Association of the Time to Immune Checkpoint Inhibitor (ICI) Initiation and Outcomes With Second Line ICI in Patients With Advanced Urothelial Carcinoma.


Journal

Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955

Informations de publication

Date de publication:
12 2022
Historique:
received: 29 07 2022
accepted: 15 08 2022
pubmed: 27 9 2022
medline: 6 12 2022
entrez: 26 9 2022
Statut: ppublish

Résumé

Early progression on first-line (1L) platinum-based therapy or between therapy lines may be a surrogate of more aggressive disease and poor outcomes in advanced urothelial carcinoma (aUC), but its prognostic role regarding immune checkpoint inhibitor (ICI) response and survival is unclear. We hypothesized that shorter time until start of second-line (2L) ICI would be associated with worse outcomes in aUC. We performed a retrospective multi-institution cohort study in patients with aUC treated with 1L platinum-based chemotherapy, who received 2L ICI. Patients receiving switch maintenance ICI were excluded. We defined time to 2L ICI therapy as the time between the start of 1L platinum-based chemotherapy to the start of 2L ICI and categorized patients a priori into 1 of 3 groups: less than 3 months versus 3-6 months versus more than 6 months. We calculated overall response rate (ORR) with 2L ICI, progression-free survival (PFS) and overall survival (OS) from the start of 2L ICI. ORR was compared among the 3 groups using multivariable logistic regression, and PFS, OS using cox regression. Multivariable models were adjusted for known prognostic factors. We included 215, 215, and 219 patients in the ORR, PFS, and OS analyses, respectively, after exclusions. ORR difference did not reach statistical significance between patients with less than 3 months versus 3-6 months versus more than 6 months to 2L ICI. However, PFS (HR 1.64; 95% CI 1.02-2.63) and OS (HR 1.77; 95% CI 1.10-2.84) was shorter among those with time to 2L ICI less than 3 months compared to those who initiated 2L ICI more than 6 months. Among patients with aUC treated with 2L ICI, time to 2L ICI less than 3 months was associated with lower, but not significantly different ORR, but shorter PFS and OS compared to 2L ICI more than 6 months. This highlights potential cross resistance mechanisms between ICI and platinum-based chemotherapy.

Sections du résumé

BACKGROUND
Early progression on first-line (1L) platinum-based therapy or between therapy lines may be a surrogate of more aggressive disease and poor outcomes in advanced urothelial carcinoma (aUC), but its prognostic role regarding immune checkpoint inhibitor (ICI) response and survival is unclear. We hypothesized that shorter time until start of second-line (2L) ICI would be associated with worse outcomes in aUC.
PATIENTS AND METHODS
We performed a retrospective multi-institution cohort study in patients with aUC treated with 1L platinum-based chemotherapy, who received 2L ICI. Patients receiving switch maintenance ICI were excluded. We defined time to 2L ICI therapy as the time between the start of 1L platinum-based chemotherapy to the start of 2L ICI and categorized patients a priori into 1 of 3 groups: less than 3 months versus 3-6 months versus more than 6 months. We calculated overall response rate (ORR) with 2L ICI, progression-free survival (PFS) and overall survival (OS) from the start of 2L ICI. ORR was compared among the 3 groups using multivariable logistic regression, and PFS, OS using cox regression. Multivariable models were adjusted for known prognostic factors.
RESULTS
We included 215, 215, and 219 patients in the ORR, PFS, and OS analyses, respectively, after exclusions. ORR difference did not reach statistical significance between patients with less than 3 months versus 3-6 months versus more than 6 months to 2L ICI. However, PFS (HR 1.64; 95% CI 1.02-2.63) and OS (HR 1.77; 95% CI 1.10-2.84) was shorter among those with time to 2L ICI less than 3 months compared to those who initiated 2L ICI more than 6 months.
CONCLUSION
Among patients with aUC treated with 2L ICI, time to 2L ICI less than 3 months was associated with lower, but not significantly different ORR, but shorter PFS and OS compared to 2L ICI more than 6 months. This highlights potential cross resistance mechanisms between ICI and platinum-based chemotherapy.

