A New Prognostic Model in Patients with Advanced Urothelial Carcinoma Treated with First-line Immune Checkpoint Inhibitors.


Journal

European urology oncology
ISSN: 2588-9311
Titre abrégé: Eur Urol Oncol
Pays: Netherlands
ID NLM: 101724904

Informations de publication

Date de publication:
06 2021
Historique:
received: 28 09 2020
revised: 25 11 2020
accepted: 03 12 2020
pubmed: 12 1 2021
medline: 2 2 2022
entrez: 11 1 2021
Statut: ppublish

Résumé

While immune checkpoint inhibitors (ICIs) are approved in the first-line (1L) setting for cisplatin-unfit patients with programmed death-ligand 1 (PD-L1)-high tumors or for platinum (cisplatin/carboplatin)-unfit patients, response rates remain modest and outcomes vary with no clinically useful biomarkers (except for PD-L1). We aimed to develop a prognostic model for overall survival (OS) in patients receiving 1L ICIs for advanced urothelial cancer (aUC) in a multicenter cohort study. Patients treated with 1L ICIs for aUC across 24 institutions and five countries (in the USA and Europe) outside clinical trials were included in this study. We used a stepwise, hypothesis-driven approach using clinician-selected covariates to develop a new risk score for patients receiving ICIs in the 1L setting. Demographics, clinicopathologic data, treatment patterns, and OS were collected uniformly. Univariate Cox regression was performed on 18 covariates hypothesized to be associated with OS based on published data. Variables were retained for multivariate analysis (MVA) if they correlated with OS (p < 0.2) and were included in the final model if p < 0.05 on MVA. Retained covariates were assigned points based on the beta coefficient to create a risk score. Stratified median OS and C-statistic were calculated. Among 984 patients, 357 with a mean age of 71 yr were included in the analysis, 27% were female, 68% had pure UC, and 13% had upper tract UC. Eastern Cooperative Oncology Group performance status ≥2, albumin <3.5 g/dl, neutrophil:lymphocyte ratio >5, and liver metastases were significant prognostic factors on MVA and were included in the risk score. C index for new 1L risk score was 0.68 (95% confidence interval 0.65-0.71). Limitations include retrospective nature and lack of external validation. We developed a new 1L ICI risk score for OS based on data from patients with aUC treated with ICIs in the USA and Europe outside of clinical trials. The score components highlight readily available factors related to tumor biology and treatment response. External validation is being pursued. With multiple new treatments under development and approved for advanced urothelial carcinoma, it can be difficult to identify the best treatment sequence for each patient. The risk score may help inform treatment discussions and estimate outcomes in patients treated with first-line immune checkpoint inhibitors, while it can also impact clinical trial design and endpoints. TAKE  HOME MESSAGE: A new risk score was developed for advanced urothelial carcinoma treated with first-line immune checkpoint inhibitors. The score assigned Eastern Cooperative Oncology Group performance status ≥2, albumin <3.5 g/dl, neutrophil:lymphocyte ratio >5, and liver metastases each one point, with a higher score being associated with worse overall survival.

