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Managing relapsed refractory lymphoma with palliative oral chemotherapy: A multicentre retrospective study

PEP‐C (prednisolone, etoposide, procarbazine and cyclophosphamide) is an orally administered daily chemotherapy regimen used with palliative intent in relapsed refractory lymphoma. To our knowledge, no data on PEP‐C have been reported since the original group described the regimen. Here we present a...

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Autores principales: Bulley, Simon J., Santarsieri, Anna, Lentell, Isabel C., O'Sullivan, Brendan, Hodson, Andrew, Firth, Oliver, Sadullah, Shalal, Follows, Annabel M., Karanth, Mamatha, Min, Sandra Young, Fowler, Alexis, Russell, James, Uttenthal, Benjamin J., Hodson, Daniel J., Follows, George A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713053/
https://www.ncbi.nlm.nih.gov/pubmed/36467809
http://dx.doi.org/10.1002/jha2.537
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author Bulley, Simon J.
Santarsieri, Anna
Lentell, Isabel C.
O'Sullivan, Brendan
Hodson, Andrew
Firth, Oliver
Sadullah, Shalal
Follows, Annabel M.
Karanth, Mamatha
Min, Sandra Young
Fowler, Alexis
Russell, James
Uttenthal, Benjamin J.
Hodson, Daniel J.
Follows, George A.
author_facet Bulley, Simon J.
Santarsieri, Anna
Lentell, Isabel C.
O'Sullivan, Brendan
Hodson, Andrew
Firth, Oliver
Sadullah, Shalal
Follows, Annabel M.
Karanth, Mamatha
Min, Sandra Young
Fowler, Alexis
Russell, James
Uttenthal, Benjamin J.
Hodson, Daniel J.
Follows, George A.
author_sort Bulley, Simon J.
collection PubMed
description PEP‐C (prednisolone, etoposide, procarbazine and cyclophosphamide) is an orally administered daily chemotherapy regimen used with palliative intent in relapsed refractory lymphoma. To our knowledge, no data on PEP‐C have been reported since the original group described the regimen. Here we present a multicentre retrospective cohort reporting our use of PEP‐C in 92 patients over an 8‐year period. We find that even heavily pretreated lymphoma can respond to PEP‐C, particularly low‐grade lymphoma (including mantle cell) and lymphoma that was sensitive to the previous line of systemic therapy (chemosensitive). These characteristics may help in the selection of patients likely to derive benefit. The median overall survival of patients with chemosensitive lymphoma treated with PEP‐C is 217 days. Within the limitations of a retrospective cohort, we find that PEP‐C is well tolerated: the most common toxicity leading to discontinuation is marrow suppression. We suggest that PEP‐C should be considered for patients with relapsed refractory lymphoma in two settings: first, where there is no licensed alternative; and second, where the licensed alternative is an intravenous drug and the patient would prefer to choose an oral chemotherapy option.
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spelling pubmed-97130532022-12-02 Managing relapsed refractory lymphoma with palliative oral chemotherapy: A multicentre retrospective study Bulley, Simon J. Santarsieri, Anna Lentell, Isabel C. O'Sullivan, Brendan Hodson, Andrew Firth, Oliver Sadullah, Shalal Follows, Annabel M. Karanth, Mamatha Min, Sandra Young Fowler, Alexis Russell, James Uttenthal, Benjamin J. Hodson, Daniel J. Follows, George A. EJHaem Short Reports PEP‐C (prednisolone, etoposide, procarbazine and cyclophosphamide) is an orally administered daily chemotherapy regimen used with palliative intent in relapsed refractory lymphoma. To our knowledge, no data on PEP‐C have been reported since the original group described the regimen. Here we present a multicentre retrospective cohort reporting our use of PEP‐C in 92 patients over an 8‐year period. We find that even heavily pretreated lymphoma can respond to PEP‐C, particularly low‐grade lymphoma (including mantle cell) and lymphoma that was sensitive to the previous line of systemic therapy (chemosensitive). These characteristics may help in the selection of patients likely to derive benefit. The median overall survival of patients with chemosensitive lymphoma treated with PEP‐C is 217 days. Within the limitations of a retrospective cohort, we find that PEP‐C is well tolerated: the most common toxicity leading to discontinuation is marrow suppression. We suggest that PEP‐C should be considered for patients with relapsed refractory lymphoma in two settings: first, where there is no licensed alternative; and second, where the licensed alternative is an intravenous drug and the patient would prefer to choose an oral chemotherapy option. John Wiley and Sons Inc. 2022-09-02 /pmc/articles/PMC9713053/ /pubmed/36467809 http://dx.doi.org/10.1002/jha2.537 Text en © 2022 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Reports
Bulley, Simon J.
Santarsieri, Anna
Lentell, Isabel C.
O'Sullivan, Brendan
Hodson, Andrew
Firth, Oliver
Sadullah, Shalal
Follows, Annabel M.
Karanth, Mamatha
Min, Sandra Young
Fowler, Alexis
Russell, James
Uttenthal, Benjamin J.
Hodson, Daniel J.
Follows, George A.
Managing relapsed refractory lymphoma with palliative oral chemotherapy: A multicentre retrospective study
title Managing relapsed refractory lymphoma with palliative oral chemotherapy: A multicentre retrospective study
title_full Managing relapsed refractory lymphoma with palliative oral chemotherapy: A multicentre retrospective study
title_fullStr Managing relapsed refractory lymphoma with palliative oral chemotherapy: A multicentre retrospective study
title_full_unstemmed Managing relapsed refractory lymphoma with palliative oral chemotherapy: A multicentre retrospective study
title_short Managing relapsed refractory lymphoma with palliative oral chemotherapy: A multicentre retrospective study
title_sort managing relapsed refractory lymphoma with palliative oral chemotherapy: a multicentre retrospective study
topic Short Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713053/
https://www.ncbi.nlm.nih.gov/pubmed/36467809
http://dx.doi.org/10.1002/jha2.537
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