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  1. Artikel ; Online: Adjusted comparison of outcomes between patients from CARTITUDE-1

    Mateos, Maria-Victoria / Weisel, Katja / Martin, Thomas / Berdeja, Jesús G / Jakubowiak, Andrzej / Stewart, A Keith / Jagannath, Sundar / Lin, Yi / Diels, Joris / Ghilotti, Francesca / Thilakarathne, Pushpike / Perualila, Nolen J / Cabrieto, Jedelyn / Haefliger, Benjamin / Erler-Yates, Nichola / Hague, Clare / Jackson, Carolyn C / Schecter, Jordan M / Strulev, Vadim /
    Nesheiwat, Tonia / Pacaud, Lida / Einsele, Hermann / Moreau, Philippe

    Haematologica

    2023  Band 108, Heft 8, Seite(n) 2192–2204

    Abstract: Ciltacabtagene autoleucel (cilta-cel) is a chimeric antigen receptor T-cell therapy studied in patients with multiple myeloma exposed to three classes of treatment in the single-arm CARTITUDE-1 study. To assess the effectiveness of cilta-cel compared to ... ...

    Abstract Ciltacabtagene autoleucel (cilta-cel) is a chimeric antigen receptor T-cell therapy studied in patients with multiple myeloma exposed to three classes of treatment in the single-arm CARTITUDE-1 study. To assess the effectiveness of cilta-cel compared to real-world clinical practice (RWCP), we performed adjusted comparisons using individual patients' data from CARTITUDE-1 and LocoMMotion, a prospective, multinational study of patients with multiple myeloma triple-class exposed of treatment. Comparisons were performed using inverse probability weighting. In CARTITUDE-1, 113 patients were enrolled, and 97 patients were infused with cilta-cel. In LocoMMotion, 248 patients were enrolled, and 170 patients were included in the comparisons versus infused patients. Ninety-two unique regimens were used in LocoMMotion, most frequently carfilzomib-dexamethasone (13.7%), pomalidomide-cyclophosphamide-dexamethasone (13.3%) and pomalidomidedexamethasone (11.3%). Adjusted comparisons showed that patients treated with cilta-cel were 3.12-fold more likely to respond to treatment than those managed by RWCP (response rate, 3.12, 95% confidence interval [95% CI]: 2.24-4.00), had their risk of progression or death reduced to by 85% (progression-free survival hazard ratio=0.15, 95% CI: 0.08-0.29), and a risk of death lowered by 80% (overall survival hazard ratio HR=0.20, 95% CI: 0.09-0.41). The incremental improvement in healthrelated quality of life from baseline for cilta-cel versus RWCP at week 52, as measured by EORTC QLQ-C30 Global Health Status, was 13.4 (95% CI: 3.5-23.6) and increased to 30.8 (95% CI: 21.8-39.8) when including death as additional information regarding patients' health status. Patients treated with cilta-cel experienced more adverse events than those managed with RWCP (any grade: 100% vs. 83.5%). The results from this study demonstrate improved efficacy outcomes of cilta-cel versus RWCP and highlight its potential as a novel and effective treatment option for patients with multiple myeloma triple-class exposed of antimyeloma treatment. CARTITUDE-1 is registered with clinicaltrials gov. Identifier: NCT03548207. LocoMMotion is registered with clinicaltrials gov. Identifier: NCT04035226.
    Mesh-Begriff(e) Humans ; Multiple Myeloma/drug therapy ; Multiple Myeloma/etiology ; Proteasome Inhibitors/therapeutic use ; Immunomodulating Agents ; Prospective Studies ; Quality of Life ; Dexamethasone/therapeutic use ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use
    Chemische Substanzen Proteasome Inhibitors ; Immunomodulating Agents ; Dexamethasone (7S5I7G3JQL)
    Sprache Englisch
    Erscheinungsdatum 2023-08-01
    Erscheinungsland Italy
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2333-4
    ISSN 1592-8721 ; 0017-6567 ; 0390-6078
    ISSN (online) 1592-8721
    ISSN 0017-6567 ; 0390-6078
    DOI 10.3324/haematol.2022.280482
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Heart-Lung Transplant via an Eighth-Time Sternotomy.

