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  1. Article ; Online: Retrospective Analysis of the Efficacy and Tolerability of Gemcitabine-Based Chemotherapy in Relapsed/Refractory Lymphoma Patients Not Eligible for Stem Cell Transplant.

    Chiu, May / Hague, Samuel / Elinder-Camburn, Anna / Merriman, Eileen / Chan, Henry

    Clinical lymphoma, myeloma & leukemia

    2022  Volume 22, Issue 11, Page(s) 835–840

    Abstract: Introduction: Gemcitabine-based regimens are effective salvage therapy for RR lymphoma patients eligible for ASCT, but there is limited data in transplant-ineligible (TIE) patients. Here, we present a retrospective analysis on the outcome of TIE adult ... ...

    Abstract Introduction: Gemcitabine-based regimens are effective salvage therapy for RR lymphoma patients eligible for ASCT, but there is limited data in transplant-ineligible (TIE) patients. Here, we present a retrospective analysis on the outcome of TIE adult patients with RR lymphoma treated with gemcitabine, cisplatin or carboplatin and dexamethasone (GDP/GDCarboP) +/- rituximab regimen in our center.
    Patients: We identified 33 patients: 54.5% diffuse large Bcell lymphoma (DLBCL), 6.1% double/triple hit lymphoma, 15% follicular lymphoma, 18% T-cell lymphoma, and 6% classical Hodgkin lymphoma. Majority of the patients had advanced-stage disease and raised LDH at relapse. The cohort's median age was 71 years. The median number of prior lines of treatment was 2, and 60.6% were refractory to their last line of treatment.
    Results: The overall response rate was 33% (complete response 15%) for the entire cohort and 62.5% for DLBCL patients not refractory to prior line of treatment. At median follow-up of 25 months, the median duration of response and overall survival in the responders were not reached. Conversely, the median overall survival for the non-responders was dismal at 5 months. Fifty-five percent required treatment alteration (dose attenuation or omission and treatment delay for >1 week) due to adverse events, 73% needed transfusion, and 70% had at least 1 hospital admission during treatment.
    Conclusion: Our real-world data showed that GDP/GDCarboP provides meaningful efficacy and durability, especially among the responders. However, dose modification and inpatient support are frequently needed, indicating the need for good supportive care and close follow-up in this frailer population.
    MeSH term(s) Adult ; Humans ; Aged ; Cisplatin/therapeutic use ; Carboplatin/therapeutic use ; Rituximab/therapeutic use ; Retrospective Studies ; Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Neoplasm Recurrence, Local/drug therapy ; Lymphoma, Non-Hodgkin/drug therapy ; Lymphoma, B-Cell/drug therapy ; Stem Cell Transplantation ; Lymphoma, Follicular/drug therapy ; Dexamethasone/adverse effects
    Chemical Substances gemcitabine (B76N6SBZ8R) ; Cisplatin (Q20Q21Q62J) ; Carboplatin (BG3F62OND5) ; Rituximab (4F4X42SYQ6) ; Dexamethasone (7S5I7G3JQL)
    Language English
    Publishing date 2022-06-29
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2540992-X
    ISSN 2152-2669 ; 2152-2650
    ISSN (online) 2152-2669
    ISSN 2152-2650
    DOI 10.1016/j.clml.2022.06.010
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Real-world experience of nintedanib for progressive fibrosing interstitial lung disease in the UK.

