Second-look surgery for ependymoma: the Italian experience

Author:

Massimino Maura1,Solero Carlo Lazzaro2,Garrè Maria Luisa3,Biassoni Veronica1,Cama Armando2,Genitori Lorenzo4,Di Rocco Concezio5,Sardi Iacopo4,Viscardi Elisabetta6,Modena Piergiorgio7,Potepan Paolo8,Barra Salvina9,Scarzello Giovanni10,Galassi Ercole11,Giangaspero Felice12,Antonelli Manila12,Gandola Lorenza13

Affiliation:

1. Pediatric,

2. Neurosurgery Unit, Fondazione IRCCS Istituto Neurologico, Carlo Besta, Milano;

3. Neurosurgery Unit, IRCCS Giannina Gaslini, and

4. Neurosurgery Unit, Ospedale Meyer, Firenze;

5. Pediatric Neurosurgery, Policlinico A. Gemelli, Roma;

6. Pediatrics and

7. Molecular Biology Unit, Centro di Riferimento Oncologico, Aviano;

8. Radiology Units, Fondazione Istituto Di Ricovero e Cura a Carattere Scientifico (IRCCS) Istituto Nazionale Tumori, and

9. Radiotherapy Unit, Istituto Nazionale per la Ricerca sul Cancro, Genova;

10. Radiotherapy Unit, Istituto Oncologico del Veneto, Padova;

11. Neurosurgery, Ospedale Bellaria, Bologna; and

12. Neuropathology, Università La Sapienza, Roma, and Neuromed, Pozzilli, Italy

13. Radiotherapy, and

Abstract

Object Complete ependymoma resection ensures a better prognosis for children with this tumor, but the complete excision of infratentorial ependymomas involves serious risks. Second-look surgery for tumor remnants may be less harmful and enable complete removal. There is a potential, although still unclear, role for neoadjuvant chemotherapy in preparation for further surgery. Methods Since 1994, the authors have adopted two successive protocols for intracranial ependymoma, both including a phase of adjuvant chemotherapy for children with surgical tumor remnants with a plan for potential second-look surgery before radiotherapy. Results In the first protocol, 9 of 63 children underwent further surgery, and 6 became tumor free with no additional sequelae. Their prognosis for progression-free survival and freedom from local relapse was comparable to that of children who were operated on only once. In the second protocol, efforts were made to achieve complete resection and 29 of 110 patients underwent reoperations: 9 after the first surgery, 17 after chemotherapy, and 3 soon after radiotherapy. Fourteen of the 29 patients became tumor free, 1 of them with worsening neurological symptoms. The outcome of the 66 patients who became tumor free after 1 operation was compared with that of the 14 who became tumor free after reoperation. The 3-year progression-free survival of the 66 patients compared with the 14 other patients was 71.4% ± 6.9% and 90% ± 9.5%, respectively; the 3-year freedom from local relapse was 84.7% ± 5.9% and 90% ± 9.5%, respectively; and the 3-year overall survival was 85.9% ± 5.4% and 87.5% ± 11.7%, respectively. Conclusions Second-look surgery proved feasible with no major morbidity, and results improved with time. Local tumor control was comparable in patients undergoing 1 or more resections.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

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