    Riggs, Kyle W / Chin, Clifford W / Bryant, Roosevelt / Zafar, Farhan / Chin, Clifford / Schecter, Marc G / Morales, David L S

    World journal for pediatric & congenital heart surgery

    2019  Band 12, Heft 1, Seite(n) 136–138

    Abstract: We report a combined heart-lung transplantation following seven prior sternotomies in a patient born with a transitional atrioventricular septal defect. Previous surgeries to repair and replace the mitral valve led to pulmonary vein stenosis and ... ...

    Abstract We report a combined heart-lung transplantation following seven prior sternotomies in a patient born with a transitional atrioventricular septal defect. Previous surgeries to repair and replace the mitral valve led to pulmonary vein stenosis and pulmonary vascular disease. Eighth-time sternotomy and significant vascular adhesions led to a prolonged operation and to placing the heart-lung block anterior to the phrenic nerves. Despite this, the patient was ready for discharge after two weeks and continues to do well over nine months later. As more patients survive multiple cardiac palliations with some developing pulmonary vascular disease, heart-lung transplantation may become relevant again.
    Mesh-Begriff(e) Adolescent ; Echocardiography ; Heart Septal Defects/diagnosis ; Heart Septal Defects/surgery ; Heart-Lung Transplantation/methods ; Humans ; Male ; Sternotomy/methods ; Tomography, X-Ray Computed
    Sprache Englisch
    Erscheinungsdatum 2019-04-24
    Erscheinungsland United States
    Dokumenttyp Case Reports ; Journal Article
    ZDB-ID 2550261-X
    ISSN 2150-136X ; 2150-1351
    ISSN (online) 2150-136X
    ISSN 2150-1351
    DOI 10.1177/2150135118815876
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Matching-Adjusted Indirect Treatment Comparison to Assess the Comparative Efficacy of Ciltacabtagene Autoleucel in CARTITUDE-1 Versus Belantamab Mafodotin in DREAMM-2, Selinexor-Dexamethasone in STORM Part 2, and Melphalan Flufenamide-Dexamethasone in HORIZON for the Treatment of Patients With Triple-Class Exposed Relapsed or Refractory Multiple Myeloma.

    Weisel, Katja / Krishnan, Amrita / Schecter, Jordan M / Vogel, Martin / Jackson, Carolyn C / Deraedt, William / Yeh, Tzu-Min / Banerjee, Arnob / Yalniz, Fevzi / Nesheiwat, Tonia / Van Sanden, Suzy / Diels, Joris / Valluri, Satish / Usmani, Saad Z / Berdeja, Jesus G / Jagannath, Sundar / Martin, Tom

    Clinical lymphoma, myeloma & leukemia

    2022  Band 22, Heft 9, Seite(n) 690–701

    Abstract: Introduction: This study estimated the comparative efficacy of ciltacabtagene autoleucel (cilta-cel; CARTITUDE-1), a chimeric antigen receptor (CAR)-T-cell therapy, versus 3 non-CAR-T therapies (belantamab mafodotin [DREAMM-2], selinexor plus ... ...

