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  1. Article: Concomitant EGFR Mutations and ALK Rearrangements in Lung Adenocarcinoma Treated With Osimertinib.

    Thomas, David / Maloney, McKenzie E / Raval, Girindra

    Cureus

    2023  Volume 15, Issue 11, Page(s) e48122

    Abstract: Lung cancer is the third most common cancer in addition to being the cancer responsible for the most annual deaths in the United States, comprising 15% of all diagnosed cancers, and 28% of all cancer deaths in 2020. Major advances in survival are because ...

    Abstract Lung cancer is the third most common cancer in addition to being the cancer responsible for the most annual deaths in the United States, comprising 15% of all diagnosed cancers, and 28% of all cancer deaths in 2020. Major advances in survival are because of gene sequencing and the advent of targeted biological therapy. The prevalence of epidermal growth factor receptor (EGFR) mutations coexisting with anaplastic lymphoma kinase (ALK) rearrangements is quite low. However, the clinical relevance and effective treatment of these cancers require further investigation. This case series describes two patients diagnosed with stage IV adenocarcinoma with coexisting EGFR and ALK rearrangements. In Case 1, a 73-year-old male presented with worsening ataxia and headaches. In Case 2, a 64-year-old female presented with worsening dyspnea. Molecular studies revealed ALK gene fusion and the L861Q EGFR mutation in Case 1 and L858R EGFR mutation and ALK gene fusion in Case 2. Both patients received a gamma knife and an EGFR-tyrosine kinase inhibitor (TKI), osimertinib. In one of the cases, following the discovery of new brain metastases, the dose of osimertinib was increased from 80 to 160 mg. The patient passed away nine months after beginning EGFR-TKI treatment, one month after increasing the dose. The second patient experienced a significant interval reduction in the size of enhancing metastasis in both the right frontal and left parietal lobe after four months of EGFR-TKI treatment. The cases of coexisting EGFR mutations and ALK rearrangements are quite rare, and treatment can be challenging. Here, EGFR-TKI had a mixed response among our patients.
    Language English
    Publishing date 2023-11-01
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2747273-5
    ISSN 2168-8184
    ISSN 2168-8184
    DOI 10.7759/cureus.48122
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Successful Treatment of Refractory Thrombotic Thrombocytopenic Purpura (TTP) With Caplacizumab: A Case Report.

    Pramanik, Debolina / Bhardwaj, Divyashish / Karmani, Vikash K / Raval, Girindra G / Kutlar, Abdullah

    Cureus

    2023  Volume 15, Issue 7, Page(s) e42423

    Abstract: We report a female patient who presented with generalized weakness, episodes of altered mental status and slurred speech, and a history of systemic lupus erythematosus. Initial investigations showed profound thrombocytopenia and schistocytosis on ... ...

    Abstract We report a female patient who presented with generalized weakness, episodes of altered mental status and slurred speech, and a history of systemic lupus erythematosus. Initial investigations showed profound thrombocytopenia and schistocytosis on peripheral blood smear. PLASMIC score was promptly calculated, and plasma exchange with steroids was initiated based on the initial high PLASMIC score. Bone marrow examination showed hypocellular marrow without any other obvious abnormalities. The patient's platelet counts initially improved but had a quick decline, on which, rituximab and subsequently caplacizumab were introduced. The patient was discharged after stabilization with plasma exchange (PLEX) therapy as needed on an outpatient basis.
    Language English
    Publishing date 2023-07-25
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2747273-5
    ISSN 2168-8184
    ISSN 2168-8184
    DOI 10.7759/cureus.42423
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Cardiovascular Toxicities Associated with Tyrosine Kinase Inhibitors.

    Sayegh, Nicolas / Yirerong, Juliet / Agarwal, Neeraj / Addison, Daniel / Fradley, Michael / Cortes, Jorge / Weintraub, Neal L / Sayed, Nazish / Raval, Girindra / Guha, Avirup

    Current cardiology reports

    2023  Volume 25, Issue 4, Page(s) 269–280

    Abstract: Purpose of review: To provide a detailed overview of cardiovascular adverse events associated with the use of tyrosine kinase inhibitors across different tumor types.: Recent findings: Despite an undeniable survival advantage of tyrosine kinase ... ...

