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Objective To evaluate the efficacy and safety of recombinant adenovirus-p53(rAdp53) injection combined with radiotherapy and hyperthermia in the treatment of unresectable advanced soft tissue sarcoma.Methods In this retrospective study, we evaluated 76 patients with unresectable advanced primary or recurrent soft tissue sarcoma treated in our hospital from November 2005 to November 2012. These patients received radiotherapy and hyperthermia with rAdp53(p53 group, n=41) or without rAdp53(control group, n=35). rAdp53((1-2)×1012 viral particles each time, once a week, 8 times on average) was injected into the tumor or infused into the pelvic cavity. Radiotherapy (2 Gy each time, 5 times a week) was performed for the planning target volume at 56.3±5.3 Gy in the p53 group and 58.1±4.2 Gy in the control group, with no significant difference between the two groups (P>0.05). Superficial or deep thermotherapy was employed 8 times on average (twice a week). Clinical features, response rate, time to progression (TTP), overall survival (OS), and adverse events were compared between the two groups (P>0.05). The Kaplan-Meier method was used to calculate OS;the log-rank test was used for survival difference analysis and univariate prognostic analysis;the chi-square test was used for comparison of categorical data. Results At 2 months after treatment, the p53 group had significantly increased response rate (partial response+ complete response+ stable disease)(85% vs. 54%, P=0.003) and local control rate (49% vs. 23%, P=0.020) as well as prolonged TTP (12 months vs. 5 months, P=0.010) and OS (48 months vs. 31 months, P=0.049), as compared with the control group. No adverse events caused by radiotherapy and hyperthermia except transient fever were seen in the two groups. Conclusions Concurrent radiotherapy and hyperthermia combined with rAdp53 injection is effective and safe for patients with advanced soft tissue sarcoma.
Objective To examine the efficacy and safety of 125I seed implantation for treating neuroblastoma (NB) in animal models.Methods A total of 45 nude mice models of neuroblastoma were constructed and divided into the 125I group.control group.and blank group at 15 mice per group. The long and short diameters of the tumor were measured every 3 days.and the tumor inhibition rate was calculated every 9 days. Apoptotic and proliferative protein expression levels in tumor tissue and peritumoral tissue.as well as endocrine markers and bone marrow of the nude mice.were analyzed. The independent sample t test was used to compare the mean scores.and ANOVA was used for comparison between multiple groups. Results Tumor volume inhibition rate was significantly higher in the 125I group than in the control group and blank group on days 9.18.and 27(all P<0.05).Caspase-3 expression in tumor tissues was significantly higher in the 125I group than in the control group and blank group (all P<0.05).whereas proliferating cell nuclear antigen (PCNA) expression was significantly lower in the 125I group than in the control group and blank group (all P<0.05).There was no significant difference in Caspase-3 and PCNA expression between the control group and blank group (all P>0.05).In addition.no significant difference in the expression of Caspase-3 and PCNA in peritumoral tissue was observed between the 125I group.control group.and blank group (all P>0.05).Cell apoptosis in tumor tissue was significantly lower in the blank group and control group than in the 125I group (all P<0.05).while there was no significant difference between the blank group and the control group (P>0.05).There was no significant difference in endocrine markers between the three groups (P>0.05).There was no significant bone marrow suppression in the 125I group.and this observation was similar to those in the control group and blank group (all P>0.05).Conclusions 125I seeds have significant toxicity to NB.125I seed implantation is safe in nude mice with NB within the therapeutic doses.
Peripheral T-cell lymphoma (PTCL) is a highly specific and invasive non-Hodgkin’s lymphoma derived from mature T-cells that leave the thymus. At present, the clinical progress in PTCLs is behind that in B-cell lymphomas, and the current treatments for PTCLs have low efficacy and poor overall prognosis. Therefore, there is currently still no standard treatment for PTCL. The efficacy of the conventional CHOP chemotherapy regimen is poor, and the value of radiotherapy in early-stage PTLC patients remains to be determined. Autologous hematopoietic stem cell transplantation is the top choice for consolidation treatment for high-risk patients, but the efficacy of novel drugs for PTCLs needs to be further confirmed. In addition, PET/CT plays a more important role in predicting the prognosis of PTCLs.
Radiotherapy is a major local treatment for cervical cancer. However, local uncontrollability due to radioresistance is still common. Therefore, the prediction of radiosensitivity is quite beneficial to develop an optimal treatment strategy for individual patients. Multiple factors could influence the radiosensitivity of cells, and p53 status is one of them. The upstream or downstream molecules of p53 could also be regulated to affect the radiosensitivity of cervical cancer. The aim of the review is to analyze the difference in p53 status between different types of cervical cancer and to discuss how p53 regulates the response to radiotherapy.
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