    Abstract Introduction: This study estimated the comparative efficacy of ciltacabtagene autoleucel (cilta-cel; CARTITUDE-1), a chimeric antigen receptor (CAR)-T-cell therapy, versus 3 non-CAR-T therapies (belantamab mafodotin [DREAMM-2], selinexor plus dexamethasone [STORM Part 2], and melphalan flufenamide plus dexamethasone [HORIZON]), each with distinct mechanisms of action, for the treatment of patients with relapsed or refractory multiple myeloma (RRMM) who were triple-class exposed to an immunomodulatory drug, proteasome inhibitor, and an anti-CD38 monoclonal antibody.
    Patients and methods: Pairwise matching-adjusted indirect treatment comparisons (MAICs) were conducted using patient-level data for cilta-cel from CARTITUDE-1 and summary level data for each comparator (2.5 mg/kg cohort in DREAMM-2, modified intention-to-treat population in STORM Part 2, and triple-class refractory patients in HORIZON). Treated patients from CARTITUDE-1 who satisfied the eligibility of the comparator trial were included. MAICs adjusted for imbalances in important prognostic factors between CARTITUDE-1 and the comparator populations. Comparative efficacy of cilta-cel versus each therapy was estimated for overall response rate, complete response or better rate, progression-free survival, and overall survival.
    Results: After adjustment, patients treated with cilta-cel demonstrated at least a 3.1-fold and at least a 10.3-fold increase in the likelihood of achieving an overall response or complete response or better, respectively, at least a 74% reduction in the risk of disease progression or death, and at least a 47% reduction in the risk of death. These results were statistically significant.
    Conclusion: Cilta-cel showed improved efficacy over each comparator for all outcomes, demonstrating its potential as an efficacious treatment for patients with triple-class exposed RRMM.
    Mesh-Begriff(e) Antibodies, Monoclonal, Humanized ; Antineoplastic Combined Chemotherapy Protocols/pharmacology ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Dexamethasone/pharmacology ; Dexamethasone/therapeutic use ; Humans ; Hydrazines ; Melphalan/pharmacology ; Melphalan/therapeutic use ; Multiple Myeloma/drug therapy ; Multiple Myeloma/etiology ; Triazoles
    Chemische Substanzen Antibodies, Monoclonal, Humanized ; Hydrazines ; Triazoles ; selinexor (31TZ62FO8F) ; Dexamethasone (7S5I7G3JQL) ; belantamab mafodotin (DB1041CXDG) ; Melphalan (Q41OR9510P)
    Sprache Englisch
    Erscheinungsdatum 2022-05-23
    Erscheinungsland United States
    Dokumenttyp Clinical Trial ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2540992-X
    ISSN 2152-2669 ; 2152-2650
    ISSN (online) 2152-2669
    ISSN 2152-2650
    DOI 10.1016/j.clml.2022.04.025
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: The clinical and cost impact of switching to fingolimod versus other first line injectable disease-modifying therapies in patients with relapsing multiple sclerosis.

    Freedman, M S / Duquette, P / Grand'Maison, F / Lee, L / Vorobeychik, G / Lara, N / Khurana, V / Nakhaipour, H R / Schecter, R / Haddad, P

    Current medical research and opinion

    2019  Band 35, Heft 5, Seite(n) 767–776

    Abstract: Background: There is limited evidence on the effectiveness and healthcare costs of switching to fingolimod versus another first line injectable therapy (FLIT) in patients with relapsing multiple sclerosis (RMS) who have already been treated with FLIT.!## ...

