The relation of radiological tumor volume response to histological response and outcome in patients with localized Ewing Sarcoma.


Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
03 2019
Historique:
received: 22 08 2018
revised: 08 01 2019
accepted: 10 01 2019
pubmed: 23 2 2019
medline: 17 4 2020
entrez: 22 2 2019
Statut: ppublish

Résumé

Magnetic resonance imaging (MRI) is the modality of choice for local staging and response evaluation of Ewing sarcoma (EwS). Aim of this study was to determine the relevance of tumor volume response (TVR) in relation to histological response (HisRes) and survival, in order to evaluate if early modification of chemotherapy might be indicated in patients with inadequate TVR. Three dimensional (3D)-tumor volume data at diagnosis, during early induction phase (1-3 courses of chemotherapy; n = 195) and/or late induction phase (4-6 courses; n = 175) from 241 localized patients were retrospectively analyzed. A distinction was made between adequate response (reduction ≥67%) and inadequate response (reduction <67% or progression). Correlations between TVR, HisRes, event free survival (EFS), and overall survival (OS) were analyzed using chi-square tests, log-rank tests, and the Cox-regression model. Early adequate TVR, noted in 41% of patients, did not correlate with EFS (P = 0.92) or OS (P = 0.38). During late induction phase 62% of patients showed an adequate TVR. EFS for patients with late adequate TVR was better (78%) than for those with inadequate late TVR (61%) (P = 0.01); OS was 80% and 69% (P = 0.26), respectively. No correlation was found between TVR and HisRes. Multivariate analysis showed that poor HisRes, pelvic location and late inadequate TVR were associated with poor outcome. Early inadequate TVR does not predict adverse outcome; therefore, changing the treatment to second line chemotherapy is not indicated in case of inadequate early TVR. Late adequate TVR and good HisRes correlate with better EFS; patients with late inadequate TVR might benefit from augmented therapy.

Sections du résumé

BACKGROUND
Magnetic resonance imaging (MRI) is the modality of choice for local staging and response evaluation of Ewing sarcoma (EwS). Aim of this study was to determine the relevance of tumor volume response (TVR) in relation to histological response (HisRes) and survival, in order to evaluate if early modification of chemotherapy might be indicated in patients with inadequate TVR.
METHODS
Three dimensional (3D)-tumor volume data at diagnosis, during early induction phase (1-3 courses of chemotherapy; n = 195) and/or late induction phase (4-6 courses; n = 175) from 241 localized patients were retrospectively analyzed. A distinction was made between adequate response (reduction ≥67%) and inadequate response (reduction <67% or progression). Correlations between TVR, HisRes, event free survival (EFS), and overall survival (OS) were analyzed using chi-square tests, log-rank tests, and the Cox-regression model.
RESULTS
Early adequate TVR, noted in 41% of patients, did not correlate with EFS (P = 0.92) or OS (P = 0.38). During late induction phase 62% of patients showed an adequate TVR. EFS for patients with late adequate TVR was better (78%) than for those with inadequate late TVR (61%) (P = 0.01); OS was 80% and 69% (P = 0.26), respectively. No correlation was found between TVR and HisRes. Multivariate analysis showed that poor HisRes, pelvic location and late inadequate TVR were associated with poor outcome.
CONCLUSIONS
Early inadequate TVR does not predict adverse outcome; therefore, changing the treatment to second line chemotherapy is not indicated in case of inadequate early TVR. Late adequate TVR and good HisRes correlate with better EFS; patients with late inadequate TVR might benefit from augmented therapy.

Identifiants

pubmed: 30790456
doi: 10.1002/cam4.2002
pmc: PMC6434194
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1086-1094

Informations de copyright

© 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

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Auteurs

Lianne M Haveman (LM)

Emma Children's Hospital, Department of Pediatric Oncology, Academic Medical Center, Amsterdam, The Netherlands.
Prinses Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Andreas Ranft (A)

Department of Pediatric Hematology and Oncology, University of Essen, Essen, Germany.
Coordinating Center for Clinical Trials, Muenster, Germany.

Henk Vd Berg (H)

Emma Children's Hospital, Department of Pediatric Oncology, Academic Medical Center, Amsterdam, The Netherlands.

Anne Smets (A)

Department of Radiology, Academic Medical Center, Amsterdam, The Netherlands.

Jarmila Kruseova (J)

Department of Pediatric Oncology, University Hospital Motol, Prague, Czech Republic.

Ruth Ladenstein (R)

Children's Cancer Research Institute, Vienna, Austria.

Benedicte Brichard (B)

Saint Luc University Hospital, Department of Pediatric Hematology and Oncology, University of Louvain, Datteln, Belgium.

Michael Paulussen (M)

Witten/Herdecke University, Vestische Kinder- und Jugendklinik, Datteln, Germany.

Thomas Kuehne (T)

Department of Pediatric Oncology and Haematology, University Children Hospital, Basel, Switzerland.

Heribert Juergens (H)

Coordinating Center for Clinical Trials, Muenster, Germany.
Department of Pediatric Hematology and Oncology, University Children's Hospital, Muenster, Germany.

Stephanie Klco-Brosius (S)

Department of Pediatric Hematology and Oncology, University of Essen, Essen, Germany.
Coordinating Center for Clinical Trials, Muenster, Germany.

Uta Dirksen (U)

Department of Pediatric Hematology and Oncology, University of Essen, Essen, Germany.
Coordinating Center for Clinical Trials, Muenster, Germany.

Johannes H M Merks (JHM)

Emma Children's Hospital, Department of Pediatric Oncology, Academic Medical Center, Amsterdam, The Netherlands.

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