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Long-Term Survival in Patients Responding to Anti-PD-1/PD-L1 Therapy and Disease Outcome upon Treatment Discontinuation.
Gauci, Marie-Léa; Lanoy, Emilie; Champiat, Stéphane; Caramella, Caroline; Ammari, Samy; Aspeslagh, Sandrine; Varga, Andrea; Baldini, Capucine; Bahleda, Rastilav; Gazzah, Anas; Michot, Jean-Marie; Postel-Vinay, Sophie; Angevin, Eric; Ribrag, Vincent; Hollebecque, Antoine; Soria, Jean-Charles; Robert, Caroline; Massard, Christophe; Marabelle, Aurélien.
Affiliation
  • Gauci ML; Gustave Roussy, Université Paris-Saclay, Département d'Innovation Thérapeutique et d'Essais Précoces, Villejuif, France.
  • Lanoy E; Gustave-Roussy, Université Paris-Saclay, Service de Biostatistique et d'Epidémiologie, Villejuif, France.
  • Champiat S; Université Paris-Saclay, Univ. Paris-Sud, UVSQ, CESP, INSERM, Villejuif, France.
  • Caramella C; Gustave Roussy, Université Paris-Saclay, Département d'Innovation Thérapeutique et d'Essais Précoces, Villejuif, France.
  • Ammari S; INSERM U981, Villejuif, France.
  • Aspeslagh S; Gustave-Roussy, Université Paris-Saclay, Service de Radiologie, Villejuif, France.
  • Varga A; Gustave-Roussy, Université Paris-Saclay, Service de Radiologie, Villejuif, France.
  • Baldini C; Gustave Roussy, Université Paris-Saclay, Département d'Innovation Thérapeutique et d'Essais Précoces, Villejuif, France.
  • Bahleda R; Gustave Roussy, Université Paris-Saclay, Département d'Innovation Thérapeutique et d'Essais Précoces, Villejuif, France.
  • Gazzah A; Gustave Roussy, Université Paris-Saclay, Département d'Innovation Thérapeutique et d'Essais Précoces, Villejuif, France.
  • Michot JM; Gustave Roussy, Université Paris-Saclay, Département d'Innovation Thérapeutique et d'Essais Précoces, Villejuif, France.
  • Postel-Vinay S; Gustave Roussy, Université Paris-Saclay, Département d'Innovation Thérapeutique et d'Essais Précoces, Villejuif, France.
  • Angevin E; Gustave Roussy, Université Paris-Saclay, Département d'Innovation Thérapeutique et d'Essais Précoces, Villejuif, France.
  • Ribrag V; Gustave Roussy, Université Paris-Saclay, Département d'Innovation Thérapeutique et d'Essais Précoces, Villejuif, France.
  • Hollebecque A; Gustave Roussy, Université Paris-Saclay, Département d'Innovation Thérapeutique et d'Essais Précoces, Villejuif, France.
  • Soria JC; Gustave Roussy, Université Paris-Saclay, Département d'Innovation Thérapeutique et d'Essais Précoces, Villejuif, France.
  • Robert C; Gustave Roussy, Université Paris-Saclay, Département d'Innovation Thérapeutique et d'Essais Précoces, Villejuif, France.
  • Massard C; Gustave Roussy, Université Paris-Saclay, Département d'Innovation Thérapeutique et d'Essais Précoces, Villejuif, France.
  • Marabelle A; Université Paris-Saclay, Univ. Paris-Sud, UVSQ, CESP, INSERM, Villejuif, France.
Clin Cancer Res ; 25(3): 946-956, 2019 02 01.
Article in En | MEDLINE | ID: mdl-30297458
ABSTRACT

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 = 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.See related commentary by Cohen and Flaherty, p. 910.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Outcome Assessment, Health Care / B7-H1 Antigen / Programmed Cell Death 1 Receptor / Antineoplastic Agents, Immunological / Cancer Survivors / Neoplasms Type of study: Observational_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2019 Document type: Article Affiliation country: Francia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Outcome Assessment, Health Care / B7-H1 Antigen / Programmed Cell Death 1 Receptor / Antineoplastic Agents, Immunological / Cancer Survivors / Neoplasms Type of study: Observational_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2019 Document type: Article Affiliation country: Francia