Literature DB >> 19543851

Atypical choroid plexus papilloma: clinical experience in the CPT-SIOP-2000 study.

Brigitte Wrede1, Martin Hasselblatt2, Ove Peters1, Peter F Thall3, Tezer Kutluk4, Albert Moghrabi5, Anita Mahajan6, Stefan Rutkowski7, Blanca Diez8, Xuemei Wang3, Torsten Pietsch9, Rolf-Dieter Kortmann10, Werner Paulus2, Astrid Jeibmann2, Johannes E A Wolff11,12,13.   

Abstract

Atypical choroid plexus papilloma (APP) represents a novel intermediate-grade subtype of choroid plexus tumor (CPT), the clinical outcome of which has not been described yet. We present the first analysis of a group of APP patients enrolled in the ongoing CPT-SIOP-2000 study of CPTs. A worldwide registration and a randomized trial for those patients who require chemotherapy started in 2000. For APP, maximal surgical resection was recommended. After surgery, patients who had undergone complete resection were observed, whereas patients with incompletely resected or metastasized APP were treated with six chemotherapy courses (etoposide and vincristine, combined with either carboplatin or cyclophosphamide). Risk-adapted radiotherapy was given only to patients older than 3 years of age. Of the 106 patients with a centrally confirmed CPT histology, 30 had APP, 42 CPP and 34 CPC. APP patients were significantly younger (median = 0.7 years) than patients with CPP or CPC (both medians = 2.3 years). Complete resection was achieved in 68 (64%) patients (79% in CPP, 63% in APP, and 47% in CPC). Metastases were present at diagnosis in 17% of APP patients, 5% of CPP patients, and 21% of CPC patients. All nine APP patients who received postoperative chemotherapy showed an early response after two cycles: two had complete remission, four had partial response, and three had stable disease. In the observation group of 15 patients, one event was seen, and all patients were alive. In the treatment group, one patient with a metastasized tumor and incompletely resected APP died. While APP was defined histologically, median percentages of both the Ki-67/MIB-1 proliferation marker and the p53 tumor suppressor protein increased across the three histological subtypes (from CPP to APP and then CPC), suggesting that the subtypes comprise an ordinal categorization of increasingly severe CPT tumors. This ordering was reiterated by clinical outcome in the 92 patients treated per the study protocol, with 5-year EFS rates of 92% in 39 CPP patients, 83% in 24 APP patients, and 28% in 29 CPC patients. A similar ordering was seen when all 106 patients were evaluated for EFS. APP responded favorably to chemotherapy. The intermediate position of APP between CPP and CPC was supported by the clinical data.

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Year:  2009        PMID: 19543851      PMCID: PMC5637399          DOI: 10.1007/s11060-009-9936-y

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  45 in total

1.  Radiation therapy and survival in choroid plexus carcinoma.

Authors:  J E Wolff; M Sajedi; M J Coppes; R A Anderson; R M Egeler
Journal:  Lancet       Date:  1999-06-19       Impact factor: 79.321

2.  Malignant evolution of choroid plexus papilloma.

Authors:  E Chow; J J Jenkins; P C Burger; D A Reardon; J W Langston; R A Sanford; R L Heideman; L E Kun; T E Merchant
Journal:  Pediatr Neurosurg       Date:  1999-09       Impact factor: 1.162

Review 3.  Choroid plexus carcinoma of childhood.

Authors:  R J Packer; G Perilongo; D Johnson; L N Sutton; G Vezina; R A Zimmerman; J Ryan; G Reaman; L Schut
Journal:  Cancer       Date:  1992-01-15       Impact factor: 6.860

Review 4.  Evidence of therapeutic efficacy of CCNU in recurrent choroid plexus papilloma.

Authors:  J Valencak; W Dietrich; M Raderer; K Dieckmann; D Prayer; J A Hainfellner; C Marosi
Journal:  J Neurooncol       Date:  2000-09       Impact factor: 4.130

5.  Diffuse craniospinal seeding from a benign fourth ventricle choroid plexus papilloma. Case report.

Authors:  R Leblanc; S Bekhor; D Melanson; S Carpenter
Journal:  J Neurosurg       Date:  1998-04       Impact factor: 5.115

6.  Chemotherapy improves the survival of patients with choroid plexus carcinoma: a meta-analysis of individual cases with choroid plexus tumors.

