2020, Number 6
Immunotherapy in Bladder Cancer: Present and Future
Language: Spanish
References: 38
Page: 1-19
PDF size: 241.41 Kb.
ABSTRACT
Bladder cancer (BC) continues to be a challenge in current urologic clinical practice. It is the seventh most frequently diagnosed tumor in men worldwide, and the eleventh, if we include both men and women.The treatment of non-muscle-invasive bladder cancer has limitations, starting with the approach: transurethral resection is not always complete, there can be failures or early recurrence after bacillus Calmette- Guérin (BCG) therapy, and side effects of treatment with BCG can force its suspension.
In cases of muscle-invasive bladder cancer (MIBC), radical cystectomy is not always a treatment option due to important perioperative comorbidity. In patients with metastatic bladder tumors, the side effects of conventional chemotherapy, as well as tumor progression, have resulted in the need for developing new therapies.
Advances in the knowledge of oncologic molecular biology have provided us with new therapeutic targets (such as cell cycle inhibitors), and specific drugs directed at them have been developed, through the use of monoclonal antibodies. At present, five drugs have been approved by the Food and Drug Administration and the European Medicines Agency for the treatment of metastatic MIBC: atezolizumab, nivolumab, and pembrolizumab stand out for their wider use in clinical practice.
The good results obtained in metastatic bladder cancer have led to the development of new lines of research for the use of those molecules at earlier disease stages and in neoadjuvant protocols. Likewise, numerous studies are being conducted on the combination of those new agents with conventional chemotherapy and radiotherapy to determine more adequate treatment regimens.
The present review article concisely describes the current state of immunotherapy in relation to bladder cancer.
REFERENCES
Brausi M, Collette L, Kurth K, van der Meijden AP, Oosterlinck W, Witjes JA, et al. Variability in the recurrence rate at first follow-up cystoscopy after TUR in stage Ta T1 transitional cell carcinoma of the bladder: a combined analysis of seven EORTC studies. Eur Urol. 2002;41(5):523–31. doi: 10.1016/s0302- 2838(02)00068-4
Rosenberg JE, Hoffman-Censits J, Powles T, van der Heijden MS, Balar AV, Necchi A, et al. Atezolizumab in patients with locally advanced and metastatic urothelial carcinoma who have progressed following treatment with platinumbased chemotherapy: a single-arm, multicentre, phase 2 trial. Lancet. 2016;387(10031):1909– 20. doi: 10.1016/S0140-6736(16)00561-4
Balar AV, Galsky MD, Rosenberg JE, Powles T, Petrylak DP, Bellmunt J, et al. Atezolizumab as first-line treatment in cisplatin-ineligible patients with locally advanced and metastatic urothelial carcinoma: a single-arm, multicentre, phase 2 trial. Lancet. 2017;389(10064):67–76. doi: 10.1016/S0140-6736(16)32455-2
Powles T, Durán I, van der Heijden MS, Loriot Y, Vogelzang NJ, De Giorgi U, et al. Atezolizumab versus chemotherapy in patients with platinum-treated locally advanced or metastatic urothelial carcinoma (IMvigor211): a multicentre, open-label, phase 3 randomised controlled trial. Lancet. 2018;391(10122):748– 57. doi: 10.1016/S0140-6736(17)33297-X
Morales A, Herr H, Steinberg G, Given R, Cohen Z, Amrhein J, et al. Efficacy and safety of MCNA in patients with nonmuscle invasive bladder cancer at high risk for recurrence and progression after failed treatment with bacillus Calmette-Guérin. J Urol. 2015;193(4):1135–43. doi: 10.1016/j.juro.2014.09.109
National Library of Medicine. Novel Therapeutic Approaches for Recurrent Non Muscle invasive Bladder Cancer. Clinical Trials. gov. [accessed 3 Oct 2020] Available from: https://www.clinicaltrials.gov/ct2/results?con d=Novel+Therapeutic+Approaches+for+Recurr ent+Non+Muscle+invasive+Bladder+Cancer&te rm=&cntry=&state=&city=&dist=
Newton MR, Askeland EJ, Andresen ED, Chehval VA, Wang X, Askeland RW, et al. Anti-interleukin-10R1 monoclonal antibody in combination with bacillus Calmette--Guérin is protective against bladder cancer metastasis in a murine orthotopic tumour model and demonstrates systemic specific anti-tumour immunity. Clin Exp Immunol. 2014;177(1):261– 8. doi: 10.1111/cei.12315
Autenrieth M, Kurtz F, Horn T, Seidl C, Morgenstern A, Bruchertseifer F, et al. Intravesikale α-Strahler-Radioimmuntherapie mit Bi-213-anti-EGFR-mAb beim Carcinoma in situ-Rezidiv nach BCG-Therapie: eine Alternative zur Zystektomie? In German Medical Science GMS Publishing House; 2015. p. DocFV06. doi: 10.3205/15oegu06
Necchi A, Briganti A, Bianchi M, Raggi D, Giannatempo P, Luciano’ R, et al. Preoperative pembrolizumab (pembro) before radical cystectomy (RC) for muscle-invasive urothelial bladder carcinoma (MIUC): Interim clinical and biomarker findings from the phase 2 PURE-01 study. JCO. 2018;36(15_suppl):4507–4507. doi: 10.1200/JCO.2018.36.15_suppl.4507
Siefker-Radtke AO, Necchi A, Park SH, García-Donas J, Huddart RA, Burgess EF, et al. First results from the primary analysis population of the phase 2 study of erdafitinib (ERDA; JNJ-42756493) in patients (pts) with metastatic or unresectable urothelial carcinoma (mUC) and FGFR alterations (FGFRalt). JCO. 2018;36(15_suppl):4503–4503. doi: 10.1200/ JCO.2018.36.15_suppl.4503
Bajwa R, Cheema A, Khan T, Amirpour A, Paul A, Chaughtai S, et al. Adverse Effects of Immune Checkpoint Inhibitors (Programmed Death-1 Inhibitors and Cytotoxic T-Lymphocyte- Associated Protein-4 Inhibitors): Results of a Retrospective Study. Journal of Clinical Medicine Research. 2019;11(4):225–36. doi: 10.14740/jocmr3750
Diem S, Keller F, Rüesch R, Maillard SA, Speiser DE, Dummer R, Siano M, Urner-Bloch U, Goldinger SM, Flatz L. Pembrolizumab-triggered Uveitis: An Additional Surrogate Marker for Responders in Melanoma Immunotherapy? J Immunother. 2016 Nov/Dec;39(9):379-382. doi: 10.1097/CJI.0000000000000143. PMID: 27662340.