Sections du résumé

BACKGROUND
While immune checkpoint inhibitors (ICIs) are approved in the first-line (1L) setting for cisplatin-unfit patients with programmed death-ligand 1 (PD-L1)-high tumors or for platinum (cisplatin/carboplatin)-unfit patients, response rates remain modest and outcomes vary with no clinically useful biomarkers (except for PD-L1).
OBJECTIVE
We aimed to develop a prognostic model for overall survival (OS) in patients receiving 1L ICIs for advanced urothelial cancer (aUC) in a multicenter cohort study.
DESIGN, SETTING, AND PARTICIPANTS
Patients treated with 1L ICIs for aUC across 24 institutions and five countries (in the USA and Europe) outside clinical trials were included in this study.
OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS
We used a stepwise, hypothesis-driven approach using clinician-selected covariates to develop a new risk score for patients receiving ICIs in the 1L setting. Demographics, clinicopathologic data, treatment patterns, and OS were collected uniformly. Univariate Cox regression was performed on 18 covariates hypothesized to be associated with OS based on published data. Variables were retained for multivariate analysis (MVA) if they correlated with OS (p < 0.2) and were included in the final model if p < 0.05 on MVA. Retained covariates were assigned points based on the beta coefficient to create a risk score. Stratified median OS and C-statistic were calculated.
RESULTS AND LIMITATIONS
Among 984 patients, 357 with a mean age of 71 yr were included in the analysis, 27% were female, 68% had pure UC, and 13% had upper tract UC. Eastern Cooperative Oncology Group performance status ≥2, albumin <3.5 g/dl, neutrophil:lymphocyte ratio >5, and liver metastases were significant prognostic factors on MVA and were included in the risk score. C index for new 1L risk score was 0.68 (95% confidence interval 0.65-0.71). Limitations include retrospective nature and lack of external validation.
CONCLUSIONS
We developed a new 1L ICI risk score for OS based on data from patients with aUC treated with ICIs in the USA and Europe outside of clinical trials. The score components highlight readily available factors related to tumor biology and treatment response. External validation is being pursued.
PATIENT SUMMARY
With multiple new treatments under development and approved for advanced urothelial carcinoma, it can be difficult to identify the best treatment sequence for each patient. The risk score may help inform treatment discussions and estimate outcomes in patients treated with first-line immune checkpoint inhibitors, while it can also impact clinical trial design and endpoints. TAKE  HOME MESSAGE: A new risk score was developed for advanced urothelial carcinoma treated with first-line immune checkpoint inhibitors. The score assigned Eastern Cooperative Oncology Group performance status ≥2, albumin <3.5 g/dl, neutrophil:lymphocyte ratio >5, and liver metastases each one point, with a higher score being associated with worse overall survival.

Identifiants

pubmed: 33423945
pii: S2588-9311(20)30214-5
doi: 10.1016/j.euo.2020.12.006
pmc: PMC8169524
mid: NIHMS1657590
pii:
doi:

Substances chimiques

Immune Checkpoint Inhibitors 0

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

464-472

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA009515
Pays : United States
Organisme : Wellcome Trust
ID : PS3416
Pays : United Kingdom
Organisme : NCATS NIH HHS
ID : UL1 TR002319
Pays : United States
Organisme : Wellcome Trust
Pays : United Kingdom

Informations de copyright

Copyright © 2020 European Association of Urology. Published by Elsevier B.V. All rights reserved.

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Auteurs

Ali Raza Khaki (AR)

Division of Medical Oncology, Department of Medicine, Fred Hutchinson Cancer Research Center, Seattle Cancer Care Alliance, University of Washington, Seattle, WA, USA.

Ang Li (A)

Section of Hematology/Oncology, Department of Medicine, Baylor College of Medicine, Houston, TX, USA.

Leonidas N Diamantopoulos (LN)

Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.

Natalie J Miller (NJ)

Department of Medicine, University of Washington, Seattle, WA, USA.

Lucia Carril-Ajuria (L)

Hospital Universitario 12 de Octubre, Madrid, Spain.

Daniel Castellano (D)

Hospital Universitario 12 de Octubre, Madrid, Spain.

Ivan De Kouchkovsky (I)

Division of Oncology, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.

Vadim Koshkin (V)

Division of Oncology, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.

Joseph Park (J)

Division of Oncology, Department of Medicine, University of Michigan, Ann Arbor, MI, USA.

Ajjai Alva (A)

Division of Oncology, Department of Medicine, University of Michigan, Ann Arbor, MI, USA.

Mehmet A Bilen (MA)

Winship Cancer Institute of Emory University, Atlanta, GA, USA.

Tyler Stewart (T)

Division of Oncology, Department of Medicine, University of California, San Diego, La Jolla, CA, USA.

Victor Santos (V)

Division of Oncology, Department of Medicine, University of Utah, Salt Lake City, UT, USA.

Neeraj Agarwal (N)

Division of Oncology, Department of Medicine, University of Utah, Salt Lake City, UT, USA.

Jayanshu Jain (J)

Department of Medicine, University of Iowa, Iowa City, IA, USA.

