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2022 ◽  
Vol 11 ◽  
Author(s):  
Fei Chen ◽  
Naifei Chen ◽  
Yangyang Gao ◽  
Lin Jia ◽  
Zheng Lyu ◽  
...  

Breast cancer is a major killer of women’s health worldwide. While breast cancer is thought to have lower immunogenicity compared with other solid tumors, combination therapy is able to improve the immunogenicity of the tumor and sensitize breast cancer cells to immunotherapy. Immunotherapy represented by immune checkpoint inhibitors (ICIs) has been largely explored in the field of breast cancer, including both early and advanced disease. Immunotherapy for triple-negative breast cancer (TNBC) has been the most studied, and the PD-L1 inhibitor atezolizumab combined with nab-paclitaxel has been used in the first-line treatment of TNBC. Immunotherapeutic data for human epidermal growth factor receptor-positive and hormone receptor-positive breast cancer are also accumulating. This review summarizes the clinical trial data of ICIs or ICI-containing therapies in different types and stages of breast cancer.


Author(s):  
Raul Weiss ◽  
George Mark ◽  
Mikhael El-Chami ◽  
Mauro Biffi ◽  
VINCENT PROBST ◽  
...  

Background: Infection remains a major complication of cardiac implantable electronic devices (CIEDs) and can lead to significant morbidity and mortality. Extrathoracic devices that avoid epicardial or transvenous leads, such as the subcutaneous implantable cardioverter-defibrillator (S-ICD), can reduce the risk of serious infection-related complications, such as bloodstream infection and infective endocarditis. While the 2017 AHA/ACC/HRS guidelines include recommendations for S-ICD use for patients at high risk of infection, currently, there are no clinical trial data that address best practices for the prevention of S-ICD infections. Therefore, an expert panel was convened to develop consensus on these topics. Methods: An expert process mapping methodology was used to achieve consensus on the appropriate steps to minimize or prevent S-ICD infections. Two face-to-face meetings of high-volume S-ICD implanters and an infectious diseases specialist, with expertise on cardiovascular implantable electronic device infections, were conducted to develop consensus on useful strategies pre-, peri-, and post-implant to reduce S-ICD infection risk. Results: Expert panel consensus of recommended steps for patient preparation, S-ICD implantation, and post-operative management were developed to provide guidance in individual patient management. Conclusion: Achieving expert panel consensus by process mapping methodology for S-ICD infection prevention was attainable, and the results should be helpful to clinicians in adopting interventions to minimize risks of S-ICD infection.


Author(s):  
Marc-André Gagnon ◽  
Matthew Herder ◽  
Janice Graham ◽  
Katherine Fierlbeck ◽  
Anna Danyliuk

Cancers ◽  
2021 ◽  
Vol 14 (1) ◽  
pp. 113
Author(s):  
Omar Alkharabsheh ◽  
Zachary Trisel ◽  
Sunil Badami ◽  
Mohammed A. Aljama ◽  
M. Hasib Sidiqi

Immune dysregulation and alteration of the bone marrow microenvironment allowing plasma cells to escape immune surveillance are well-known factors associated with the proliferation of clonal plasma cells and development of multiple myeloma (MM). Whilst immunotherapeutic approaches are now commonplace in a wide spectrum of malignancies, this aberration of myeloma development gives rise to the biological rationale for the use of immune checkpoint inhibitors (ICIs) in MM. However, the initial experience with these agents has been challenging with limited single agent efficacy, significant toxicity, and side effects. Herein, we review the biological and immunological aspects of MM and ICIs. We discuss the basic biology of immune checkpoint inhibitors, mechanisms of resistance, and drug failure patterns, review the published clinical trial data for ICIs in MM, and look towards the future of ICIs for MM treatment.


2021 ◽  
Vol 16 ◽  
Author(s):  
Jingang Jiang ◽  
Ziwen Gao ◽  
Shichang Song ◽  
Xiaoyang Yu ◽  
Yang Zeng

Background: Today, living standards and medical technology are improving, and the aging global population is increasing. Moreover, more and more older adults are suffering from knee diseases. This will seriously affect patients’ daily life and their mental state. In many studies, repetitive physical exercises and motor activities in real-world environments have been shown to help improve knee muscle strength and restore damaged nerves. Therefore, physical knee therapy is very necessary. The use of rehabilitation training devices for movement therapy has shown great potentia Objective: The structural features, functions and development status of the knee rehabilitation training device are introduced Method: This review explores the structure and function of various current knee rehabilitation devices based on structural and kinematic properties of the knee joint in relation to requirements of physical knee rehabilitation. This paper aims to present a systematic guideline and to outline a reference for future designers of rehabilitation devices. Results: By analyzing the structure and movement of the knee joint and combining the strategies of physical knee rehabilitation, movement requirements during knee rehabilitation training are concluded. According to the structure, drive form, transmission mode and rehabilitation environment of knee rehabilitation devices, the devices are classified and compared; some typical features are summarized; some current problems are analyzed; and the future trends and development directions of rehabilitation devices are discussed. Conclusion: Current rehabilitation equipment has a variety of structures and functions, but a good balance between weight and volume is hardly maintained. The protection of the body needs to be further improved. Many knee rehabilitation devices are only concepts, not physical objects, and lack clinical trial data. Power sources and drives are large and heavy, which can compress the knee joint and place a burden on the patient. Strong and light-weight materials should be chosen to assist knee rehabilitation. It will be a good development in the future