    Abstract Background: There is limited evidence on the effectiveness and healthcare costs of switching to fingolimod versus another first line injectable therapy (FLIT) in patients with relapsing multiple sclerosis (RMS) who have already been treated with FLIT.
    Objective: The objectives of the study were to assess the annualized relapse rate (ARR), socio-demographic and clinical characteristics, persistence and adherence rates, healthcare resource utilization and cost among patients with RMS who either switch to fingolimod or another FLIT in routine clinical practice.
    Methods: A multicenter, observational, retrospective chart review was conducted across eight clinics in Canada between 1 May 2011 and 30 June 2013. The data was collected from two cohorts: patients who switched to fingolimod and patients who switched to FLIT from a previous FLIT.
    Results and conclusions: A total of 124 patients were included in the study: 82 and 42 switched to fingolimod and FLIT, respectively. There were no significant differences in the patient characteristics at the date of switch except for number of previous disease-modifying therapies (DMTs) which was higher in the fingolimod cohort (fingolimod: 1.52; FLIT: 1.10, p < .001). The ARR during the first year of switching was numerically higher in the FLIT cohort compared to the fingolimod cohort (FLIT: 0.9 [95% CI 0.3-1.6]; fingolimod: 0.3 [95% CI 0.1-0.5]). The negative binomial model adjusted for the number of previous DMTs confirmed a statistically significant difference in ARR between the fingolimod and FLIT cohorts at 12 months of follow-up (p = .012). In the fingolimod cohort, 20.7% of patients experienced at least one relapse compared to 38.1% in the FLIT cohort. In both groups, a high proportion of patients (>90%) showed good treatment adherence (≥80% of prescribed doses).
    Mesh-Begriff(e) Adult ; Female ; Fingolimod Hydrochloride/therapeutic use ; Health Care Costs ; Humans ; Immunosuppressive Agents/therapeutic use ; Injections ; Male ; Middle Aged ; Multiple Sclerosis/drug therapy ; Recurrence ; Retrospective Studies
    Chemische Substanzen Immunosuppressive Agents ; Fingolimod Hydrochloride (G926EC510T)
    Sprache Englisch
    Erscheinungsdatum 2019-01-21
    Erscheinungsland England
    Dokumenttyp Comparative Study ; Journal Article ; Multicenter Study ; Observational Study ; Research Support, Non-U.S. Gov't
    ZDB-ID 80296-7
    ISSN 1473-4877 ; 0300-7995
    ISSN (online) 1473-4877
    ISSN 0300-7995
    DOI 10.1080/03007995.2019.1565818
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel: Supervised therapy in San Francisco.

    Schecter, G F

    Clinics in chest medicine

    1997  Band 18, Heft 1, Seite(n) 165–168

    Abstract: DOT is challenging, rewarding, and the best way we have of ensuring patients' adherence to treatment. Although labor intensive, the team approach with well-defined roles for the RN, DCI, and outreach worker is efficient and effective. Although the human ... ...

    Abstract DOT is challenging, rewarding, and the best way we have of ensuring patients' adherence to treatment. Although labor intensive, the team approach with well-defined roles for the RN, DCI, and outreach worker is efficient and effective. Although the human touch-a welcoming, tolerant, and caring approach to the patient-is the single key element, the use of incentives and enablers makes DOT more attractive to patients and the program more successful. An organized approach is necessary, yet flexibility must be maintained. Each patient has unique needs. Using other programs to help, such as school-based nurserun clinics or methadone sites, is more convenient for the patient and increases adherence. Helping patients access other services is important. And, finally, recognizing and appreciating the hard work and skills of the DOT staff contribute to maintaining high staff morale and esprit de corps.
    Mesh-Begriff(e) Communicable Disease Control ; Community Health Services ; Humans ; Medical Staff/psychology ; Morale ; Patient Care Team ; Patient Compliance ; San Francisco ; Tuberculosis/drug therapy ; Tuberculosis/prevention & control
    Sprache Englisch
    Erscheinungsdatum 1997-03
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Review
    ZDB-ID 447455-7
    ISSN 1557-8216 ; 0272-5231
    ISSN (online) 1557-8216
    ISSN 0272-5231
    DOI 10.1016/s0272-5231(05)70366-x
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: Evaluation of a change in cytomegalovirus prevention strategy following pediatric solid organ transplantation.

    Pangonis, Scott / Paulsen, Grant / Andersen, Heidi / Flores, Francisco / Miethke, Alexander / Peters, Anna / Kocoshis, Samuel / Lazear, Danielle / Garr, BreAnn / Schecter, Marc / Chin, Clifford / Hemmelgarn, Trina / Danziger-Isakov, Lara

    Transplant infectious disease : an official journal of the Transplantation Society

    2019  Band 22, Heft 2, Seite(n) e13232

    Abstract: Background: An optimal cytomegalovirus (CMV) prevention strategy following solid organ transplantation (SOT) remains uncertain. This study reports on the rates of CMV events following a change in a local prevention guideline involving increased ... ...

