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  1. Article ; Online: Drug-induced radiation recall reactions and non-anticancer drugs: A descriptive analysis from VigiBase®.

    Aubin-Beale, Eyrian / Giorgi, Lorene / Beurrier, Mathilde / Granel-Brocard, Florence / Gillet, Pierre / Fresse, Audrey

    Fundamental & clinical pharmacology

    2023  Volume 37, Issue 3, Page(s) 673–679

    Abstract: Radiation recall reactions are inflammatory reactions confined to previously irradiated tissues, often of drug-induced etiology, particularly with anticancer therapies. Other drugs, in particular COVID-19 vaccines, may also be involved. To describe ... ...

    Abstract Radiation recall reactions are inflammatory reactions confined to previously irradiated tissues, often of drug-induced etiology, particularly with anticancer therapies. Other drugs, in particular COVID-19 vaccines, may also be involved. To describe radiation recall reactions under non-anticancer drugs more precisely, we extracted the cases of radiation recall reactions associated with non-anticancer drugs from WHO pharmacovigilance database VigiBase®. We performed two analyses from this extraction: a global analysis and an analysis focusing on vaccination-related issues. We extracted 120 cases corresponding to 269 drugs, of which 130 were non-anticancer (22 vaccines). Among the non-anticancer drugs, tozinameran was the most reported treatment (4.46% of cases), followed by levofloxacin (2.97%) and folinic acid (2.60%), dexamethasone (2.23), and ChAdOx1 nCoV-19 vaccine and prednisone (1.86% each). Among vaccines, tozinameran (54.55% of cases) was the most reported, followed by ChAdOx1 nCoV-19 (22.73%), HPV and inactivated influenza vaccine (9.09% each), and elasomeran (4.55%). Our study first describes the occurrence of radiation recall reactions during non-anticancer treatment. It also highlights a potential safety signal with COVID-19 vaccines.
    MeSH term(s) Humans ; COVID-19 Vaccines ; ChAdOx1 nCoV-19 ; COVID-19/epidemiology ; COVID-19/prevention & control ; BNT162 Vaccine ; Radiodermatitis ; Influenza Vaccines
    Chemical Substances COVID-19 Vaccines ; ChAdOx1 nCoV-19 (B5S3K2V0G8) ; BNT162 Vaccine ; Influenza Vaccines
    Language English
    Publishing date 2023-01-11
    Publishing country England
    Document type Journal Article
    ZDB-ID 639134-5
    ISSN 1472-8206 ; 0767-3981
    ISSN (online) 1472-8206
    ISSN 0767-3981
    DOI 10.1111/fcp.12866
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Does Preventive Negative Pressure Wound Therapy (NPWT) reduce local complications following Lymph Node Dissection (LND) in the management of metastatic skin tumors?

    Poirier, Antoine / Albuisson, Eliane / Bihain, Florence / Granel-Brocard, Florence / Perez, Manuela

    Journal of plastic, reconstructive & aesthetic surgery : JPRAS

    2022  Volume 75, Issue 12, Page(s) 4403–4409

    Abstract: Introduction: Axillary and inguinal lymph node dissection (LND) are performed in metastatic skin tumors with several local complications, such as lymphorrhea, lymphoceles, and lymphedema. The purpose of this study is to determine whether negative ... ...

