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Dive into the research topics where Carol Burian is active.

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Featured researches published by Carol Burian.


Journal of Clinical Oncology | 2003

Extended Follow-Up of Patients With Hairy Cell Leukemia After Treatment With Cladribine

Grant R. Goodman; Carol Burian; James A. Koziol; Alan Saven

PURPOSE Hairy cell leukemia (HCL) is an uncommon, indolent, chronic B-cell lymphoproliferative disorder involving the marrow and spleen. Therapy for HCL includes splenectomy, interferon alfa-2a and alfa-2b, pentostatin, and cladribine. The purpose of this article was to report the extended follow-up of HCL patients treated with cladribine. PATIENTS AND METHODS Two hundred nine patients with HCL who were treated with cladribine had at least 7 years of follow-up. A course of cladribine constituted a 7-day continuous intravenous infusion at a dose of 0.1 mg/kg/d. RESULTS Of the 207 assessable patients who had at least 7 years of follow-up, 196 (95%) achieved a complete response (CR) and 11 (5%) achieved a partial response (PR) after a single course of cladribine (overall response rate, 100%). The median first-response duration for all responders was 98 months. Seventy-six patients (37%) experienced relapse after their first course of cladribine. The median time to first relapse for all responders was 42 months. Time to treatment failure of CRs compared with PRs was statistically significant (P <.0005). The overall survival rate was 97% recorded at 108 months. Forty-seven patients developed 58 second malignancies. The observed-to-expected ratio for second malignancies was 2.03 (95% confidence interval, 1.49 to 2.71). CONCLUSION These results confirm previous observations that single courses of cladribine administered to patients with HCL induce high response rates, the majority of which are CRs. Most patients enjoy long-lasting complete remissions, and those patients who experience relapse can be successfully re-treated with cladribine.


British Journal of Haematology | 1998

Bolus administration of cladribine in the treatment of Waldenström macroglobulinaemia

Eva S. Liu; Carol Burian; William E. Miller; Alan Saven

This phase II clinical trial evaluated bolus cladribine as a single agent in Waldenström macroglobulinaemia (WM).


Blood | 2010

Very long-term eradication of minimal residual disease in patients with hairy cell leukemia after a single course of cladribine

Darren Sigal; Robert W. Sharpe; Carol Burian; Alan Saven

Cladribine induces protracted remissions in patients with hairy cell leukemia (HCL). However, many long-term responders ultimately relapse. We sought to determine whether long-term complete responders subsequent to a single 7-day course of cladribine were without minimal residual disease (MRD) and potentially cured of HCL. From the 358-person Scripps Clinic cladribine database, we identified 19 patients in continuous and complete hematologic response (median age, 75 years; median time from diagnosis, 18 years; and median time from cladribine, 16 years). Nine of 19 (47%) patient samples had no evidence of residual disease; 7 of 19 (37%) samples had MRD; and 3 of 19 (16%) had morphologic evidence of HCL in hematoxylin and eosin-stained bone marrow sections. These results indicate that HCL is potentially curable after cladribine treatment. In addition, patients with MRD and even gross morphologic disease can live many years without manifesting hematologic relapses.


Blood | 2014

Clinical characteristics and long-term outcome of young hairy cell leukemia patients treated with cladribine: a single-institution series

Joshua D. Rosenberg; Carol Burian; Jill Waalen; Alan Saven

Hairy cell leukemia (HCL) is a rare, indolent B-cell disorder in which single courses of cladribine induce high rates of complete responses. We report on 88 young HCL patients (≤40 years of age at diagnosis) treated with cladribine from the Scripps Clinic HCL Database, of whom 83 were evaluable for response. Seventy-three patients (88%) achieved an initial complete response and 10 (12%) a partial response, with a median response duration of 57 months. Forty-eight patients (58%) relapsed, with a median time to first relapse for all responders of 54 months. Eight patients developed 11 second primary malignancies with an excess frequency of 1.60 (95% confidence interval, 0.80-2.89). Thirteen (15%) patients died with a mortality ratio compared with age-matched normals of 1.85 (95% confidence interval, 1.07-3.18). Median overall survival for all patients following the first cladribine course was 231 months, and 251 months from diagnosis. Single courses of cladribine induce high rates of complete and durable responses in the majority of young HCL patients and are therefore recommended for HCL patients regardless of age.


Blood | 1998

Long-term follow-up of patients with hairy cell leukemia after cladribine treatment

Alan Saven; Carol Burian; James A. Koziol; Lawrence D. Piro


Blood | 1999

Cladribine Activity in Adult Langerhans-Cell Histiocytosis

Alan Saven; Carol Burian


Blood | 1999

Filgrastim for Cladribine-Induced Neutropenic Fever in Patients With Hairy Cell Leukemia

Alan Saven; Carol Burian; Jasvant Adusumalli; James A. Koziol


Journal of Clinical Oncology | 2008

Potential curability of cladribine in selected patients with hairy cell leukemia

Darren Sigal; R. W. Sharpe; Carol Burian; Alan Saven


Blood | 2016

Drug Sensitivity Across Acute Myeloid Leukemia Subtypes Using an in Vitro Assay

Levanto Schachter; Irene M. Hutchins; Jill Waalen; Carol Burian; Darren Finlay; Kristiina Vuori; Giovanni Paternostro; Marin Feldman Xavier; Carrie Costantini; William E. Miller; Jeffrey Andrey; James Mason


Biology of Blood and Marrow Transplantation | 2016

Predictive Drug Sensitivity Testing with Patient-Derived Cultured Leukemia Cells

Richard Gopez Ancheta; Carol Burian; William E. Miller; Darren Finlay; Kristiina Vuori; Giovanni Paternostro; James Mason

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James A. Koziol

Scripps Research Institute

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