David J. Straus

ORCID: 0000-0001-8364-6816
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About
Contact & Profiles
Research Areas
  • Lymphoma Diagnosis and Treatment
  • Chronic Lymphocytic Leukemia Research
  • Lung Cancer Treatments and Mutations
  • Viral-associated cancers and disorders
  • CNS Lymphoma Diagnosis and Treatment
  • Cutaneous lymphoproliferative disorders research
  • CAR-T cell therapy research
  • Chronic Myeloid Leukemia Treatments
  • T-cell and Retrovirus Studies
  • HER2/EGFR in Cancer Research
  • Acute Lymphoblastic Leukemia research
  • Multiple and Secondary Primary Cancers
  • Medical Imaging Techniques and Applications
  • Monoclonal and Polyclonal Antibodies Research
  • Cancer Genomics and Diagnostics
  • PARP inhibition in cancer therapy
  • Histone Deacetylase Inhibitors Research
  • Ovarian cancer diagnosis and treatment
  • Cancer Treatment and Pharmacology
  • Radiopharmaceutical Chemistry and Applications
  • Protein Degradation and Inhibitors
  • Neutropenia and Cancer Infections
  • Immune Cell Function and Interaction
  • Sarcoma Diagnosis and Treatment
  • Childhood Cancer Survivors' Quality of Life

Memorial Sloan Kettering Cancer Center
2016-2025

Cornell University
2009-2024

Kettering University
2020-2023

University of California, San Diego
2021

Weill Cornell Medicine
2018

Leukemia and Lymphoma Society
2005-2017

University of Rochester Medical Center
2016

Fred Hutch Cancer Center
2016

Cancer Research Center
2016

NewYork–Presbyterian Hospital
2016

Brentuximab vedotin is an anti-CD30 antibody-drug conjugate that has been approved for relapsed and refractory Hodgkin's lymphoma.We conducted open-label, multicenter, randomized phase 3 trial involving patients with previously untreated stage III or IV classic lymphoma, in which 664 were assigned to receive brentuximab vedotin, doxorubicin, vinblastine, dacarbazine (A+AVD) 670 bleomycin, (ABVD). The primary end point was modified progression-free survival (the time progression, death,...

10.1056/nejmoa1708984 article EN New England Journal of Medicine 2017-12-10

To determine the antitumor activity of novel proteasome inhibitor bortezomib in patients with indolent and mantle-cell lymphoma (MCL).Patients MCL were eligible. Bortezomib was given at a dose 1.5 mg/m2 on days 1, 4, 8, 11. Patients required to have received no more than three prior chemotherapy regimens, least 1 month since treatment, 3 months from rituximab, 7 corticosteroids; absolute neutrophil count 1,500/microL (500/microL if documented bone marrow involvement); platelet...

10.1200/jco.2005.02.050 article EN Journal of Clinical Oncology 2004-12-22

Abstract Nonparametric maximum likelihood estimation of the probability failing from a particular cause by time t in presence other acting causes (i.e., cause-specific failure probability) is discussed. A commonly used incorrect approach to take 1 minus Kaplan-Meier (KM) estimator (1 – KM), whereby patients who fail extraneous are treated as censored observations. Examples showing extent bias using 1-KM presented clinical oncology data. This can be quite large if data uncensored or...

10.1080/01621459.1993.10476289 article EN Journal of the American Statistical Association 1993-06-01

PURPOSE In studies of diffuse large B-cell lymphoma, positron emission tomography with [(18)F]fluorodeoxyglucose (FDG-PET) performed after two to four cycles chemotherapy has demonstrated prognostic significance. However, some patients treated immunochemotherapy experience a favorable long-term outcome despite positive interim FDG-PET scan. To clarify the significance scans, we prospectively studied FDG-positive disease within risk-adapted sequential program. PATIENTS AND METHODS From March...

10.1200/jco.2009.26.5942 article EN Journal of Clinical Oncology 2010-03-09

Purpose Four US National Clinical Trials Network components (Southwest Oncology Group, Cancer and Leukemia Group B/Alliance, Eastern Cooperative the AIDS Malignancy Consortium) conducted a phase II Intergroup clinical trial that used early interim fluorodeoxyglucose positron emission tomography (FDG-PET) imaging to determine utility of response-adapted therapy for stage III IV classic Hodgkin lymphoma. Patients Methods The Southwest S0816 (Fludeoxyglucose F 18-PET/CT Imaging Combination...

