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فهرست مطالب jalil beheshti

  • Belal Delshad, Hamed Abadijoo, Hossein Simaee, MohammadAli Khayamian, Mohammadreza Ghaderinia, Seyed Mojtaba Yazdanparast, Jalil Beheshti, Khosro Shamsi, Maryam Avatefi Afkham, Sepideh Mansouri, MohammadEsmaeil Akbari, Mohammad Abdolahad
    Background

    Intraoperative radiation therapy (IORT), is a promising method which has been widely applied in breast cancer lumpectomy. Although its effect on destructing remaining cancer cells was approved, maintaining or draining post intraoperative radiation therapy wound fluids (PIWF) is challenging.Moreover, the roles of immune cells in interaction with PIWFs have not been studied before which is the main investigation of this paper.

    Methods

    Surgical wound fluids were collected from 24 IDC patients one day afterlumpectomy. The patients were divided into control and IORT groups. The collected wound fluids were centrifuged for 20 minutes at 2000 rpm. The concentration of tumor-associated cytokines and inflammasomes were recorded using the immunoassays.

    Results

    PIWFs stimulate the residue of cancer cells in cavity sides causing disease progression. Here we have focused on the effect of PIWFs on the proactivation or deactivation of WBCs in the tumor bed environment. By sequential imaging in time-transient intervals from the interaction between WBCs and cancer cells, PIWFs have no additive proactivating effect on immune cells.

    Conclusion

    PIWFs have significant roles in proliferation of cancer cells but did not show an observable role in pro-activating immune cells against cancer cells. The functions of immune cells did not show any independent proactivation in the presence of PIWFs with respect to their activation in the presence of blood serum. It seems that draining the PIWFs may be required. In future research, we will use tumor samples of the patients instead of cell lines to better investigate the personalized immune-tumor interactions of patients.

    Keywords: Breast cancer, tumor microenvironment, Intraoperative radiation therapy, Immune system, cytokines}
  • Alireza Negahi, MohammadEsmaeil Akbari *, Paniz Motaghi O, Atieh Akbari, Hooman Riazi, Mahnaz Akbari, Najmeh Dabbagh, Jalil Beheshti
    Background

     Adequate treatment for all resectable early gastric cancers (EGCs) is gastrectomy with regional lymphadenectomy. The number of positive resected lymph nodes during lymphadenectomy can be a reliable predictor of survival of GC.

    Objectives

     We aimed at assessing the prognostic significance of Dissected Lymph Node Count (DLNC), positive LNC (PLNC), and Lymph Node Ratio (LNR) in patients with EGC.

    Methods

     In the current retrospective cohort, 201 patients with resectable EGC were included. Demographic variables, clinicopathological characteristics of tumors (including numbers of total dissected nodes and positive, negative nodes), history of receiving adjuvant cancer therapies, and 1- and 5-year survivals were noted.

    Results

     DLNC, PLNC, and LNR were associated with differentiation and depth of tumor, lymph node status, and risk of death (P-value for all < 0.05). There was no correlation between either of these measures with preoperative symptoms, lymphovascular invasion, and recurrence. DLNC, PLNC, and LNR showed prognostic significance only in patients, who did not receive comprehensive therapy (P-value < 0.001 for all). A significantly higher LNR was seen in patients with more than 1-year survival compared to others (P-value = 0.011). A significantly lower DLNC and higher PLNC were seen in patients, who survived over 5 years (P-value of 0.002 and 0.047, respectively).

    Conclusions

     LNR, DLNC, and PLNC are significant prognostic factors for EGC. According to our findings, choosing the optimal approach, through which fewer negative lymph nodes are dissected, is crucial in increasing overall survival and extended lymphadenectomy cannot necessarily benefit patients.

    Keywords: Locoregional Dissection, Overall Survival, Lymph Node Count, Lymph Node Ratio, Lymph Node Resection, Lymphadenectomy, Gastric Cancer}
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