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Dive into the research topics where Benjamin Lichtiger is active.

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Featured researches published by Benjamin Lichtiger.


Transfusion | 1996

Clinical toxicity and laboratory effects of granulocyte-colony-stimulating factor (filgrastim) mobilization and blood stem cell apheresis from normal donors, and analysis of charges for the procedures.

Paolo Anderlini; Donna Przepiorka; D. Seong; P. Miller; J. Sundberg; Benjamin Lichtiger; Frank Norfleet; K. W. Chan; Richard E. Champlin; Martin Korbling

BACKGROUND: Apheresis of granulocyte‐colony‐stimulating factor (filgrastim)‐mobilized blood stem cells from normal donors is now being used in place of a marrow harvest in transplantation. How the adverse effects of and charges for this procedure compare with those of the standard marrow harvest is not known.


Leukemia | 1997

Treatment of neutropenia-related fungal infections with granulocyte colony-stimulating factor-elicited white blood cell transfusions: a pilot study.

M. C. Dignani; Elias Anaissie; Jeane P. Hester; Stephen J. O'Brien; S. E. Vartivarian; J. H. Rex; H. Kantarjian; David Jendiroba; Benjamin Lichtiger; Borje S. Andersson; Emil J. Freireich

Neutropenia-related fungal infections can be life-threatening despite antifungal therapy. We evaluated the role of recombinant granulocyte colony-stimulating factor (rG-CSF)-elicited white blood cell (WBC) transfusions in patients with neutropenia-related fungal infections. Adult patients with hematologic malignancies, absolute neutrophil counts (ANC) <500/μl and fungal infections refractory to amphotericin b, received daily transfusions of rg-csf-elicited and irradiated wbc transfusions from related donors. donors received 5 μg/kg/day of rg-csf subcutaneously. donors achieved a mean anc of 29.4 × 103 per microliter. The mean yield of neutrophils per transfusion was 41 × 109 (range, 10–116). Fifteen patients received a median of eight transfusions (range, 3–16). Fourteen patients had received rG-CSF for a median of 12 days. The median ANC baseline was 20/μl. Eleven patients had favorable responses and eight of them remained free of infection 3 weeks after therapy. Favorable responses occurred among patients with better Zubrod performance status (median, 3 vs 4) and shorter duration of both profound neutropenia (median, 15 vs 25 days) and active infection (median, 8 vs 17 days). The mean 1- and 24-h post-transfusion ANCs were 594/μl (range, 98–1472/μl) and 396/μl (range, 50–1475/μl), respectively. Adverse reactions were observed in nine of 35 donors and in the recipients of six of 130 transfusions. rG-CSF-elicited WBC transfusions may be a safe and promising approach for treating neutropenia-related fungal infections.


Cancer | 1970

Spindle-cell variant of squamous carcinoma. A light and electron microscopic study of 13 cases.

Benjamin Lichtiger; Bruce Mackay; Carl F. Tessmer

Thirteen spindle‐cell tumors of the upper respiratory tract, oral cavity, and skin of face have been studied with light and electron microscopy. Five were primary neoplasms, and 8 had recurred following radiation therapy. The primary lesions were superficially located, and, in light microscopic sections, sites of apparent continuity between tumor and overlying epithelium were observed. The electron micrographs demonstrated the presence in many tumor cells of aggregates of keratohyaline and slender bundles of tonofilaments, and occasional premelanosomes were seen. Desmosomes were present, but were few in number and poorly developed. No evidence could be found to support the concept of malignant connective tissue component. Findings justify designation of this group of tumors as spindle‐cell variants of squamous carcinomas.


Cancer | 2004

Impact of high-dose granulocyte transfusions in patients with cancer with candidemia: retrospective case-control analysis of 491 episodes of Candida species bloodstream infections.

Amar Safdar; Hend A. Hanna; Maha Boktour; Dimitrios P. Kontoyiannis; Ray Hachem; Benjamin Lichtiger; Emil J. Freireich; Issam Raad

The efficacy and feasibility of donor granulocyte transfusion therapy (GTX) have changed considerably over the past four decades. The authors sought to determine the impact of high‐dose (approximately 5.5 × 1010 cells) GTX in patients with candidemia.


