Impact of performance status on treatment outcomes: A real-world study of advanced urothelial cancer treated with immune checkpoint inhibitors.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
15 03 2020
Historique:
received: 27 08 2019
revised: 07 10 2019
accepted: 27 10 2019
pubmed: 13 12 2019
medline: 10 10 2020
entrez: 13 12 2019
Statut: ppublish

Résumé

Immune checkpoint inhibitors (ICIs) represent an appealing treatment for patients with advanced urothelial cancer (aUC) and a poor performance status (PS). However, the benefit of ICIs for patients with a poor PS remains unknown. It was hypothesized that a poor Eastern Cooperative Oncology Group (ECOG) PS (≥2 vs 0-1) would correlate with shorter overall survival (OS) in patients receiving ICIs. In this retrospective cohort study, clinicopathologic, treatment, and outcome data were collected for patients with aUC who were treated with ICIs at 18 institutions (2013-2019). The overall response rate (ORR) and OS were compared for patients with an ECOG PS of 0 to 1 and patients with an ECOG PS ≥ 2 at ICI initiation. The association between a new ICI in the last 30 and 90 days of life (DOL) and death location was also tested. Of the 519 patients treated with ICIs, 395 and 384 were included in OS and ORR analyses, respectively, with 26% and 24% having a PS ≥ 2. OS was higher in those with a PS of 0 to 1 than those with a PS ≥ 2 who were treated in the first line (median, 15.2 vs 7.2 months; hazard ratio [HR], 0.62; P = .01) but not in subsequent lines (median, 9.8 vs 8.2 months; HR, 0.78; P = .27). ORRs were similar for patients with a PS of 0 to 1 and patients with a PS ≥ 2 in both lines. Of the 288 patients who died, 10% and 32% started ICIs in the last 30 and 90 DOL, respectively. ICI initiation in the last 30 DOL was associated with increased odds of death in a hospital (odds ratio, 2.89; P = .04). Despite comparable ORRs, ICIs may not overcome the negative prognostic role of a poor PS, particularly in the first-line setting, and the initiation of ICIs in the last 30 DOL was associated with hospital death location.

Sections du résumé

BACKGROUND
Immune checkpoint inhibitors (ICIs) represent an appealing treatment for patients with advanced urothelial cancer (aUC) and a poor performance status (PS). However, the benefit of ICIs for patients with a poor PS remains unknown. It was hypothesized that a poor Eastern Cooperative Oncology Group (ECOG) PS (≥2 vs 0-1) would correlate with shorter overall survival (OS) in patients receiving ICIs.
METHODS
In this retrospective cohort study, clinicopathologic, treatment, and outcome data were collected for patients with aUC who were treated with ICIs at 18 institutions (2013-2019). The overall response rate (ORR) and OS were compared for patients with an ECOG PS of 0 to 1 and patients with an ECOG PS ≥ 2 at ICI initiation. The association between a new ICI in the last 30 and 90 days of life (DOL) and death location was also tested.
RESULTS
Of the 519 patients treated with ICIs, 395 and 384 were included in OS and ORR analyses, respectively, with 26% and 24% having a PS ≥ 2. OS was higher in those with a PS of 0 to 1 than those with a PS ≥ 2 who were treated in the first line (median, 15.2 vs 7.2 months; hazard ratio [HR], 0.62; P = .01) but not in subsequent lines (median, 9.8 vs 8.2 months; HR, 0.78; P = .27). ORRs were similar for patients with a PS of 0 to 1 and patients with a PS ≥ 2 in both lines. Of the 288 patients who died, 10% and 32% started ICIs in the last 30 and 90 DOL, respectively. ICI initiation in the last 30 DOL was associated with increased odds of death in a hospital (odds ratio, 2.89; P = .04).
CONCLUSIONS
Despite comparable ORRs, ICIs may not overcome the negative prognostic role of a poor PS, particularly in the first-line setting, and the initiation of ICIs in the last 30 DOL was associated with hospital death location.

Identifiants

pubmed: 31829450
doi: 10.1002/cncr.32645
pmc: PMC7050422
mid: NIHMS1062430
doi:

Substances chimiques

B7-H1 Antigen 0
CD274 protein, human 0
PDCD1 protein, human 0
Programmed Cell Death 1 Receptor 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1208-1216

Subventions

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

Informations de copyright

© 2019 American Cancer Society.