    Abstract Introduction: Axillary and inguinal lymph node dissection (LND) are performed in metastatic skin tumors with several local complications, such as lymphorrhea, lymphoceles, and lymphedema. The purpose of this study is to determine whether negative pressure wound therapy (NPWT) applied as a preventive measure could improve outcomes.
    Materials and methods: A monocentric study included patients who underwent axillary or inguinal LND from May 2010 to March 2020, with a retrospective evaluation of prospectively collected data. Patients were divided into two groups: the conventional wound care (CWC) and the NPWT groups. Patients were systematically reviewed at D7, D30, and at 1 year postoperative, and data regarding lymphorrhea, lymphoceles, and lymphedema were collected.
    Results: A total of 109 axillary and inguinal LND were performed. NPWT was applied on 68 LND and CWC on 41 LND. The variables, diabetes, smoking, gender, associated treatments, and primary pathology (melanoma, squamous cell carcinoma, or Merkel tumors) were similar in both groups. Analyses have shown a significant difference in the rate of scar disunion during the first month between the two groups (p=0.045 between D1 and D7; p=0.011 between D8 and D30), as well as the presence of lymphorrhea (p=0.000 between D1 and D7; p=0.002 between D8 and D30). The rate of lymphoedema was significantly reduced in the NPWT group versus CWC (p=0.000 between D8 and D30; p=0.034 between D31 and 1 year).
    Conclusion: NPWT reduces local complications (scar disunion, lymphorrhea, and lymphedema) during the first year following LND in the management of node metastatic skin tumors.
    MeSH term(s) Humans ; Lymphocele/etiology ; Negative-Pressure Wound Therapy ; Retrospective Studies ; Cicatrix/complications ; Lymph Node Excision/adverse effects ; Skin Neoplasms/surgery ; Lymphedema/prevention & control ; Lymphedema/complications ; Lymphatic Diseases ; Lymph Nodes
    Language English
    Publishing date 2022-08-24
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2217750-4
    ISSN 1878-0539 ; 1748-6815 ; 0007-1226
    ISSN (online) 1878-0539
    ISSN 1748-6815 ; 0007-1226
    DOI 10.1016/j.bjps.2022.08.054
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: A flare-up of rheumatoid arthritis followed by adrenocorticotropic insufficiency induced by pembrolizumab: A case-report.

    Garon-Czmil, Julie / Abs, Diane / Granel-Brocard, Florence / Gillet, Pierre / Yelehe-Okouma, Mélissa

    Therapie

    2020  Volume 76, Issue 5, Page(s) 510–512

    MeSH term(s) Antibodies, Monoclonal, Humanized/adverse effects ; Arthritis, Rheumatoid/drug therapy ; Humans
    Chemical Substances Antibodies, Monoclonal, Humanized ; pembrolizumab (DPT0O3T46P)
    Language English
    Publishing date 2020-11-24
    Publishing country France
    Document type Case Reports ; Letter
    ZDB-ID 603474-3
    ISSN 1958-5578 ; 0040-5957
    ISSN (online) 1958-5578
    ISSN 0040-5957
    DOI 10.1016/j.therap.2020.11.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Personalized follow-up of circulating DNA in resected stage III/IV melanoma: PERCIMEL multicentric prospective study protocol.

    Geoffrois, Lionnel / Harlé, Alexandre / Sahki, Nassim / Sikanja, Aleksandra / Granel-Brocard, Florence / Hervieu, Alice / Mortier, Laurent / Jeudy, Géraldine / Michel, Catherine / Nardin, Charlée / Huin-Schohn, Cécile / Merlin, Jean-Louis

    BMC cancer

    2023  Volume 23, Issue 1, Page(s) 554

    Abstract: Background: With more than 15,000 new cases /year in France and 2,000 deaths, cutaneous melanoma represents approximately 4% of incidental cancers and 1.2% of cancer related deaths. In locally advanced (stage III) or resectable metastatic (stage IV) ... ...

