29 research outputs found

    Pouvons-nous irradier les patientes atteintes d’un cancer du sein et de la covid-19 ? RĂ©sultats d’une Ă©tude prospective

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    International audiencePurposeThe coronavirus disease 2019 (covid-19) caused by the severe acute respiratory syndrome coronavirus 2 (Sars-Cov-2) is at the origin of a global pandemic. This pandemic has prompted the current health system to reorganize and rethink the care offered by health establishments. We report the early and late toxicity in patients infected with covid-19 treated at the same time for early-stage breast cancer.Material and methodsThis is a monocentric prospective study of patients treated in our hospital between March and June 2020 who were diagnosed with covid-19 infection. The inclusion criteria were to be irradiated for early-stage breast cancer and to have a positive covid diagnosis on a polymerase chain reaction (PCR) test and/or a lung computed tomography (CT) scan and/or suggestive clinical symptoms. All of them needed 6 months follow-up clinic after the end of the radiotherapy with clinical examination, mammogram, as well as CT scan to evaluate the lung status. Radiotherapy consisted of breast or chest wall irradiation with or without lymph node irradiation, with protocols adapted to pandemic situation. The treatment-related toxicity was graded according to the Common Toxicology Criteria for Adverse Events (version 4.03).ResultsAll 350 patients treated for early-stage breast cancer were studied. Of them, 16 presented clinical symptoms of covid-19 infection, and of them 12 had clinical, CT scan and PCR confirmation. This entire cohort of 12 patients with median age of 56 years (range: 42–72 years) underwent their radiotherapy. During the radiotherapy, nine patients presented radiodermatitis: eight grade 1 (66%) and one grade 2 (8%). Two patients with lymph nodes irradiation presented grade 2 oesophagitis. Late toxicity was evaluated 6 months after the end of the radiotherapy, and there was no radiation or covid lung sequel on the CT scans. One patient presented covid-related dyspnoea, and two had fibrosis.ConclusionThe half-year follow-up of prospective covid-19 cohort, treated for early-stage breast cancer demonstrated an acceptable toxicity profile with few low-grade adverse events. It seems that the covid-19 infection does not appear to increase the side effects of radiotherapy. Therefore radiotherapy should not be delayed.Objectif de l’étudeLa Coronavirus Disease (covid-19) causĂ©e par le Severe Acute Respiratory Syndrome Coronavirus 2 (Sars-Cov-2) est Ă  l’origine d’une pandĂ©mie mondiale. Cette pandĂ©mie a incitĂ© le systĂšme de santĂ© actuel Ă  se rĂ©organiser et Ă  repenser les soins offerts par les Ă©tablissements de santĂ©. Nous rapportons la toxicitĂ© prĂ©coce et tardive chez les patientes atteintes par la covid-19 prises en charge en mĂȘme temps pour un cancer du sein de stade prĂ©coce.MatĂ©riel et mĂ©thodesIl s’agissait d’une Ă©tude prospective monocentrique portant sur des patientes prises en charge dans notre hĂŽpital entre mars et juin 2020, avec un diagnostic de covid-19. Les critĂšres d’inclusion Ă©taient patientes irradiĂ©es pour un cancer du sein de stade prĂ©coce avec un diagnostic de covid selon un test par polymerase chain reaction (PCR) et/ou une tomodensitomĂ©trie pulmonaire et/ou des symptĂŽmes cliniques Ă©vocateurs. Toutes les patientes ont eu un contrĂŽle de suivi Ă  6 mois de la fin de la radiothĂ©rapie avec un examen clinique, une mammographie, ainsi qu’une tomodensitomĂ©trie pour Ă©valuer l’état pulmonaire. La radiothĂ©rapie consistait en une irradiation du sein ou de la paroi thoracique avec ou sans irradiation des ganglions lymphatiques, avec des protocoles adaptĂ©s Ă  la situation pandĂ©mique. La toxicitĂ© liĂ©e au traitement a Ă©tĂ© classĂ©e selon les Common Terminology Criteria for Adverse Events version 4.03.RĂ©sultatsToutes les 350 patientes prises en charge pour un stade prĂ©coce d’un cancer du sein ont Ă©tĂ© prises en compte. Parmi elles, 16 ont souffert de symptĂŽmes cliniques de covid-19 et parmi ces derniĂšres, 12 ont eu une confirmation clinique, tomodensitomĂ©trique et PCR. Toute cette cohorte de 12 patientes d’un Ăąge mĂ©dian de 56 ans (intervalle : 42–72 ans) a Ă©tĂ© irradiĂ©e. Au cours de la radiothĂ©rapie, neuf patientes ont eu une radiodermite: de grade 1 dans huit cas (soit 66 %), et de grade 2 chez une (soit 8 %). Deux patientes recevant une irradiation ganglionnaire ont souffert d’une Ɠsophagite de grade 2. La toxicitĂ© tardive Ă©valuĂ©e 6 mois aprĂšs la fin de la radiothĂ©rapie n’a pas retrouvĂ© de sĂ©quelles pulmonaires liĂ©es Ă  la radiothĂ©rapie ou Ă  la covid-19 sur les tomodensitomĂ©tries. Cliniquement, une patiente souffrait d’une dyspnĂ©e et deux d’une fibrose liĂ©e Ă  la covid-19.ConclusionAvec un suivi minimum de 6 mois de la cohorte prospective atteinte de covid-19, prise en charge pour un stade prĂ©coce d’un cancer du sein, a dĂ©montrĂ© un profil de toxicitĂ© acceptable avec peu d’évĂ©nements indĂ©sirables de bas grade. La covid-19 ne semble pas augmenter les effets secondaires de la radiothĂ©rapie. En consĂ©quence, la radiothĂ©rapie ne doit pas ĂȘtre retardĂ©e

