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  1. Article ; Online: Intention-to-treat outcomes utilising a stringent event definition in children and young people treated with tisagenlecleucel for r/r ALL through a national access scheme.

    Oporto Espuelas, Macarena / Burridge, Saskia / Kirkwood, Amy A / Bonney, Denise / Watts, Kelly / Shenton, Geoff / Jalowiec, Katarzyna A / O'Reilly, Maeve A / Roddie, Claire / Castleton, Anna / Clesham, Katherine / Nicholson, Emma / Alajangi, Rajesh / Prabhu, Shilpa / George, Lindsay / Uttenthal, Ben / Gabelli, Maria / Neill, Lorna / Besley, Caroline /
    Chaganti, Sridhar / Wynn, Robert F / Bartram, Jack / Chiesa, Robert / Lucchini, Giovanna / Pavasovic, Vesna / Rao, Anupama / Rao, Kanchan / Silva, Juliana / Samarasinghe, Sujith / Vora, Ajay / Clark, Peter / Cummins, Michelle / Marks, David I / Amrolia, Persis / Hough, Rachael / Ghorashian, Sara

    Blood cancer journal

    2024  Volume 14, Issue 1, Page(s) 66

    Abstract: CAR T-cell therapy has transformed relapsed/refractory (r/r) B-cell precursor ...

    Abstract CAR T-cell therapy has transformed relapsed/refractory (r/r) B-cell precursor acute lymphoblastic leukaemia (B-ALL) management and outcomes, but following CAR T infusion, interventions are often needed. In a UK multicentre study, we retrospectively evaluated tisagenlecleucel outcomes in all eligible patients, analysing overall survival (OS) and event-free survival (EFS) with standard and stringent definitions, the latter including measurable residual disease (MRD) emergence and further anti-leukaemic therapy. Both intention-to-treat and infused cohorts were considered. We collected data on feasibility of delivery, manufacture, toxicity, cause of therapy failure and followed patients until death from any cause. Of 142 eligible patients, 125 received tisagenlecleucel, 115/125 (92%) achieved complete remission (CR/CRi). Severe cytokine release syndrome and neurotoxicity occurred in 16/123 (13%) and 10/123 (8.1%), procedural mortality was 3/126 (2.4%). The 2-year intent to treat OS and EFS were 65.2% (95%CI 57.2-74.2%) and 46.5% (95%CI 37.6-57.6%), 2-year intent to treat stringent EFS was 35.6% (95%CI 28.1-44.9%). Median OS was not reached. Sixty-two responding patients experienced CAR T failure by the stringent event definition. Post failure, 1-year OS and standard EFS were 61.2% (95%CI 49.3-75.8) and 55.3% (95%CI 43.6-70.2). Investigation of CAR T-cell therapy for B-ALL delivered on a country-wide basis, including following patients beyond therapy failure, provides clinicians with robust outcome measures. Previously, outcomes post CAR T-cell therapy failure were under-reported. Our data show that patients can be successfully salvaged in this context with good short-term survival.
    MeSH term(s) Child ; Humans ; Adolescent ; Receptors, Chimeric Antigen ; Intention to Treat Analysis ; Retrospective Studies ; Receptors, Antigen, T-Cell ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/therapy ; Immunotherapy, Adoptive/adverse effects ; Antigens, CD19
    Chemical Substances tisagenlecleucel (Q6C9WHR03O) ; Receptors, Chimeric Antigen ; Receptors, Antigen, T-Cell ; Antigens, CD19
    Language English
    Publishing date 2024-04-15
    Publishing country United States
    Document type Multicenter Study ; Journal Article
    ZDB-ID 2600560-8
    ISSN 2044-5385 ; 2044-5385
    ISSN (online) 2044-5385
    ISSN 2044-5385
    DOI 10.1038/s41408-024-01038-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Radial access for peripheral vascular intervention: the S.M.A.R.T. RADIANZ Vascular Stent System.

    Subramanian, Vinayak / Sauguet, Antoine / Werner, Martin / Sbarzaglia, Paolo / Hausegger, Klaus A / Goyault, Gilles / Guerra, Mercedes / Deloose, Koen / Kahlberg, Andrea / Balestriero, Giovanni / Brodmann, Marianne / Binkert, Christoph / Goueffic, Yann / Groezinger, Gerd / Schwindt, Arne / Schlager, Oliver / Bertoglio, Luca / Adams, George / Sultana, Nusrath /
    Coscas, Raphaël

    Expert review of medical devices

    2023  Volume 20, Issue 9, Page(s) 715–720

    Abstract: ... a transradial approach (TRA). The S.M.A.R.T. RADIANZ Vascular Stent System is among the RADIANZ suite ... of peripheral vascular intervention (PVI) using TRA (2) Detailed description of the S.M.A.R.T. RADIANZ Vascular ...