    Abstract Background: With more than 15,000 new cases /year in France and 2,000 deaths, cutaneous melanoma represents approximately 4% of incidental cancers and 1.2% of cancer related deaths. In locally advanced (stage III) or resectable metastatic (stage IV) melanomas, medical adjuvant treatment is proposed and recent advances had shown the benefit of anti-PD1/PDL1 and anti-CTLA4 immunotherapy as well as anti-BRAF and anti-MEK targeted therapy in BRAF V600 mutated tumors. However, the recurence rate at one year is approximately 30% and justify extensive research of predictive biomarkers. If in metastatic disease, the follow-up of circulating tumor DNA (ctDNA) has been demonstrated, its interest in adjuvant setting remains to be precised, especially because of a lower detection rate. Further, the definition of a molecular response could prove useful to personalized treatment.
    Methods: PERCIMEL is an open prospective multicentric study executed through collaboration of the Institut de Cancérologie de Lorraine (non-profit comprehensive cancer center) and 6 French university and community hospitals. A total of 165 patients with resected stage III and IV melanoma, eligible to adjuvant imunotherapy or anti-BRAF/MEK kinase inhibitors will be included. The primary endpoint is the presence of ctDNA, 2 to 3 weeks after surgery, defined as mutated ctDNA copy number calculated as the allelic fraction of a clonal mutation relative to total ctDNA. Secondary endpoints are recurrence-free survival, distant metastasis-free survival and specific survival. We will follow ctDNA along treatment, quantitatively through ctDNA mutated copy number variation, qualitatively through the presence of cfDNA and its clonal evolution. Relative and absolute variations of ctDNA during follow-up will be also analyzed. PERCIMEL study aims at provide scientific evidence that ctDNA quantitative and qualitative variations can be used to predict the recurrence of patients with melanoma treated with adjuvant immunotherapy or kinase inhibitors, thus defining the notion of molecular recurrence.
    MeSH term(s) Humans ; Melanoma/genetics ; Melanoma/therapy ; Melanoma/pathology ; Skin Neoplasms/drug therapy ; Skin Neoplasms/genetics ; Prospective Studies ; Cell-Free Nucleic Acids ; Follow-Up Studies ; DNA Copy Number Variations ; Protein Kinase Inhibitors ; Proto-Oncogene Proteins B-raf/genetics ; Mutation ; Melanoma, Cutaneous Malignant
    Chemical Substances Cell-Free Nucleic Acids ; Protein Kinase Inhibitors ; Proto-Oncogene Proteins B-raf (EC 2.7.11.1)
    Language English
    Publishing date 2023-06-16
    Publishing country England
    Document type Journal Article
    ZDB-ID 2041352-X
    ISSN 1471-2407 ; 1471-2407
    ISSN (online) 1471-2407
    ISSN 1471-2407
    DOI 10.1186/s12885-023-11029-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Sweet syndrome and erythema nodosum in a case of anal canal cancer during concomitant radiochemotherapy.

    Moreau, Estelle / Peiffert, Didier / Schmutz, Jean Luc / Granel-Brocard, Florence / Bursztejn, Anne-Claire

    European journal of dermatology : EJD

    2019  Volume 29, Issue 5, Page(s) 539–540

    MeSH term(s) Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Anus Neoplasms/therapy ; Chemoradiotherapy/adverse effects ; Erythema Nodosum/diagnosis ; Erythema Nodosum/etiology ; Female ; Fluorouracil/administration & dosage ; Fluorouracil/adverse effects ; Humans ; Middle Aged ; Mitomycin/administration & dosage ; Mitomycin/adverse effects ; Sweet Syndrome/diagnosis ; Sweet Syndrome/etiology
    Chemical Substances Mitomycin (50SG953SK6) ; Fluorouracil (U3P01618RT)
    Language English
    Publishing date 2019-10-16
    Publishing country France
    Document type Case Reports ; Journal Article
    ZDB-ID 1128666-0
    ISSN 1952-4013 ; 1167-1122
    ISSN (online) 1952-4013
    ISSN 1167-1122
    DOI 10.1684/ejd.2019.3628
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Simultaneous response of cutaneous and lung squamous cell carcinoma with cemiplimab.

    Escobar, Gabriela Fortes / Granel-Brocard, Florence / Schmutz, Jean-Luc / Cervantes, Pierre / Ben Mahmoud, Sinan / Bursztejn, Anne-Claire

    Dermatologic therapy

    2020  Volume 33, Issue 6, Page(s) e13951

    MeSH term(s) Antibodies, Monoclonal, Humanized ; Carcinoma, Squamous Cell ; Humans ; Lung ; Skin Neoplasms
    Chemical Substances Antibodies, Monoclonal, Humanized ; cemiplimab (6QVL057INT)
    Language English
    Publishing date 2020-07-16
    Publishing country United States
    Document type Letter
    ZDB-ID 1354801-3
    ISSN 1529-8019 ; 1396-0296
    ISSN (online) 1529-8019
    ISSN 1396-0296
    DOI 10.1111/dth.13951
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Colite ulcérée sévère lors d’un traitement par ipilimumab sans récidive après cure d’infliximab et relai secondaire par pembrolizumab.

