TY - JOUR
T1 - Long-term survival in patients responding to anti-PD-1/PD-L1 therapy and disease outcome upon treatment discontinuation
AU - Gauci, Marie Léa
AU - Lanoy, Emilie
AU - Champiat, Stéphane
AU - Caramella, Caroline
AU - Ammari, Samy
AU - Aspeslagh, Sandrine
AU - Varga, Andrea
AU - Baldini, Capucine
AU - Bahleda, Rastilav
AU - Gazzah, Anas
AU - Michot, Jean Marie
AU - Postel-Vinay, Sophie
AU - Angevin, Eric
AU - Ribrag, Vincent
AU - Hollebecque, Antoine
AU - Soria, Jean Charles
AU - Robert, Caroline
AU - Massard, Christophe
AU - Marabelle, Aurélien
N1 - Publisher Copyright:
© 2018 American Association for Cancer Research.
PY - 2019/2/1
Y1 - 2019/2/1
N2 - Purpose: Anti-PD-(L)1 can provide overall survival (OS) benefits over conventional treatments for patients with many different cancer types. However, the long-term outcome of cancer patients responding to these therapies remains unknown. This study is an exploratory study that aimed to describe the long-term survival of patients responding to anti-PD-(L)1 monotherapy across multiple cancer types. Patients and Methods: Data from patients treated with an anti-PD-(L)1 monotherapy in a phase I trial at Gustave Roussy were retrospectively analyzed over a period of 5 years. All cancer types (n ¼ 19) were included. Clinical and biological factors associated with response, long-term survival, and secondary refractory disease were studied. Results: Among 262 eligible patients, the overall objective response rate was 29%. The median progression-free survival of responder patients (RP) at 3 months was 30 months, and the median OS of RP was not reached after a median follow-up of 34 months. In RPs, 3- and 5-year OS percentages were 84% and 64%, respectively. No death occurred in the 21 complete responders (CR) during the overall follow-up. However, many partial responders (PR) showed subsequent tumor relapses to treatment. Long responders (response ≥2 years) represented 11.8% of the overall population. These findings should be validated in further prospective studies. Conclusions: There are currently no differences in therapeutic strategies between CRs and PRs to anti-PD-(L)1. We found a striking difference in OS between these two types of responses. Our results are in favor of evaluating patient stratification strategies and intensification of treatments when tumor lesions of a partial responder to immunotherapy stop improving.
AB - Purpose: Anti-PD-(L)1 can provide overall survival (OS) benefits over conventional treatments for patients with many different cancer types. However, the long-term outcome of cancer patients responding to these therapies remains unknown. This study is an exploratory study that aimed to describe the long-term survival of patients responding to anti-PD-(L)1 monotherapy across multiple cancer types. Patients and Methods: Data from patients treated with an anti-PD-(L)1 monotherapy in a phase I trial at Gustave Roussy were retrospectively analyzed over a period of 5 years. All cancer types (n ¼ 19) were included. Clinical and biological factors associated with response, long-term survival, and secondary refractory disease were studied. Results: Among 262 eligible patients, the overall objective response rate was 29%. The median progression-free survival of responder patients (RP) at 3 months was 30 months, and the median OS of RP was not reached after a median follow-up of 34 months. In RPs, 3- and 5-year OS percentages were 84% and 64%, respectively. No death occurred in the 21 complete responders (CR) during the overall follow-up. However, many partial responders (PR) showed subsequent tumor relapses to treatment. Long responders (response ≥2 years) represented 11.8% of the overall population. These findings should be validated in further prospective studies. Conclusions: There are currently no differences in therapeutic strategies between CRs and PRs to anti-PD-(L)1. We found a striking difference in OS between these two types of responses. Our results are in favor of evaluating patient stratification strategies and intensification of treatments when tumor lesions of a partial responder to immunotherapy stop improving.
UR - http://www.scopus.com/inward/record.url?scp=85060959641&partnerID=8YFLogxK
U2 - 10.1158/1078-0432.CCR-18-0793
DO - 10.1158/1078-0432.CCR-18-0793
M3 - Article
C2 - 30297458
AN - SCOPUS:85060959641
SN - 1078-0432
VL - 25
SP - 946
EP - 956
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 3
ER -