Even after SARS-CoV-2 booster, there is increased COVID-19 breakthrough infection in patients with plasma cell disorders DOI Creative Commons
Nathanael R. Fillmore, Jennifer La, Julie Wu

et al.

Blood Advances, Journal Year: 2023, Volume and Issue: 7(21), P. 6767 - 6770

Published: Aug. 30, 2023

Language: Английский

Multidisciplinary recommendations for the management of CAR-T recipients in the post-COVID-19 pandemic era DOI Creative Commons
Tingting Zhang,

Weiwei Tian,

Shuang Wei

et al.

Experimental Hematology and Oncology, Journal Year: 2023, Volume and Issue: 12(1)

Published: July 27, 2023

Abstract The outbreak of coronavirus disease 2019 (COVID-19) posed an unprecedented challenge on public health systems. Despite the measures put in place to contain it, COVID-19 is likely continue experiencing sporadic outbreaks for some time, and individuals will remain susceptible recurrent infections. Chimeric antigen receptor (CAR)-T recipients are characterized by durable B-cell aplasia, hypogammaglobulinemia loss T-cell diversity, which lead increased proportion severe/critical cases a high mortality rate after infection. Thus, treatment decisions have become much more complex require greater caution when considering CAR immunotherapy. Hence, we reviewed current understanding reported clinical experience management CAR-T therapy. After panel discussion, proposed rational procedure pertaining with aim maximizing benefit therapy post pandemic era.

Language: Английский

Citations

10

Managing Infection Complications in the Setting of Chimeric Antigen Receptor T cell (CAR-T) Therapy DOI Creative Commons
Nausheen Ahmed, Olalekan O. Oluwole, Zahra Mahmoudjafari

et al.

Clinical Hematology International, Journal Year: 2024, Volume and Issue: 6(2)

Published: April 29, 2024

Chimeric antigen receptor T-cell (CAR T-cell) therapy has changed the paradigm of management non-Hodgkin's lymphoma (NHL) and Multiple Myeloma. Infection complications have emerged as a concern that can arise in setting lead to morbidity mortality. In this review, we classified infection into three categories, pre-infusion phase from time pre- lymphodepletion (LD) up day zero, early infusion 30 post-infusion, late after onwards. Infections arising are closely related previous chemotherapy bridging therapy. more likely LD chemo expected brief period grade 3-4 neutropenia. particularly worrisome because they associated with adverse risk features including prolonged neutropenia, dysregulation humoral adaptive immunity lymphopenia, hypogammaglobinemia, B cell aplasia. Bacterial, respiratory other viral infections, protozoal fungal infections occur during . We recommend enhanced supportive care prompt recognition treatment neutropenia growth factor support, surveillance testing for specific viruses appropriate instance, hypogammaglobulinemia repletion extended antimicrobial prophylaxis those at higher (e.g. high dose steroid use cytopenia). Finally, re-immunizing patients post CAR-T based on CDC transplant guidelines.

Language: Английский

Citations

3

Multiple myeloma and infections in the era of novel treatment modalities DOI
Mobil Akhmedov,

P. A. Zeynalovа,

А. А. Феденко

et al.

Leukemia Research, Journal Year: 2024, Volume and Issue: 143, P. 107544 - 107544

Published: June 25, 2024

Language: Английский

Citations

3

Outcomes of COVID‐19 in multiple myeloma patients treated with daratumumab DOI Creative Commons
Dian Jin, Jingsong He,

Wenjun Wu

et al.

Cancer Science, Journal Year: 2023, Volume and Issue: 115(1), P. 237 - 246

Published: Oct. 26, 2023

Despite concerns about an increased risk of adverse outcomes following coronavirus disease (COVID-19) in multiple myeloma patients treated with anti-CD38 Abs, the impact COVID-19 on this group is unclear. We tried to evaluate clinical these patients. collected data from 1036 and enrolled 509 cases COVID-19. divided into daratumumab or nondaratumumab cohorts based whether they had received daratumumab-based treatment within 6 months infection. applied a propensity score matching method reduce bias baseline characteristics, then compared incidence between two cohorts. A total 117 were cohort, 392 cohort. After matching, 204 matched. The proportions who developed pneumonia (59.8% vs. 34.3%, p < 0.001), hospitalized (33.3% 11.8%, 0.001) severe (23.5% 6.9%, = higher matched By multivariate analysis, exposure was independent factor for disease. An ECOG performance status >2 history chronic kidney factors COVID-19-related mortality among therapy. This study suggested that exposed at

Language: Английский

Citations

7

Charting a path forward: Promising outcomes of convalescent plasma therapy in the care of severely B‐cell depleted patients with persistent COVID‐19 DOI
Tsofia Inbar, Eldad J. Dann, Omer Kerner

et al.

Transfusion, Journal Year: 2024, Volume and Issue: 64(3), P. 443 - 448

Published: Feb. 8, 2024

Abstract Background Patients with severe B‐cell depletion related to hematological malignancies or targeted therapy suffer from impaired antibody responses SARS‐CoV‐2 and are at risk for prolonged COVID‐19. In this population, COVID‐19 convalescent plasma (CCP) may provide passive immunity, enhance immune response, promote virus neutralization. This study evaluated outcomes of depleted patients persistent treated CCP. Study Design Methods analysis included all consecutive severely COVID‐19, receiving CCP Rambam between 01.2022–02.2023. Persistent was defined as the presence symptoms ≥14 days in negative nucleocapsid test results. Results Twenty met inclusion criteria, 17 whom had malignancies, two suffered rheumatoid arthritis one both. Twelve received anti‐CD‐20 treatment, ‐ CAR‐T cells three underwent stem cell transplantation. The median duration 27.5 (range 14–97); 12 mild‐to‐moderate 8 infection. Sixteen required hospitalization. majority other therapies before Within a 1–16) post‐infusion, 19/20 clinically improved. No CCP‐associated adverse events were documented. recurred 3 improved patients. Two died on 1 90 following first infusion. Discussion is safe associated rapid clinical improvement. subset immunocompromised could particularly benefit administration.

