Multicentre, retrospective study of the efficacy and safety of nivolumab for recurrent and metastatic salivary gland carcinoma.
Multicentre, retrospective study of the efficacy and safety of nivolumab for recurrent and metastatic salivary gland carcinoma.
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DOI:
10.1038/s41598-020-73965-6
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发表时间:
2020-10-12
影响因子:
4.6
通讯作者:
Tada Y
中科院分区:
文献类型:
--
作者:
Niwa K;Kawakita D;Nagao T;Takahashi H;Saotome T;Okazaki M;Yamazaki K;Okamoto I;Hirai H;Saigusa N;Fushimi C;Masubuchi T;Miura K;Okazaki SI;Matsui H;Okada T;Iwaki S;Matsuki T;Hanyu K;Tsukahara K;Oridate N;Tada Y
Although immune-checkpoint inhibitors (ICIs) are effective against various cancers, little is known regarding their role in salivary gland carcinoma (SGC) treatment. Therefore, we evaluated the efficacy and safety of nivolumab monotherapy in patients with recurrent and/or metastatic SGC. In this multicentre retrospective study, nivolumab (240 mg) was administered every 2 weeks. The overall response rate (ORR), progression-free survival (PFS), overall survival (OS), and safety were examined; the correlation between treatment outcomes and clinicopathological factors was analysed. Twenty-four patients were enrolled; the most common histopathology was salivary duct carcinoma. Eleven tumours were PD-L1-positive; no tumour was microsatellite instability-high. The ORR was 4.2%, and the median PFS and OS were 1.6 and 10.7 months, respectively. One patient continued nivolumab for 28 months without disease progression. One patient showed grade 4 increase in creatine phosphokinase levels and grade 3 myositis. Biomarker analysis revealed significantly increased OS in patients with performance status of 0; modified Glasgow prognostic score of 0; low neutrophil-to-lymphocyte ratio, lactate dehydrogenase, and C-reactive protein; and high lymphocyte-to-monocyte ratio and in patients who received systemic therapy following nivolumab. Although nivolumab’s efficacy against SGC was limited, some patients achieved long-term disease control. Further studies are warranted on ICI use for SGC.
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影响因子:
8.4
作者:
Eisenhauer, E. A.;Therasse, P.;Verweij, J.
通讯作者:
Verweij, J.
影响因子:
15.9
作者:
Ho, Allen S.;Ochoa, Angelica;Morris, Luc G. T.
通讯作者:
Morris, Luc G. T.
DOI:
10.1002/hed.25035
发表时间:
2018-03
期刊:
Head & neck
影响因子:
--
作者:
Boon E;van Boxtel W;Buter J;Baatenburg de Jong RJ;van Es RJJ;Bel M;Fiets E;Oosting SF;Slingerland M;Hoeben A;Tesselaar MET;Jonker MA;Flucke UE;Nationwide Network and Registry of Histopathology and Cytopathology (PALGA) Group;van der Graaf WTA;van Herpen CML
通讯作者:
van Herpen CML
DOI:
10.1158/1078-0432.ccr-19-3758
发表时间:
2020-06-15
期刊:
Clinical cancer research : an official journal of the American Association for Cancer Research
影响因子:
--
作者:
Linxweiler M;Kuo F;Katabi N;Lee M;Nadeem Z;Dalin MG;Makarov V;Chowell D;Dogan S;Ganly I;Hakimi AA;Wong RJ;Riaz N;Ho AL;Chan TA;Morris LGT
通讯作者:
Morris LGT
影响因子:
50.5
作者:
Delyon, J.;Mateus, C.;Robert, C.
通讯作者:
Robert, C.