    Yelehe-Okouma, Mélissa / Granel-Brocard, Florence / Hudziak, Hervé / Schmutz, Jean-Luc / Gillet, Pierre

    Therapie

    2017  Volume 73, Issue 3, Page(s) 291–293

    Title translation Severe ipilimumab-induced ulcerative colitis remitting after infliximab therapy and secondary switching with pembrolizumab.
    MeSH term(s) Aged ; Antibodies, Monoclonal, Humanized/therapeutic use ; Antineoplastic Agents, Immunological/adverse effects ; Antineoplastic Agents, Immunological/therapeutic use ; Colitis, Ulcerative/chemically induced ; Colitis, Ulcerative/diagnostic imaging ; Colitis, Ulcerative/drug therapy ; Crohn Disease/chemically induced ; Crohn Disease/diagnostic imaging ; Humans ; Infliximab/adverse effects ; Infliximab/therapeutic use ; Ipilimumab/adverse effects ; Ipilimumab/therapeutic use ; Male ; Melanoma/complications ; Melanoma/drug therapy
    Chemical Substances Antibodies, Monoclonal, Humanized ; Antineoplastic Agents, Immunological ; Ipilimumab ; Infliximab (B72HH48FLU) ; pembrolizumab (DPT0O3T46P)
    Language French
    Publishing date 2017-11-16
    Publishing country France
    Document type Case Reports ; Letter
    ZDB-ID 603474-3
    ISSN 1958-5578 ; 0040-5957
    ISSN (online) 1958-5578
    ISSN 0040-5957
    DOI 10.1016/j.therap.2017.10.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Apport du panel multiparamétrique CD3 CD4 CD8 CD7 CD26 CD158k dans la détection et le suivi par cytométrie en flux des cellules de Sézary.

    Callet, Jonas / Latger-Cannard, Véronique / Gérard, Delphine / Salignac, Sylvain / Granel-Brocard, Florence / Campidelli, Arnaud / Bursztejn, Anne-Claire / Broséus, Julien / Vial, Jean-Philippe / Lesesve, Jean-François

    Annales de biologie clinique

    2021  Volume 79, Issue 3, Page(s) 233–240

    Abstract: The Sezary syndrome has been defined by a triad combining erythrodermia, generalized lymphadenopathy, and the presence of circulating Sezary cells > 1 × ... ...

    Title translation Use of the multiparametric panel CD3/CD4/CD8/CD7/CD26/CD158k in the detection and use of flow cytometry of Sezary cells.
    Abstract The Sezary syndrome has been defined by a triad combining erythrodermia, generalized lymphadenopathy, and the presence of circulating Sezary cells > 1 × 10
    MeSH term(s) Antigens, CD ; Biomarkers, Tumor ; CD8-Positive T-Lymphocytes ; Dipeptidyl Peptidase 4 ; Flow Cytometry ; Humans ; Retrospective Studies ; Skin Neoplasms/diagnosis
    Chemical Substances Antigens, CD ; Biomarkers, Tumor ; Dipeptidyl Peptidase 4 (EC 3.4.14.5)
    Language French
    Publishing date 2021-06-24
    Publishing country France
    Document type Journal Article
    ZDB-ID 418098-7
    ISSN 1950-6112 ; 0003-3898
    ISSN (online) 1950-6112
    ISSN 0003-3898
    DOI 10.1684/abc.2021.1651
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Risk of irAEs in patients with autoimmune diseases treated by immune checkpoint inhibitors for stage III or IV melanoma: results from a matched case-control study.