    Elias Fonsalada Kritische Ausgabe

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    Cancer of the anal canal: Diagnosis, staging and follow-up with MRI

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    International audienceAlthough a rare disease, anal cancer is increasingly being diagnosed in patients with risk factors, mainly anal infection with the human papilloma virus. Magnetic resonance imaging (MRI) with external phased-array coils is recommended as the imaging modality of choice to grade anal cancers and to evaluate the response assessment after chemoradiotherapy, with a high contrast and good anatomic resolution of the anal canal. MRI provides a performant evaluation of size, extent and signal characteristics of the anal tumor before and after treatment, as well as lymph node involvement and extension to the adjacent organs. MRI is also particularly helpful in the assessment of complications after treatment, and in the diagnosis for relapse of the diseases

    PET/CT imaging: what radiologists need to know

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    Positron emission tomography (PET)/computed tomography (CT) imaging is frequently requested in Oncology. Radiologists and nuclear medicine physicians are often asked to perform a panel of imaging examinations as part of the initial staging or follow-up of cancer patients. Medical imaging must therefore integrate polyvalent skills enabling imaging specialists to understand and interpret all types of images. In this context, PET imaging combined with non-enhanced CT, and diagnostic quality contrast-enhanced CT scan and optimisation of CT settings, is part of this multidisciplinary approach requiring the specific skills of a radiologist and a nuclear medicine physician. This approach must therefore be conducted in both directions: radiologists and nuclear medicine physicians should both know how to correlate PET and CT images, while preserving the specificities of each discipline. Radiologists need to be aware of several aspects of PET imaging: PET technology, the examination procedure and injection of iodinated contrast agent for high quality diagnostic CT, ideally followed by double interpretation of CT images, PET images and fused images. Radiologists should be familiar with PET imaging, as this procedure may be associated with several pitfalls and artefacts that need interpretation by a trained specialist. The authors analyse the examination technique of PET combined with non-enhanced and/or contrast-enhanced CT and the proposals for optimal interpretation of normal or pathological PET/CT fusion images

    Treatment of liver metastases from uveal melanoma by combined surgery-chemotherapy.

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    AIMS: To investigate sporadic results demonstrating prolonged survival after surgical resection and/or intraarterial chemotherapy (IACH) for liver metastases from uveal melanoma. METHODS: From December 1992 to March 1997 every patient with liver metastases from uveal melanoma was enrolled in a prospective study including: (1) aggressive surgical approach removing as much liver disease as possible; (2) implantation of an intraaterial catheter; (3) intraarterial chemotherapy for 6 months. 75 patients were enrolled: 38 men, 37 women, mean age 51 years (range: 18-72), mean time from initial diagnosis of uveal melanoma to liver metastases 37 months (ranged: 1-168). RESULTS: Disseminated disease in both lobes was present in all but one patient. Macroscopically curative surgery was possible in 27.5%. Significant tumour reduction was performed in 49.3% and a simple biopsy was possible in 23.2%. Eight patients did not receive chemotherapy and died soon after. IACH included Fotemustine and/or DTIC-Platinum for 4-9 cycles. Overall median survival was 9 months; very similar to non-operated historical controls. In the 61 patients receiving complete treatment surgery plus chemotherapy, median survival improved to 10 months. When curative resection was possible, survival increased to 22 months (P < 0.001). CONCLUSIONS: Aggressive surgical resection, when possible, appears to be the best method of improving survival of liver metastases from uveal melanoma. New drug combinations are also required to improve survival
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