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A Preliminary Report: Radical Surgery and Stem Cell Transplantation for the Treatment of Patients With Pancreatic Cancer.
Omazic, Brigitta; Ayoglu, Burcu; Löhr, Matthias; Segersvärd, Ralf; Verbeke, Caroline; Magalhaes, Isabelle; Potacova, Zuzana; Mattsson, Jonas; Terman, Alexei; Ghazi, Sam; Albiin, Nils; Kartalis, Nikolaos; Nilsson, Peter; Poiret, Thomas; Zhenjiang, Liu; Heuchel, Rainer; Schwenk, Jochen M; Permert, Johan; Maeurer, Markus J; Ringden, Olle.
Afiliación
  • Omazic B; *Division of Clinical Immunology and Transfusion Medicine ¶Center for Allogeneic Stem Cell Transplantation ∥Division of Therapeutic Immunology (TIM) Departments of §Laboratory Medicine, Division of Pathology ‡Surgical Gastroenterology #Radiology, Karolinska Institutet, Karolinska University Hospital Huddinge †Affinity Proteomics, SciLifeLab, School of Biotechnology, KTH-Royal Institute of Technology, Stockholm, Sweden.
J Immunother ; 40(4): 132-139, 2017 May.
Article en En | MEDLINE | ID: mdl-28338506
We examined the immunologic effects of allogeneic hematopoietic stem cell transplantation (HSCT) in the treatment of pancreatic ductal adenocarcinoma, a deadly disease with a median survival of 24 months for resected tumors and a 5-year survival rate of 6%. After adjuvant chemotherapy, 2 patients with resected pancreatic ductal adenocarcinoma underwent HSCT with HLA-identical sibling donors. Comparable patients who underwent radical surgery, but did not have a donor, served as controls (n=6). Both patients developed humoral and cellular (ie, HLA-A*01:01-restricted) immune responses directed against 2 novel tumor-associated antigens (TAAs), INO80E and UCLH3 after HSCT. Both TAAs were highly expressed in the original tumor tissue suggesting that HSCT promoted a clinically relevant, long-lasting cellular immune response. In contrast to untreated controls, who succumbed to progressive disease, both patients are tumor-free 9 years after diagnosis. Radical surgery combined with HSCT may cure pancreatic adenocarcinoma and change the cellular immune repertoire capable of responding to clinically and biologically relevant TAAs.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Immunother Asunto de la revista: ALERGIA E IMUNOLOGIA / NEOPLASIAS / TERAPEUTICA Año: 2017 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Immunother Asunto de la revista: ALERGIA E IMUNOLOGIA / NEOPLASIAS / TERAPEUTICA Año: 2017 Tipo del documento: Article País de afiliación: Suecia
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