Language: Английский

Citations

2

Risk of infection in patients with multiple myeloma treated with T-cell redirecting approaches: a call out for clinicians DOI
Tommaso Lupia,

Lorenzo Cani,

Sara Bringhen

et al.

Clinical Lymphoma Myeloma & Leukemia, Journal Year: 2024, Volume and Issue: 24(9), P. 592 - 603

Published: May 4, 2024

Language: Английский

Citations

2

The patients with multiple myeloma were infected with COVID-19 during autologous stem cell transplantation: case report and literature review DOI Creative Commons
Chang Su, Lijun Huang, Liang Liang

et al.

Infectious Agents and Cancer, Journal Year: 2024, Volume and Issue: 19(1)

Published: May 27, 2024

Abstract This paper introduces two cases of multiple myeloma, COVID-19 infection during autologous stem cell transplantation, the treatment process, and different results patients, which provides a reference for how to carry out ASCT safely normalization stage.

Language: Английский

Citations

2

Immunogenicity and effectiveness of COVID-19 booster vaccination among people living with HIV: a systematic review and meta-analysis DOI Creative Commons

Meng-Qun Cheng,

Rong Li,

Zhiying Weng

et al.

Frontiers in Medicine, Journal Year: 2023, Volume and Issue: 10

Published: Oct. 9, 2023

Background The effect of booster vaccinations with the coronavirus virus disease (COVID-19) vaccine on people living HIV (PLWH) remains unknown. In this study, we aimed to investigate immunogenicity and effectiveness doses COVID-19 in PLWH. Methods Literature research was done through PubMed, Embase, Cochrane Review, Web Science databases up 4 July 2023. Pooled estimates were calculated compared using DerSimonian Laird method for a random effects model. Randomized control trials observational studies both considered inclusion. Results We included 35 eligible covering 30,154 pooled immune response rate (IRR) PLWH after vaccination 97.25% (95% confidence interval [CI], 93.81–99.49), similar healthy (HC) (risk ratio [RR] = 0.98, 95% CI, 0.96–1.00). IRR CD4 + T-cell counts ≤ 200 86.27 65.35–99.07). For Omicron variants, dose 74.07% 58.83–89.30), risk reduced by 10% HC (RR 0.90, 0.80–1.00). found be comparable ( p ≥ 0.05). Subgroup analyses revealed that mRNA vaccines produced relatively high other vaccines. addition, results showed appeared further reduce COVID-19-related infections, hospitalizations, deaths primary vaccination. Conclusion It shown provided still desirable moderate count 200. Importantly, humoral responses HC, observed SARS-CoV-2 variant. Our review strongly emphasizes eliciting protective IRR. Furthermore, appears infection, hospitalization, death However, more evidence is needed confirm its effectiveness.

Language: Английский

Citations

6

Tixagevimab/Cilgavimab as Pre-Exposure Prophylaxis against COVID-19 for Multiple Myeloma Patients: A Prospective Study in the Omicron Era DOI Creative Commons
Ioannis Ntanasis‐Stathopoulos, Charalampos Filippatos, Maria Gavriatopoulou

et al.

Diseases, Journal Year: 2023, Volume and Issue: 11(3), P. 123 - 123

Published: Sept. 18, 2023

Background: tixagevimab/cilgavimab, distributed under the name "Evusheld", was first available pre-exposure prophylaxis for COVID-19 other than vaccination. It received an EUA from FDA after sufficient trial data showed efficacy in preventing SARS-CoV-2 infections and subsequent severe disease. Its potential benefits high-risk immunocompromised patients generated a lot of interest. Individuals with multiple myeloma fall into this category, as they are characterized by attenuated immune responses and, some cases, vaccines have limited efficacy. Methods: single-center, prospective study included consecutive myeloma. All individuals were considered due to their underlying Baseline demographic clinical characteristics, well regarding infection antibodies, collected. Patients administered two intramuscular 150 mg doses Evusheld monitored during follow-up period. Results: one hundred eleven analysis, median age 64 years (range 58-69) fifty-three females (47.7%). Fourteen (12.6%) had prior history all vaccinated either three or four mRNA-based vaccines. An increase observed neutralizing-antibody levels before tixagevimab/cilgavimab administration, 92.6% 97.3%. The high sustainable, level 95.4% at 3 months post administration. Overall, nine (8.1%) diagnosed period, 31 days. There no SARS-CoV-2- infection-related hospitalizations deaths. monoclonal antibody combination tolerated, infusion-related reactions major adverse events, pain injection site only reported 33 (30%). Conclusions: (Evusheld) seemed beneficial myeloma, who presented low incidence initial Omicron wave. No new safety concerns emerged. However, novel combinations antibodies against circulating variants deemed necessary view emergence tolerance.

Language: Английский

Citations

4

Pre-exposure prophylaxis with tixagevimab/cilgavimab for coronavirus disease 2019 (COVID-19) during the Omicron BA.5 wave at a single institution in Japan DOI
Ichiro Kawashima,

Hideto Hyuga,

Ayato Nakadate

et al.

International Journal of Hematology, Journal Year: 2023, Volume and Issue: 118(6), P. 731 - 736

Published: Sept. 25, 2023

Language: Английский

Citations

4