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Is radiotherapy required in first-line treatment of stage I diffuse anaplastic Wilms tumor? A report of SIOP-RTSG, AIEOP, JWiTS, and UKCCSG.
Fajardo, Raquel Dávila; van den Heuvel-Eibrink, Marry M; van Tinteren, Harm; Spreafico, Filippo; Acha, Thomas; Bergeron, Christophe; de Camargo, Beatriz; Oldenburger, Foppe; Rübe, Christian; Oue, Takaharu; Vokuhl, Christian; de Krijger, Ronald R; Vujanic, Gordan; Sebire, Neil; Coulomb-L'Hermine, Aurore; Collini, Paola; Gandola, Lorenza; Pritchard-Jones, Kathy; Graf, Norbert; Janssens, Geert O; van Grotel, Martine.
Affiliation
  • Fajardo RD; Department of Radiation Oncology, University Medical Centre Utrecht, Utrecht, The Netherlands.
  • van den Heuvel-Eibrink MM; Department of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • van Tinteren H; Department of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Spreafico F; Department of Statistics, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Acha T; Pediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Bergeron C; Department of Pediatric Oncology, Hospital Materno-Infantil, Málaga, Spain.
  • de Camargo B; Department of Pediatric Oncology, Centre Leon Berard, Lyon, France.
  • Oldenburger F; Department of Pediatric Hematology and Oncology, Instituto Nacional Do Cancer (INCA), Rio de Janeiro, Brazil.
  • Rübe C; Department of Radiation Oncology, Academic Medical Center, Amsterdam, The Netherlands.
  • Oue T; Department of Radio-Oncology, University Hospital of Saarland, Homburg, Germany.
  • Vokuhl C; Department of Pediatric Surgery, Hyogo College of Medicine, Nishinomiya City, Hyogo Prefecture, Osaka, Japan.
  • de Krijger RR; Institute of Pediatric Pathology, University of Kiel, Kiel, Germany.
  • Vujanic G; Department of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Sebire N; Department of Pathology, Sidra Medicine, Doha, Qatar.
  • Coulomb-L'Hermine A; Department of Histopathology, Great Ormond Street Hospital, London, UK.
  • Collini P; Department of Pathology, Hopitaux Universitaires Est Parisien, Paris, France.
  • Gandola L; Department of Pathology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Pritchard-Jones K; Department of Radiation Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Graf N; Institute of Child Health, University College London, London, UK.
  • Janssens GO; Department of Pediatric Oncology, University Hospital of Saarland, Homburg, Germany.
  • van Grotel M; Department of Radiation Oncology, University Medical Centre Utrecht, Utrecht, The Netherlands.
Pediatr Blood Cancer ; 67(2): e28039, 2020 02.
Article in En | MEDLINE | ID: mdl-31625685
ABSTRACT

BACKGROUND:

As a significant proportion of relapses occurred in the tumor bed or abdomen on patients with the fifth National Wilms Tumor Study stage I anaplastic Wilms tumor (WT), flank radiotherapy was added for stage I anaplastic WT in the subsequent study of the Children's Oncology Group (AREN0321). Preliminary results revealed reduction of relapse rate and improved survival. In cases treated with preoperative chemotherapy, such as in International Society of Pediatric Oncology (SIOP), the value of radiotherapy has never been studied. The aim of this observational study is to describe the pattern of recurrence and survival of patients with stage I diffuse anaplastic WT (DAWT) after induction chemotherapy.

METHODS:

Retrospective data analysis of the pattern of relapse and survival of all patients with stage I DAWT were included in recent SIOP, L'Associazone Italiana Ematologica Oncologia Pediatrica (AIEOP), Japan Wilms Tumor Study Group (JWiTS), United Kingdom Children's Cancer Study Group (UKCCSG) renal tumor registries. Postoperative treatment consisted of actinomycin D, vincristine, and doxorubicin for 28 weeks without local irradiation.

RESULTS:

One hundred nine cases with stage I DAWT were identified, of which 95 cases received preoperative chemotherapy. Of these, seven patients underwent preoperative true-cut biopsy. Sixteen of the 95 patients relapsed (17%), six locally, four at distant site, and six combined, and all treated according to SIOP 2001 relapse protocol, which resulted in a 5-year overall survival of 93%.

CONCLUSION:

Despite 13% locoregional relapse rate, an excellent rescue rate was achieved after salvage treatment, in patients with stage I DAWT whose first-line treatment comprised three-drug chemotherapy (including doxorubicin), without flank irradiation. Therefore, we continue not to advocate the use of radiotherapy in first-line treatment after preoperative chemotherapy in stage I DAWT in the next SIOP protocol.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antineoplastic Combined Chemotherapy Protocols / Wilms Tumor / Kidney Neoplasms Type of study: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child, preschool / Female / Humans / Infant / Male Language: En Journal: Pediatr Blood Cancer Journal subject: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Year: 2020 Type: Article Affiliation country: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antineoplastic Combined Chemotherapy Protocols / Wilms Tumor / Kidney Neoplasms Type of study: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child, preschool / Female / Humans / Infant / Male Language: En Journal: Pediatr Blood Cancer Journal subject: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Year: 2020 Type: Article Affiliation country: Netherlands