Evidence of pseudoprogression in patients treated with PD1/PDL1 antibodies across tumor types.


Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
04 2020
Historique:
received: 06 09 2019
revised: 14 11 2019
accepted: 05 12 2019
pubmed: 20 2 2020
medline: 15 5 2021
entrez: 20 2 2020
Statut: ppublish

Résumé

PD(L)1 antibodies (anti-PD(L)-1) have been a major breakthrough in several types of cancer. Novel patterns of response and progression have been described with anti-PD(L)-1. We aimed at characterizing pseudoprogression (PSPD) among patients with various solid tumor types treated by anti-PD(L)-1. All consecutive patients (pts) enrolled in phase 1 trials with advanced solid tumors and lymphomas treated in phase I clinical trials evaluating monotherapy by anti-PD(L)-1 at Gustave Roussy were analyzed. We aimed to assess prevalence and outcome of PSPD across tumor types. We also intended to describe potential clinical and pathological factors associated with PSPD. A total of 169 patients treated with anti-PD(L)-1 were included in the study. Most frequent tumor types included melanoma (n = 57) and non-small cell lung cancer (n = 19). At first tumor evaluation 77 patients (46%) presented with immune unconfirmed progressive disease. Six patients (8%) experienced PSPD: 2 patients with partial response; 4 patients with stable disease. Increase in target lesions in the first CT-scan was more frequently associated to PSPD (67% vs 33%; P = .04). Patients with a PSPD had a superior survival when compared to patients progressing (median OS: 10.7 months vs 8.7 months; P = .07). A small subset of PSPD patients may experience response after an initial progression. Assessment of the current strategy for immune-related response evaluations may require further attention.

Sections du résumé

BACKGROUND
PD(L)1 antibodies (anti-PD(L)-1) have been a major breakthrough in several types of cancer. Novel patterns of response and progression have been described with anti-PD(L)-1. We aimed at characterizing pseudoprogression (PSPD) among patients with various solid tumor types treated by anti-PD(L)-1.
METHODS
All consecutive patients (pts) enrolled in phase 1 trials with advanced solid tumors and lymphomas treated in phase I clinical trials evaluating monotherapy by anti-PD(L)-1 at Gustave Roussy were analyzed. We aimed to assess prevalence and outcome of PSPD across tumor types. We also intended to describe potential clinical and pathological factors associated with PSPD.
RESULTS
A total of 169 patients treated with anti-PD(L)-1 were included in the study. Most frequent tumor types included melanoma (n = 57) and non-small cell lung cancer (n = 19). At first tumor evaluation 77 patients (46%) presented with immune unconfirmed progressive disease. Six patients (8%) experienced PSPD: 2 patients with partial response; 4 patients with stable disease. Increase in target lesions in the first CT-scan was more frequently associated to PSPD (67% vs 33%; P = .04). Patients with a PSPD had a superior survival when compared to patients progressing (median OS: 10.7 months vs 8.7 months; P = .07).
CONCLUSIONS
A small subset of PSPD patients may experience response after an initial progression. Assessment of the current strategy for immune-related response evaluations may require further attention.

Identifiants

pubmed: 32074405
doi: 10.1002/cam4.2797
pmc: PMC7163099
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
B7-H1 Antigen 0
Biomarkers, Tumor 0
CD274 protein, human 0
PDCD1 protein, human 0
Programmed Cell Death 1 Receptor 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2643-2652

Informations de copyright

© 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

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Auteurs

Patricia Martin-Romano (P)

Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France.

Eduardo Castanon (E)

Oncology Department, Clínica Universidad de Navarra, Madrid, Spain.

Samy Ammari (S)

Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France.
Department of Radiology, Gustave Roussy Cancer Campus, Villejuif, France.

Stéphane Champiat (S)

Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France.

Antoine Hollebecque (A)

Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France.

Sophie Postel-Vinay (S)

Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France.
INSERM, VILLEJUIF, France.

Capucine Baldini (C)

Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France.

Andrea Varga (A)

Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France.

Jean Marie Michot (JM)

Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France.

Perrine Vuagnat (P)

Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France.

Aurélien Marabelle (A)

Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France.
INSERM, VILLEJUIF, France.

Jean-Charles Soria (JC)

Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France.
INSERM, VILLEJUIF, France.

Charles Ferté (C)

Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France.
INSERM, VILLEJUIF, France.

Christophe Massard (C)

Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France.
INSERM, VILLEJUIF, France.

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