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Auteurs

Ali Raza Khaki (AR)

Division of Oncology, Department of Medicine, University of Washington, Seattle, Washington.

Ang Li (A)

Division of Hematology, Department of Medicine, University of Washington, Seattle, Washington.

Leonidas N Diamantopoulos (LN)

Division of Oncology, Department of Medicine, University of Washington, Seattle, Washington.

Mehmet A Bilen (MA)

Department of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, Georgia.

Victor Santos (V)

Department of Medicine, University of Utah, Salt Lake City, Utah.

John Esther (J)

Department of Medicine, University of Utah, Salt Lake City, Utah.

Rafael Morales-Barrera (R)

Vall d'Hebron Institute of Oncology, Vall d'Hebron University Hospital, Autonomous University of Barcelona, Barcelona, Spain.

Michael Devitt (M)

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

Ariel Nelson (A)

Division of Hematology/Oncology, Department of Medicine, Case Comprehensive Cancer Center, Cleveland, Ohio.

Christopher J Hoimes (CJ)

Division of Hematology/Oncology, Department of Medicine, Case Comprehensive Cancer Center, Cleveland, Ohio.

Evan Shreck (E)

Department of Medical Oncology, Montefiore Medical Center, Bronx, New York.
Department of Urology, Montefiore Medical Center, Bronx, New York.

Hussein Assi (H)

Section of Hematology Oncology, Department of Medicine, University of Oklahoma Stephenson Cancer Center, Oklahoma City, Oklahoma.

Benjamin A Gartrell (BA)

Department of Medical Oncology, Montefiore Medical Center, Bronx, New York.
Department of Urology, Montefiore Medical Center, Bronx, New York.

Alex Sankin (A)

Department of Medical Oncology, Montefiore Medical Center, Bronx, New York.
Department of Urology, Montefiore Medical Center, Bronx, New York.

Alejo Rodriguez-Vida (A)

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

Mark Lythgoe (M)

Department of Surgery and Cancer, Imperial College London, London, United Kingdom.

David J Pinato (DJ)

Department of Surgery and Cancer, Imperial College London, London, United Kingdom.

Alexandra Drakaki (A)

Division of Hematology/Oncology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California.

Monika Joshi (M)

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

Pedro Isaacsson Velho (P)

Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland.

Noah Hahn (N)

Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland.

Sandy Liu (S)

Division of Hematology/Oncology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California.

Lucia Alonso Buznego (L)

Marques de Valdecilla University Hospital, Instituto de Investigacion Sanitaria Valdecilla, Santander, Spain.

Ignacio Duran (I)

Marques de Valdecilla University Hospital, Instituto de Investigacion Sanitaria Valdecilla, Santander, Spain.

Marcus Moses (M)

Department of Medicine and Oncology, Tulane University, New Orleans, Louisiana.

Jayanshu Jain (J)

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

Jure Murgic (J)

Department of Oncology and Nuclear Medicine, University Hospital Center, Sisters of Charity Zagreb School of Medicine, Zagreb, Croatia.

Praneeth Baratam (P)

College of Medicine, Drexel University, Philadelphia, Pennsylvania.

Pedro Barata (P)

Department of Medicine and Oncology, Tulane University, New Orleans, Louisiana.

Abhishek Tripathi (A)

Section of Hematology Oncology, Department of Medicine, University of Oklahoma Stephenson Cancer Center, Oklahoma City, Oklahoma.

Yousef Zakharia (Y)

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

Matthew D Galsky (MD)

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

Guru Sonpavde (G)

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

Evan Y Yu (EY)

Division of Oncology, Department of Medicine, University of Washington, Seattle, Washington.

Veena Shankaran (V)

Division of Oncology, Department of Medicine, University of Washington, Seattle, Washington.

Gary H Lyman (GH)

Division of Oncology, Department of Medicine, University of Washington, Seattle, Washington.
Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.

Petros Grivas (P)

Division of Oncology, Department of Medicine, University of Washington, Seattle, Washington.

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