Authors:  Brigitte Wrede; Ping Liu; Johannes Ernst Alexander Wolff
Journal:  J Neurooncol       Date:  2007-06-19       Impact factor: 4.130

7.  Response of a recurrent choroid plexus tumor to combination chemotherapy.

Authors:  B L Maria; M L Graham; L C Strauss; M D Wharam
Journal:  J Neurooncol       Date:  1985       Impact factor: 4.130

Review 8.  Carcinoma of the choroid plexus: a pediatric experience.

Authors:  J Y Pierga; C Kalifa; M J Terrier-Lacombe; J L Habrand; J Lemerle
Journal:  Med Pediatr Oncol       Date:  1993

9.  Malignant progression in choroid plexus papillomas.

Authors:  Astrid Jeibmann; Brigitte Wrede; Ove Peters; Johannes E Wolff; Werner Paulus; Martin Hasselblatt
Journal:  J Neurosurg       Date:  2007-09       Impact factor: 5.115

10.  Metastatic choroid plexus papilloma: a case report.

Authors:  Andrew W McEvoy; Malcolm Galloway; Thomas Revesz; Neil D Kitchen
Journal:  J Neurooncol       Date:  2002-02       Impact factor: 4.130

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  38 in total

1.  Estimating progression-free survival in paediatric brain tumour patients when some progression statuses are unknown.

Authors:  Ying Yuan; Peter F Thall; Johannes E Wolff
Journal:  J R Stat Soc Ser C Appl Stat       Date:  2012-01-01       Impact factor: 1.864

2.  Regional distribution and cell type-specific subcellular localization of Prothymosin alpha in brain.

Authors:  Sebok Kumar Halder; Hiroshi Ueda
Journal:  Cell Mol Neurobiol       Date:  2011-07-13       Impact factor: 5.046

3.  Bevacizumab use in disseminated choroid plexus papilloma.

Authors:  Mark Daniel Anderson; Brett J Theeler; Marta Penas-Prado; Morris D Groves; W K Alfred Yung
Journal:  J Neurooncol       Date:  2013-06-13       Impact factor: 4.130

4.  A unique presentation of an adolescent with disseminated atypical choroid plexus papilloma.

Authors:  R N Rivière; D L Johnston; E Story
Journal:  J Neurooncol       Date:  2018-05-16       Impact factor: 4.130

5.  Uncommon low-grade brain tumors.

Authors:  Thankamma Ajithkumar; Naduni Imbulgoda; Elliott Rees; Fiona Harris; Gail Horan; Amos Burke; Sarah Jefferies; Stephen Price; Justin Cross; Kieren Allinson
Journal:  Neuro Oncol       Date:  2019-02-14       Impact factor: 12.300

6.  Methylation of the hTERT promoter is frequent in choroid plexus tumors but not of independent prognostic value.

Authors:  Vincent Ruland; Stefan Hartung; Uwe Kordes; Johannes E Wolff; Werner Paulus; Martin Hasselblatt
Journal:  J Neurooncol       Date:  2014-05-14       Impact factor: 4.130

7.  Choroid plexus tumor epidemiology and outcomes: implications for surgical and radiotherapeutic management.

Authors:  Donald M Cannon; Pranshu Mohindra; Vinai Gondi; Tim J Kruser; Kevin R Kozak
Journal:  J Neurooncol       Date:  2014-10-01       Impact factor: 4.130

8.  Cross-Species Genomics Identifies TAF12, NFYC, and RAD54L as Choroid Plexus Carcinoma Oncogenes.

Authors:  Yiai Tong; Diana Merino; Birgit Nimmervoll; Kirti Gupta; Yong-Dong Wang; David Finkelstein; James Dalton; David W Ellison; Xiaotu Ma; Jinghui Zhang; David Malkin; Richard J Gilbertson
Journal:  Cancer Cell       Date:  2015-05-11       Impact factor: 31.743

9.  The role of chemotherapy and surgical removal in the treatment of Choroid Plexus carcinomas and atypical papillomas.

Authors:  Annalisa Passariello; Maria Tufano; Pietro Spennato; Lucia Quaglietta; Antonio Verrico; Roberta Migliorati; Giuseppe Cinalli
Journal:  Childs Nerv Syst       Date:  2015-04-12       Impact factor: 1.475

10.  Central nervous system tumors in the first year of life: a clinical and pathologic experience from a single cancer center.

Authors:  Maysa Al-Hussaini; Maisa Swaidan; Usama Al-Jumaily; Awni Musharbash
Journal:  Childs Nerv Syst       Date:  2013-03-24       Impact factor: 1.475

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