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Worsening and newly diagnosed paraneoplastic syndromes following anti-PD-1 or anti-PD-L1 immunotherapies, a descriptive study.


ABSTRACT: BACKGROUND:Paraneoplastic syndromes (PNS) are autoimmune disorders specifically associated with cancer. There are few data on anti-PD-1 or anti-PD-L1 immunotherapy in patients with a PNS. Our objective was to describe the outcome for patients with a pre-existing or newly diagnosed PNS following the initiation of anti-PD-1 or anti-PD-L1 immunotherapy. METHODS:We included all adult patients (aged ?18) treated with anti-PD-1 or anti-PD-L1 immunotherapy for a solid tumor, diagnosed with a PNS, and registered in French pharmacovigilance databases. Patients were allocated to cohorts 1 and 2 if the PNS had been diagnosed before vs. after the initiation of immunotherapy, respectively. FINDINGS:Of the 1304 adult patients screened between June 27th, 2014, and January 2nd, 2019, 32 (2.45%) had a PNS and were allocated to either cohort 1 (n?=?16) or cohort 2 (n?=?16). The median (range) age was 64 (45-88). The tumor types were non-small-cell lung cancer (n?=?15, 47%), melanoma (n?=?6, 19%), renal carcinoma (n?=?3, 9%), and other malignancies (n?=?8, 25%). Eleven (34%) patients presented with a neurologic PNS, nine (28%) had a rheumatologic PNS, eight (25%) had a connective tissue PNS, and four (13%) had other types of PNS. The highest severity grade for the PNS was 1-2 in 10 patients (31%) and???3 in 22 patients (69%). Four patients (13%) died as a result of the progression of a neurologic PNS (encephalitis in three cases, and Lambert-Eaton syndrome in one case). Following the initiation of immunotherapy, the PNS symptoms worsened in eight (50%) of the 16 patients in cohort 1. INTERPRETATION:Our results show that PNSs tend to be worsened or revealed by anti-PD-1 or anti-PD-L1 immunotherapy. Cases of paraneoplastic encephalitis are of notable concern, in view of their severity. When initiating immunotherapy, physicians should carefully monitor patients with a pre-existing PNS.

SUBMITTER: Manson G 

PROVIDER: S-EPMC6892018 | biostudies-literature | 2019 Dec

REPOSITORIES: biostudies-literature

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Worsening and newly diagnosed paraneoplastic syndromes following anti-PD-1 or anti-PD-L1 immunotherapies, a descriptive study.

Manson Guillaume G   Maria Alexandre Thibault Jacques ATJ   Poizeau Florence F   Danlos François-Xavier FX   Kostine Marie M   Brosseau Solenn S   Aspeslagh Sandrine S   Du Rusquec Pauline P   Roger Maxime M   Pallix-Guyot Maud M   Ruivard Marc M   Dousset Léa L   Grignou Laurianne L   Psimaras Dimitri D   Pluvy Johan J   Quéré Gilles G   Grados Franck F   Duval Fanny F   Bourdain Frederic F   Maigne Gwenola G   Perrin Julie J   Godbert Benoit B   Taifas Beatris Irina BI   Forestier Alexandra A   Voisin Anne-Laure AL   Martin-Romano Patricia P   Baldini Capucine C   Marabelle Aurélien A   Massard Christophe C   Honnorat Jérôme J   Lambotte Olivier O   Michot Jean-Marie JM  

Journal for immunotherapy of cancer 20191203 1


<h4>Background</h4>Paraneoplastic syndromes (PNS) are autoimmune disorders specifically associated with cancer. There are few data on anti-PD-1 or anti-PD-L1 immunotherapy in patients with a PNS. Our objective was to describe the outcome for patients with a pre-existing or newly diagnosed PNS following the initiation of anti-PD-1 or anti-PD-L1 immunotherapy.<h4>Methods</h4>We included all adult patients (aged ≥18) treated with anti-PD-1 or anti-PD-L1 immunotherapy for a solid tumor, diagnosed wi  ...[more]

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