Neoadjuvant in situ immunomodulation enhances systemic antitumor immunity against highly metastatic tumors

2021 ◽  
pp. canres.0939.2021
Author(s):  
Takaaki Oba ◽  
Ryutaro Kajihara ◽  
Toshihiro Yokoi ◽  
Elizabeth A Repasky ◽  
Fumito Ito
2004 ◽  
Vol 64 (11) ◽  
pp. 4024-4029 ◽  
Author(s):  
Martijn H. M. G. M. den Brok ◽  
Roger P. M. Sutmuller ◽  
Robbert van der Voort ◽  
Erik J. Bennink ◽  
Carl G. Figdor ◽  
...  

2015 ◽  
Vol 9 ◽  
pp. CMO.S23252 ◽  
Author(s):  
Hiromi Kumon ◽  
Katsumi Sasaki ◽  
Yuichi Ariyoshi ◽  
Takuya Sadahira ◽  
Shin Ebara ◽  
...  

A 63-year-old man with metastatic castration-resistant prostate cancer (CRPC) was successfully treated for two years with in situ gene therapy using an adenovirus vector carrying the human REIC/Dkk-3 gene (Ad-REIC), following chemotherapy. Ad-REIC mediates simultaneous induction of cancer-selective apoptosis and augmentation of antitumor immunity, and a Phase I/IIa clinical study on Ad-REIC has been conducted at Okayama University Hospital since January 2011. At the time of enrollment in December 2012, the patient presented with rapid progression of lymph node (LN) metastases. Two scheduled Ad-REIC injections and 10 additional Ad-REIC injections into metastatic pelvic and para-aortic LNs under CT guidance, with an average four weeks’ interval, exhibited the potent direct and indirect effects of Ad-REIC as a therapeutic cancer vaccine. During the next 12 months, three additional injections into para-aortic LNs showing regrowth achieved adequate control of all metastatic LNs with prostate-specific antigen (PSA) decline, without any particular adverse events.


2014 ◽  
Vol 2014 ◽  
pp. 1-28 ◽  
Author(s):  
Dan A. Erkes ◽  
Senthamil R. Selvan

Haptens are small molecule irritants that bind to proteins and elicit an immune response. Haptens have been commonly used to study allergic contact dermatitis (ACD) using animal contact hypersensitivity (CHS) models. However, extensive research into contact hypersensitivity has offered a confusing and intriguing mechanism of allergic reactions occurring in the skin. The abilities of haptens to induce such reactions have been frequently utilized to study the mechanisms of inflammatory bowel disease (IBD) to induce autoimmune-like responses such as autoimmune hemolytic anemia and to elicit viral wart and tumor regression. Hapten-induced tumor regression has been studied since the mid-1900s and relies on four major concepts: (1)ex vivohaptenation, (2)in situhaptenation, (3) epifocal hapten application, and (4) antigen-hapten conjugate injection. Each of these approaches elicits unique responses in mice and humans. The present review attempts to provide a critical appraisal of the hapten-mediated tumor treatments and offers insights for future development of the field.


Nano Today ◽  
2021 ◽  
Vol 38 ◽  
pp. 101109
Author(s):  
Xue Yang ◽  
Ying Yang ◽  
Jiayi Bian ◽  
Jiajia Wei ◽  
Zheng Wang ◽  
...  

2004 ◽  
Vol 17 (11) ◽  
pp. 1309-1313 ◽  
Author(s):  
Kevin M Kernek ◽  
Matteo Brunelli ◽  
Thomas M Ulbright ◽  
John N Eble ◽  
Guido Martignoni ◽  
...  

2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Yurina Maeshima ◽  
Tomo Osako ◽  
Hidetomo Morizono ◽  
Mayu Yunokawa ◽  
Yumi Miyagi ◽  
...  

Abstract Background Accurate diagnosis of metastatic tumors in the breast is crucial because the therapeutic approach is essentially different from primary tumors. A key morphological feature of metastatic tumors is their lack of an in situ carcinoma component. Here, we present a unique case of metastatic ovarian carcinoma spreading into mammary ducts and mimicked an in situ component of primary carcinoma. To our knowledge, this is the second case (and the first adult case) confirming the in situ-mimicking growth pattern of a metastatic tumor using immunohistochemistry. Case presentation A 69-year-old Japanese woman was found to have a breast mass with microcalcifications. She had a known history of ovarian mixed serous and endocervical-type mucinous (seromucinous) carcinoma. Needle biopsy specimen of the breast tumor revealed adenocarcinoma displaying an in situ-looking tubular architecture in addition to invasive micropapillary and papillary architectures with psammoma bodies. From these morphological features, metastatic serous carcinoma and invasive micropapillary carcinoma of breast origin were both suspected. In immunohistochemistry, the cancer cells were immunoreactive for WT1, PAX8, and CA125, and negative for GATA3, mammaglobin, and gross cystic disease fluid protein-15. Therefore, the breast tumor was diagnosed to be metastatic ovarian serous carcinoma. The in situ-looking architecture showed the same immunophenotype, but was surrounded by myoepithelium confirmed by immunohistochemistry (e.g. p63, cytokeratin 14, CD10). Thus, the histogenesis of the in situ-like tubular foci was could be explained by the spread of metastatic ovarian cancer cells into existing mammary ducts. Conclusion Metastatic tumors may spread into mammary duct units and mimic an in situ carcinoma component of primary breast cancer. This in situ-mimicking growth pattern can be a potential pitfall in establishing a correct diagnosis of metastasis to the breast. A panel of breast-related and extramammary organ/tumor-specific immunohistochemical markers may be helpful in distinguishing metastatic tumors from primary tumors.


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