- |||||||||| Rituxan (rituximab) / Biogen, Zenyaku Holdings, Roche
Triple autologous stem cell transplantation for primary CNS lymphoma (Y2) - Sep 30, 2023 - Abstract #DGHO2023DGHO_1492; Six cycles of E-KRd treatment induce substantial bone remineralization in osteolytic lesions in patients with newly diagnosed MM. Salvage therapy with the R-DeVIC regimen (rituximab 375 mg/m
- |||||||||| Blincyto (blinatumomab) / Astellas, Amgen, Besponsa (inotuzumab ozogamicin) / Pfizer, UCB
Complete remission after sequential Inotuzumab, Blinatumomab and chemotherapy with concurrent donor lymphocyte infusions in relapsed pre-B-ALL after allogeneic stem cell transplantation. (Hall F) - Sep 30, 2023 - Abstract #DGHO2023DGHO_1098; A cytoreductive therapy with Doxorubicin 45mg/m 2 , Vincristine 2mg and a second DLI-application (1.5x10 7 CD3+cells/kg) followed in month four...Temporary, a hepatic GvHD grade I was observed, which was treated with budesonide orally...In conclusion, our case demonstrates that co-administration of DLI, InO, Blina and chemotherapy is feasible without severe GvHD. Given these promising results, this
- |||||||||| Akynzeo oral (netupitant/palonesteron FDC) / Helsinn, Roche, Otsuka, Mundipharma, Immedica
Assessing the Benefit of NEPA (Fixed Combination of Netupitant/Palonosetron) for Preventing Chemotherapy-induced Nausea and Vomiting (CINV) in Patients at Increased Emetic Risk Receiving Moderately Emetogenic Chemotherapy (Hall 4) - Sep 30, 2023 - Abstract #DGHO2023DGHO_1066; P4 Background: In patients receiving moderately emetogenic chemotherapy (MEC), antiemetic guidelines lack evidence to recommend an NK 1 receptor antagonist (RA) for all patients; therefore, they endorse a 5-HT 3 RA + dexamethasone (DEX)...A generalized linear model will analyze CR over 3 cycles of MEC with logit link function, binomial distribution, and with study treatment, carboplatin use, and the country as factors...Enrollment is open; as of April 26, 2023, 287 patients have been randomized. In Germany, 96 of 100 patients have been enrolled by five study centres.
- |||||||||| Carvykti (ciltacabtagene autoleucel) / J&J
First phase 3 results from CARTITUDE-4: Cilta-cel versus standard of care (PVd or DPd) in lenalidomide-refractory multiple myeloma (Hall A) - Sep 30, 2023 - Abstract #DGHO2023DGHO_819; P3 Introduction: CARTITUDE-4 is a global, phase 3, randomized, controlled trial (NCT04181827) of cilta-cel, a dual-binding, BCMA-targeting CAR-T cell therapy, vs standard of care (SOC; pomalidomide, bortezomib, and dexamethasone [PVd] or daratumumab, pomalidomide, and dexamethasone [DPd]) in lenalidomide (len)-refractory patients (pts). A single cilta-cel infusion significantly improved PFS vs SOC in len-refractory pts with 1
- |||||||||| Keytruda (pembrolizumab) / Merck (MSD)
Long-term complete remission in a patient with EBV-triggered hemophagocytic lymphohistiocytosis and Hodgkin (X2) - Sep 30, 2023 - Abstract #DGHO2023DGHO_668; This patient case highlights the fact that genetic testing for very rare inherited immunodeficiency-associated syndromes should be included in the workup of patients with unclear HLH. We therefore started dexamethasone aiming to restore liver function...At this time, an EBV reactivation was diagnosed, which we treated with addition of Rituximab...Brentuximab was added as HL therapy, but patient
- |||||||||| Sarclisa (isatuximab-irfc) / Sanofi
Expression-linked and R-ISS-Adapted Stratification for first line therapy in multiple myeloma patients (ELIAS) (Y2) - Sep 30, 2023 - Abstract #DGHO2023DGHO_563; The primary objective is to show non-inferiority of the experimental arm compared to the control arm with standard of care regarding the rate of patients with minimal residual disease (MRD) negativity combined with at least a complete remission response according to IMWG criteria at week 40 after start of induction therapy (18 weeks after randomization). Furthermore, we aim to detect possible differences in MRD negativity at specific points of time and to characterize both arms with respect to OS and PFS since randomization, PFS during second-line treatment since relapse, time to next treatment, and overall response rate.
- |||||||||| dexamethasone / Generic mfg.
Journal: Lithium-induced subacute diencephalic angio endotheliopathy. (Pubmed Central) - Sep 30, 2023 The patient deceased one month after discharge, mainly due to Diabetes Insipidusassociated hypernatremia. Dissecting the "Pandora's box" represented by complex MRI findings (SDAE and sinus thrombosis) in lithium-induced neurotoxicity is fundamental in timely recognizing this threating but potentially reversible clinical picture.
- |||||||||| dexamethasone / Generic mfg.
Journal: Exposure to low-intensity noise exacerbates nonalcoholic fatty liver disease by activating hypothalamus pituitary adrenal axis. (Pubmed Central) - Sep 30, 2023 In vivo (n?=?5) and in vitro models challenged with dexamethasone (DEX) were used to verify the role of hypothalamus pituitary adrenal (HPA) axis activation in hepatic lipid metabolism...Thus, three-month exposure to 75?dB SPL noise was sufficient to exacerbate NAFLD progress in mice, where activation of HPA axis played a critical role. Depression played an intermediate role and contributed to HPA axis activation up-stream of the exacerbation.
- |||||||||| dexamethasone / Generic mfg.
Journal: Capsular phimosis with intraocular lens tilt and decentration. (Pubmed Central) - Sep 28, 2023 A 34-year-old woman with quiescent bilateral intermediate uveitis maintained on once-daily dexamethasone 0.1% eyedrops, complicated by left cataract and glaucoma controlled with a single antiglaucoma medication, presented for cataract surgery...Discuss how you would manage this problem, explaining your decisions. How would you be able to avoid the same problem when operating on her fellow eye?
- |||||||||| Thymoglobulin (anti-thymocyte globulin (rabbit)) / Sanofi
Trial completion date, Trial primary completion date, Post-transplantation: Methods of T Cell Depletion Trial (MoTD) (clinicaltrials.gov) - Sep 28, 2023 P2, N=400, Recruiting, Trial completion date: Dec 2023 --> Dec 2024 Trial completion date: Jun 2025 --> Jan 2026 | Trial primary completion date: Jun 2025 --> Jan 2026
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