Myeloablative anti-CD20 radioimmunotherapy +/- high-dose chemotherapy followed by autologous stem cell support for relapsed/refractory B-cell lymphoma results in excellent long-term survival

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Myeloablative anti-CD20 radioimmunotherapy +/- high-dose chemotherapy followed by autologous stem cell support for relapsed/refractory B-cell lymphoma results in excellent long-term survival. / Wagner, Julia Y; Schwarz, Kathleen; Schreiber, Susanne; Schmidt, Burkhard; Wester, Hans-Jürgen; Schwaiger, Markus; Peschel, Christian; von Schilling, Christoph; Scheidhauer, Klemens; Keller, Ulrich.

in: ONCOTARGET, Jahrgang 4, Nr. 6, 01.06.2013, S. 899-910.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Wagner, JY, Schwarz, K, Schreiber, S, Schmidt, B, Wester, H-J, Schwaiger, M, Peschel, C, von Schilling, C, Scheidhauer, K & Keller, U 2013, 'Myeloablative anti-CD20 radioimmunotherapy +/- high-dose chemotherapy followed by autologous stem cell support for relapsed/refractory B-cell lymphoma results in excellent long-term survival', ONCOTARGET, Jg. 4, Nr. 6, S. 899-910.

APA

Wagner, J. Y., Schwarz, K., Schreiber, S., Schmidt, B., Wester, H-J., Schwaiger, M., Peschel, C., von Schilling, C., Scheidhauer, K., & Keller, U. (2013). Myeloablative anti-CD20 radioimmunotherapy +/- high-dose chemotherapy followed by autologous stem cell support for relapsed/refractory B-cell lymphoma results in excellent long-term survival. ONCOTARGET, 4(6), 899-910.

Vancouver

Bibtex

@article{c7eacea4ed53497393b7e907ac232c0f,
title = "Myeloablative anti-CD20 radioimmunotherapy +/- high-dose chemotherapy followed by autologous stem cell support for relapsed/refractory B-cell lymphoma results in excellent long-term survival",
abstract = "BACKGROUND: Radioimmunotherapy (RIT) has been used to treat relapsed/refractory CD20+ Non-Hodgkin lymphoma (NHL). Myeloablative anti-CD20 RIT followed by autologous stem cell infusion (ASCT) enables high radiation doses to lymphoma sites. We performed a phase I/II trial to assess feasibility and survival.METHODS: Twenty-three patients with relapsed/refractory NHL without complete remission (CR) to salvage chemotherapy were enrolled to evaluate RIT with Iodine-131 labelled rituximab (131I-rituximab) in a myeloablative setting. Biodistribution and dosimetric studies were performed to determine 131I activity required to induce a total body dose of 21-27Gy to critical organs. In 6/23 patients RIT was combined with high-dose chemotherapy. 8/23 patients received a sequential high-dose chemotherapy with a second ASCT. The median follow-up is 9.5 years.RESULTS: 6.956-19.425GBq of 131I was delivered to achieve the limiting organ dose to lungs or kidneys. No grade III/IV non-hematologic toxicity was seen with RIT alone. Significant grade III/IV toxicity (mucositis, fever, infection, one therapy related death) was observed in patients treated with RIT combined with high-dose chemotherapy. The overall response rate was 87% (64% CR). The median progression-free (PFS) and overall survival (OS) is 47.5 and 101.5 months. An international prognostic index score >1 was predictive for OS.CONCLUSION: Myeloablative RIT with 131I-rituximab followed by ASCT is feasible, well-tolerated and effective in high risk CD20+ NHL. Combination of RIT and high-dose chemotherapy increased toxicity significantly. Long-term results for PFS and OS are encouraging.",
keywords = "Adult, Aged, Antibodies, Monoclonal, Murine-Derived, Antineoplastic Combined Chemotherapy Protocols, Combined Modality Therapy, Disease-Free Survival, Female, Humans, Iodine Radioisotopes, Lymphoma, B-Cell, Male, Middle Aged, Neoplasm Recurrence, Local, Peripheral Blood Stem Cell Transplantation, Radioimmunotherapy, Radiopharmaceuticals, Risk Factors, Survival Analysis, Transplantation, Autologous",
author = "Wagner, {Julia Y} and Kathleen Schwarz and Susanne Schreiber and Burkhard Schmidt and Hans-J{\"u}rgen Wester and Markus Schwaiger and Christian Peschel and {von Schilling}, Christoph and Klemens Scheidhauer and Ulrich Keller",
year = "2013",
month = jun,
day = "1",
language = "English",
volume = "4",
pages = "899--910",
journal = "ONCOTARGET",
issn = "1949-2553",
publisher = "IMPACT JOURNALS LLC",
number = "6",