    Abstract Introduction: Radial access is the standard of care for nearly all cardiac catheterization procedures. It improves patient satisfaction, reduces the length of stay, and is associated with fewer complications. However, few devices and tools are available for the treatment of peripheral arterial disease via a transradial approach (TRA). The S.M.A.R.T. RADIANZ Vascular Stent System is among the RADIANZ suite of products, which is aimed at expanding the portfolio of devices to treat peripheral arterial disease.
    Areas covered: In this Expert review, the following areas will be covered: (1) Current Landscape of peripheral vascular intervention (PVI) using TRA (2) Detailed description of the S.M.A.R.T. RADIANZ Vascular Stent System. (3) Ongoing clinical trials to evaluate safety of this approach. (4) Future directions and current regulatory status.
    Expert opinion: TRA for PVI is a promising approach. It holds the possibility of substantially improving the care of patients with peripheral arterial disease (PAD). Numerous challenges must be overcome to realize the full potential of a radial-to-peripheral (RTP) approach. The length of devices and the small sheath size are the main constraints of this approach. The results of the ongoing RADIANCY trial will demonstrate the safety, in selected patients, of the RADIANZ suite of products.
    MeSH term(s) Humans ; Treatment Outcome ; Radial Artery/surgery ; Endovascular Procedures ; Catheterization, Peripheral/methods ; Peripheral Arterial Disease/surgery ; Stents
    Language English
    Publishing date 2023-07-24
    Publishing country England
    Document type Journal Article
    ZDB-ID 2250857-0
    ISSN 1745-2422 ; 1743-4440
    ISSN (online) 1745-2422
    ISSN 1743-4440
    DOI 10.1080/17434440.2023.2240227
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: C16orf72/HAPSTR1/TAPR1 functions with BRCA1/Senataxin to modulate replication-associated R-loops and confer resistance to PARP disruption.

    Sharma, Abhishek Bharadwaj / Ramlee, Muhammad Khairul / Kosmin, Joel / Higgs, Martin R / Wolstenholme, Amy / Ronson, George E / Jones, Dylan / Ebner, Daniel / Shamkhi, Noor / Sims, David / Wijnhoven, Paul W G / Forment, Josep V / Gibbs-Seymour, Ian / Lakin, Nicholas D

    Nature communications

    2023  Volume 14, Issue 1, Page(s) 5003

    Abstract: ... associated R-loops. C16orf72 is critical to facilitate replication fork restart, suppress DNA damage and ... this identifies a C16orf72/Senataxin/BRCA1-dependent pathway to suppress replication-associated R-loop ...

    Abstract While the toxicity of PARP inhibitors to cells with defects in homologous recombination (HR) is well established, other synthetic lethal interactions with PARP1/PARP2 disruption are poorly defined. To inform on these mechanisms we conducted a genome-wide screen for genes that are synthetic lethal with PARP1/2 gene disruption and identified C16orf72/HAPSTR1/TAPR1 as a novel modulator of replication-associated R-loops. C16orf72 is critical to facilitate replication fork restart, suppress DNA damage and maintain genome stability in response to replication stress. Importantly, C16orf72 and PARP1/2 function in parallel pathways to suppress DNA:RNA hybrids that accumulate at stalled replication forks. Mechanistically, this is achieved through an interaction of C16orf72 with BRCA1 and the RNA/DNA helicase Senataxin to facilitate their recruitment to RNA:DNA hybrids and confer resistance to PARP inhibitors. Together, this identifies a C16orf72/Senataxin/BRCA1-dependent pathway to suppress replication-associated R-loop accumulation, maintain genome stability and confer resistance to PARP inhibitors.
    MeSH term(s) DNA Damage ; DNA Helicases/genetics ; Poly(ADP-ribose) Polymerase Inhibitors/pharmacology ; R-Loop Structures/genetics ; RNA ; BRCA1 Protein/genetics ; Intracellular Signaling Peptides and Proteins/genetics
    Chemical Substances DNA Helicases (EC 3.6.4.-) ; Poly(ADP-ribose) Polymerase Inhibitors ; RNA (63231-63-0) ; BRCA1 Protein ; Intracellular Signaling Peptides and Proteins
    Language English
    Publishing date 2023-08-17
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-023-40779-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Revisiting the 4 R’s