    Abstract Purpose of review: To provide a detailed overview of cardiovascular adverse events associated with the use of tyrosine kinase inhibitors across different tumor types.
    Recent findings: Despite an undeniable survival advantage of tyrosine kinase inhibitors (TKIs) in patients with hematologic or solid malignancies, the accompanying off-target cardiovascular adverse events can be life-threatening. In patients with B cell malignancies, the use of Bruton tyrosine kinase inhibitors has been associated with atrial and ventricular arrhythmias, as well as hypertension. Cardiovascular toxic profiles are heterogeneous among the several approved breakpoint cluster region (BCR)-ABL TKIS. Notably, imatinib might be cardioprotective. Vascular endothelial growth factor TKIs, constituting the central axis in the treatment of several solid tumors, including renal cell carcinoma and hepatocellular carcinoma, have strongly been associated with hypertension and arterial ischemic events. Epidermal growth factor TKIs as therapy for advanced non-small cell lung cancer (NSCLC) have been reported to be infrequently associated with heart failure and QT prolongation. While tyrosine kinase inhibitors have been demonstrated to increase overall survival across different types of cancers, special consideration should be given to cardiovascular toxicities. High-risk patients can be identified by undergoing a comprehensive workup at baseline.
    MeSH term(s) Humans ; Tyrosine Kinase Inhibitors ; Protein Kinase Inhibitors/adverse effects ; Carcinoma, Non-Small-Cell Lung/chemically induced ; Vascular Endothelial Growth Factor A ; Lung Neoplasms/chemically induced ; Hypertension
    Chemical Substances Tyrosine Kinase Inhibitors ; Protein Kinase Inhibitors ; Vascular Endothelial Growth Factor A
    Language English
    Publishing date 2023-02-16
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2055373-0
    ISSN 1534-3170 ; 1523-3782
    ISSN (online) 1534-3170
    ISSN 1523-3782
    DOI 10.1007/s11886-023-01845-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: TNF-α inhibitors: are they carcinogenic?

    Raval, Girindra / Mehta, Paulette

    Drug, healthcare and patient safety

    2010  Volume 2, Page(s) 241–247

    Abstract: Biologic therapy has increasingly been used in the treatment of chronic diseases. Tumor necrosis factor (TNF) is a cytokine implicated in the pathogenesis of rheumatoid arthritis and inflammatory bowel disease. Anti-TNF therapy is being used in the ... ...

    Abstract Biologic therapy has increasingly been used in the treatment of chronic diseases. Tumor necrosis factor (TNF) is a cytokine implicated in the pathogenesis of rheumatoid arthritis and inflammatory bowel disease. Anti-TNF therapy is being used in the treatment of these conditions. Since the introduction of anti-TNF agents, there have been many case reports of development of malignancy after the initiation of anti-TNF therapy. With increasing case reports, there is growing concern that anti-TNF therapy, albeit useful in the treatment of these chronic conditions, might be associated with the development of malignancy in patients. In this review we examine the different anti-TNF agents and different studies to evaluate any possible association between use of any anti-TNF agent and development of malignancy.
    Language English
    Publishing date 2010-12-06
    Publishing country New Zealand
    Document type Journal Article
    ZDB-ID 2520700-3
    ISSN 1179-1365 ; 1179-1365
    ISSN (online) 1179-1365
    ISSN 1179-1365
    DOI 10.2147/DHPS.S7829
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Ethno-demographic disparities in humoral responses to the COVID-19 vaccine among healthcare workers.

    Ahluwalia, Pankaj / Vashisht, Ashutosh / Singh, Harmanpreet / Sahajpal, Nikhil Shri / Mondal, Ashis K / Jones, Kimya / Farmaha, Jaspreet / Bloomquist, Ryan / Carlock, Caroline Marie / Fransoso, Drew / Sun, Christina / Day, Tyler / Prah, Comfort / Vuong, Trinh / Ray, Patty / Bradshaw, Danielle / Galvis, Marisol Miranda / Fulzele, Sadanand / Raval, Girindra /
    Moore, Justin Xavier / Cortes, Jorge / James, Jeffrey N / Kota, Vamsi / Kolhe, Ravindra

    Journal of medical virology

    2023  Volume 95, Issue 9, Page(s) e29067

    Abstract: The COVID-19 pandemic had a profound impact on global health, but rapid vaccine administration resulted in a significant decline in morbidity and mortality rates worldwide. In this study, we sought to explore the temporal changes in the humoral immune ... ...

    Abstract The COVID-19 pandemic had a profound impact on global health, but rapid vaccine administration resulted in a significant decline in morbidity and mortality rates worldwide. In this study, we sought to explore the temporal changes in the humoral immune response against SARS-CoV-2 healthcare workers (HCWs) in Augusta, GA, USA, and investigate any potential associations with ethno-demographic features. Specifically, we aimed to compare the naturally infected individuals with naïve individuals to understand the immune response dynamics after SARS-CoV-2 vaccination. A total of 290 HCWs were included and assessed prospectively in this study. COVID status was determined using a saliva-based COVID assay. Neutralizing antibody (NAb) levels were quantified using a chemiluminescent immunoassay system, and IgG levels were measured using an enzyme-linked immunosorbent assay method. We examined the changes in antibody levels among participants using different statistical tests including logistic regression and multiple correspondence analysis. Our findings revealed a significant decline in NAb and IgG levels at 8-12 months postvaccination. Furthermore, a multivariable analysis indicated that this decline was more pronounced in White HCWs (odds ratio [OR] = 2.1, 95% confidence interval [CI] = 1.07-4.08, p = 0.02) and IgG (OR = 2.07, 95% CI = 1.04-4.11, p = 0.03) among the whole cohort. Booster doses significantly increased IgG and NAb levels, while a decline in antibody levels was observed in participants without booster doses at 12 months postvaccination. Our results highlight the importance of understanding the dynamics of immune response and the potential influence of demographic factors on waning immunity to SARS-CoV-2. In addition, our findings emphasize the value of booster doses to ensure durable immunity.
    MeSH term(s) Humans ; COVID-19 Vaccines ; COVID-19/prevention & control ; Pandemics ; SARS-CoV-2 ; Antibodies, Neutralizing ; Health Personnel ; Immunoglobulin G
    Chemical Substances COVID-19 Vaccines ; Antibodies, Neutralizing ; Immunoglobulin G
    Language English
    Publishing date 2023-09-07
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ZDB-ID 752392-0
    ISSN 1096-9071 ; 0146-6615
    ISSN (online) 1096-9071
    ISSN 0146-6615
    DOI 10.1002/jmv.29067
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: TNF-alpha inhibitor etanercept and hematologic malignancies: report of a case and review of the literature.

    Nair, Bijay / Raval, Girindra / Mehta, Paulette

    American journal of hematology

    2007  Volume 82, Issue 11, Page(s) 1022–1024

    Abstract: We report here a 57-year-old man treated with etanercept for 6 months for psoriasis who developed myelodysplasia with acute myeloid leukemia. Leukemia cells had distinct karyotype associated with poor prognosis. The patient did not respond to cytosine ... ...

    Abstract We report here a 57-year-old man treated with etanercept for 6 months for psoriasis who developed myelodysplasia with acute myeloid leukemia. Leukemia cells had distinct karyotype associated with poor prognosis. The patient did not respond to cytosine arabinoside 100 mg/m(2) continuous infusion over 7 days with daunorubicin 45 mg/m(2) daily for 3 days. He also did not respond to salvage induction therapy with gemtuzumab (6 mg/m(2) on day 1 and 4 mg/m(2) on day 8) and intravenous continuous infusion cytosine arabinoside 200 mg/m(2). We review other cases of lymphoma and leukemia associated with tumor necrosis factor inhibitors and suggest mechanisms by which inhibition of the TNF-alpha family may predispose to cancer. We also suggest that all patients being considered for TNF-alpha treatment be screened for hematologic malignancies or premalignancies with blood counts and bone marrow aspirates/biopsies if indicated.
    MeSH term(s) Arthritis, Psoriatic/drug therapy ; Etanercept ; Humans ; Immunoglobulin G/adverse effects ; Leukemia, Myeloid, Acute/chemically induced ; Male ; Middle Aged ; Myelodysplastic Syndromes/chemically induced ; Receptors, Tumor Necrosis Factor ; Tumor Necrosis Factor-alpha/antagonists & inhibitors
    Chemical Substances Immunoglobulin G ; Receptors, Tumor Necrosis Factor ; Tumor Necrosis Factor-alpha ; Etanercept (OP401G7OJC)
    Language English
    Publishing date 2007-11
    Publishing country United States
    Document type Case Reports ; Journal Article ; Review
    ZDB-ID 196767-8
    ISSN 1096-8652 ; 0361-8609
    ISSN (online) 1096-8652
    ISSN 0361-8609
    DOI 10.1002/ajh.20926
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Unexplained hemolytic anemia with multiorgan failure.