    Abstract Background: An optimal cytomegalovirus (CMV) prevention strategy following solid organ transplantation (SOT) remains uncertain. This study reports on the rates of CMV events following a change in a local prevention guideline involving increased surveillance, earlier transition to oral valganciclovir, and decreased CMV-immunoglobulin use.
    Methods: A retrospective cohort study utilizing historical controls evaluated the rates of CMV invasive disease pre- and post-intervention among pediatric heart, liver, and kidney recipients. Outcomes were recorded for the 4 years pre- and post-intervention, 9/2009-10/2017. Logistic regression was used to estimate the risk of a CMV event.
    Results: There was no difference in the rates of CMV invasive disease between the two study groups (P = 1). An increase in the detection of CMV events occurred (P = .04), predominantly asymptomatic CMV infection. This increase was independently associated with increased surveillance testing among high-risk heart and liver recipients, aOR 1.08 (1.06-1.12). Surprisingly, 28.9% of CMV events occurred during antiviral prophylaxis.
    Conclusions: Modification of the local CMV prevention guideline did not result in an increase in CMV invasive disease. CMV events occurred while on prophylaxis, highlighting a potential difference from adult solid organ transplant (SOT) and emphasizing the potential need for monitoring on prophylaxis in the pediatric population.
    Mesh-Begriff(e) Adolescent ; Antibodies, Viral/administration & dosage ; Antiviral Agents/administration & dosage ; Child ; Child, Preschool ; Cytomegalovirus ; Cytomegalovirus Infections/prevention & control ; Female ; Ganciclovir/administration & dosage ; Humans ; Immunoglobulins, Intravenous/administration & dosage ; Infant ; Logistic Models ; Male ; Organ Transplantation/adverse effects ; Primary Prevention/methods ; Retrospective Studies
    Chemische Substanzen Antibodies, Viral ; Antiviral Agents ; Immunoglobulins, Intravenous ; cytomegalovirus-specific hyperimmune globulin (129L90A25N) ; Ganciclovir (P9G3CKZ4P5)
    Sprache Englisch
    Erscheinungsdatum 2019-12-30
    Erscheinungsland Denmark
    Dokumenttyp Journal Article ; Observational Study
    ZDB-ID 1476094-0
    ISSN 1399-3062 ; 1398-2273
    ISSN (online) 1399-3062
    ISSN 1398-2273
    DOI 10.1111/tid.13232
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Artikel ; Online: Developing an adolescent and adult Fontan Management Programme.

    Lubert, Adam M / Alsaied, Tarek / Trout, Andrew T / Dillman, Jonathan R / Palermo, Joseph J / Eichelbrenner, Felicia / Kleier, Kelly / Lorts, Angela / Anwar, Nadeem / Schecter, Marc G / Tiao, Gregory M / Chin, Clifford / Feldman, David S / Jenkins, Meredith / Morales, David Ls / Opotowsky, Alexander R / Bucuvalas, John C / Veldtman, Gruschen R / Goldstein, Stuart L

    Cardiology in the young

    2021  Band 32, Heft 2, Seite(n) 230–235

    Abstract: Patients with single-ventricle CHD undergo a series of palliative surgeries that culminate in the Fontan procedure. While the Fontan procedure allows most patients to survive to adulthood, the Fontan circulation can eventually lead to multiple cardiac ... ...

