12 research outputs found

    Sentinel lymph node in the treatment of anal canal carcinoma. Where are we now?

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    L’intérêt théorique de la recherche et de l’étude du (des) ganglion(s) sentinelle(s) chez les patients atteints de carcinomes épidermoïdes du canal anal de petite taille est de surseoir à l’irradiation des creux inguinaux en l’absence de métastases identifiables et de prévenir la morbidité induite par ce traitement. L’absence de standardisation des indications et certaines difficultés techniques constituent un frein au développement de cette technique. Ces différents aspects sont développés dans ce travail.The theoretical advantage of the identification, removal and analysis of sentinel lymph nodes in patients with small anal canal carcinoma is to rule out external beam radiotherapy of the inguinal lymph nodes areas and therefore to prevent late induced morbidity in the absence of occult metastases. This approach is not widely accepted to date because of some technical limitations and because of remaining uncertainty regarding best clinical indications. The aim of this article is to discuss these different aspects

    Radiation therapy of anal canal carcinoma

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    La radio(chimio)thérapie correspond au traitement de référence des carcinomes épidermoïdes du canal anal localisés qui représentent la majorité des cas. Elle a pour objectif d’obtenir une stérilisation tumorale définitive tout en conservant un sphincter anal fonctionnel. Cet article a pour objectif de préciser les indications et les modalités de la radiothérapie pelvienne dans cette situation. Il sera également question des nouvelles modalités d’irradiation (Radiothérapie Conformationnelle avec Modulation d’Intensité ; Tomothérapie hélicoïdale et irradiation avec modulation d’intensité volumétrique par Arc thérapie) qui permettent à la fois une meilleure définition des volumes cibles et une meilleure protection des organes à risque (intestin grêle, recto-sigmoïde, vessie, organes génitaux notamment). Cette dernière réduit la toxicité induite, ce qui permet d’envisager une réduction de la durée totale du traitement (réduction de la durée de la pause thérapeutique entre les 2 séquences de radiothérapie, voire suppression de cette pause avec traitement continu). La réduction de la toxicité devrait également permettre d’augmenter la dose totale délivrée dans le volume cible. L’intérêt d’une telle stratégie mérite d’être évalué.Radio(chemo)therapy is the standard treatment of localized epidermoid carcinomas of the anal canal, which represent the majority of cases. The aim of treatment is to obtain tumor sterilization while preserving functional anal sphincter. This article concerns the indications and the modalities of radiotherapy in this situation, with special attention to the new available radiation techniques (conformational static field intensity modulated radiotherapy; helicoidal tomotherapy; volumetric modulated arc therapy). These developments mainly allow to reduce the dose to normal tissues and organs at risk thereby minimizing the risk of toxicity. The reduction of the induced morbidity should allow to shorten the classical 2 to 6 weeks gap period between the two sequences of radiotherapy and therefore the total duration of treatment. It also should allow dose escalation to the tumor volume potentially leading to improved locoregional control

    Identification of a Proliferation Gene Cluster Associated with HPV E6/E7 Expression Level and Viral DNA Load in Invasive Cervical Carcinoma

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    Specific HPV DNA sequences are associated with more than 90% of invasive carcinomas of the uterine cervix. Viral E6 and E7 oncogenes are key mediators in cell transformation by disrupting TP53 and RB pathways. To investigate molecular mechanisms involved in the progression of invasive cervical carcinoma, we performed a gene expression study on cases selected according to viral and clinical parameters. Using Coupled Two-Way Clustering and Sorting Points Into Neighbourhoods methods, we identified a Cervical Cancer Proliferation Cluster composed of 163 highly correlated transcripts, many of which corresponded to E2F pathway genes controlling cell proliferation, whereas no primary TP53 targets were present in this cluster. The average expression level of the genes of this cluster was higher in tumours with an early relapse than in tumours with a favourable course (P=0.026). Moreover, we found that E6/E7 mRNA expression level was positively correlated with the expression level of the cluster genes and with viral DNA load. These findings suggest that HPV E6/E7 expression level plays a key role in the progression of invasive carcinoma of the uterine cervix via the deregulation of cellular genes controlling tumour cell proliferation. HPV expression level may thus correspond to a biological marker useful for prognosis assessment and specific therapy of the disease

    Outcome in Advanced Ovarian Cancer following an Appropriate and Comprehensive Effort at Upfront Cytoreduction: A Twenty-Year Experience in a Single Cancer Institute

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    Objectives. The purpose of this retrospective evaluation of advanced-stage ovarian cancer patients was to compare outcome with published findings from other centers and to discuss future options for the management of advanced ovarian carcinoma patients. Methods. A retrospective series of 340 patients with a mean age of 58 years (range: 17–88) treated for FIGO stage III and IV ovarian cancer between January 1985 and January 2005 was reviewed. All patients had primary cytoreductive surgery, without extensive bowel, peritoneal, or systematic lymph node resection, thereby allowing initiation of chemotherapy without delay. Chemotherapy consisted of cisplatin-based chemotherapy in combination with alkylating agents before 2000, whereas carboplatin and paclitaxel regimes were generally used after 1999-2000. Overall survival and disease-free survival were analyzed by the Kaplan-Meier method and the log-rank test. Results. With a mean followup of 101 months (range: 5 to 203), 280 events (recurrence or death) were observed and 245 patients (72%) had died. The mortality and morbidity related to surgery were low. The main prognostic factor for overall survival was postoperative residual disease (P < .0002), while the main prognostic factor for disease-free survival was histological tumor type (P < .0007). Multivariate analysis identified three significant risk factors: optimal surgery (RR = 2.2 for suboptimal surgery), menopausal status (RR = 1.47 for postmenopausal women), and presence of a taxane in the chemotherapy combination (RR = 0.72). Conclusion. These results confirm that optimal surgery defined by an appropriate and comprehensive effort at upfront cytoreduction limits morbidity related to the surgical procedure and allows initiation of chemotherapy without any negative impact on survival. The impact of neoadjuvant chemotherapy to improve resectability while lowering the morbidity of the surgical procedure is discussed
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