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Adjuvant immunotherapy in patients with high-risk muscle-invasive urothelial carcinoma: The potential impact of informative censoring.
Martini, Alberto; Yu, Menggang; Raggi, Daniele; Joshi, Himanshu; Fallara, Giuseppe; Montorsi, Francesco; Necchi, Andrea; Galsky, Matthew D.
Afiliação
  • Martini A; Department of Urology, Vita-Salute San Raffaele University, Milan, Italy.
  • Yu M; Department of Biostatistics and Medical Informatics, University of Wisconsin, Madison, Wisconsin.
  • Raggi D; Department of Oncology, Vita-Salute San Raffaele University, Milan, Italy.
  • Joshi H; Department of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Fallara G; Department of Urology, Vita-Salute San Raffaele University, Milan, Italy.
  • Montorsi F; Department of Urology, Vita-Salute San Raffaele University, Milan, Italy.
  • Necchi A; Department of Oncology, Vita-Salute San Raffaele University, Milan, Italy.
  • Galsky MD; Division of Hematology/Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
Cancer ; 128(15): 2892-2897, 2022 08 01.
Article em En | MEDLINE | ID: mdl-35553053
ABSTRACT

BACKGROUND:

The results of 2 studies exploring adjuvant immune checkpoint inhibition (aCPI) in high-risk muscle-invasive urothelial cancer have yielded conflicting results. A trial employing placebo as the control arm demonstrated a significant prolongation in disease-free survival (DFS) whereas a trial employing observation as the control arm (IMvigor010) demonstrated no prolongation in DFS with CPI. Here, the authors aimed to estimate the aCPI benefit and to model the potential impact of informative censoring on trial results.

METHODS:

Survival data from 1518 patients was reconstructed from Kaplan-Meier curves. A network meta-analysis approach was used to estimate aCPI benefit through the restricted mean disease-free survival time (RMDFST). To estimate the potential impact of informative censoring on IMvigor010, a simulation was performed. The minimum proportion of informative censoring on the observation arm that could account for the lack of observed improvement in DFS was estimated. Random variability from the time of censoring to progression was modeled using the exponential distribution.

RESULTS:

Patients receiving aCPI had better DFS ΔRMDFST at 36 months of 2.2 (95% CI, 0.6-3.7, P = .006) months relative to observation/placebo. In IMvigor010, in the observation arm, 20.5% of patients were censored due to consent withdrawal, protocol violation and/or noncompliance, or lost to follow-up versus 8.2% in the treatment arm. On simulation, it was found that the lack of observed improvement in DFS could have resulted from as few as 14% of the censored patients on observation arm not being censored at random (simulated DFS with 14% informative censoring hazard ratio, 0.83; 95% CI, 0.69-0.99; P = .049).

CONCLUSIONS:

Phase 3 trials comparing adjuvant therapies to observation are at risk for informative censoring that could potentially impact interpretation of study results.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Bexiga Urinária / Carcinoma de Células de Transição Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Bexiga Urinária / Carcinoma de Células de Transição Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article