scholarly journals Bullous lichen planus and anti-programmed cell death-1 therapy: Case report and literature review

2020 ◽  
Vol 147 (3) ◽  
pp. 221-227 ◽  
Author(s):  
C. de Lorenzi ◽  
R. André ◽  
A. Vuilleumier ◽  
G. Kaya ◽  
M. Abosaleh
2018 ◽  
Vol 32 (7) ◽  
pp. e260-e261 ◽  
Author(s):  
T. Ogawa ◽  
Y. Ishitsuka ◽  
K. Iwamoto ◽  
H. Koguchi-Yoshioka ◽  
R. Tanaka ◽  
...  

2020 ◽  
Vol 11 (4) ◽  
pp. 1006-1009 ◽  
Author(s):  
Susumu Kurihara ◽  
Yoichi Oikawa ◽  
Ritsuko Nakajima ◽  
Atsushi Satomura ◽  
Ryuhei Tanaka ◽  
...  

2015 ◽  
Vol 64 (6) ◽  
pp. 765-767 ◽  
Author(s):  
Juan Martin-Liberal ◽  
Andrew JS Furness ◽  
Kroopa Joshi ◽  
Karl S. Peggs ◽  
Sergio A. Quezada ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Wen Dong ◽  
Pengfei Lei ◽  
Xin Liu ◽  
Qin Li ◽  
Xiangyang Cheng

Multiple gene-driven programmed cell death 1 ligand 1 (PD-L1)-expressing non-small-cell lung cancer (NSCLC) is very rare. Previous studies have shown that patients with NSCLC with anaplastic lymphoma kinase (ALK) gene rearrangement rarely benefit from PD-L1 inhibitors. Besides the secondary mutations in ALK gene, other mechanisms might contribute to tumor resistance to ALK tyrosine kinase inhibitors (ALK-TKIs). Herein, we present a case of PD-L1-overexpressing lung adenocarcinoma that harbors both EML4-ALK gene rearrangement and BRAF mutation. In particular, a second molecular analysis after resistance to first- and second-generation ALK-TKIs revealed a high PD-L1 expression and tumor mutation burden. Therefore, treatment with nivolumab monotherapy, an anti-PD-1 inhibitor, was started and the patient achieved complete remission. This case report suggested that PD-1 inhibitors might be an effective treatment option for patients with multiple gene-driven PD-L1-expressing NSCLC harboring ALK gene rearrangement.


2021 ◽  
Vol 12 ◽  
Author(s):  
Zi-yun Qiao ◽  
Zi-jie Zhang ◽  
Zi-cheng Lv ◽  
Huan Tong ◽  
Zhi-feng Xi ◽  
...  

Programmed cell death 1 (PD-1) blockade is considered contraindicated in liver transplant (LT) recipients due to potentially lethal consequences of graft rejection and loss. Though post-transplant PD-1 blockade had already been reported, pre-transplant use of PD-1 blockade has not been thoroughly investigated. This study explores the safety and efficacy of neoadjuvant PD-1 blockade in patients with hepatocellular carcinoma (HCC) after registration on the waiting list. Seven transplant recipients who underwent neoadjuvant PD-1 blockade combined with lenvatinib and subsequent LT were evaluated. The objective response rate (ORR) and disease control rate (DCR) was 71% and 85% according to the mRECIST criteria. Additionally, a literature review contained 29 patients were conducted to summarize the PD-1 blockade in LT for HCC. Twenty-two LT recipients used PD-1 inhibitors for recurrent HCC. 9.1% (2/22) and 4.5% (1/22) recipients achieved complete remission (CR) and partial remission (PR), respectively; 40.9% (9/22) recipients had progressive disease (PD). Allograft rejection occurred in 45% of patients. In total, seven patients from our center and three from the literature used pretransplant anti-PD-1 antibodies, eight patients (80%) had a PR, and the disease control rate was 100%. Biopsy-proven acute rejection (BPAR) incidence was 30% (3 in 10 patients), two patients died because of BPAR. This indicated that neoadjuvant PD-1-targeted immunotherapy plus tyrosine kinase inhibitors (TKI) exhibited promising efficacy with tolerable mortality in transplant recipients under close clinical monitoring.


2019 ◽  
Vol 2019 ◽  
pp. 1-5
Author(s):  
Ken Yajima ◽  
Yushi Akise

Immune checkpoint inhibitors, such as anti-programmed cell death-1 (anti-PD-1), have been widely used in the treatment of malignancies. However, these drugs can cause immune-related adverse events resembling autoimmune diseases. There are some reports of Graves’ disease (GD) induced by anti-cytotoxic T-lymphocyte-associated antigen 4 antibodies, but reports which discussed GD induced by anti-PD-1 antibodies are very rare. We report the case of a 61-year-old man with bladder cancer who presented with severe diarrhea, fatigue, palpitation, body weight loss, and hyperthyroidism after the fifth treatment with the anti-PD-1 monoclonal antibody pembrolizumab. His thyroid function prior to pembrolizumab administration had been subclinical hyperthyroidism, despite a negative thyroid-stimulating hormone receptor antibody (TRAb) level. On admission, pembrolizumab administration was discontinued. Graves’ disease was diagnosed based on a positive TRAb test result and the ultrasonographic finding of increased blood flow in the superior thyroid artery. Based on colonoscopy findings, the cause of diarrhea was diagnosed as active colitis. His diarrhea was improved with prednisolone, and thyroid function was treated with potassium iodide and thiamazole. This case report of GD with positive TRAb induced by the anti-PD-1 antibody pembrolizumab may contribute to the understanding of the mechanism underlying the association between GD and autoimmune activation via PD-1.


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