10.1200/jco.2015.63.1119 article EN Journal of Clinical Oncology 2016-04-12

Five-year follow-up in a trial involving patients with previously untreated stage III or IV classic Hodgkin's lymphoma showed long-term progression-free survival benefits first-line therapy brentuximab vedotin, CD30-directed antibody–drug conjugate, plus doxorubicin, vinblastine, and dacarbazine (A+AVD), as compared bleomycin, (ABVD). A planned interim analysis indicated potential benefit regard to overall survival; data from median of 6 years are now available.

10.1056/nejmoa2206125 article EN New England Journal of Medicine 2022-07-13

We conducted a phase II study evaluating pembrolizumab plus gemcitabine, vinorelbine, and liposomal doxorubicin (pembro-GVD) as second-line therapy for relapsed or refractory (rel/ref) classical Hodgkin lymphoma (cHL) (ClinicalTrials.gov identifier: NCT03618550).Transplant eligible patients with rel/ref cHL following first-line were treated two to four cycles of (200 mg intravenous [IV], day 1), gemcitabine (1,000 mg/m2 IV, days 1 8), vinorelbine (20 (15 mg/m2, given on 21-day cycles. The...

10.1200/jco.21.01056 article EN Journal of Clinical Oncology 2021-06-25

Patients with follicular lymphoma (FL) frequently require multiple treatments during their disease course; however, survival based on lines of treatment remains poorly described in the post-rituximab era. Also, Follicular Lymphoma International Prognostic Index (FLIPI) score was developed to predict at diagnosis, yet it unknown whether increase FLIPI following an initial observation period is associated less-favorable outcomes. To address these knowledge gaps, we retrospectively studied 1088...

10.1038/s41408-020-00340-z article EN cc-by Blood Cancer Journal 2020-07-17

This study investigated the efficacy, toxicity, and pharmacokinetic interactions resulting from simultaneous combination chemotherapy highly active antiretroviral therapy (HAART) for patients with human immunodeficiency virus (HIV)-associated non-Hodgkin's lymphoma (NHL). In addition, effects on viral load, CD4 counts, opportunistic infections were examined use of combined HAART.Sixty-five previously untreated measurable disease at any stage HIV-associated NHL intermediate or high grade...

10.1200/jco.2001.19.8.2171 article EN Journal of Clinical Oncology 2001-04-15

PURPOSE This phase III, placebo-controlled, randomized trial was designed to investigate efficacy and safety of two doses denileukin diftitox (DD; DAB(389)-interleukin-2 [IL-2]), a recombinant fusion protein targeting IL-2 receptor-expressing malignant T lymphocytes, in patients with stage IA CD25 assay-positive cutaneous T-cell lymphoma (CTCL), including the mycosis fungoides Sézary syndrome forms disease, who had received up three prior therapies. The primary end point overall response...

10.1200/jco.2009.26.2386 article EN Journal of Clinical Oncology 2010-03-09

Review of prognostic factors at Memorial Hospital in New York City has shown that adult patients with large-cell lymphoma (diffuse histiocytic by Rappaport classification) who have high lactic dehydrogenase (LDH) and/or bulky mediastinal or abdominal disease are destined to do poorly conventional combination chemotherapy, a 2-year disease-free survival about 20%. Patients relapse after chemotherapy similar poor prognosis. Thirty-one such were studied evaluate the efficacy intensive...

10.1200/jco.1988.6.8.1303 article EN Journal of Clinical Oncology 1988-08-01

Limited data exist regarding the activity of bendamustine in Hodgkin lymphoma (HL). This phase II study evaluated efficacy relapsed and refractory HL.Patients with HL who were ineligible for autologous stem-cell transplantation (ASCT), or whom this treatment failed, received 120 mg/m(2) as a 30-minute infusion on days 1 2 every 28 growth factor support. The primary end point was overall response rate (ORR). A secondary referral to allogeneic (alloSCT) patients deemed eligible alloSCT at time...

10.1200/jco.2012.45.3308 article EN Journal of Clinical Oncology 2012-12-18

The initial promising results with alternating chemotherapy regimens (mechlorethamine, vincristine, procarbazine, and prednisone/doxorubicin, bleomycin, vinblastine, dacarbazine [MOPP/ABVD]; lomustine, melphalan, vindesine [CAD] plus MOPP ABV) combined intermediate-dose radiation therapy (RT) have been sustained further follow-up; 82.2% of patients (152 185) achieved a complete remission (CR), overall survival is 71.7% +/- 4.4% at 8 years (median follow-up 55 months among the survivors). No...

10.1200/jco.1990.8.7.1173 article EN Journal of Clinical Oncology 1990-07-01
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