Outcome of SIOP patients with low- or intermediate-risk Wilms tumour relapsing after initial vincristine and actinomycin-D therapy only: the SIOP 93-01 and 2001 protocols

Purpose - Society of International Pediatric Oncology - Renal Tumor Study Group (SIOP-RTSG) treatment recommendations for relapsed Wilms tumour (WT) are stratified by the intensity of first-line treatment. To explore the evidence for the treatment of patients relapsing after vincristine and actinomy...

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Hauptverfasser: Groenendijk, Alissa (VerfasserIn) , van Tinteren, Harm (VerfasserIn) , Jiang, Yilin (VerfasserIn) , de Krijger, Ronald R. (VerfasserIn) , Vujanic, Gordan M. (VerfasserIn) , Godzinski, Jan (VerfasserIn) , Rübe, Christian (VerfasserIn) , Schenk, Jens-Peter (VerfasserIn) , Morosi, Carlo (VerfasserIn) , Pritchard-Jones, Kathy (VerfasserIn) , Al-Saadi, Reem (VerfasserIn) , Vaidya, Sucheta J. (VerfasserIn) , Verschuur, Arnauld C. (VerfasserIn) , Ramírez-Villar, Gema L. (VerfasserIn) , Graf, Norbert (VerfasserIn) , de Camargo, Beatriz (VerfasserIn) , Drost, Jarno (VerfasserIn) , Perotti, Daniela (VerfasserIn) , van den Heuvel-Eibrink, Marry M. (VerfasserIn) , Brok, Jesper (VerfasserIn) , Spreafico, Filippo (VerfasserIn) , Mavinkurve-Groothuis, Annelies M. C. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 15 January 2022
In: European journal of cancer
Year: 2022, Jahrgang: 163, Pages: 88-97
ISSN:1879-0852
DOI:10.1016/j.ejca.2021.12.014
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.ejca.2021.12.014
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S0959804921012855
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Verfasserangaben:Alissa Groenendijk, Harm van Tinteren, Yilin Jiang, Ronald R. de Krijger, Gordan M. Vujanic, Jan Godzinski, Christian Rübe, Jens-Peter Schenk, Carlo Morosi, Kathy Pritchard-Jones, Reem Al-Saadi, Sucheta J. Vaidya, Arnauld C. Verschuur, Gema L. Ramírez-Villar, Norbert Graf, Beatriz de Camargo, Jarno Drost, Daniela Perotti, Marry M. van den Heuvel-Eibrink, Jesper Brok, Filippo Spreafico, Annelies M.C. Mavinkurve-Groothuis
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Zusammenfassung:Purpose - Society of International Pediatric Oncology - Renal Tumor Study Group (SIOP-RTSG) treatment recommendations for relapsed Wilms tumour (WT) are stratified by the intensity of first-line treatment. To explore the evidence for the treatment of patients relapsing after vincristine and actinomycin-D (VA) treatment for primary WT, we retrospectively evaluated rescue treatment and survival of this patient group. - Patients and methods - We included 109 patients with relapse after VA therapy (no radiotherapy) for stage I-II primary low- or intermediate-risk WT from the SIOP 93-01 and SIOP 2001 studies. Univariate Cox regression analysis was performed to study the effect of relapse treatment intensity on event-free survival (EFS) and overall survival (OS). Relapse treatment intensity was classified into vincristine, actinomycin-D, and either doxorubicin or epirubicin (VAD), and more intensive therapies (ifosfamide/carboplatin/etoposide [ICE]/≥ 4 drugs/high-dose chemotherapy with haematopoietic stem cell transplantation [HD HSCT]). - Results - Relapse treatment regimens included either VAD, or cyclophosphamide/carboplatin/etoposide/doxorubicin (CyCED), or ICE backbones. Radiotherapy was administered in 62 patients and HD HSCT in 15 patients. Overall, 5-year EFS and OS after relapse were 72.3% (95% confidence interval [CI]: 64.0-81.6%) and 79.3% (95% CI: 71.5-88.0%), respectively. Patients treated with VAD did not fare worse when compared with patients treated with more intensive therapies (hazard ratio EFS: 0.611 [95% CI: 0.228-1.638] [p-value = 0.327] and hazard ratio OS: 0.438 [95% CI: 0.126-1.700] [p-value = 0.193]). - Conclusion - Patients with relapsed WT after initial VA-only treatment showed no inferior EFS and OS when treated with VAD regimens compared with more intensive rescue regimens. A subset of patients relapsing after VA may benefit from less intensive rescue treatment than ICE/CyCED-based regimens and deserve to be pinpointed by identifying additional (molecular) prognostic factors in future studies.
Beschreibung:Gesehen am 01.07.2022
Beschreibung:Online Resource
ISSN:1879-0852
DOI:10.1016/j.ejca.2021.12.014