    Shifra Z. Goldenberg / Jenna M. Parker / Stephen M. Chege / Alison L. Greggor / Matt Hunt / Nadine Lamberski / Kellie A. Leigh / Hendrik H. Nollens / Kirstie A. Ruppert / Chris Thouless / George Wittemyer / Megan A. Owen

    Frontiers in Conservation Science, Vol

    Improving post-release outcomes for rescued mammalian wildlife by fostering behavioral competence during rehabilitation

    2022  Volume 3

    Abstract: ... of what has been termed “the 4th R”, research. Similar to conservation breeding and headstarting, rescue and ...

    Abstract Rescue, rehabilitation, and release (‘rescue-rehab-release’) of wildlife is an increasingly widespread practice across ecosystems, largely driven by habitat loss, wildlife exploitation and a changing climate. Despite this, its conservation value has not been realized, in part due to the scarcity of what has been termed “the 4th R”, research. Similar to conservation breeding and headstarting, rescue and rehabilitation entails close association of humans and the wildlife in their care over impressionable and extended periods. However, unlike these interventions, rescue and rehabilitation require an initial, and sometimes sustained, focus on crisis management and veterinary needs which can impede the development of natural behaviors and promote habituation to humans, both of which can compromise post-release survival and recruitment. In this perspective, we discuss the pathways toward, and implications of, behavioral incompetence and highlight opportunities for testable interventions to curtail negative outcomes post-release, without compromising the health or welfare of rescued individuals. We propose that practitioners ‘switch gears’ from triage to fostering behavioral competence as early in the rehabilitation process as is possible, and that research be implemented in order to develop an evidence-base for best practices that can be shared amongst practitioners. We focus on four mammalian species to illustrate specific contexts and considerations for fostering behavioral competence by building on research in the conservation translocation literature. Finally, we discuss a way forward that calls for greater cross-pollination among translocation scenarios involving extended time under human care during developmentally sensitive periods.
    Keywords wildlife rescue ; rehabilitation ; behavioral competence ; post-release monitoring ; behavioral training ; reintroduction biology ; General. Including nature conservation ; geographical distribution ; QH1-199.5
    Subject code 333
    Language English
    Publishing date 2022-08-01T00:00:00Z
    Publisher Frontiers Media S.A.
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article ; Online: Author Correction: C16orf72/HAPSTR1/TAPR1 functions with BRCA1/Senataxin to modulate replication-associated R-loops and confer resistance to PARP disruption.

    Sharma, Abhishek Bharadwaj / Ramlee, Muhammad Khairul / Kosmin, Joel / Higgs, Martin R / Wolstenholme, Amy / Ronson, George E / Jones, Dylan / Ebner, Daniel / Shamkhi, Noor / Sims, David / Wijnhoven, Paul W G / Forment, Josep V / Gibbs-Seymour, Ian / Lakin, Nicholas D

    Nature communications

    2023  Volume 14, Issue 1, Page(s) 7784

    Language English
    Publishing date 2023-11-27
    Publishing country England
    Document type Published Erratum
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-023-43353-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Joseph R. Bertino, Scientist and Clinical Oncologist.

    Chabner, Bruce A / Canellos, George P

    Journal of clinical oncology : official journal of the American Society of Clinical Oncology

    2022  Volume 40, Issue 14, Page(s) 1511–1513

    MeSH term(s) Health Personnel ; Humans ; Oncologists ; Physicians
    Language English
    Publishing date 2022-04-04
    Publishing country United States
    Document type Journal Article
    ZDB-ID 604914-x
    ISSN 1527-7755 ; 0732-183X
    ISSN (online) 1527-7755
    ISSN 0732-183X
    DOI 10.1200/JCO.21.02693
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: The effect of COVID rehabilitation for ongoing symptoms Post HOSPitalisation with COVID-19 (PHOSP-R): protocol for a randomised parallel group controlled trial on behalf of the PHOSP consortium.

