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Pseudorelapse and cancer stem cells in ovarian cancer
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Cancer Science & Therapy

ISSN: 1948-5956

Open Access

Pseudorelapse and cancer stem cells in ovarian cancer


32nd Euro Congress on Cancer Science & Therapy

March 07-08, 2019 | Barcelona, Spain

Martin Orlando Rosas Delgado, Pedro Alejandro Lucero Diaz, Jose Antonio Matute Briceno, Alejandro Camacho, Juan Pablo Marquez Manriquez and Salvador Icedo Zamora

Sonora Cancer Research Center (CICS), USA

Posters & Accepted Abstracts: J Cancer Sci Ther

Abstract :

Little information exists about the early, middle and late image effects after antigen-specific multi-peptide immunotherapy and immunomodulation in epithelial ovarian cancer. Most of the potential effects in pseudorelapse are mainly unknown for the oncologists and radiologists, specifically in the follow up by images such as CT scan and PET scan after immune interventions are mainly unexplored clinically. We studied 30 high-grade serous carcinomas. We selected two relevant clinical image methods to demonstrate that immune infiltration attacking biologically and clinically relevant proteins involved in cancer stem cells and prognosis produce atypical image in patients with pseudo-progression and in patients with pseudo-relapse after successful immune based treatment. We demonstrated that patients treated with this approach have atypical image. We found by PET scan bright images, multiple lymphadenopathies and necrosis nests after treatment compatible with better prognosis. 30 PET scans and CT scans were analyzed for number of enlarged lymph nodes, lesions brightness size were analyzed by four operators. Moreover, we analyzed by granzyme B ELISPOT the immune response against predicted Th1 and CD8 epitopes from the bad prognosis proteins during, before and after treatment. We performed univariate and multivariate analysis for clinical correlations. 100% of the patients showed the same pattern in the PET and CT scan by meaning of multiple lymphadenopathies and bright areas in the previously ??occult? microscopic cancer stem cells. We found that the four bad prognosis proteins were over expressed in tumor as following Fascin-1 (90%), SURV (90%), BCL2 (75%) and Sox2 (0%). We found after treatment a media expression of CD8 cells of 40%. Epithelial ovarian cancer is highly infiltrated by CD8 cells that induce bright color on the lesions by Pet and CT scan and we need to validate this data to have the proof of principle and avoid over treatment in epithelial ovarian cancer and importantly learn to distinguish true relapse versus pseudorelapse due immune infiltration which usually is currently unknown or misinterpreted by radiologists and oncologists..

Biography :

E-mail: drmrosas@hotmail.com

 

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Citations: 3968

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