Long-Term Oncological Outcomes in Patients Diagnosed With Nonmetastatic Plasmacytoid Variant of Bladder Cancer: A 20-Year University of Texas MD Anderson Cancer Center Experience

Akshay Sood, Jan K. Rudzinski, Craig V. Labbate, Patrick J. Hensley, Kelly K. Bree, Charles C. Guo, Omar Alhalabi, Matthew T. Campbell, Arlene O. Siefker-Radtke, Neema Navai, Colin P.N. Dinney, Jianjun Gao, Ashish M. Kamat

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Purpose: The treated natural history of nonmetastatic plasmacytoid variant of bladder cancer (PV-BCa) is poorly understood owing to its rarity. We sought to examine the disease recurrence and metastasis patterns in this select group of patients in order to identify opportunities for intervention. Materials and Methods: We conducted a natural language processing algorithmeaugmented retrospective chart review of 56 consecutive patients who were treated with curative intent for nonmetastatic PV-BCa at our institution between 1998 and 2018. Kaplan-Meier and multivariable Cox regression methods were used for survival analyses. Results: The stage at presentation was: ≤ cT2N0 in 22 (39.3%), cT3N0 in 15 (26.8%), cT4N0 in 13 (23.2%), and ≥ cN1 in 6 patients (10.7%). Forty-nine patients (87.5%) received chemotherapy, and 42 (75%) were able to undergo the planned surgery. Notably, only 4 patients (7.2%) had pT0 stage, while 22 (52.4%) had pND disease at the time of surgery. At 36-month follow-up, 28.4% of patients (95% CI: 22.1%-34.5%) were alive and 22.2% (95% CI: 16.1%-28.5%) were free of metastatic disease. The benefit of surgical extirpation was stage specific: successful completion of surgery was associated with improved metastasis-free survival (at 36 months 32.4% vs 0%, log-rank P < .001) in patients with localized or locally advanced disease (≤cT2N0/cT3N0); however, in patients with regionally advanced disease (cT4N0/≥cN1), consolidative surgery following chemotherapy was not associated with improved metastasis-free survival (12.5% vs 10% at 36 months, log-rank P [ .49). The median time to metastasis from primary treatment end was 6.5 months (IQR: 2.9-14.7). The predominant site of recurrence/metastasis was the peritoneum (76.1%), either in isolation or along with extraperitoneal lesions. Salvage immunotherapy in these patients significantly reduced the risk of death (HR [ 0.11, P [ .001). Conclusions: PV-BCa is a disease with high lethality. Despite multimodal treatment, a vast majority of patients develop atypical intraperitoneal metastasis soon after therapy and rapidly succumb to it. Clinical trials evaluating utility of hyperthermic intraperitoneal chemotherapy and/or immunotherapy may be warranted in this high-risk population.

Original languageEnglish
Pages (from-to)241-255
Number of pages15
JournalJournal of Urology
Volume211
Issue number2
DOIs
StatePublished - Feb 1 2024

Bibliographical note

Publisher Copyright:
© 2023 by AMERICAN UROLOGICAL ASSOCIATION EDUCATION AND RESEARCH, INC.

Funding

Support: This research was supported by the Wayne B. Duddlesten Professorship in Cancer Research and the Raymond and Maria Floyd Bladder Cancer Research Foundation Grant to A.M.K. and NIH/NCI UTMD Anderson SPORE in Genitourinary Cancer (Bladder; P50CA091846) to C.P.N.D. J.J.G. is supported by the Doris Duke Clinical Scientist Development Award (#2018097), the MD Anderson Physician Scientist Award, Khalifa Physician Scientist Award, Andrew Sabin Family Foundation Fellows Award, MD Anderson Faculty Scholar Award, the David H. Koch Center for Applied Research of Genitourinary Cancers, Wendy and Leslie Irvin Barnhart Fund, Joan and Herb Kelleher Charitable Foundation, KCA Advanced Discovery Award, the Williams TNT Fund, the V Foundation Translational Award, the DOD KCRP Translational Research Partnership Award, and NIH/NCI R01 CA254988-01A1. The work was also supported in part by the Cancer Center Support Grant to MD Anderson Cancer Center (Grant P30 CA016672) from the National Cancer Institute, by MD Anderson's Prometheus informatics system, and by the Department of Genitourinary Medical Oncology's Eckstein and Alexander Laboratories.

FundersFunder number
Alexander Laboratories
Markey Cancer Center's Cancer Center SupportP30 CA016672
Department of Genitourinary Medical Oncology's Eckstein
Doris Duke Clinical Scientist Development Award2018097
Joan and Herb Kelleher Charitable Foundation
Williams TNT Fund
National Institutes of Health (NIH)
U.S. Department of DefenseR01 CA254988-01A1
U.S. Department of Defense
National Childhood Cancer Registry – National Cancer InstituteP50CA091846
National Childhood Cancer Registry – National Cancer Institute
V Foundation for Cancer Research
Andrew Sabin Family Foundation

    Keywords

    • bladder cancer
    • chemotherapy
    • immunotherapy
    • plasmacytoid

    ASJC Scopus subject areas

    • Urology

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