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Practice Guideline
. 2022 Apr;24(4):613-624.
doi: 10.1007/s12094-022-02815-w. Epub 2022 Mar 26.

SEOM-SOGUG clinical guideline for localized muscle invasive and advanced bladder cancer (2021)

Affiliations
Practice Guideline

SEOM-SOGUG clinical guideline for localized muscle invasive and advanced bladder cancer (2021)

Begoña P Valderrama et al. Clin Transl Oncol. 2022 Apr.

Abstract

Most muscle-invasive bladder cancer (BC) are urothelial carcinomas (UC) of transitional origin, although histological variants of UC have been recognized. Smoking is the most important risk factor in developed countries, and the basis for prevention. UC harbors high number of genomic aberrations that make possible targeted therapies. Based on molecular features, a consensus classification identified six different MIBC subtypes. Hematuria and irritative bladder symptoms, CT scan, cystoscopy and transurethral resection are the basis for diagnosis. Radical cystectomy with pelvic lymphadenectomy is the standard approach for muscle-invasive BC, although bladder preservation is an option for selected patients who wish to avoid or cannot tolerate surgery. Perioperative cisplatin-based neoadjuvant chemotherapy is recommended for cT2-4aN0M0 tumors, or as adjuvant in patients with pT3/4 and or pN + after radical cystectomy. Follow-up is particularly important after the availability of new salvage therapies. It should be individualized and adapted to the risk of recurrence. Cisplatin-gemcitabine is considered the standard first line for metastatic tumors. Carboplatin should replace cisplatin in cisplatin-ineligible patients. According to the EMA label, pembrolizumab or atezolizumab could be an option in cisplatin-ineligible patients with high PD-L1 expression. For patients whose disease respond or did not progress after first-line platinum chemotherapy, maintenance with avelumab prolongs survival with respect to the best supportive care. Pembrolizumab also increases survival versus vinflunine or taxanes in patients with progression after chemotherapy who have not received avelumab, as well as enfortumab vedotin in those progressing to first-line chemotherapy followed by an antiPDL1/PD1. Erdafitinib may be considered in this setting in patients with FGFR alterations. An early onset of supportive and palliative care is always strongly recommended.

Keywords: Bladder cancer; Muscle-invasive; Urothelial.

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Conflict of interest statement

AGLL reports Advisory Board and Speaker from Roche, Pfizer and Astellas; Speaker from MSD and BMS and Speaker and Other from AstraZecena. BPV reports Advisory Board, Speaker and Other from Astellas, Roche, BMS and Merk-Pfizer; Advisory Board and Other from Ipsen; Advisory Board and Speaker from EUSA and MSD and Advisory Board from Sanofi. IPF report Advisory Board, Speaker and Other from Pfizer; Speaker and Other from Ipsen and Roche; Advisory Board from EUSA and BMS and Speaker from Novartis and MSD. OFC reports Advisory Board and Speaker from Ipsen and Astellas; Advisory Board from BMS and Pfizer-Merck and Speaker from AstraZeneca. AGA has received research funding from Astellas, travel grants from Astellas, Jansen, Sanofi, BMS, Roche, Pfizer and Ipsen and honoraria for speaker engagements, advisory boards and continuous medical education from Janssen, Astellas, Sanofi, Bayer, Roche, Ipsen, BMS, MSD, Pfizer, Eusa Pharma, Eisai and AstraZeneca. JAA reports honoraria from Astellas, Pfizer and BMS; conulting or advisory role from Pfizer, Astellas, Janssen-Cilag, MSD Oncology, BMS, Merck, AstraZeneca, Bayer and Eisai and Research Funding from BMS. RMB, SVE, CCD and MDS have nothing to disclose.

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