Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
1.
Bull Cancer ; 110(2S): S56-S66, 2023 Feb.
Article in French | MEDLINE | ID: mdl-35662519

ABSTRACT

Autologous and allogeneic hematopoietic stem cell transplantation (HSCT) can lead to early cardiac complications as well as late sequelae. A cardiac evaluation is essential in the pre-transplant assessment given the patient's comorbidities and previous chemotherapy treatments received. Various thresholds of cardiac function are recommended as eligibility criteria. The rise of haplo-identical transplantation with the use of post-transplant high-dose cyclophosphamide (PT-Cy) as a prophylaxis against graft-versus-host disease (GVHD) is accompanied by a resurgence of cardiological concerns. Arrhythmias are also a concern and the list of drugs implicated in this complication is growing. The rare occurrence of cardiac GVHD has been reported, although the entity is not well defined. Finally, although long-term follow-up recommendations exist, they are not accompanied by specific targets for cardiovascular risk factors, the presence of which is nevertheless increased after HSCT. In the framework of the Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-TC) practice harmonization workshops held in Lille in September 2019, the prophylaxis, the diagnostic approach and the treatments of cardiac complication following HSCT were reviewed after analysis of published studies.


Subject(s)
Graft vs Host Disease , Hematopoietic Stem Cell Transplantation , Humans , Hematopoietic Stem Cell Transplantation/adverse effects , Bone Marrow Transplantation , Cyclophosphamide , Graft vs Host Disease/etiology , Graft vs Host Disease/prevention & control , Comorbidity
2.
Bull Cancer ; 107(12S): S116-S121, 2020 Dec.
Article in French | MEDLINE | ID: mdl-32631612

ABSTRACT

INTRODUCTION: Allogeneic stem cell transplantation is currently the only curative therapy for hematological disorders. This treatment can lead to complications, of which ophtalmological involvement. METHODS: We reviewed the literature and established accessible and convenient recommendations for hematologists and ophthalmologists. RESULTS: Ophtalmological follow-up should be done in every patient having had an allogeneic transplantation, by the hematologist questioning and by the ophthalmologist physical exam. Complications due to graft-versus-host disease (GVHD) or not due to GVHD are cited, as well as therapeutic options. DISCUSSION: Screening and treatment of ophthalmologic complications in allogeneic stem cells transplantation recipients requires a close collaboration between hematologists and ophthalmologists. The management of these patients by caregivers trained in these questions is encouraged.


Subject(s)
Eye Diseases/etiology , Hematopoietic Stem Cell Transplantation/adverse effects , Eye Diseases/diagnosis , Eye Diseases/therapy , Graft vs Host Disease/complications , Hematologic Diseases/therapy , Hematology , Humans , Ophthalmologists , Societies, Medical , Transplantation, Homologous/adverse effects
3.
Bull Cancer ; 107(12S): S122-S129, 2020 Dec.
Article in French | MEDLINE | ID: mdl-32532421

ABSTRACT

Stomatological complications of allogeneic hematopoietic stem cell transplantation (HSCT) are frequent and very uncomfortable for patients. The primary complication is the graft versus host disease reaction. Other side effects of the procedure include infections, taste disorders and carcinogenic risks. Various local treatments are used but remain imperfect. Within the framework of the 10th workshop of practice harmonization of the Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-TC) held in Lille in September 2019, diagnostic approaches and treatments of tongue and oral complications following allogeneic HSCT were reviewed according to the analysis of published studies.


Subject(s)
Hematopoietic Stem Cell Transplantation/adverse effects , Mouth Diseases/etiology , Acute Disease , Candidiasis, Oral/diagnosis , Candidiasis, Oral/etiology , Candidiasis, Oral/therapy , Carcinoma, Squamous Cell/etiology , Chronic Disease , Dental Caries/etiology , Dental Caries/prevention & control , Gout/etiology , Graft vs Host Disease/complications , Humans , Mouth Diseases/diagnosis , Mouth Diseases/therapy , Mouth Neoplasms/etiology , Periodontal Diseases/etiology , Societies, Medical , Tongue Diseases/diagnosis , Tongue Diseases/etiology , Tongue Diseases/therapy , Transplantation Conditioning/adverse effects , Transplantation, Homologous/adverse effects
4.
Bull Cancer ; 107(1S): S44-S51, 2020 Jan.
Article in French | MEDLINE | ID: mdl-31570213

ABSTRACT

The modalities of mobilization of hematopoietic stem cells in autologous transplantation have evolved in recent years. The Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-TC) organized the 9th hematopoietic stem cell transplantation clinical practices harmonization workshop series in September 2018 in Lille, France, to conduct a review of current practices of the society centers and of international recommendations. The cell dose objectives have been revised. The modalities of mobilization including the use of plerixafor have been specified allowing reaching the objectives of collection while limiting the number of apheresis. Collections failures have become exceptional.