    Plaçais, Léo / Dalle, Stéphane / Dereure, Olivier / Trabelsi, Sabiha / Dalac, Sophie / Legoupil, Delphine / Montaudié, Henri / Arnault, Jean-Philippe / De Quatrebarbes, Julie / Saiag, Philippe / Brunet-Possenti, Florence / Lesimple, Thierry / Maubec, Eve / Aubin, François / Granel-Brocard, Florence / Grob, Jean-Jacques / Stoebner, Pierre-Emmanuel / Allayous, Clara / Oriano, Bastien /
    Dutriaux, Caroline / Mortier, Laurent / Lebbe, Céleste

    Annals of the rheumatic diseases

    2022  Volume 81, Issue 10, Page(s) 1445–1452

    Abstract: Objective: To quantify the risk of immune-related adverse events (irAEs) in patients with pre-existing autoimmune disease (pAID) treated by immune checkpoint inhibitors (ICIs) for stage III or IV melanoma.: Methods: Case-control study performed on a ... ...

    Abstract Objective: To quantify the risk of immune-related adverse events (irAEs) in patients with pre-existing autoimmune disease (pAID) treated by immune checkpoint inhibitors (ICIs) for stage III or IV melanoma.
    Methods: Case-control study performed on a French multicentric prospective cohort of patients with melanoma, matched for irAE risk factors and oncological staging. Risk of irAE was assessed by logistic regression.
    Results: 110 patients with pAID were included and matched with 330 controls, from March 2013 to October 2020. Over a median follow-up period of 7.2 months for cases and 6.9 months for controls, the ORs of developing all-grade and grade ≥3 irAEs among cases compared with controls were 1.91 (95% CI (1.56 to 2.27)) and 1.44 (95% CI (1.08 to 1.82)), respectively. Patients with pAID had an increased risk of multiple irAEs (OR 1.46, 95% CI (1.15 to 2.67)) and a shorter time to irAE onset. In contrast, there were no difference in irAE-related mortality nor in the rate of treatment discontinuation, and a landmark analysis revealed a better survival at 24 months among cases (p=0.02). Thirty per cent of cases experienced a pAID flare during follow-up, and baseline immunosuppression did not prevent irAE occurrence. Last, we report associations between the pAID clinical subsets and organ-specific irAEs.
    Conclusion: In our study, patients with pAID were at greater risk of all-grade, severe and multiple irAEs, yet had a better 24-month survival than controls. Thus, patients with pAID should be eligible for ICI therapy but benefit from a close monitoring for irAE occurrence, especially during the first months of therapy.
    MeSH term(s) Antineoplastic Agents, Immunological/adverse effects ; Autoimmune Diseases/chemically induced ; Autoimmune Diseases/drug therapy ; Case-Control Studies ; Humans ; Immune Checkpoint Inhibitors/adverse effects ; Immune System Diseases ; Melanoma/drug therapy ; Prospective Studies ; Retrospective Studies
    Chemical Substances Antineoplastic Agents, Immunological ; Immune Checkpoint Inhibitors
    Language English
    Publishing date 2022-07-04
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 7090-7
    ISSN 1468-2060 ; 0003-4967
    ISSN (online) 1468-2060
    ISSN 0003-4967
    DOI 10.1136/ard-2022-222186
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Hidradénite neutrophilique eccrine associée à une leucémie aiguë myéloïde.

    Bonhomme, Axelle / Liegeon, Anne-Laure / Granel-Brocard, Florence / Barbaud, Annick / Schmutz, Jean-Luc

    Presse medicale (Paris, France : 1983)

    2015  Volume 44, Issue 6 Pt 1, Page(s) 688–689

    Title translation Neutrophilic eccrine hidradenitis associated with acute myeloid leukemia.
    MeSH term(s) Female ; Hidradenitis/etiology ; Humans ; Leukemia, Myeloid, Acute/complications ; Middle Aged
    Language French
    Publishing date 2015-06
    Publishing country France
    Document type Case Reports ; Letter
    ZDB-ID 120943-7
    ISSN 2213-0276 ; 0032-7867 ; 0755-4982 ; 0301-1518
    ISSN (online) 2213-0276
    ISSN 0032-7867 ; 0755-4982 ; 0301-1518
    DOI 10.1016/j.lpm.2015.02.018
    Database MEDical Literature Analysis and Retrieval System OnLINE

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