Blood | 2011

Targeting neuropilin-1 in human leukemia and lymphoma

Katja Karjalainen; Diana E. Jaalouk; Carlos E. Bueso-Ramos; Amado J. Zurita; Akihiko Kuniyasu; Bedrich L. Eckhardt; Frank C. Marini; Benjamin Lichtiger; Susan O'Brien; Hagop M. Kantarjian; Jorge Cortes; Erkki Koivunen; Wadih Arap; Renata Pasqualini

Targeted drug delivery offers an opportunity for the development of safer and more effective therapies for the treatment of cancer. In this study, we sought to identify short, cell-internalizing peptide ligands that could serve as directive agents for specific drug delivery in hematologic malignancies. By screening of human leukemia cells with a combinatorial phage display peptide library, we isolated a peptide motif, sequence Phe-Phe/Tyr-Any-Leu-Arg-Ser (F(F)/(Y)XLRS), which bound to different leukemia cell lines and to patient-derived bone marrow samples. The motif was internalized through a receptor-mediated pathway, and we next identified the corresponding receptor as the transmembrane glycoprotein neuropilin-1 (NRP-1). Moreover, we observed a potent anti-leukemia cell effect when the targeting motif was synthesized in tandem to the pro-apoptotic sequence (D)(KLAKLAK)₂. Finally, our results confirmed increased expression of NRP-1 in representative human leukemia and lymphoma cell lines and in a panel of bone marrow specimens obtained from patients with acute lymphoblastic leukemia or acute myelogenous leukemia compared with normal bone marrow. These results indicate that NRP-1 could potentially be used as a target for ligand-directed therapy in human leukemias and lymphomas and that the prototype CGFYWLRSC-GG-(D)(KLAKLAK)₂ is a promising drug candidate in this setting.


Journal of Clinical Oncology | 1998

Costs of Blood Transfusion: A Process-Flow Analysis

Scott B. Cantor; David V. Hudson; Benjamin Lichtiger; Edward B. Rubenstein

PURPOSE To determine the cost of transfusing 2 units (U) of packed RBCs at a comprehensive cancer center. METHODS We performed a process-flow analysis to identify all costs of transfusing 2 U of allogeneic packed RBCs on an outpatient basis to patients with either (1) solid tumor who did not undergo bone marrow transplantation (BMT), (2) solid tumor who underwent BMT, (3) hematologic malignancy who did not undergo BMT, (4) hematologic malignancy who underwent allogeneic BMT, or (5) hematologic malignancy who underwent autologous BMT. We conducted structured interviews to determine the personnel time used and physical resources necessary at all steps of the transfusion process. RESULTS The mean cost of a 2-U transfusion of allogeneic packed RBCs was


Urology | 1991

Fibrin glue for partial nephrectomy

A. Keith Levinson; David A. Swanson; Frank J. Greskovich; Robert A. Stephenson; Benjamin Lichtiger

548,


Transfusion | 1998

Evaluation and comparison of three mobilization methods for the collection of granulocytes

David Jendiroba; Benjamin Lichtiger; Elias Anaissie; V. Reddy; Stephen J. O'Brien; H. Kantarjian; Emil J. Freireich

565,


Surgery | 2010

Two-surgeon technique of parenchymal transection contributes to reduced transfusion rate in patients undergoing major hepatectomy: Analysis of 1,557 consecutive liver resections

Martin Palavecino; Yoji Kishi; Yun S. Chun; David L. Brown; Vijaya Gottumukkala; Benjamin Lichtiger; Steven A. Curley; Eddie K. Abdalla; Jean Nicolas Vauthey

569,


Transfusion | 2002

Detecting bacteria in platelet concentrates by use of reagent strips

Jochewed Werch; Paulette Mhawech; C.E. Stager; E.I. Banez; Benjamin Lichtiger

569, and

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Fleur M. Aung

University of Texas MD Anderson Cancer Center

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Aida Narvios

University of Texas MD Anderson Cancer Center

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Emil J. Freireich

University of Texas MD Anderson Cancer Center

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Yang O. Huh

University of Texas MD Anderson Cancer Center

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Richard E. Champlin

University of Texas MD Anderson Cancer Center

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Virgil Reddy

University of Texas MD Anderson Cancer Center

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Benjamin Drewinko

University of Texas at Austin

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Fernando Martinez

University of Texas MD Anderson Cancer Center

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Saroj Vadhan-Raj

University of Texas MD Anderson Cancer Center

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Uday Popat

University of Texas MD Anderson Cancer Center

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