Subject(s)
Hematopoietic Stem Cell Mobilization/methods , Hematopoietic Stem Cell Transplantation , Algorithms , Antigens, CD34/analysis , Antineoplastic Agents/adverse effects , Antineoplastic Agents/pharmacology , Benzylamines , Blood Component Removal/methods , Bone Marrow/drug effects , Cell Count , Cell Separation/methods , Cyclams , Granulocyte Colony-Stimulating Factor/adverse effects , Granulocyte Colony-Stimulating Factor/pharmacology , Hematopoietic Cell Growth Factors/pharmacology , Hematopoietic Stem Cell Mobilization/standards , Heterocyclic Compounds/pharmacology , Humans , Practice Patterns, Physicians' , Risk Factors , Transplantation, Autologous
5.
Bull Cancer ; 106(1S): S1-S9, 2019 Jan.
Article in French | MEDLINE | ID: mdl-30580913

ABSTRACT

Allogeneic hematopoietic cell transplantation (HCT) is part of the standard of care for many hematological diseases. Over the last decades, significant advances in patient and donor selection, conditioning regimens as well as supportive care of patients undergoing allogeneic HCT leading to improved overall survival have been made. In view of many new treatment options in cellular and molecular targeted therapies, the place of allogeneic transplantation in therapy concepts must be reviewed. Most aspects of HCT are well standardized by national guidelines or laws as well as by certification labels such as FACT-JACIE. However, the requirements for human resources, construction and layout of a unit treating patients during the transplantation procedure and for different complications are not well defined. Here, we describe the process of planning a transplant unit in order to open a discussion that could lead to more precise guidelines in the field of personnel and infrastructural requirements for hospitals caring for people with severe immunosuppression.


Subject(s)
Bone Marrow Transplantation/standards , Health Facility Environment/standards , Hematologic Diseases/therapy , Hematopoietic Stem Cell Transplantation/standards , Air/standards , Cell- and Tissue-Based Therapy/standards , Diet, Healthy/standards , Donor Selection/standards , France , Health Personnel/standards , Hospital Units/standards , Humans , Hygiene , Immunosuppression Therapy/standards , Monitoring, Physiologic/methods , Protective Clothing/standards , Societies, Medical , Sterilization/standards , Transplantation, Homologous/standards , Visitors to Patients
6.
Blood Coagul Fibrinolysis ; 28(2): 145-151, 2017 Mar.
Article in English | MEDLINE | ID: mdl-27100303

ABSTRACT

Home therapy for uncomplicated mild/moderate bleeding can decrease healthcare burden, promote self-esteem, reduce complications, and provide near-normal quality of life. To evaluate recombinant activated factor VII (rFVIIa) as home therapy for joint bleeds in Algeria, Morocco, Oman, Saudi Arabia, and United Arab Emirates. Twenty-seven patients aged more than 2 years with congenital haemophilia and inhibitors were monitored for up to 8 months after a first haemarthrosis episode treated with rFVIIa. Assessments were made by patients/caregivers with a standardized diary. The main measures included home-managed bleeds, haemostasis, and pain relief within 9 h after first injection. Additional analyses included convenience, time to pain resolution, and doses given within 48 h. Of 132 bleeds, 84 (63.6%) were managed at home. Of these, successful haemostasis (partial or complete) was achieved at 9 h in 87.8%, with pain relief for 84.0%. For all treatment settings, successful haemostasis at 9 h was achieved for 86.3% of bleeds, with pain relief achieved for 74.8% of bleeds. Higher initial dosing was associated with fewer injections. Median time to complete haemostasis was 48 h (spontaneous bleeds) and 24 h (traumatic bleeds). Median time to complete pain relief was 24 h for both bleed types. Satisfaction with treatment was high. No safety concerns were reported. Results from this observational study agree with previous data on the safety and efficacy of home treatment with rFVIIa and will help to increase awareness and aggregate experience, fostering confidence in home management of haemophilia patients with inhibitors in developing countries.


Subject(s)
Factor VIIa/therapeutic use , Hemarthrosis/therapy , Hemophilia A/complications , Hemophilia B/complications , Recombinant Proteins/therapeutic use , Developing Countries , Feasibility Studies , Humans
SELECTION OF CITATIONS
SEARCH DETAIL