    Dixon, Giles / Hague, Samuel / Mulholland, Sarah / Adamali, Huzaifa / Khin, Aye Myat Noe / Thould, Hannah / Connon, Roisin / Minnis, Paul / Murtagh, Eoin / Khan, Fasihul / Toor, Sameen / Lawrence, Alexandra / Naqvi, Marium / West, Alex / Coker, Robina K / Ward, Katie / Yazbeck, Leda / Hart, Simon / Garfoot, Theresa /
    Newman, Kate / Rivera-Ortega, Pilar / Stranks, Lachlan / Beirne, Paul / Bradley, Jessica / Rowan, Catherine / Agnew, Sarah / Ahmad, Mahin / Spencer, Lisa G / Aigbirior, Joshua / Fahim, Ahmed / Wilson, Andrew M / Butcher, Elizabeth / Chong, Sy Giin / Saini, Gauri / Zulfikar, Sabrina / Chua, Felix / George, Peter M / Kokosi, Maria / Kouranos, Vasileios / Molyneaux, Philip / Renzoni, Elisabetta / Vitri, Benedetta / Wells, Athol U / Nicol, Lisa M / Bianchi, Stephen / Kular, Raman / Liu, HuaJian / John, Alexander / Barth, Sarah / Wickremasinghe, Melissa / Forrest, Ian A / Grimes, Ian / Simpson, A John / Fletcher, Sophie V / Jones, Mark G / Kinsella, Emma / Naftel, Jennifer / Wood, Nicola / Chalmers, Jodie / Crawshaw, Anjali / Crowley, Louise E / Dosanjh, Davinder / Huntley, Christopher C / Walters, Gareth I / Gatheral, Timothy / Plum, Catherine / Bikmalla, Shiva / Muthusami, Raja / Stone, Helen / Rodrigues, Jonathan C L / Tsaneva-Atanasova, Krasimira / Scotton, Chris J / Gibbons, Michael A / Barratt, Shaney L

    ERJ open research

    2024  Volume 10, Issue 1

    Abstract: Background: Nintedanib slows progression of lung function decline in patients with progressive fibrosing (PF) interstitial lung disease (ILD) and was recommended for this indication within the United Kingdom (UK) National Health Service in Scotland in ... ...

    Abstract Background: Nintedanib slows progression of lung function decline in patients with progressive fibrosing (PF) interstitial lung disease (ILD) and was recommended for this indication within the United Kingdom (UK) National Health Service in Scotland in June 2021 and in England, Wales and Northern Ireland in November 2021. To date, there has been no national evaluation of the use of nintedanib for PF-ILD in a real-world setting.
    Methods: 26 UK centres were invited to take part in a national service evaluation between 17 November 2021 and 30 September 2022. Summary data regarding underlying diagnosis, pulmonary function tests, diagnostic criteria, radiological appearance, concurrent immunosuppressive therapy and drug tolerability were collected
    Results: 24 UK prescribing centres responded to the service evaluation invitation. Between 17 November 2021 and 30 September 2022, 1120 patients received a multidisciplinary team recommendation to commence nintedanib for PF-ILD. The most common underlying diagnoses were hypersensitivity pneumonitis (298 out of 1120, 26.6%), connective tissue disease associated ILD (197 out of 1120, 17.6%), rheumatoid arthritis associated ILD (180 out of 1120, 16.0%), idiopathic nonspecific interstitial pneumonia (125 out of 1120, 11.1%) and unclassifiable ILD (100 out of 1120, 8.9%). Of these, 54.4% (609 out of 1120) were receiving concomitant corticosteroids, 355 (31.7%) out of 1120 were receiving concomitant mycophenolate mofetil and 340 (30.3%) out of 1120 were receiving another immunosuppressive/modulatory therapy. Radiological progression of ILD combined with worsening respiratory symptoms was the most common reason for the diagnosis of PF-ILD.
    Conclusion: We have demonstrated the use of nintedanib for the treatment of PF-ILD across a broad range of underlying conditions. Nintedanib is frequently co-prescribed alongside immunosuppressive and immunomodulatory therapy. The use of nintedanib for the treatment of PF-ILD has demonstrated acceptable tolerability in a real-world setting.
    Language English
    Publishing date 2024-01-15
    Publishing country England
    Document type Journal Article
    ZDB-ID 2827830-6
    ISSN 2312-0541
    ISSN 2312-0541
    DOI 10.1183/23120541.00529-2023
    Database MEDical Literature Analysis and Retrieval System OnLINE

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