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DC Field | Value | Language |
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dc.contributor.author | Aragon-Ching, J. B. | - |
dc.contributor.author | Petrylak, D. P. | - |
dc.contributor.author | Sridhar, Srikala S. | - |
dc.contributor.author | Gupta, S. | - |
dc.contributor.author | Grivas, P. | - |
dc.contributor.author | Powles, T. | - |
dc.contributor.author | Gurney, Howard | - |
dc.contributor.author | Jacob, N. | - |
dc.contributor.author | Tyroller, K. | - |
dc.contributor.author | Guenther, S. | - |
dc.contributor.author | Bellmunt, J. | - |
dc.date.accessioned | 2024-04-23T04:29:43Z | - |
dc.date.available | 2024-04-23T04:29:43Z | - |
dc.date.issued | 2024 | - |
dc.identifier.citation | Journal of Clinical Oncology 42(4, Supplement)2024 | - |
dc.identifier.uri | https://wslhd.intersearch.com.au/wslhdjspui/handle/1/9459 | - |
dc.description.abstract | BACKGROUND: Avelumab 1L maintenance is recommended as standard of care by international treatment guidelines for pts with aUC that has not progressed with 1L platinum-based chemotherapy, based on level 1 evidence from the phase 3 JAVELIN Bladder 100 trial (NCT02603432). In the trial, avelumab 1L maintenance + best supportive care (BSC) significantly prolonged overall survival (OS) and progression-free survival (PFS) vs BSC alone (median OS, 23.8 vs 15.0 mo; HR, 0.76 [95% CI, 0.63-0.91]; 2-sided p=0.0036). The longterm safety of avelumab 1L maintenance was also demonstrated. It is estimated that 25% of the world's population will have BMI >=30 by 2035, and high BMI is a risk factor for bladder cancer. We report post hoc analyses of long-term outcomes from JAVELIN Bladder 100 in pts with high BMI (>=30) at baseline. Method(s): Eligible pts with unresectable locally advanced or metastatic UC without progression after 4-6 cycles of 1L platinum-based chemotherapy were randomized 1:1 to receive avelumab 10 mg/kg every 2 wk + BSC (n=350) or BSC alone (n=350). The primary endpoint was OS; secondary endpoints included PFS and safety. RESULTS: At data cutoff (June 4, 2021), median follow-up was >=38 mo in both arms. In the avelumab + BSC and BSC alone arms, 67 and 55 pts had high BMI at baseline, respectively. In these pts, median OS was 20.8 mo (95% CI, 16.9-34.4) with avelumab + BSC vs 12.7mo(95% CI, 8.1-26.6) with BSC alone (HR, 0.77[95% CI, 0.49-1.21]); 2-y OS rates were 47.8% vs 37.6%, respectively. Median PFS by investigator was 5.6 mo (95% CI, 3.7-7.5) with avelumab + BSC vs 2.1 mo (95% CI, 1.9-4.0) with BSC alone (HR, 0.64 [95% CI, 0.42-0.97]); 2-y PFS rates were 23.5% vs 11.3%, respectively. Long-term safety in pts with high BMI was generally consistent with the overall safety population (Table). CONCLUSIONS: This exploratory analysis shows the long-term efficacy and tolerability of avelumab 1L maintenance in pts with high BMI in JAVELIN Bladder 100, with no new safety concerns identified. These results further support the use of avelumab 1L maintenance as standard of care in pts with aUC who are progression free after 1L platinum-based chemotherapy, including pts with high BMI. | - |
dc.subject | Oncology | - |
dc.title | Avelumab first-line (1L) maintenance for advanced urothelial carcinoma (aUC): Long- term outcomes from the JAVELIN Bladder 100 trial in patients (pts) with high body mass index (BMI) | - |
dc.type | Journal Article | - |
dc.type | Conference Abstract | - |
dc.identifier.doi | https://doi.org/10.1200/JCO.2024.42.4_suppl.600 | - |
dc.subject.keywords | urinary bladder neoplams | - |
dc.subject.keywords | carcinoma, transitional cell | - |
dc.subject.keywords | avelumab | - |
dc.identifier.journaltitle | Journal of Clinical Oncology | - |
dc.identifier.department | Crown Princess Mary Cancer Centre | - |
dc.identifier.department | Oncology | - |
dc.contributor.wslhd | Sridhar, Srikala S. | - |
dc.contributor.wslhd | Gurney, Howard | - |
dc.type.studyortrial | Controlled Study | - |
dc.type.studyortrial | Major Clinical Study | - |
dc.identifier.affiliation | Inova Schar Cancer Institute, Fairfax, VA | - |
dc.identifier.affiliation | Yale Cancer Center, New Haven, CT | - |
dc.identifier.affiliation | Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada | - |
dc.identifier.affiliation | Cleveland Clinic Taussig Cancer Institute, Cleveland, OH | - |
dc.identifier.affiliation | Division of Hematology & Oncology, University of Washington & Fred Hutchinson Cancer Center, Seattle, WA | - |
dc.identifier.affiliation | Barts Cancer Institute, Cancer Research UK Experimental Cancer Medicine Centre, Queen Mary University of London, London, United Kingdom | - |
dc.identifier.affiliation | Faculty of Medicine, Health and Human Sciences, Macquarie University, Sydney, NSW, Australia | - |
dc.identifier.affiliation | Crown Princess Mary Cancer Centre, Westmead Hospital, Macquarie Park, Australia | - |
dc.identifier.affiliation | The Healthcare Business of Merck KGaA, Darmstadt, Germany | - |
dc.identifier.affiliation | EMD Serono, Billerica, MA | - |
dc.identifier.affiliation | Dana-Farber Cancer Institute, Boston, MA | - |
dc.identifier.facility | Blacktown | - |
dc.identifier.facility | Westmead | - |
dc.identifier.conferencename | 2024 ASCO Genitourinary Cancers Symposium. San Francisco, CA United States. | - |
Appears in Collections: | Blacktown Mount Druitt Hospital |
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