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1.
Cancer Radiother ; 11(8): 461-4, 2007 Dec.
Article in English | MEDLINE | ID: mdl-17689126

ABSTRACT

BACKGROUND: The current retrospective study aimed to identify some determinants of survival in metastatic NPC. METHODS: The study concerned 95 patients with metastatic nasopharyngeal carcinoma treated between 1993 and 2001. Statistical comparison between patients subgroups survival was carried out employing the log-Rank test (statistical significance was defined as p45 years and25 years), gender, performance status at diagnosis of metastatic disease (PS 0-1 or 2-3), time of metastasis diagnosis(at presentation or later), number of metastatic sites (single or multiple), specific metastatic sites(bone, liver, lung, distant nodes), number of bone metastasis (single or multiple), disease free survival (DFI) (6 months), prior chemotherapy, radiotherapy of metastatic sites. RESULTS: Negative prognostic factors in univariate analysis were: poor PS (>or=1), multiple metastatic sites, multiple bone metastasis, previous chemotherapy, visceral or node metastasis and non irradiated metastasis. Poor PS, multiple metastatic sites, and prior chemotherapy were independently significant negative prognostic factors in multivariable analysis. CONCLUSIONS: In this study we identified new prognostic factors in univariate and multivariate analysis. A regular and careful follow-up of patients treated for NPC is then recommended in order to detect early metastatic dissemination (with minimal localizations) while patients have still a good PS.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Nasopharyngeal Neoplasms/drug therapy , Nasopharyngeal Neoplasms/pathology , Nasopharyngeal Neoplasms/radiotherapy , Adult , Aged , Bleomycin/administration & dosage , Cisplatin/administration & dosage , Combined Modality Therapy , Epirubicin/administration & dosage , Female , Humans , Male , Middle Aged , Multivariate Analysis , Neoplasm Metastasis , Neoplasm Staging , Prognosis , Retrospective Studies , Tunisia
2.
Cancer Radiother ; 10(8): 545-9, 2006 Dec.
Article in French | MEDLINE | ID: mdl-16807035

ABSTRACT

PURPOSE: The objective of this retrospective study was to discuss the epidemioclinical criteria and the therapeutic results of metastatic nasopharyngeal carcinoma. PATIENTS AND METHODS: The current study concerned 95 patients with histologically proven nasopharyngeal carcinoma who were metastatic at diagnosis or who had developed late metastasis. We reviewed the epidemioclinical records of all the patients. Patients were treated with chemotherapy (BEC regimen: bleomycin, epirubicin and cisplatin or PBF regimen: bleomycin, 5-fluorouacil and cisplatin) and radiotherapy of pauci metastatic localizations (single or double) or bone metastasis with high risk of compression or fracture+/-associated with locoregional radiotherapy for patients who were metastatic at diagnosis. Response was assessed according to the WHO criteria. Overall survival was calculated according to the Kaplan-Meier method. A long-term disease-free survival was defined from 36 months. RESULTS: There were 34 patients who were metastatic at diagnosis and 61 patients who had developed late metastasis. The mean age was 41.5 years (sex-ratio: 3.1). Bone metastases were the most frequent (83%). Objective and complete response rates were respectively 75% and 70%, and 32% and 16% for BEC and PBF regimens. Twenty-five patients received radiotherapy for pauci metastatic localizations, among whom 19 patients who were metastatic at diagnosis received locoregional irradiation. The overall survival probability was of 15% for three years. Eleven patients were long survivors (extremes: 36 and 134 months). CONCLUSION: Therapeutic results were comparable to those reported in other series using platin combination chemotherapy. Radiotherapy of metastasis yielded to long-term survival.


Subject(s)
Nasopharyngeal Neoplasms , Adolescent , Adult , Aged , Antibiotics, Antineoplastic/administration & dosage , Antimetabolites, Antineoplastic/administration & dosage , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Bleomycin/administration & dosage , Bone Neoplasms/secondary , Cisplatin/administration & dosage , Combined Modality Therapy , Disease-Free Survival , Epirubicin/administration & dosage , Female , Fluorouracil/administration & dosage , Follow-Up Studies , Humans , Male , Middle Aged , Nasopharyngeal Neoplasms/diagnosis , Nasopharyngeal Neoplasms/drug therapy , Nasopharyngeal Neoplasms/epidemiology , Nasopharyngeal Neoplasms/mortality , Nasopharyngeal Neoplasms/radiotherapy , Neoplasm Metastasis , Radiotherapy Dosage , Retrospective Studies , Survival Analysis , Time Factors , Treatment Outcome
3.
Cancer Radiother ; 9(8): 587-9, 2005 Dec.
Article in French | MEDLINE | ID: mdl-16236540

