Dissociated Responses in Patients with Metastatic Solid Tumors Treated with Immunotherapy.


Journal

Drugs in R&D
ISSN: 1179-6901
Titre abrégé: Drugs R D
Pays: New Zealand
ID NLM: 100883647

Informations de publication

Date de publication:
Dec 2021
Historique:
accepted: 01 09 2021
pubmed: 26 9 2021
medline: 23 11 2021
entrez: 25 9 2021
Statut: ppublish

Résumé

Immune checkpoint inhibitors have been demonstrated to improve overall survival. Atypical patterns of response have been reported, including dissociated response (DR). We evaluated the prevalence of DR. Patients had to have a baseline computed tomography (CT) scan and at least one follow-up CT scan and two target lesions (TLs). Three types of DR were evaluated using RECIST1.1: DR1, defined as at least one progressive and one responding TL; DR2, defined as at least one progressive and one stable TL; and DR3, defined as at least one stable and one responding TL. A total of 1244 measurements of 272 TLs were performed in 100 patients. Forty-nine out of the 272 TLs (18%) had received old or recent radiotherapy, and 42 (15%) had been biopsied. An objective response was observed in 22 patients (22%) and on 52 TLs (19%). DR1 were observed in 8% of patients. At the tumor measurement level, the response rate was lower in the case of prior radiotherapy (29% vs 34%, p = 0.01) and higher in the case of prior biopsy (40% vs 32%, p = 0.02). A DR was observed in 8% of patients. Response rate was lower in the case of prior radiotherapy and higher in the case of prior biopsy.

Sections du résumé

BACKGROUND BACKGROUND
Immune checkpoint inhibitors have been demonstrated to improve overall survival. Atypical patterns of response have been reported, including dissociated response (DR). We evaluated the prevalence of DR.
PATIENTS AND METHODS METHODS
Patients had to have a baseline computed tomography (CT) scan and at least one follow-up CT scan and two target lesions (TLs). Three types of DR were evaluated using RECIST1.1: DR1, defined as at least one progressive and one responding TL; DR2, defined as at least one progressive and one stable TL; and DR3, defined as at least one stable and one responding TL.
RESULTS RESULTS
A total of 1244 measurements of 272 TLs were performed in 100 patients. Forty-nine out of the 272 TLs (18%) had received old or recent radiotherapy, and 42 (15%) had been biopsied. An objective response was observed in 22 patients (22%) and on 52 TLs (19%). DR1 were observed in 8% of patients. At the tumor measurement level, the response rate was lower in the case of prior radiotherapy (29% vs 34%, p = 0.01) and higher in the case of prior biopsy (40% vs 32%, p = 0.02).
CONCLUSIONS CONCLUSIONS
A DR was observed in 8% of patients. Response rate was lower in the case of prior radiotherapy and higher in the case of prior biopsy.

Identifiants

pubmed: 34562258
doi: 10.1007/s40268-021-00362-3
pii: 10.1007/s40268-021-00362-3
pmc: PMC8602606
doi:

Substances chimiques

Immunologic Factors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

399-406

Informations de copyright

© 2021. The Author(s).

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Auteurs

Pauline Vaflard (P)

Department of Drug Development and Innovation (D3i), Institut Curie, Paris and Saint-Cloud, 26 rue d'Ulm, 75005, Paris, France.

Xavier Paoletti (X)

Versailles St Quentin University and Institut Curie, Saint-Cloud, France.
INSERM U900 Research unit, Saint-Cloud, France.

Vincent Servois (V)

Department of Radiology, Institut Curie, Paris, France.

Patricia Tresca (P)

Department of Drug Development and Innovation (D3i), Institut Curie, Paris and Saint-Cloud, 26 rue d'Ulm, 75005, Paris, France.

Elvire Pons-Tostivint (E)

Department of Medical Oncology, Claudius Regaud Institute, IUCT-Oncopole, Toulouse, France.

Marie-Paule Sablin (MP)

Department of Drug Development and Innovation (D3i), Institut Curie, Paris and Saint-Cloud, 26 rue d'Ulm, 75005, Paris, France.

Francesco Ricci (F)

Department of Drug Development and Innovation (D3i), Institut Curie, Paris and Saint-Cloud, 26 rue d'Ulm, 75005, Paris, France.

Delphine Loirat (D)

Department of Drug Development and Innovation (D3i), Institut Curie, Paris and Saint-Cloud, 26 rue d'Ulm, 75005, Paris, France.

Ségolène Hescot (S)

Department of Drug Development and Innovation (D3i), Institut Curie, Paris and Saint-Cloud, 26 rue d'Ulm, 75005, Paris, France.

Nouritza Torossian (N)

Department of Drug Development and Innovation (D3i), Institut Curie, Paris and Saint-Cloud, 26 rue d'Ulm, 75005, Paris, France.

Diana Bello Roufai (D)

Department of Drug Development and Innovation (D3i), Institut Curie, Paris and Saint-Cloud, 26 rue d'Ulm, 75005, Paris, France.

Maud Kamal (M)

Department of Drug Development and Innovation (D3i), Institut Curie, Paris and Saint-Cloud, 26 rue d'Ulm, 75005, Paris, France.

Edith Borcoman (E)

Department of Drug Development and Innovation (D3i), Institut Curie, Paris and Saint-Cloud, 26 rue d'Ulm, 75005, Paris, France.

Christophe Le Tourneau (C)

Department of Drug Development and Innovation (D3i), Institut Curie, Paris and Saint-Cloud, 26 rue d'Ulm, 75005, Paris, France. Christophe.LeTourneau@curie.fr.
INSERM U900 Research unit, Saint-Cloud, France. Christophe.LeTourneau@curie.fr.
Paris-Saclay University, Paris, France. Christophe.LeTourneau@curie.fr.

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