    Abstract Patients with single-ventricle CHD undergo a series of palliative surgeries that culminate in the Fontan procedure. While the Fontan procedure allows most patients to survive to adulthood, the Fontan circulation can eventually lead to multiple cardiac complications and multi-organ dysfunction. Care for adolescents and adults with a Fontan circulation has begun to transition from a primarily cardiac-focused model to care models, which are designed to monitor multiple organ systems, and using clues from this screening, identify patients who are at risk for adverse outcomes. The complexity of care required for these patients led our centre to develop a multidisciplinary Fontan Management Programme with the primary goals of earlier detection and treatment of complications through the development of a cohesive network of diverse medical subspecialists with Fontan expertise.
    Mesh-Begriff(e) Adolescent ; Adult ; Fontan Procedure/adverse effects ; Heart Defects, Congenital/surgery ; Humans ; Palliative Care ; Univentricular Heart
    Sprache Englisch
    Erscheinungsdatum 2021-05-10
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 1078466-4
    ISSN 1467-1107 ; 1047-9511
    ISSN (online) 1467-1107
    ISSN 1047-9511
    DOI 10.1017/S104795112100175X
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel ; Online: Meta-analysis of ciltacabtagene autoleucel versus physician's choice therapy for the treatment of patients with relapsed or refractory multiple myeloma.

    Costa, Luciano J / Hari, Parameswaran / Berdeja, Jesus G / De Stefano, Valerio / Gay, Francesca / Hooper, Becky / Bartlett, Meaghan / Haltner, Anja / Rosta, Emily / Kumar, Shaji / Martin, Thomas / Mateos, Maria-Victoria / Moreau, Philippe / Usmani, Saad Z / Olyslager, Yunsi / Schecter, Jordan M / Roccia, Tito / Garrett, Ashraf / Lee, Sam /
    Nesheiwat, Tonia / Pacaud, Lida / Zhou, Changwei / Samjoo, Imtiaz A / Lin, Yi / Diels, Joris / Valluri, Satish / Weisel, Katja

    Current medical research and opinion

    2022  Band 38, Heft 10, Seite(n) 1759–1767

    Abstract: Objective: ...

    Abstract Objective:
    Mesh-Begriff(e) Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Humans ; Multiple Myeloma/drug therapy ; Physicians
    Sprache Englisch
    Erscheinungsdatum 2022-08-10
    Erscheinungsland England
    Dokumenttyp Journal Article ; Meta-Analysis
    ZDB-ID 80296-7
    ISSN 1473-4877 ; 0300-7995
    ISSN (online) 1473-4877
    ISSN 0300-7995
    DOI 10.1080/03007995.2022.2100651
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel ; Online: Linezolid in the treatment of multidrug-resistant tuberculosis.

    Schecter, G F / Scott, C / True, L / Raftery, A / Flood, J / Mase, S

    Clinical infectious diseases : an official publication of the Infectious Diseases Society of America

    2010  Band 50, Heft 1, Seite(n) 49–55

    Abstract: Background: Linezolid is a new antibiotic with activity against Mycobacterium tuberculosis in vitro and in animal studies. Several small case series suggest that linezolid is poorly tolerated because of the side effects of anemia/thrombocytopenia and ... ...