Yousef Zakharia (Y)

Division of Oncology, Department of Medicine, University of Iowa, Iowa City, IA, USA.

Rafael Morales-Barrera (R)

Vall d'Hebron Institute of Oncology, Vall d' Hebron University Hospital, Universitat Autònoma de Barcelona, Barcelona, Spain.

Michael Devitt (M)

Division of Hematology/Oncology, Department of Medicine, University of Virginia School of Medicine, Charlottesville, VA, USA.

Ariel Nelson (A)

Division of Medical Oncology, Seidman Cancer Center at Case Comprehensive Cancer Center, Cleveland, OH, USA; Division of Hematology and Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.

Christopher J Hoimes (CJ)

Division of Medical Oncology, Seidman Cancer Center at Case Comprehensive Cancer Center, Cleveland, OH, USA; Division of Medical Oncology, Duke University, Durham, NC, USA.

Evan Shreck (E)

Departments of Medical Oncology and Urology, Montefiore Medical Center, Bronx, NY, USA.

Benjamin A Gartrell (BA)

Departments of Medical Oncology and Urology, Montefiore Medical Center, Bronx, NY, USA.

Alex Sankin (A)

Departments of Medical Oncology and Urology, Montefiore Medical Center, Bronx, NY, USA.

Abhishek Tripathi (A)

Stephenson Cancer Center, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.

Roubini Zakopoulou (R)

Department of Clinical Therapeutics, Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Aristotelis Bamias (A)

2nd Propaedeutic Department of Internal Medicine, ATTIKON University Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Alejo Rodriguez-Vida (A)

Medical Oncology Department, Hospital del Mar Research Institute, Barcelona, Spain.

Alexandra Drakaki (A)

Division of Hematology/Oncology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.

Sandy Liu (S)

Division of Hematology/Oncology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.

Vivek Kumar (V)

Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Mark P Lythgoe (MP)

Department of Surgery and Cancer, Imperial College London, London, UK.

David J Pinato (DJ)

Department of Surgery and Cancer, Imperial College London, London, UK.

Jure Murgic (J)

Department of Oncology and Nuclear Medicine, University Hospital Center Sestre Milosrdnice, School of Dental Medicine, Zagreb, Croatia.

Ana Fröbe (A)

Department of Oncology and Nuclear Medicine, University Hospital Center Sestre Milosrdnice, School of Dental Medicine, Zagreb, Croatia.

Monika Joshi (M)

Division of Hematology/Oncology, Department of Medicine, Penn State Cancer Institute, Hershey, PA, USA.

Pedro Isaacsson Velho (P)

Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA.

Noah Hahn (N)

Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA.

Lucia Alonso Buznego (L)

Hospital Universitario Marques de Valdecilla, IDIVAL, Santander, Spain.

Ignacio Duran (I)

Hospital Universitario Marques de Valdecilla, IDIVAL, Santander, Spain.

Marcus Moses (M)

Department of Medicine, Section of Hematology/Oncology, Tulane University, New Orleans, LA, USA.

Pedro Barata (P)

Department of Medicine, Section of Hematology/Oncology, Tulane University, New Orleans, LA, USA.

Matthew D Galsky (MD)

Division of Oncology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Guru Sonpavde (G)

Genitourinary Oncology Program, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

Evan Y Yu (EY)

Division of Medical Oncology, Department of Medicine, Fred Hutchinson Cancer Research Center, Seattle Cancer Care Alliance, University of Washington, Seattle, WA, USA.

Veena Shankaran (V)

Division of Medical Oncology, Department of Medicine, Fred Hutchinson Cancer Research Center, Seattle Cancer Care Alliance, University of Washington, Seattle, WA, USA.

Gary H Lyman (GH)

Division of Medical Oncology, Department of Medicine, Fred Hutchinson Cancer Research Center, Seattle Cancer Care Alliance, University of Washington, Seattle, WA, USA.

Petros Grivas (P)

Division of Medical Oncology, Department of Medicine, Fred Hutchinson Cancer Research Center, Seattle Cancer Care Alliance, University of Washington, Seattle, WA, USA. Electronic address: pgrivas@uw.edu.

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