaries. Bethesda, MD: National Cancer Institute (US); 2002
- 4 Rehman Y, Rosenberg JE. Abiraterone acetate: oral androgen biosynthesis inhibitor for treatment of castration-resistant prostate cancer. Drug Des Devel Ther 2012; 6: 13-18
- 5 Facchini G, Caffo O, Ortega C. et al. Very early PSA response to abiraterone in mCRPC patients: a novel prognostic factor predicting overall survival. Front Pharmacol 2016; 7: 123
- 6 Miller D, Ippolito B, Hernandez I, Davies B. The costs of delayed generic drug entry: evidence from a controversial prostate cancer drug patent. J Gen Intern Med 2022; 37 (03) 668-670
- 7 Wang C, Hu C, Gao D. et al. Pharmacokinetics and bioequivalence of generic and branded abiraterone acetate tablet: a single-dose, open-label, and replicate designed study in healthy Chinese male volunteers. Cancer Chemother Pharmacol 2019; 83 (03) 509-517
- 8 Meredith PA. Generic drugs. Drug-Safety 1996; 15: 233-242
- 9 Sankaran H, Sengupta S, Purohit V. et al. A comparison of asparaginase activity in generic formulations of E. coli derived L-asparaginase: in-vitro study and retrospective analysis of asparaginase monitoring in pediatric patients with leukemia. Br J Clin Pharmacol 2020; 86 (06) 1081-1088
- 10 Johnson S, Dhamne C, Sankaran H. et al. A prospective, open-label, randomised, parallel design study of 4 generic formulations of intramuscular L-asparaginase in childhood precursor B-cell acute lymphoblastic leukaemia (ALL). Cancer Chemother Pharmacol 2022; 90 (06) 445-453
- 11 Vial J, Cohen M, Sassiat P, Thiébaut D. Pharmaceutical quality of docetaxel generics versus originator drug product: a comparative analysis. Curr Med Res Opin 2008; 24 (07) 2019-2033
- 12 Xu XS, Ryan CJ, Stuyckens K. et al. Correlation between prostate-specific antigen kinetics and overall survival in abiraterone acetate-treated castration-resistant prostate cancer patients. Clin Cancer Res 2015; 21 (14) 3170-3177
- 13 Miyake H, Hara T, Tamura K. et al. Independent association between time to prostate-specific antigen (PSA) nadir and PSA progression-free survival in patients with docetaxel-naïve, metastatic castration-resistant prostate cancer receiving abiraterone acetate, but not enzalutamide. Urol Oncol 2017; 35 (06) 432-437
- 14 Nakayama M, Kobayashi H, Takahara T, Oyama R, Imanaka K, Yoshizawa K. Association of early PSA decline and time to PSA progression in abiraterone acetate-treated metastatic castration-resistant prostate cancer; a post-hoc analysis of Japanese phase 2 trials. BMC Urol 2016; 16 (01) 27
- 15 Fizazi K, Scher HI, Molina A. et al; COU-AA-301 Investigators. Abiraterone acetate for treatment of metastatic castration-resistant prostate cancer: final overall survival analysis of the COU-AA-301 randomised, double-blind, placebo-controlled phase 3 study. Lancet Oncol 2012; 13 (10) 983-992
- 16 Raju R, Sahu A, Klevansky M, Torres J. Real-world data on outcomes in metastatic castrate-resistant prostate cancer patients treated with abiraterone or enzalutamide: a regional experience. Front Oncol 2021; 11: 656146
- 17 Halabi S, Armstrong AJ, Sartor O. et al. Prostate-specific antigen changes as surrogate for overall survival in men with metastatic castration-resistant prostate cancer treated with second-line chemotherapy. J Clin Oncol 2013; 31 (31) 3944-3950
- 18 Demirci A, Bilir C, Gülbağcı B. et al. Comparison of real-life data of abiraterone acetate and enzalutamide in metastatic castration-resistant prostate cancer. Sci Rep 2021; 11 (01) 14131
- 19 Indurlal P, Ives H, Garey JS, McGuinness M, Pacheco AV, Wilfong LS. Financial impact of generic therapeutic interchange of abiraterone in the oncology care model for the U.S. Oncology Network. J Clin Oncol 2022; 40 (16, suppl): e17019-e17019
- 20 Rescigno P, Lorente D, Ferraldeschi R. et al. Association between PSA declines at 4 weeks and OS in patients treated with abiraterone acetate (AA) for metastatic castration resistant prostate cancer (mCRPC) after docetaxel. J Clin Oncol 2015; 33 (7, suppl): 215-215