Author(s):  
Sarah E. Murphy ◽  
Tihana Bicanic

Candida species are the leading cause of invasive fungal infections worldwide and are associated with acute mortality rates of ~50%. Mortality rates are further augmented in the context of host immunosuppression and infection with drug-resistant Candida species. In this review, we outline antifungal drugs already in clinical use for invasive candidiasis and candidaemia, their targets and mechanisms of resistance in clinically relevant Candida species, encompassing not only classical resistance, but also heteroresistance and tolerance. We describe novel antifungal agents and targets in pre-clinical and clinical development, including their spectrum of activity, antifungal target, clinical trial data and potential in treatment of drug-resistant Candida. Lastly, we discuss the use of combination therapy between conventional and repurposed agents as a potential strategy to combat the threat of emerging resistance in Candida.


Hematology ◽  
2021 ◽  
Vol 2021 (1) ◽  
pp. 92-99
Author(s):  
Carol Mathew ◽  
Marc Zumberg

Abstract Although much less common than deep vein thrombosis of the lower extremities or lungs, clots in unusual locations, including the splanchnic, cerebral, retinal, upper-extremity, and renal locations, present with significant morbidity and mortality. In the last 2 decades, treatment of clots in these unusual locations is primarily managed medically, with interventional and surgical approaches reserved for more severe or refractory cases. The hematologist is well positioned to provide consultation to organ-specific specialties (ie, neurosurgery, hepatology, ophthalmology), especially because acquired and congenital hypercoagulability plays a major role, and anticoagulation is often the primary treatment. Historically, treatment has been based on expert opinion, but systematic reviews and meta-analyses have recently been published. Various societies have produced guidelines for the treatment of clots in unusual locations; however, randomized clinical trial data remain scarce. In the last few years, increasing data have emerged concerning the efficacy of the direct oral anticoagulants in treating clots in unusual locations. Cases have recently been described highlighting atypical thrombosis associated with COVID-19 infection as well as with the ChAdOx1 nCoV-19 (AstraZeneca) vaccine and Johnson and Johnson's Janssen Ad26.COV2.S vaccine. This article reviews clots in unusual locations with an emphasis on the splanchnic (mesenteric, portal, splenic, hepatic) and cerebral circulation. Through a case-based approach, key questions are posed, and data are presented to help guide diagnosis and treatment.


2021 ◽  
Vol 22 (24) ◽  
pp. 13185
Author(s):  
Nina Dedic ◽  
Heather Dworak ◽  
Courtney Zeni ◽  
Grazia Rutigliano ◽  
Oliver D. Howes

Trace amine-associated receptor 1 (TAAR1) has emerged as a promising therapeutic target for neuropsychiatric disorders due to its ability to modulate monoaminergic and glutamatergic neurotransmission. In particular, agonist compounds have generated interest as potential treatments for schizophrenia and other psychoses due to TAAR1-mediated regulation of dopaminergic tone. Here, we review unmet needs in schizophrenia, the current state of knowledge in TAAR1 circuit biology and neuropharmacology, including preclinical behavioral, imaging, and cellular evidence in glutamatergic, dopaminergic and genetic models linked to the pathophysiology of psychotic, negative and cognitive symptoms. Clinical trial data for TAAR1 drug candidates are reviewed and contrasted with antipsychotics. The identification of endogenous TAAR1 ligands and subsequent development of small-molecule agonists has revealed antipsychotic-, anxiolytic-, and antidepressant-like properties, as well as pro-cognitive and REM-sleep suppressing effects of TAAR1 activation in rodents and non-human primates. Ulotaront, the first TAAR1 agonist to progress to randomized controlled clinical trials, has demonstrated efficacy in the treatment of schizophrenia, while another, ralmitaront, is currently being evaluated in clinical trials in schizophrenia. Coupled with the preclinical findings, this provides a rationale for further investigation and development of this new pharmacological class for the treatment of schizophrenia and other psychiatric disorders.


2021 ◽  
Author(s):  
Olivia Sanchez-Graillet ◽  
Arne Kramer-Sunderbrink ◽  
Philipp Cimiano

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