ABSTRACT

PURPOSE: The aim of this work is to study the epidemiological, clinical and evolutive characteristics of the erysipela in patients treated for nasopharyngeal carcinoma (NPC). PATIENTS AND METHODS: Between January 1993 and June 2003, 212 patients were treated for NPC in the radiotherapy department of Sfax hospital. Twenty-two patients among them have presented an erysipela. A neoadjuvant chemotherapy was used for 16 patients with N2-N3 disease. Locoregional radiotherapy was delivered for all of patients. RESULTS: The mean age was 35 years (range: 10 and 69), sex-ratio was 1.2. The median delay between the appearance of erysipela and the end of the treatment was 16 months. The main localisation was the face. The main clinical manifestations were fever in 86% of cases and erythema in 77% of cases. Immediate evolution was favorable in all cases after antibiotherapy. Recurrences were observed in 45% in cases. CONCLUSION: Erysipela is a common skin infection readly found in patients with venous insufficiency. In our study we found a significant correlation between the frequency of erysipela and dystrophic complications. The incidence of erysipela in the face and cervical region after radiotherapy is unknown.


Subject(s)
Erysipelas/etiology , Nasopharyngeal Neoplasms/drug therapy , Nasopharyngeal Neoplasms/radiotherapy , Adolescent , Adult , Aged , Child , Face/pathology , Female , Humans , Male , Middle Aged , Neoadjuvant Therapy , Recurrence , Sex Ratio
4.
J Med Virol ; 75(4): 593-602, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15714486

ABSTRACT

Nasopharyngeal carcinoma (NPC) in Tunisia is characterized by its bimodal age distribution involving juvenile patients of 10-24 years and adult patients of 40-60 years. Three serological techniques were compared for primary diagnosis (N = 117) and post-treatment monitoring (N = 21) of NPC patients separated in two age groups. Immunofluorescence assay (IFA) was used as the "gold standard" for detection of IgG and IgA antibodies reactive with Epstein-Barr virus (EBV) early (EA) and viral capsid (VCA) antigens. Results were compared with ELISA measuring IgG and IgA antibody reactivity to defined EBNA1, EA, and VCA antigens. Immunoblot was used to reveal the molecular diversity underlying the anti-EBV IgG and IgA antibody responses. The results indicate that young NPC patients have significantly more restricted anti-EBV IgG and IgA antibody responses with aberrant IgG VCA/EA levels in 78% compared to 91.7% in elder patients. IgA VCA/EA was detected in 50% of young patients versus 89.4% for the elder group (P < 0.001). Immunoblot revealed a reduced overall diversity of EBV antigen recognition for both IgG and IgA in young patients. A good concordance was observed between ELISA and IFA for primary NPC diagnosis with 81-91% overall agreement. Even better agreement (95-100%) was found for antibody changes during follow-up monitoring, showing declining reactivity in patients in remission and increasing reactivity in patients with persistent disease or relapse. ELISA for IgA anti-VCA-p18 and immunoblot proved most sensitive for predicting tumor relapse. VCA-p18 IgA ELISA seems suitable for routine diagnosis and early detection of NPC complication.


Subject(s)
Aging/immunology , Carcinoma/diagnosis , Herpesvirus 4, Human/immunology , Immunoglobulin A/blood , Immunoglobulin G/blood , Nasopharyngeal Neoplasms/diagnosis , Adolescent , Adult , Aged , Antigens, Viral/immunology , Carcinoma/virology , Child , Enzyme-Linked Immunosorbent Assay , Epstein-Barr Virus Infections/diagnosis , Epstein-Barr Virus Infections/virology , Female , Fluorescent Antibody Technique , Humans , Immunoblotting , Male , Middle Aged , Nasopharyngeal Neoplasms/virology , Tunisia
5.
Eur J Cancer ; 39(16): 2349-54, 2003 Nov.
Article in English | MEDLINE | ID: mdl-14556927

ABSTRACT

Standard therapy for nasopharyngeal carcinoma (NPC) in children has generally followed the guidelines established for adults. We report here, the treatment outcomes in 32 children and adolescents with NPC and we discuss treatment approaches. Between 1993 and 1997, 32 NPC patients aged

Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Nasopharyngeal Neoplasms/drug therapy , Nasopharyngeal Neoplasms/radiotherapy , Adolescent , Adult , Bleomycin/administration & dosage , Child , Cisplatin/administration & dosage , Combined Modality Therapy , Epirubicin/administration & dosage , Female , Humans , Male , Neoplasm Metastasis , Quality of Life , Survival Analysis , Treatment Outcome
6.
Clin Cancer Res ; 6(10): 3932-6, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11051240