    Daynes, Enya / Baldwin, Molly / Greening, Neil J / Yates, Thomas / Bishop, Nicolette C / Mills, George / Roberts, Matthew / Hamrouni, Malik / Plekhanova, Tatiana / Vogiatzis, Ioannis / Echevarria, Carlos / Nathu, Rashmita / McAuley, Hamish J C / Latimer, Lorna / Glennie, Jennifer / Chambers, Francesca / Penfold, Ruth / Hume, Emily / Megaritis, Dimitrios /
    Alexiou, Charikleia / Potthoff, Sebastian / Hogg, Mitchell James / Haighton, Catherine / Nichol, Bethany / Leavy, Olivia C / Richardson, Matthew / Elneima, Omer / Singapuri, Amisha / Sereno, Marco / Saunders, Ruth M / Harris, Victoria C / Nolan, Claire M / Bolton, Charlotte / Houchen-Wolloff, Linzy / Harrison, Ewen M / Lone, Nazir / Quint, Jennifer / Chalmers, James D / Ho, Ling-Pei / Horsley, Alex / Marks, Michael / Poinasamy, Krisnah / Ramen, Betty / Wain, Louise V / Brightling, Christopher / Man, William D-C / Evans, Rachael / Singh, Sally J

    Trials

    2023  Volume 24, Issue 1, Page(s) 61

    Abstract: Introduction: Many adults hospitalised with COVID-19 have persistent symptoms such as fatigue, breathlessness and brain fog that limit day-to-day activities. These symptoms can last over 2 years. Whilst there is limited controlled studies on ... ...

    Abstract Introduction: Many adults hospitalised with COVID-19 have persistent symptoms such as fatigue, breathlessness and brain fog that limit day-to-day activities. These symptoms can last over 2 years. Whilst there is limited controlled studies on interventions that can support those with ongoing symptoms, there has been some promise in rehabilitation interventions in improving function and symptoms either using face-to-face or digital methods, but evidence remains limited and these studies often lack a control group.
    Methods and analysis: This is a nested single-blind, parallel group, randomised control trial with embedded qualitative evaluation comparing rehabilitation (face-to-face or digital) to usual care and conducted within the PHOSP-COVID study. The aim of this study is to determine the effectiveness of rehabilitation interventions on exercise capacity, quality of life and symptoms such as breathlessness and fatigue. The primary outcome is the Incremental Shuttle Walking Test following the eight week intervention phase. Secondary outcomes include measures of function, strength and subjective assessment of symptoms. Blood inflammatory markers and muscle biopsies are an exploratory outcome. The interventions last eight weeks and combine symptom-titrated exercise therapy, symptom management and education delivered either in a face-to-face setting or through a digital platform ( www.yourcovidrecovery.nhs.uk ). The proposed sample size is 159 participants, and data will be intention-to-treat analyses comparing rehabilitation (face-to-face or digital) to usual care.
    Ethics and dissemination: Ethical approval was gained as part of the PHOSP-COVID study by Yorkshire and the Humber Leeds West Research NHS Ethics Committee, and the study was prospectively registered on the ISRCTN trial registry (ISRCTN13293865). Results will be disseminated to stakeholders, including patients and members of the public, and published in appropriate journals. Strengths and limitations of this study • This protocol utilises two interventions to support those with ongoing symptoms of COVID-19 • This is a two-centre parallel-group randomised controlled trial • The protocol has been supported by patient and public involvement groups who identified treatments of symptoms and activity limitation as a top priority.
    MeSH term(s) Adult ; Humans ; COVID-19 ; Quality of Life ; Single-Blind Method ; Dyspnea ; Fatigue/diagnosis ; Fatigue/etiology ; Randomized Controlled Trials as Topic
    Language English
    Publishing date 2023-01-26
    Publishing country England
    Document type Clinical Trial Protocol ; Journal Article
    ZDB-ID 2040523-6
    ISSN 1745-6215 ; 1468-6694 ; 1745-6215
    ISSN (online) 1745-6215
    ISSN 1468-6694 ; 1745-6215
    DOI 10.1186/s13063-023-07093-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: OMERACT 2020: A virtual (R)evolution.

    Grosskleg, Shawna / Beaton, Dorcas / Conaghan, Phil / Hofstetter, Catherine / Maxwell, Lara / Shea, Bev / Tugwell, Peter / Bingham, Clifton O / Antonietta D'Agostino, Maria / March, Lyn / Singh, Jasvinder A / Strand, Vibeke / Wells, George / Simon, Lee

    Seminars in arthritis and rheumatism

    2021  Volume 51, Issue 3, Page(s) 588–592

    MeSH term(s) Humans ; Rheumatic Diseases ; Rheumatology
    Language English
    Publishing date 2021-04-20
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 120247-9
    ISSN 1532-866X ; 0049-0172
    ISSN (online) 1532-866X
    ISSN 0049-0172
    DOI 10.1016/j.semarthrit.2021.04.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Protocol for inferring epithelial-to-mesenchymal transition trajectories from single-cell RNA sequencing data using R.

