Patterns of progression in patients treated for immuno-oncology antibodies combination

Alice Bernard-Tessier, Capucine Baldini, Eduardo Castanon, Patricia Martin, Stéphane Champiat, Antoine Hollebecque, Sophie Postel-Vinay, Andreea Varga, Rastilav Bahleda, Anas Gazzah, Jean Marie Michot, Vincent Ribrag, Jean Pierre Armand, Aurélien Marabelle, Jean Charles Soria, Christophe Massard, Samy Ammari

    Résultats de recherche: Contribution à un journalArticleRevue par des pairs

    14 Citations (Scopus)

    Résumé

    Background: New patterns of progression under immune-oncology (IO) antibodies (mAb) have been described such as pseudoprogression. Except for melanoma, variations between studies reveal difficulties to establish their prevalence. Methods: This retrospective study enrolled patients participating in IO phase I trials at Gustave Roussy cancer center for solid tumors excluding melanoma. Radiological assessment according to iRECIST was correlated with prospectively registered patient characteristics and outcomes. Pseudoprogression (PsPD) was defined as RECIST-defined progression followed by stabilization or decrease at the next imaging, and dissociated response (DisR) as concomitant decrease in some tumor lesions and increase in others at a same timepoint. Results: Among 360 patients included, 74% received IO mAb combination: 45% with another IO mAb, 20% with targeted therapy and 10% with radiotherapy. The overall response rate was 19.7%. PsPD were observed in 10 (2.8%) patients and DisR in 12 (3.3%) patients. Atypical responses (AR), including PsPD and DisR, were not associated with any patient’s baseline characteristics. Compare with typical responder patients, patients experiencing AR presented a shorter iPFS (HR 0.34; p < 0.001) and OS (HR 0.27; p = 0.026). Among the 203 patients who progressed in 12 weeks, 80 (39.4%) patients were treated beyond progression. PD was confirmed in 80% of cases, while 10% of patients presented a response. Conclusion: Pseudoprogression and dissociated response are uncommon patterns of progression. Their prevalence should be balanced with the rate of real progressing patients treated beyond progression. Prognosis or on-treatment biomarkers are needed to identify early patients who will benefit from immunotherapy.

    langue originaleAnglais
    Pages (de - à)221-232
    Nombre de pages12
    journalCancer Immunology, Immunotherapy
    Volume70
    Numéro de publication1
    Les DOIs
    étatPublié - 1 janv. 2021

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