Salivary gland cancer in Finland 1991–96: an evaluation of 237 cases

2005 ◽  
Vol 125 (2) ◽  
pp. 207-214 ◽  
Author(s):  
Heikki Luukkaa ◽  
Pekka Klemi ◽  
Ilmo Leivo ◽  
Petri Koivunen ◽  
Jussi Laranne ◽  
...  
2021 ◽  
pp. 455-469
Author(s):  
Janakiraman Subramanian ◽  
Lara Kujtan

Author(s):  
Stefanie D. Krens ◽  
Wim Boxtel ◽  
Maike J. M. Uijen ◽  
Frank G. A. Jansman ◽  
Ingrid M. E. Desar ◽  
...  

Cancer ◽  
2017 ◽  
Vol 124 (1) ◽  
pp. 118-124 ◽  
Author(s):  
Michi Sawabe ◽  
Hidemi Ito ◽  
Taishi Takahara ◽  
Isao Oze ◽  
Daisuke Kawakita ◽  
...  

Head & Neck ◽  
2015 ◽  
Vol 38 (S1) ◽  
pp. E446-E451 ◽  
Author(s):  
Aaron D. Falchook ◽  
Jose P. Zevallos ◽  
Bhishamjit S. Chera

2018 ◽  
Vol 66 (3) ◽  
pp. e27543 ◽  
Author(s):  
Martin Zamani ◽  
Christian Grønhøj ◽  
Jakob Schmidt Jensen ◽  
Christian von Buchwald ◽  
Birgitte Wittenborg Charabi ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Thomas J. W. Klein Nulent ◽  
Robert J. J. van Es ◽  
Stefan M. Willems ◽  
Arthur. J. A. T. Braat ◽  
Lot A. Devriese ◽  
...  

Abstract Background Advanced salivary gland cancers become difficult to treat when they are technically irresectable and radiotherapy limits are exceeded. There is also an unmet need to improve palliative systemic therapy. Salivary glands depict the Prostate-Specific Membrane Antigen (PSMA) on 68Ga-PSMA-PET/CT, a transmembrane protein that is targeted for diagnosis and treatment of advanced prostate cancer. Some salivary gland carcinomas also express PSMA. Methods This study aimed to retrospectively evaluate the effectiveness of 177Lu-PSMA-617 therapy for recurrent or metastatic salivary gland cancers, as a last resort treatment. Patients with serious tumour-related discomfort for whom no regular option was available were selected and critically re-assessed by the tumour board. Radionuclide therapy eligibility was confirmed when tumour targeting was greater than liver SUVmax on 68Ga-PSMA-PET/CT. The protocol aimed at four cycles of 6.0–7.4 GBq 177Lu-PSMA-617 every 6–8 weeks. Clinical response was evaluated by questionnaires and radiological response by 68Ga-PSMA-PET/CT. Results Six patients were treated with 177Lu-PSMA: four adenoid cystic carcinomas, one adenocarcinoma NOS and one acinic cell carcinoma. In two patients, radiological response was observed, showing either stable disease or a partial response, and four patients reported immediate relief of tumour-related symptoms. Most reported side effects were grade 1–2 fatigue, nausea, bone pain and xerostomia. Four patients prematurely discontinued therapy: three due to disease progression and one due to demotivating (grade 1) side-effects. Conclusions Palliative 177Lu-PSMA therapy for salivary gland cancer may lead to rapid relief of tumour-associated discomfort and may even induce disease stabilization. It is safe, relatively well tolerated and can be considered when regular treatment options fail.


Author(s):  
VG. Zanella ◽  
VP. Wagner ◽  
TR. Schmidt ◽  
S. Thieme ◽  
C. Correa ◽  
...  

2021 ◽  
Author(s):  
Yoshihiro Aizawa ◽  
Kentaro Takada ◽  
Jun Aoyama ◽  
Daisuke Sano ◽  
Shoji Yamanaka ◽  
...  

Abstract Salivary gland carcinoma (SGC) has poor prognosis depending on the histological subtype. However, due to the scarcity of preclinical experimental models, its pathogenesis remains largely unknown, hampering the development of new treatment modalities for patients with these malignancies. Here, we first report the establishment of a large collection of human SGC experimental models for multiple histological subtypes using patient-derived xenograft (PDX) and organoid culture techniques with our previously optimized method. Additionally, we successfully generated organoids by culturing established PDXs (PDX-derived organoids). Through passaging, each pre-clinical model was confirmed to maintain the pathological characteristics of the original tumor and the genetic traits of corresponding histological subtypes. Finally, we confirmed that these organoids were available for pharmacologic studies. Thus, our comprehensive models of SGC could be a powerful resource for the development of novel therapeutic agents and investigating the pathogenesis of these malignancies.


Head & Neck ◽  
2009 ◽  
Vol 32 (8) ◽  
pp. 1019-1027 ◽  
Author(s):  
Heikki Luukkaa ◽  
Pekka Klemi ◽  
Ilmo Leivo ◽  
Antti A. Mäkitie ◽  
Jonathan Irish ◽  
...  

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