    Najafi, Annice / Jolly, Mohit Kumar / George, Jason T

    STAR protocols

    2024  Volume 5, Issue 1, Page(s) 102819

    Abstract: ... process and possesses prognostic value within the cancer context. Here, we present COMET, an R package ...

    Abstract The epithelial-to-mesenchymal transition (EMT) provides crucial insights into the metastatic process and possesses prognostic value within the cancer context. Here, we present COMET, an R package for inferring EMT trajectories and inter-state transition rates from single-cell RNA sequencing data. We describe steps for finding the optimal number of EMT genes for a specific context, estimating EMT-related trajectories, optimal fitting of continuous-time Markov chain to inferred trajectories, and estimating inter-state transition rates.
    MeSH term(s) Humans ; Epithelial-Mesenchymal Transition/genetics ; Neoplasms/pathology ; Sequence Analysis, RNA
    Language English
    Publishing date 2024-01-05
    Publishing country United States
    Document type Journal Article
    ISSN 2666-1667
    ISSN (online) 2666-1667
    DOI 10.1016/j.xpro.2023.102819
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: PD-L1 expression predicts efficacy in the phase II SPiReL trial with MVP-S, pembrolizumab, and low-dose CPA in R/R DLBCL.

    Amitai, Irina / Roos, Kim / Rashedi, Iran / Jiang, Yidi / Mangoff, Kathryn / Klein, Gail / Forward, Nicholas / Stewart, Douglas / Laneuville, Pierre / Bence-Bruckler, Isabelle / Mangel, Joy / Tomlinson, George / Berinstein, Neil L

    European journal of haematology

    2023  Volume 111, Issue 2, Page(s) 191–200

    Abstract: Background: Patients with relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL) have ... limited treatment options.: Methods: R/R DLBCL patients, who were mostly ineligible for ASCT due to age ...

    Abstract Background: Patients with relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL) have limited treatment options.
    Methods: R/R DLBCL patients, who were mostly ineligible for ASCT due to age or comorbidities, were treated with maveropepimut-S (MVP-S, previously DPX-Survivac) a survivin directed T cell educating therapy, pembrolizumab, and intermittent low-dose cyclophosphamide.
    Findings: We identified, using univariate analysis, a subset of patients with enhanced ORR, PFS and DOR. Patients with baseline CD20+/PD-L1 expression had an ORR of 46% (6/13) and the disease control rate was 10/13 (77%). The PFS and OS of the positive CD20+/PD-L1 patients were 7.1 months and 17.4 months, whereas in the intent-to-treat (ITT) population of 25 enrolled patients, the ORR was 28% (7/25), median PFS and OS were 4.2 months and 10.1 months respectively. A total of 6/7 clinical responders occurred in CD20+/PD-L1 patients. The regimen was well-tolerated, requiring only minor dose modifications and one discontinuation. Grade 1 or 2 injection site reactions occurred in 14/25, (56%). Statistically significant associations were also seen between PFS and; injection site reactions; and ELISpot response to survivin peptides, both identifying the mechanistic importance of specific immune responses to survivin.
    Interpretation: This immunotherapy combination was found to be active and safe in this clinically challenging patient population.
    MeSH term(s) Humans ; Survivin/therapeutic use ; B7-H1 Antigen/metabolism ; Injection Site Reaction ; Lymphoma, Non-Hodgkin/drug therapy ; Lymphoma, Large B-Cell, Diffuse/diagnosis ; Lymphoma, Large B-Cell, Diffuse/drug therapy ; Lymphoma, Large B-Cell, Diffuse/pathology
    Chemical Substances pembrolizumab (DPT0O3T46P) ; Survivin ; B7-H1 Antigen
    Language English
    Publishing date 2023-05-08
    Publishing country England
    Document type Clinical Trial, Phase II ; Journal Article
    ZDB-ID 392482-8
    ISSN 1600-0609 ; 0902-4441
    ISSN (online) 1600-0609
    ISSN 0902-4441
    DOI 10.1111/ejh.13982
    Database MEDical Literature Analysis and Retrieval System OnLINE

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