Pseudoprogression in patients with uterine leiomyosarcoma treated with first-line single-agent doxorubicin.

Disease progression Doxorubicin Leiomyosarcomas Pseudoprogression Radiological response Sarcomas Systemic therapy Uterine neoplasms

Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
10 2023
Historique:
received: 11 03 2023
revised: 13 07 2023
accepted: 24 07 2023
medline: 18 9 2023
pubmed: 22 8 2023
entrez: 21 8 2023
Statut: ppublish

Résumé

To evaluate the incidence of pseudoprogression in patients with metastatic or inoperable uterine leiomyosarcoma (LMS) treated with first-line single-agent doxorubicin. The Royal Marsden NHS Foundation Trust Sarcoma Unit database was searched to identify all patients with metastatic or inoperable LMS treated with first-line doxorubicin from January 2006 to January 2022. Patients with available computed tomography scans performed at baseline and during doxorubicin therapy were included. Response evaluation criteria in solid tumours v1.1 and Choi criteria were applied. Any increase in the sum of the longest diameter that decreased on the subsequent scan was labelled as pseudoprogression. The total number of patients evaluated was 52. In total, 19% (n = 10) of patients treated with doxorubicin showed pseudoprogression. However, pseudoprogression at the time of the second scan was not associated with time to doxorubicin failure. Choi criteria identified 30% (n = 3) of pseudoprogressors as responding. Despite the use of doxorubicin as first-line therapy for soft-tissue sarcomas for over 40 years, pseudoprogression has not been described. This retrospective study shows that pseudoprogression occurs in 19% of patients with metastatic/inoperable uterine LMS treated with first-line doxorubicin. Choi criteria were not consistently able to differentiate pseudoprogression from true progression. It is imperative that oncologists and radiologists are aware of this as symptomatically stable/improving patients may benefit from continued treatment despite initial radiological growth in tumour size.

Identifiants

pubmed: 37604068
pii: S0959-8049(23)00363-5
doi: 10.1016/j.ejca.2023.113261
pii:
doi:

Substances chimiques

Doxorubicin 80168379AG

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

113261

Subventions

Organisme : Department of Health
Pays : United Kingdom

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Lucy-Rose Howroyd (LR)

Royal Marsden Hospital, Fulham Road, London SW3 6JJ, UK. Electronic address: Rose.Howroyd@nhs.net.

Isabel Cornell (I)

Royal Marsden Hospital, Fulham Road, London SW3 6JJ, UK. Electronic address: Isabel.Cornell@nhs.net.

Charlotte Benson (C)

Royal Marsden Hospital, Fulham Road, London SW3 6JJ, UK.

Andrea Napolitano (A)

Royal Marsden Hospital, Fulham Road, London SW3 6JJ, UK.

Matthew Blackledge (M)

Institute of Cancer Research, 123 Old Brompton Road, London SW7 3RP, UK.

Timothy Sumhonmun (T)

Institute of Cancer Research, 123 Old Brompton Road, London SW7 3RP, UK.

Eleanor Moskovic (E)

Royal Marsden Hospital, Fulham Road, London SW3 6JJ, UK.

Christian Kelly-Morland (C)

Royal Marsden Hospital, Fulham Road, London SW3 6JJ, UK.

Margaret Adejolu (M)

Royal Marsden Hospital, Fulham Road, London SW3 6JJ, UK.

Robin L Jones (RL)

Royal Marsden Hospital, Fulham Road, London SW3 6JJ, UK; Institute of Cancer Research, 123 Old Brompton Road, London SW7 3RP, UK.

Christina Messiou (C)

Royal Marsden Hospital, Fulham Road, London SW3 6JJ, UK; Institute of Cancer Research, 123 Old Brompton Road, London SW7 3RP, UK. Electronic address: Christina.Messiou@rmh.nhs.uk.

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Classifications MeSH