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Outcomes of Consolidative Nephrectomy following Primary Immunotherapy in Advanced Renal Cell Carcinoma: A Multicenter Analysis.
Hakimi, Kevin; Saidian, Ava; Panian, Justine; Barata, Pedro; Berg, Stephanie; Chang, Steven L; Saliby, Renee M; Dzimitrowicz, Hannah; Emamekhoo, Hamid; Gross, Evan; Kilari, Deepak; Lam, Elaine; Nguyen, Mimi; Meagher, Margaret; Wang, Luke; Rauterkus, Grant P; D'Andrea, Vincent; Yim, Kendrick; Psutka, Sarah; Thapa, Bicky; Weise, Nicole; Zhang, Tian; McKay, Rana R; Derweesh, Ithaar H.
Affiliation
  • Hakimi K; Department of Urology, UC San Diego School of Medicine, San Diego, CA.
  • Saidian A; Department of Urology, UC San Diego School of Medicine, San Diego, CA.
  • Panian J; Deparment of Internal Medicine, Division of Hematology and Medical Oncology, UC San Diego School of Medicine, San Diego, CA.
  • Barata P; Department of Hematology and Medical Oncology, Tulane University School of Medicine, New Orleans, LA.
  • Berg S; Department of Hematology and Medical Oncology, Loyola University Medical Center, Maywood, IL.
  • Chang SL; Division of Urology, Brigham and Women's Hospital, Boston, MA.
  • Saliby RM; Lark Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Dzimitrowicz H; Department of Medicine, Duke University School of Medicine, Durham, NC.
  • Emamekhoo H; Department of Hematology and Medical Oncology, University of Wisconsin School of Medicine, Madison, WI.
  • Gross E; Department of Hematology and Medical Oncology, University of Washington School of Medicine, Seattle, WA.
  • Kilari D; Division of Hematology and Medical Oncology, Medical College of Wisconsin, Milwaukee, WI.
  • Lam E; Department of Hematology and Medical Oncology, University of Colorado School of Medicine, Aurora, CO.
  • Nguyen M; Department of Urology, UC San Diego School of Medicine, San Diego, CA.
  • Meagher M; Department of Urology, UC San Diego School of Medicine, San Diego, CA.
  • Wang L; Department of Urology, UC San Diego School of Medicine, San Diego, CA.
  • Rauterkus GP; Department of Hematology and Medical Oncology, Tulane University School of Medicine, New Orleans, LA.
  • D'Andrea V; Lark Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Yim K; Lark Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Psutka S; Department of Hematology and Medical Oncology, University of Washington School of Medicine, Seattle, WA.
  • Thapa B; Division of Hematology and Medical Oncology, Medical College of Wisconsin, Milwaukee, WI.
  • Weise N; Deparment of Internal Medicine, Division of Hematology and Medical Oncology, UC San Diego School of Medicine, San Diego, CA.
  • Zhang T; Department of Hematology and Medical Oncology, University of Texas Southwestern Medical Center, Dallas, TX.
  • McKay RR; Deparment of Internal Medicine, Division of Hematology and Medical Oncology, UC San Diego School of Medicine, San Diego, CA.
  • Derweesh IH; Department of Urology, UC San Diego School of Medicine, San Diego, CA. Electronic address: iderweesh@gmail.com.
Clin Genitourin Cancer ; 21(6): 694-702, 2023 12.
Article in En | MEDLINE | ID: mdl-37558529
ABSTRACT

BACKGROUND:

To evaluate effect and outcomes of combination primary immunotherapy (IO) and nephrectomy for advanced renal cell carcinoma (RCC).

METHODS:

We conducted a multicenter, retrospective analysis of patients with advanced/metastatic RCC who received IO followed by nephrectomy. Primary outcome was Bifecta (negative surgical margins and no 30-day surgical complications). Secondary outcomes included progression-free survival (PFS) following surgery, reduction in tumor/thrombus size, RENAL score, and clinical/pathologic downstaging. Cox regression multivariable analysis was conducted for predictors of Bifecta and PFS. Kaplan-Meier analysis assessed PFS, comparing Bifecta and non-Bifecta groups.

RESULTS:

A total of 56 patients were analyzed (median age 63 years; median follow-up 22.5 months). A total of 40 (71.4%) patients were intermediate IMDC risk. Patients were treated with immunotherapy for median duration of 8.1 months. Immunotherapy resulted in reductions in tumor size (P < .001), thrombus size (P = .02), and RENAL score (P < .001); 38 (67.9%) patients were clinically downstaged on imaging (P < .001) and 25 (44.6%) patients were pathologically downstaged following surgery (P < .001). Bifecta was achieved in 38 (67.9%) patients. Predictors for bifecta achievement included decreasing tumor size (HR 1.08, P = .043) and pathological downstaging (HR 2.13, P = .047). Bifecta (HR 5.65, P = .009), pathologic downstaging (HR 5.15, P = .02), and increasing reduction in tumor size (HR 1.2, P = .007) were associated with improved PFS. Bifecta patients demonstrated improved 2-year PFS (84% vs. 71%, P = .019).

CONCLUSIONS:

Primary immunotherapy reduced tumor/thrombus size and complexity. Pathologically downstaged patients were more likely to achieve bifecta, and these patients displayed improved 2-year PFS. Our study supports further inquiry in the use of CRN following primary immunotherapy for advanced renal cancer.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombosis / Carcinoma, Renal Cell / Kidney Neoplasms Type of study: Clinical_trials / Prognostic_studies Limits: Humans / Middle aged Language: En Journal: Clin Genitourin Cancer Journal subject: NEOPLASIAS / UROLOGIA Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombosis / Carcinoma, Renal Cell / Kidney Neoplasms Type of study: Clinical_trials / Prognostic_studies Limits: Humans / Middle aged Language: En Journal: Clin Genitourin Cancer Journal subject: NEOPLASIAS / UROLOGIA Year: 2023 Document type: Article Affiliation country: