Seema Singhal

ORCID: 0000-0002-8644-7684
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About
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Research Areas
  • Multiple Myeloma Research and Treatments
  • Hematopoietic Stem Cell Transplantation
  • Acute Myeloid Leukemia Research
  • Protein Degradation and Inhibitors
  • Cancer Treatment and Pharmacology
  • Peptidase Inhibition and Analysis
  • Acute Lymphoblastic Leukemia research
  • Chronic Myeloid Leukemia Treatments
  • Endometrial and Cervical Cancer Treatments
  • Chronic Lymphocytic Leukemia Research
  • Neutropenia and Cancer Infections
  • Lymphoma Diagnosis and Treatment
  • Uterine Myomas and Treatments
  • Ovarian cancer diagnosis and treatment
  • Renal Transplantation Outcomes and Treatments
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Cancer therapeutics and mechanisms
  • Amyloidosis: Diagnosis, Treatment, Outcomes
  • Cervical Cancer and HPV Research
  • Endometriosis Research and Treatment
  • Polyomavirus and related diseases
  • Antifungal resistance and susceptibility
  • HIV/AIDS drug development and treatment
  • Blood disorders and treatments
  • Mesenchymal stem cell research

All India Institute of Medical Sciences
2012-2024

Northwestern University
2012-2023

All India Institute of Medical Sciences Bhopal
2012-2023

All India Institute of Medical Sciences Raipur
2012-2023

Indraprastha Apollo Hospitals
2019-2023

Northwestern Medicine
2006-2023

Freeman Hospital
2022

Institute of Medical Sciences
2021

Robert H. Lurie Comprehensive Cancer Center of Northwestern University
2005-2020

Satguru Partap Singh Hospital
2020

Bortezomib, a boronic acid dipeptide, is novel proteasome inhibitor that has been shown in preclinical and phase 1 studies to have antimyeloma activity.In this multicenter, open-label, nonrandomized, 2 trial, we enrolled 202 patients with relapsed myeloma was refractory the therapy they had received most recently. Patients 1.3 mg of bortezomib per square meter body-surface area twice weekly for weeks, followed by week without treatment, up eight cycles (24 weeks). In suboptimal response,...

10.1056/nejmoa030288 article EN New England Journal of Medicine 2003-06-25

Patients with myeloma who relapse after high-dose chemotherapy have few therapeutic options. Since increased bone marrow vascularity imparts a poor prognosis in myeloma, we evaluated the efficacy of thalidomide, which has antiangiogenic properties, patients refractory disease.

10.1056/nejm199911183412102 article EN New England Journal of Medicine 1999-11-18

To determine the frequency, characteristics, and reversibility of peripheral neuropathy from bortezomib treatment advanced multiple myeloma.Peripheral was assessed in two phase II studies 256 patients with relapsed and/or refractory myeloma treated 1.0 or 1.3 mg/m2 intravenous bolus on days 1, 4, 8, 11, every 21 days, for up to eight cycles. Peripheral evaluated at baseline, during study, after study by patient-reported symptoms using Functional Assessment Cancer Therapy Scale/Gynecologic...

10.1200/jco.2005.04.7779 article EN Journal of Clinical Oncology 2006-06-06

Multiple myeloma (MM) is caused by the neoplastic proliferation of plasma cells. These cells proliferate and produce monoclonal immunoglobulin in bone marrow causing skeletal damage, a hallmark multiple myeloma. Other MM-related complications include hypercalcemia, renal insufficiency, anemia, infections. The NCCN Myeloma Panel members have developed guidelines for management patients with various cell dyscrasias, including solitary plasmacytoma, smoldering myeloma, systemic light chain...

10.6004/jnccn.2017.0023 article EN Journal of the National Comprehensive Cancer Network 2017-02-01
María‐Victoria Mateos Hilary Blacklock Fredrik Schjesvold Albert Oriol David Simpson and 95 more Anupkumar George Hartmut Goldschmidt Alessandra Larocca Asher Chanan‐Khan Daniel W. Sherbenou Irit Avivi Noam Benyamini Shinsuke Iida Morio Matsumoto Kenshi Suzuki Vincent Ribrag Saad Z. Usmani Sundar Jagannath Enrique M. Ocio Paula Rodríguez‐Otero Jesús F. San Miguel Uma Kher Mohammed Z.H. Farooqui Jason J. Z. Liao Patricia Marinello Sagar Lonial Andrew J. Nicol George Grigoriadis John Catalano Richard LeBlanc Mohamed Elemary Nizar J. Bahlis Thierry Façon Lionel Karlin Vincent Ribrag Michel Attal Hartmut Goldschmidt Monika Engelhardt Katja Weisel Andréas Mackensen Arnon Nagler Dina Ben Yehuda Irit Avivi Noam Benyamini Hila Magen‐Nativ Antonio Palumbo Michèle Cavo Kensei Tobinai Shinsuke Iida Takaai Chou Kenshi Suzuki Hiroshi Kosugi Masafumi Taniwaki Kazutaka Sunami Morio Matsumoto Kiyoshi Ando Peter Ganly Hilary Blacklock David Simpson Anupkumar George Fredrik Schjesvold Bjørn Tore Gjertsen Juan José Lahuerta Joan Bladé Albert Oriol Rocafiguera María‐Victoria Mateos Paula Rodríguez‐Otero Sarah Larson Djordje Atanackovic Srinivas Devarakonda Jacob D. Bitran Jeffrey A. Zonder Neil Morganstein Mohammad Hay Asher Chanan‐Khan Gene Saylors Ebenezer A. Kio Ira Oliff Dean Kirkel Mikhail Shtivelband Carrie Yuen Andrew J. Yee Jatin J. Shah Myo Htut Shahzad Raza Saurabh Chhabra Patrick J. Stiff Parameswaran Hari Bruce Bank Ehsan Malek Cristina Gasparetto Ycaoub Faroun Daniel W. Sherbenou William Kreisle Seema Singhal Jacalyn Rosenblatt Saad Z. Usmani Wes Lee Hana Safah Jose Lutzky

10.1016/s2352-3026(19)30110-3 article EN The Lancet Haematology 2019-07-18

The NCCN Guidelines for Multiple Myeloma provide recommendations diagnosis, evaluation, treatment, including supportive-care, and follow-up patients with myeloma. These Insights highlight the important updates/changes specific to myeloma therapy options in 2018 version of Guidelines.

10.6004/jnccn.2018.0002 article EN Journal of the National Comprehensive Cancer Network 2018-01-01

The NCCN Guidelines for Multiple Myeloma provide recommendations diagnosis, workup, treatment, follow-up, and supportive care patients with monoclonal gammopathy of renal significance, solitary plasmacytoma, smoldering myeloma, multiple myeloma. These Insights highlight some the important updates changes in 1.2020 version Myeloma.

10.6004/jnccn.2019.0049 article EN Journal of the National Comprehensive Cancer Network 2019-10-01

Multiple myeloma (MM) is a malignant neoplasm of plasma cells that accumulate in bone marrow, leading to destruction and marrow failure.The American Cancer Society estimates 20,580 new cases MM will occur the United States 2009, including 11,680 men 8900 women, with an estimated 10,580 deaths. 1 The mean age affected individuals 62 years for (75% > 70 years) 61 women (79% years).The treatment has dramatically improved over past decade.The 5-year survival rate reported Surveillance...

10.6004/jnccn.2009.0061 article EN Journal of the National Comprehensive Cancer Network 2009-10-01

Abstract BACKGROUND Bortezomib is a potent, reversible proteasome inhibitor that has been approved for the treatment of recurrent and/or refractory multiple myeloma, but its activity in patients with renal impairment not studied to date. METHODS Response rates, safety, and 20S were assessed relation baseline creatinine clearance (CrCl) among myeloma ( n = 256 patients) who treated bortezomib 2 Phase II trials. was administered by intravenous bolus on Days 1, 4, 8, 11 21‐day cycle at doses,...

10.1002/cncr.20888 article EN Cancer 2005-02-02

Abstract BACKGROUND. Low voriconazole levels have been associated with a higher failure rate in patients confirmed fungal infections. METHODS. Steady‐state plasma trough were measured after at least 5 days of therapy 87 hematologic malignancies on 201 separate occasions (1–5 per patient; median, 2). Most (90%) had undergone allogeneic hematopoietic stem cell transplantation. The daily dose, administered 2 divided doses, was 200 mg (n = 4), 400 151), 500 20), 600 18), and 800 8);...

10.1002/cncr.22568 article EN Cancer 2007-03-09

Summary Total Therapy 1, the first tandem autotransplant trial for newly diagnosed patients with multiple myeloma, was designed to increase frequency of complete response (CR) and thereby extend survival. With a median follow‐up 12 years, 62 231 initially enrolled are alive (17% at 15 years); 31 remain event free (7% years) including 16 94 (41%) that achieved CR. Currently less frequently had cytogenetic abnormalities (CAs) baseline ( P = 0·002), postenrolment < 0·001) relapse 0·004);...

10.1111/j.1365-2141.2006.06271.x article EN British Journal of Haematology 2006-08-29
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