WebMar 23, 2024 · The eligibility criteria for first-line patients included ineligibility for cisplatin-based therapy 1 (defined as meeting at least one of the following criteria: Eastern Cooperative Oncology Group Performance Status 2 or 3, creatinine clearance <60 mL/min, grade ≥2 audiometric hearing loss, grade ≥2 peripheral neuropathy, or New York Heart ... WebFeb 23, 2024 · Our team uses the following nephrotoxicity mitigation strategies: • Decompression if acute obstructive uropathy is present. • Nephrology consultation …
Testing Anti-Cancer Drugs Erdafitinib With or Without …
WebOct 14, 2024 · Inclusion Criteria: Histologically confirmed transitional cell urothelial carcinoma. Participants with mixed histologies are required to have a dominant (ie, 50% at least) transitional cell pattern. ... Refuse cisplatin therapy (does not apply in France) or are ineligible for cisplatin therapy per modified Galsky criteria with exclusion of ... WebFeb 16, 2024 · Notes: # The Galsky criteria; 10 ##Many patients had multiple metastatic sites; ¶ Other regimens consisted of 3 gemcitabine plus pacliaxel, 1 gemcitabine … hull cheese
Health-related Quality of Life with Adjuvant Nivolumab After …
WebAug 9, 2024 · The criteria to assess cisplatin fitness is the Galsky criteria published in the Journal of Clinical Oncology in 2011, based on consensus agreement of different medical oncologists who treat patients with urothelial cancer. You covered them well. Age is not 1 of those criteria. It’s mainly patients with higher ECOG performance status in whom ... WebAmong cisplatin-eligible patients, cisplatin + gemcitabine has a median overall survival of 13.8 months, and among cisplatin-ineligible patients (as defined by the Galsky criteria determining patients to be unfit for cisplatin – ECOG >=2, CrCl < 60 mL/min, Grade >=2 hearing loss, Grade >= 2 neuropathy, NY Heart Association Class III heart ... WebKey eligibility criteria included stage cT2-4aN0-1M0, ≥20% tumor content at TURBT and cisplatin-ineligibility (Galsky criteria) or refusal. Primary endpoint was safety manifested as rate of ≥G3 treatment related adverse events (TRAE) assessed in each cohort with CTCAE v5.0. Key secondary endpoints included the % of pts who had RC > 6 weeks ... holiday parks down under