ABSTRACT

EBV-associated nasopharyngeal carcinomas (NPCs) from Southeast Asia and North Africa have many common clinical and biological characteristics. However, they differ with regard to their age distribution. In Asia, NPC mainly affects patients in the 4th or 5th decade of their life, whereas in North Africa an additional peak of incidence is found between the ages of 10 and 20. The p53 gene is rarely mutated in NPC. However, several groups have reported a consistent accumulation of p53 in Asian NPCs. To determine whether p53 was also accumulated in North African NPCs, we investigated its expression, by immunohistochemistry, in a series of 90 Tunisian biopsies. Bc12 and CD95, two proteins involved in the regulation of cell survival and apoptosis, were investigated in the same study. We found accumulation of p53 in 81% of the cases for patients over 30 years of age, but in only 38% of specimens for younger patients (P = 0.00013). There was a trend toward a higher frequency of Bc12 detection in patients over 30, but it was not statistically significant. CD95 expression was detected in all biopsies, generally at a high level, even at advanced stages of the disease. The changing frequency of p53 accumulation, below and over 30, suggests that NPC cells often achieve malignant transformation through different pathways in both age groups.


Subject(s)
Age Factors , Carcinoma/epidemiology , Carcinoma/genetics , Gene Frequency , Genes, p53/genetics , Nasopharyngeal Neoplasms/epidemiology , Nasopharyngeal Neoplasms/genetics , Adolescent , Adult , Africa, Northern , Aged , Apoptosis , Carcinoma/pathology , Cell Survival , Child , Female , Humans , Immunohistochemistry , Male , Middle Aged , Nasopharyngeal Neoplasms/pathology , Proto-Oncogene Proteins c-bcl-2/biosynthesis , Tumor Suppressor Protein p53/biosynthesis , Tunisia , fas Receptor/biosynthesis
7.
Cancer Radiother ; 4(6): 469-72, 2000.
Article in French | MEDLINE | ID: mdl-11191855

ABSTRACT

Radio-induced tumor have been known for a long time to occur after treatment of cancer during childhood. This entity is exceptional following radiotherapy of the cavum. Skull and facial osteosarcoma were described after treatment of UCNT. We report two observations of radio-induced tumors arising, respectively three and seven years after treatment of UCNT. The first one is a temporoparietal glioblastoma and the second is a rhino- and pharyngeal myxoma. The two patients are alive after treatment of the second tumor. The delay of appearance of these tumors, their situation in the field's irradiated and dose received suggests their radio-induced nature. However, the cytogenetic study is necessary to confirm the implication of radiotherapy in the genesis of these cancers.


Subject(s)
Brain Neoplasms/etiology , Carcinoma/radiotherapy , Glioblastoma/etiology , Myxoma/etiology , Nasopharyngeal Neoplasms/radiotherapy , Neoplasms, Radiation-Induced , Adult , Brain Neoplasms/pathology , Female , Glioblastoma/pathology , Humans , Magnetic Resonance Imaging , Middle Aged , Myxoma/pathology
8.
Bull Cancer ; 84(3): 273-6, 1997 Mar.
Article in French | MEDLINE | ID: mdl-9207873

ABSTRACT

Between January 1994 and June 1995, 19 cases of nasopharyngeal carcinoma, classified N2-N3 (AJC/UICC 1987) were treated by neoadjuvant chemotherapy including cisplatin 100 mg/m2 on day 1 and epirubicin 80 mg/m2 on day 1. Following course started on day 21. A clinical and scannographic evaluation was made after 3 courses of chemotherapy. Fifty-eight percent of the patients were N3. Seventy-four percent were T3-T4. Tolerance to chemotherapy was good in 100% of the cases. A functional improvement was obtained in 14 among 16 patients who were initially symptomatic. For lymph nodes, an objective response (OR) was observed in all patients. The response was complete (CR) in 53%. A regression of primary tumor was obtained in 68% of the patients, but it was complete in 16% only. Sixty-nine percent of the patients has have a tumoral OR have a lymph node CR. Ninety percent of the patients with a complete lymph node response have a tumoral regression more than 50%. A correlation seems likely between the importance of the tumoral and the lymph node responses.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Carcinoma/drug therapy , Nasopharyngeal Neoplasms/drug therapy , Adolescent , Adult , Aged , Carcinoma/mortality , Carcinoma/pathology , Chemotherapy, Adjuvant , Child , Cisplatin/administration & dosage , Cisplatin/adverse effects , Combined Modality Therapy , Epirubicin/administration & dosage , Epirubicin/adverse effects , Female , Humans , Lymphatic Metastasis , Middle Aged , Nasopharyngeal Neoplasms/mortality , Nasopharyngeal Neoplasms/pathology , Neoplasm Staging , Survival Analysis , Treatment Outcome
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