    Raval, Girindra / Straughen, Joel E / McMillin, Gwendolyn A / Bornhorst, Joshua A

    Clinical chemistry

    2011  Volume 57, Issue 11, Page(s) 1485–1488

    MeSH term(s) Anemia, Hemolytic/chemically induced ; Anemia, Hemolytic/diagnosis ; Cadmium Poisoning/complications ; Cadmium Poisoning/diagnosis ; Fatal Outcome ; Humans ; Male ; Middle Aged ; Multiple Organ Failure/chemically induced ; Multiple Organ Failure/diagnosis
    Language English
    Publishing date 2011-10-28
    Publishing country England
    Document type Case Reports ; Journal Article
    ZDB-ID 80102-1
    ISSN 1530-8561 ; 0009-9147
    ISSN (online) 1530-8561
    ISSN 0009-9147
    DOI 10.1373/clinchem.2010.160119
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: New cancers after autotransplantations for multiple myeloma.

    Mahindra, Anuj / Raval, Girindra / Mehta, Paulette / Brazauskas, Ruta / Zhang, Mei-Jie / Zhong, Xiaobo / Bird, Jennifer M / Freytes, César O / Hale, Gregory A / Herzig, Roger / Holmberg, Leona A / Kamble, Rammurti T / Kumar, Shaji / Lazarus, Hillard M / Majhail, Navneet S / Marks, David I / Moreb, Jan S / Olsson, Richard / Saber, Wael /
    Savani, Bipin N / Schiller, Gary J / Tay, Jason / Vogl, Dan T / Waller, Edmund K / Wiernik, Peter H / Wirk, Baldeep / Lonial, Sagar / Krishnan, Amrita Y / Dispenzieri, Angela / Brandenburg, Nancy A / Gale, Robert Peter / Hari, Parameswaran N

    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation

    2014  Volume 21, Issue 4, Page(s) 738–745

    Abstract: We describe baseline incidence and risk factors for new cancers in 4161 persons receiving autotransplants for multiple myeloma in the United States from 1990 to 2010. Observed incidence of invasive new cancers was compared with expected incidence ... ...

    Abstract We describe baseline incidence and risk factors for new cancers in 4161 persons receiving autotransplants for multiple myeloma in the United States from 1990 to 2010. Observed incidence of invasive new cancers was compared with expected incidence relative to the US population. The cohort represented 13,387 person-years at-risk. In total, 163 new cancers were observed, for a crude incidence rate of 1.2 new cancers per 100 person-years and cumulative incidences of 2.6% (95% confidence interval [CI], 2.09 to 3.17), 4.2% (95% CI, 3.49 to 5.00), and 6.1% (95% CI, 5.08 to 7.24) at 3, 5, and 7 years, respectively. The incidence of new cancers in the autotransplantation cohort was similar to age-, race-, and gender-adjusted comparison subjects with an observed/expected (O/E) ratio of 1.00 (99% CI, .81 to 1.22). However, acute myeloid leukemia and melanoma were observed at higher than expected rates with O/E ratios of 5.19 (99% CI, 1.67 to 12.04; P = .0004), and 3.58 (99% CI, 1.82 to 6.29; P < .0001), respectively. Obesity, older age, and male gender were associated with increased risks of new cancers in multivariate analyses. This large data set provides a baseline for comparison and defines the histologic type specific risk for new cancers in patients with MM receiving postautotransplantation therapies, such as maintenance.
    MeSH term(s) Adolescent ; Autografts ; Child ; Child, Preschool ; Female ; Humans ; Incidence ; Infant ; Infant, Newborn ; Male ; Multiple Myeloma/epidemiology ; Multiple Myeloma/therapy ; Neoplasms, Second Primary/epidemiology ; Retrospective Studies ; Risk Factors ; Sex Factors ; Stem Cell Transplantation ; United States/epidemiology
    Language English
    Publishing date 2014-12-31
    Publishing country United States
    Document type Clinical Trial ; Journal Article ; Multicenter Study ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S. ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 1474865-4
    ISSN 1523-6536 ; 1083-8791
    ISSN (online) 1523-6536
    ISSN 1083-8791
    DOI 10.1016/j.bbmt.2014.12.028
    Database MEDical Literature Analysis and Retrieval System OnLINE

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