}

RIS

TY - JOUR

T1 - Myeloablative anti-CD20 radioimmunotherapy +/- high-dose chemotherapy followed by autologous stem cell support for relapsed/refractory B-cell lymphoma results in excellent long-term survival

AU - Wagner, Julia Y

AU - Schwarz, Kathleen

AU - Schreiber, Susanne

AU - Schmidt, Burkhard

AU - Wester, Hans-Jürgen

AU - Schwaiger, Markus

AU - Peschel, Christian

AU - von Schilling, Christoph

AU - Scheidhauer, Klemens

AU - Keller, Ulrich

PY - 2013/6/1

Y1 - 2013/6/1

N2 - BACKGROUND: Radioimmunotherapy (RIT) has been used to treat relapsed/refractory CD20+ Non-Hodgkin lymphoma (NHL). Myeloablative anti-CD20 RIT followed by autologous stem cell infusion (ASCT) enables high radiation doses to lymphoma sites. We performed a phase I/II trial to assess feasibility and survival.METHODS: Twenty-three patients with relapsed/refractory NHL without complete remission (CR) to salvage chemotherapy were enrolled to evaluate RIT with Iodine-131 labelled rituximab (131I-rituximab) in a myeloablative setting. Biodistribution and dosimetric studies were performed to determine 131I activity required to induce a total body dose of 21-27Gy to critical organs. In 6/23 patients RIT was combined with high-dose chemotherapy. 8/23 patients received a sequential high-dose chemotherapy with a second ASCT. The median follow-up is 9.5 years.RESULTS: 6.956-19.425GBq of 131I was delivered to achieve the limiting organ dose to lungs or kidneys. No grade III/IV non-hematologic toxicity was seen with RIT alone. Significant grade III/IV toxicity (mucositis, fever, infection, one therapy related death) was observed in patients treated with RIT combined with high-dose chemotherapy. The overall response rate was 87% (64% CR). The median progression-free (PFS) and overall survival (OS) is 47.5 and 101.5 months. An international prognostic index score >1 was predictive for OS.CONCLUSION: Myeloablative RIT with 131I-rituximab followed by ASCT is feasible, well-tolerated and effective in high risk CD20+ NHL. Combination of RIT and high-dose chemotherapy increased toxicity significantly. Long-term results for PFS and OS are encouraging.

AB - BACKGROUND: Radioimmunotherapy (RIT) has been used to treat relapsed/refractory CD20+ Non-Hodgkin lymphoma (NHL). Myeloablative anti-CD20 RIT followed by autologous stem cell infusion (ASCT) enables high radiation doses to lymphoma sites. We performed a phase I/II trial to assess feasibility and survival.METHODS: Twenty-three patients with relapsed/refractory NHL without complete remission (CR) to salvage chemotherapy were enrolled to evaluate RIT with Iodine-131 labelled rituximab (131I-rituximab) in a myeloablative setting. Biodistribution and dosimetric studies were performed to determine 131I activity required to induce a total body dose of 21-27Gy to critical organs. In 6/23 patients RIT was combined with high-dose chemotherapy. 8/23 patients received a sequential high-dose chemotherapy with a second ASCT. The median follow-up is 9.5 years.RESULTS: 6.956-19.425GBq of 131I was delivered to achieve the limiting organ dose to lungs or kidneys. No grade III/IV non-hematologic toxicity was seen with RIT alone. Significant grade III/IV toxicity (mucositis, fever, infection, one therapy related death) was observed in patients treated with RIT combined with high-dose chemotherapy. The overall response rate was 87% (64% CR). The median progression-free (PFS) and overall survival (OS) is 47.5 and 101.5 months. An international prognostic index score >1 was predictive for OS.CONCLUSION: Myeloablative RIT with 131I-rituximab followed by ASCT is feasible, well-tolerated and effective in high risk CD20+ NHL. Combination of RIT and high-dose chemotherapy increased toxicity significantly. Long-term results for PFS and OS are encouraging.

KW - Adult

KW - Aged

KW - Antibodies, Monoclonal, Murine-Derived

KW - Antineoplastic Combined Chemotherapy Protocols

KW - Combined Modality Therapy

KW - Disease-Free Survival

KW - Female

KW - Humans

KW - Iodine Radioisotopes

KW - Lymphoma, B-Cell

KW - Male

KW - Middle Aged

KW - Neoplasm Recurrence, Local

KW - Peripheral Blood Stem Cell Transplantation

KW - Radioimmunotherapy

KW - Radiopharmaceuticals

KW - Risk Factors

KW - Survival Analysis

KW - Transplantation, Autologous

M3 - SCORING: Journal article

C2 - 23765188

VL - 4

SP - 899

EP - 910

JO - ONCOTARGET

JF - ONCOTARGET

SN - 1949-2553

IS - 6

ER -