    Abstract Background: Linezolid is a new antibiotic with activity against Mycobacterium tuberculosis in vitro and in animal studies. Several small case series suggest that linezolid is poorly tolerated because of the side effects of anemia/thrombocytopenia and peripheral neuropathy. To characterize our clinical experience with linezolid, the California Department of Public Health Tuberculosis Control Branch's Multidrug-Resistant Tuberculosis (MDR-TB) Service reviewed cases in which the MDR-TB treatment regimens included linezolid therapy.
    Methods: Record review was performed for 30 patients treated with linezolid as part of an MDR-TB regimen. Data were collected on clinical and microbiological characteristics, linezolid tolerability, and treatment outcomes. The dosage of linezolid was 600 mg daily. Vitamin B6 at a dosage of 50-100 mg daily was used to mitigate hematologic toxicity.
    Results: During 2003-2007, 30 patients received linezolid for the treatment of MDR-TB. Patients had isolates resistant to a median of 5 drugs (range, 2-13 drugs). Of the 30 cases, 29 (97%) were pulmonary; of these 29, 21 (72%) had positive results of acid-fast bacilli smear, and 16 (55%) were cavitary. Culture conversion occurred in all pulmonary cases at a median of 7 weeks. At data censure (31 December 2008), 22 (73%) of 30 patients had successfully completed treatment. Five continued to receive treatment. There were no deaths. Three patients had a poor outcome, including 2 defaults and 1 treatment failure. Side effects occurred in 9 patients, including peripheral and optic neuropathy, anemia/thrombocytopenia, rash, and diarrhea. However, only 3 patients stopped linezolid treatment because of side effects.
    Conclusions: Linezolid was well tolerated, had low rates of discontinuation, and may have efficacy in the treatment of MDR-TB.
    Mesh-Begriff(e) Acetamides/adverse effects ; Acetamides/therapeutic use ; Adolescent ; Adult ; Aged ; Antitubercular Agents/adverse effects ; Antitubercular Agents/therapeutic use ; Female ; Humans ; Linezolid ; Male ; Middle Aged ; Mycobacterium tuberculosis/drug effects ; Oxazolidinones/adverse effects ; Oxazolidinones/therapeutic use ; Retrospective Studies ; Treatment Outcome ; Tuberculosis, Multidrug-Resistant/drug therapy ; Tuberculosis, Multidrug-Resistant/microbiology
    Chemische Substanzen Acetamides ; Antitubercular Agents ; Oxazolidinones ; Linezolid (ISQ9I6J12J)
    Sprache Englisch
    Erscheinungsdatum 2010-01-01
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 1099781-7
    ISSN 1537-6591 ; 1058-4838
    ISSN (online) 1537-6591
    ISSN 1058-4838
    DOI 10.1086/648675
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel ; Online: Enduring efficacy and tolerability of daratumumab in combination with lenalidomide and dexamethasone in patients with relapsed or relapsed/refractory multiple myeloma (GEN503): final results of an open-label, phase 1/2 study.

    Plesner, Torben / Arkenau, Hendrik-Tobias / Gay, Francesca / Minnema, Monique C / Boccadoro, Mario / Moreau, Philippe / Cavenagh, Jamie / Perrot, Aurore / Laubach, Jacob P / Krejcik, Jakub / Ahmadi, Tahamtan / de Boer, Carla / Chen, Diana / Chiu, Christopher / Schecter, Jordan M / Richardson, Paul G

    British journal of haematology

    2019  Band 186, Heft 3, Seite(n) e35–e39

    Mesh-Begriff(e) Angiogenesis Inhibitors/administration & dosage ; Angiogenesis Inhibitors/adverse effects ; Antibodies, Monoclonal/administration & dosage ; Antibodies, Monoclonal/adverse effects ; Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Dexamethasone/administration & dosage ; Dexamethasone/adverse effects ; Female ; Humans ; Lenalidomide/administration & dosage ; Lenalidomide/adverse effects ; Male ; Multiple Myeloma/drug therapy ; Neoplasm Recurrence, Local ; Progression-Free Survival
    Chemische Substanzen Angiogenesis Inhibitors ; Antibodies, Monoclonal ; daratumumab (4Z63YK6E0E) ; Dexamethasone (7S5I7G3JQL) ; Lenalidomide (F0P408N6V4)
    Sprache Englisch
    Erscheinungsdatum 2019-03-31
    Erscheinungsland England
    Dokumenttyp Clinical Trial, Phase I ; Clinical Trial, Phase II ; Letter ; Research Support, Non-U.S. Gov't
    ZDB-ID 80077-6
    ISSN 1365-2141 ; 0007-1048
    ISSN (online) 1365-2141
    ISSN 0007-1048
    DOI 10.1111/bjh.15879
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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