TY - JOUR
T1 - Better than RECIST and Faster than iRECIST
T2 - Defining the Immunotherapy Progression Decision Score to Better Manage Progressive Tumors on Immunotherapy
AU - Belkouchi, Younes
AU - Talbot, Hugues
AU - Lassau, Nathalie
AU - Lawrance, Littisha
AU - Farhane, Siham
AU - Feki-Mkaouar, Rahma
AU - Hadchiti, Joya
AU - Dawi, Lama
AU - Vibert, Julien
AU - Cournéde, Paul Henry
AU - Cousteix, Clara
AU - Mazza, Camille
AU - Kind, Michele
AU - Italiano, Antoine
AU - Marabelle, Aurelien
AU - Ammari, Samy
AU - Champiat, Stephane
N1 - Publisher Copyright:
©2023 American Association for Cancer Research.
PY - 2023/4/15
Y1 - 2023/4/15
N2 - Purpose: The objective of the study is to propose the immunotherapy progression decision (iPD) score, a practical tool based on patient features that are available at the first evaluation of immunotherapy treatment, to help oncologists decide whether to continue the treatment or switch rapidly to another therapeutic line when facing a progressive disease patient at the first evaluation. Experimental Design: This retrospective study included 107 patients with progressive disease at first evaluation according to RECIST 1.1. Clinical, radiological, and biological data at baseline and first evaluation were analyzed. An external validation set consisting of 31 patients with similar baseline characteristics was used for the validation of the score. Results: Variables were analyzed in a univariate study. The iPD score was constructed using only independent variables, each considered as a worsening factor for the survival of patients. The patients were stratified in three groups: good prognosis (GP), poor prognosis (PP), and critical prognosis (CP). Each group showed significantly different survivals (GP: 11.4, PP: 4.4, CP: 2.3 months median overall survival, P < 0.001, log-rank test). Moreover, the iPD score was able to detect the pseudoprogressors better than other scores. On the validation set, CP patients had significantly worse survival than PP and GP patients (P < 0.05, log-rank test). Conclusions: The iPD score provides oncologists with a new evaluation, computable at first progression, to decide whether treatment should be continued (for the GP group), or immediately changed for the PP and CP groups. Further validation on larger cohorts is needed to prove its efficacy in clinical practice.
AB - Purpose: The objective of the study is to propose the immunotherapy progression decision (iPD) score, a practical tool based on patient features that are available at the first evaluation of immunotherapy treatment, to help oncologists decide whether to continue the treatment or switch rapidly to another therapeutic line when facing a progressive disease patient at the first evaluation. Experimental Design: This retrospective study included 107 patients with progressive disease at first evaluation according to RECIST 1.1. Clinical, radiological, and biological data at baseline and first evaluation were analyzed. An external validation set consisting of 31 patients with similar baseline characteristics was used for the validation of the score. Results: Variables were analyzed in a univariate study. The iPD score was constructed using only independent variables, each considered as a worsening factor for the survival of patients. The patients were stratified in three groups: good prognosis (GP), poor prognosis (PP), and critical prognosis (CP). Each group showed significantly different survivals (GP: 11.4, PP: 4.4, CP: 2.3 months median overall survival, P < 0.001, log-rank test). Moreover, the iPD score was able to detect the pseudoprogressors better than other scores. On the validation set, CP patients had significantly worse survival than PP and GP patients (P < 0.05, log-rank test). Conclusions: The iPD score provides oncologists with a new evaluation, computable at first progression, to decide whether treatment should be continued (for the GP group), or immediately changed for the PP and CP groups. Further validation on larger cohorts is needed to prove its efficacy in clinical practice.
UR - http://www.scopus.com/inward/record.url?scp=85152603279&partnerID=8YFLogxK
U2 - 10.1158/1078-0432.CCR-22-0890
DO - 10.1158/1078-0432.CCR-22-0890
M3 - Article
C2 - 36719966
AN - SCOPUS:85152603279
SN - 1078-0432
VL - 29
SP - 1528
EP - 1534
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 8
ER -