Identifiants

pubmed: 36155169
pii: S1558-7673(22)00174-4
doi: 10.1016/j.clgc.2022.08.006
pmc: PMC10233855
mid: NIHMS1900255
pii:
doi:

Substances chimiques

Immune Checkpoint Inhibitors 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

558-567

Subventions

Organisme : NCI NIH HHS
ID : P30 CA023100
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA094880
Pays : United States

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

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Auteurs

Rafee Talukder (R)

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

Dimitrios Makrakis (D)

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

Genevieve Ihsiu Lin (GI)

Department of Epidemiology, University of Washington, Seattle, WA.

Leonidas N Diamantopoulos (LN)

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

Scott Dawsey (S)

Department of Hematology and Oncology, Taussig Cancer Institute, Cleveland Clinic Foundation, Cleveland, OH.

Shilpa Gupta (S)

Department of Hematology and Oncology, Taussig Cancer Institute, Cleveland Clinic Foundation, Cleveland, OH.

Lucia Carril-Ajuria (L)

Department of Medical Oncology, Hospital Universitario, Madrid, Spain.

Daniel Castellano (D)

Department of Medical Oncology, Hospital Universitario, Madrid, Spain.

Ivan de Kouchkovsky (I)

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

Tanya Jindal (T)

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

Vadim S Koshkin (VS)

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

Joseph J Park (JJ)

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

Ajjai Alva (A)

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

Mehmet A Bilen (MA)

Winship Cancer Institute of Emory University, Atlanta, GA.

Tyler F Stewart (TF)

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

Rana R McKay (RR)

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

Nishita Tripathi (N)

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

Neeraj Agarwal (N)

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

Naomi Vather-Wu (N)

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

Yousef Zakharia (Y)

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

Rafael Morales-Barrera (R)

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

Michael E Devitt (ME)

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

Alessio Cortellini (A)

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

Claudia Angela Maria Fulgenzi (CAM)

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

David J Pinato (DJ)

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

Ariel Nelson (A)

Division of Hematology and Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.

Christopher J Hoimes (CJ)

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

Kavita Gupta (K)

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

Benjamin A Gartrell (BA)

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

Alex Sankin (A)

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

Abhishek Tripathi (A)

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

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.

Jure Murgic (J)

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

Ana Fröbe (A)

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

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.

Sandy Liu (S)

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

Eric Lu (E)

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

Vivek Kumar (V)

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

Giuseppe Di Lorenzo (GD)

Oncology University of Molise and ASL, Salerno, Italy.

Monika Joshi (M)

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

Pedro Isaacsson-Velho (P)

Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD; Division of Oncology, Hospital Moinhos de Vento, Porto Alegre, Brazil.

Lucia Alonso Buznego (LA)

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

Ignacio Duran (I)

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

Marcus Moses (M)

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

Pedro Barata (P)

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

Guru Sonpavde (G)

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

Jonathan L Wright (JL)

Fred Hutchinson Cancer Center, Seattle, WA; Department of Urology, University of Washington, Seattle, WA.

Evan Y Yu (EY)

Division of Medical Oncology, Department of Medicine, University of Washington, Seattle, WA; Fred Hutchinson Cancer Center, Seattle, WA.

Robert Bruce Montgomery (RB)

Division of Medical Oncology, Department of Medicine, University of Washington, Seattle, WA; Fred Hutchinson Cancer Center, Seattle, WA.

Andrew C Hsieh (AC)

Division of Medical Oncology, Department of Medicine, University of Washington, Seattle, WA; Fred Hutchinson Cancer Center, Seattle, WA.

Petros Grivas (P)

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

Ali Raza Khaki (AR)

Division of Oncology, Department of Medicine, Stanford University, Palo Alto, CA. Electronic address: alikhaki@stanford.edu.

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