Phase I Dose Escalation trials in cancer immunotherapy: Modifying the Bayesian Logistic Regression Model for Cytokine Release Syndrome

Abstract

We extend Bayesian Logistic Regression to model the dose-toxicity re- lationship in the setting of phase I dose-escalation/ dose-finding trials for cancer immunotherapies. Immunotherapy drugs are associated with Cytokine Release Syn- drome, a systemic immune system reaction that can be mitigated when initial lower doses of the drug are administered to generate immune tolerance. This changes the classic dose-finding problem of determining an optimal safe dose, to a more complex problem where the search is for both the optimal safe dose and the dose regimen that allows patients to quickly and safely reach that dose without CRS. As part of solving this methodological challenge, we show how to jointly model CRS and non-CRS toxicities, which have distinct mechanisms, while controlling for the overall toxicity rate to make dose-escalation decisions.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

Research funded by Cogitars GmbH and its subsidiary company, Cogitars UK Ltd, https://cogitars.com

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Only simulated data was used

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All simulated data used in analyses are available upon reasonable request to the authors

留言 (0)

沒有登入
gif