{Reference Type}: Journal Article
{Title}: Combined use of tyrosine kinase inhibitors with PD-(L)1 blockade increased the risk of thyroid dysfunction in PD-(L)1 blockade: a prospective study.
{Author}: Kobayashi T;Iwama S;Yamagami A;Izuchi T;Suzuki K;Otake K;Yasuda Y;Ando M;Onoue T;Miyata T;Sugiyama M;Hagiwara D;Suga H;Banno R;Hase T;Nishio N;Mori S;Shimokata T;Sano T;Niimi K;Yoshikawa N;Akamatsu S;Ando Y;Akiyama M;Sone M;Ishii M;Arima H;
{Journal}: Cancer Immunol Immunother
{Volume}: 73
{Issue}: 8
{Year}: 2024 Jun 4
{Factor}: 6.63
{DOI}: 10.1007/s00262-024-03733-2
{Abstract}: <B>BACKGROUND: </B>Anti-programmed cell death-1 (ligand-1) antibody [PD-(L)1-Ab] can cause destructive thyroiditis and/or hypothyroidism. In addition, tyrosine kinase inhibitors (TKIs) frequently induce hypothyroidism. The aim of this prospective study is to examine the incidence and clinical characteristics of thyroid dysfunction induced by combination therapy of a PD-(L)1-Ab and TKI [PD-(L)1-Ab/TKI].<BR><B>METHODS: </B>A total of 757 patients treated with PD-(L)1-Ab or PD-(L)1-Ab/TKI were evaluated for anti-thyroid antibodies (ATAs) at baseline and for thyroid function for 48 weeks after treatment initiation and then observed until the last visit.<BR><B>RESULTS: </B>The cumulative incidences of destructive thyroiditis [4/23 (17.4%) vs. 45/734 (6.1%) patients, p < 0.001], isolated hypothyroidism [10/23 (43.5%) vs. 29/734 (4.0%) patients, p < 0.001], and all thyroid dysfunction [14/23 (60.9%) vs. 74/734 (10.1%) patients, p < 0.001] were significantly higher in the PD-(L)1-Ab/TKI group than PD-(L)1-Ab group, respectively. All patients positive for ATAs at baseline developed thyroid dysfunction after PD-(L)1-Ab/TKI treatment, a significantly higher incidence than that in those negative for ATAs at baseline [4/4 (100%) vs. 10/19 (52.6%) patients, p = 0.026].<BR><B>CONCLUSIONS: </B>The addition of TKIs increased the risk of thyroid dysfunction induced by PD-(L)1-Ab, with the risk being higher in patients positive for baseline ATAs.