Page 5 - CUA 2020_Onco_Testis-Kidney-Urothelial
P. 5

2020 CUA ABSTRACTS
                                                              2020 CUA ABSTRACTS






       Moderated Poster Session 3: Uro-Oncology












       MP-3.1                                                MP-3.3
       PDL1 expression by tumor proportion score in immunohistochemistry   Ureteric stents for malignant ureteric obstruction – assessing the
       on the tumor tissue of urothelial carcinoma locally advanced or   factors associated with encrustation and inadequate drainage: A
       metastatic treated by immune checkpoint inhibitors    cohort study
                                                                        1
                              1
                  1
                                                                                  2
                                           2
       Quang Loc Bui , Ahmed Khalil , Hong Son Trinh , Carolina Saldana ,   Shreyas Gandhi , Alex Koziarz , Jason Y. Lee 1
                                                         3
                             5
                  4
                                        6
                                                                                                           2
       Aurelien Gobert , Maya Nourieh , Eva Comperat , Olivier Cussenot 7  1 Department of Urology, University of Toronto, Toronto, ON, Canada;  Faculty
       1 Oncology Medical, Tenon Hospital, Paris, France;  Oncology Service,   of Medicine, University of Toronto, Toronto, ON, Canada
                                            2
       Viet Duc Hospital, Hanoi, Viet Nam;  Oncology Medical, Henri-Mondor   Introduction: Malignant ureteric obstruction (MUO) is a challenging clini-
                                 3
                       4
                                                                             1
       Hospital, Paris, France;  Oncology Medical, Pitié Salpêtrière Hospital, Paris,   cal entity for urologists.  Currently, no definitive guidelines exist regarding
            5
                                              6
       France;  Pathology, Henri-Mondor Hospital, Paris, France;  Pathology, Tenon   optimal management of MUO, including the required frequency of stent
                                                                   2,3
       Hospital, Paris, France;  Urology, Tenon Hospital, Paris, France  changes. Therefore, we evaluated the association of clinical factors at
                       7
       Introduction: The benefit of immune checkpoint inhibitors (ICIs) is modest,   initial stent implantation with prognosis and stent management in patients
       with a tumor response rate of 23– 29% in locally advance or metastatic   with MUO.
       urothelial carcinoma.  The expression of PD-L1 is perhaps a predictive   Methods: A single-center, retrospective cohort study was conducted among
                      1,2
       factor of tumor response of ICIs.                     all patients with MUO managed with a ureteral stent from August 2015 to
       Methods: We conducted a non-interventional, retrospective, multicenter   December 2019. A multivariable regression model was used to evalu-
       study in three university hospitals in Paris. All patients were diagnosed with   ate patient factors associated with the following primary outcomes: stent
       locally advanced or metastatic urothelial carcinoma and treated by anti-  encrustation requiring need for stent change, need for antegrade decom-
       PD1 or anti-PDL1 for at least one cycle. We classified all patients into two   pression due to inadequate drainage, and time to first stent change.
       groups according to RECIST 1.1 criteria: the clinical benefit group, which   Results: Fifty patients (72% female) were included with mean age of 63.9
       included stable disease, partial response or complete response; and the   years. Mean followup was one year. The most common indication for stent-
       progression group. We collected paraffin tissue blocks of these patients.   ing was acute kidney injury (46%), followed by hydronephrosis without
       Then we determined the expression of PDL-1 by immunohistochemistry   creatinine elevation (42%), and pain (6%). Ten patients (20%) required
       using the tumor proportion score (TPS).               antegrade decompression following first stent check. Median (interquartile
       Results: From January 1, 2015 to June 30, 2019, 23 patients were enrolled   range [IQR]) time to first stent change was 91 (84–104) days. History of
       in our study. For the primary endpoint, the mean PDL1 expression did   bowel resection (p=0.018) and diabetes mellitus (p<0.00001) was associ-
       not differ between the clinical benefit group and the progression group   ated with increased frequency of stent change when controlling for stent
       (TPS 32.83%; 95% confidence interval [CI] 3.5–67.3 vs. 26.35; 95% CI   location, creatinine at stent insertion, and indication. Initial ureteric obstruc-
       7.8–48.0, respectively); the difference of PDL1 expression was 6.48% (95%   tion at the mid-ureter was associated with fewer number of stent changes
       CI -46.2–28.3). Concerning the secondary endpoint, overall survival from   (p=0.035). There was no association of stent location, creatinine at stent
       diagnosis did not differ significantly either in the TPS ≥50% group or in   insertion, indication, history bowel resection, or diabetes mellitus with risk
       the TPS <50% group (hazard ratio [HR] 0.75; 95% CI 0.19–2.99; p=0.69).   for future antegrade decompression, risk for encrustation at first check, or
       Patients in the clinical benefit group received ICIs earlier compared to the   time to first change.
       progression disease group, with a significant difference of 1.5 lines (95%   Conclusions: History of bowel resection and diabetes mellitus is associated
       CI 0.8–2.3). Half (50%) of the patients received the ICIs first-line and 50%   with greater number of stent changes due to encrustation. Patients with
       second-line, benefiting the clinical group. On average, the progression   this history may require more frequent stent surveillance, as encrustation
       disease group received ICIs as third-line treatment.  rates may be higher.
       Conclusions: Our results suggest that PDL1 expression is not a predictive   References
       factor of tumor response in the locally advanced or metastatic urothelial   1.   O’Connor E, Nason GJ, Kiely E. Urological management of extramural
       carcinoma patients treated by ICIs.                       malignant ureteric obstruction: A survey of Irish urologists. Curr Urol
       References                                                2017;11:21-5. https://doi.org/10.1159/000447190
       1.   Balar AV, Galsky MD, Rosenberg JE, et al. Atezolizumab as first-line   2.   Sountoulides P, Pardalidis N, Sofikitis N. Endourologic management
           treatment in cisplatin-ineligible patients with locally advanced and   of malignant ureteral obstruction: Indications, results, and quality
           metastatic urothelial carcinoma: A single-arm, multicenter, phase   of life issues. J Endourol 2010;24:129-42. https://doi.org/10.1089/
           2 trial. Lancet 2017 07;389:67-76. https://doi.org/10.1016/S0140-  end.2009.0157
           6736(16)32455-2                                   3.   Lang EK, Winer AG, Abbey-Mensah G, et al. Long-term results of
       2.   Powles T, Durán I, van der Heijden MS, et al. Atezolizumab vs. che-  metallic stents for malignant ureteral obstruction in advanced cervi-
           motherapy in patients with platinum-treated locally advanced or meta-  cal malignancy. J Endourol 2013;27:646-51. https://doi.org/10.1089/
           static urothelial carcinoma (IMvigor211): A multicenter, open-label,   end.2012.0552
           phase 3 randomized controlled trial. Lancet 2018 24;391:748-57.
           https://doi.org/10.1016/S0140-6736(17)33297-X
                                                CUAJ • June 2020 • Volume 14, Issue 6(Suppl2)                 S91
                                                  © 2020 Canadian Urological Association
   1   2   3   4   5   6   7   8   9   10