Sunitinib administered prior to radiotherapy in patients with non-resectable glioblastoma: results of a Phase II study

Fecha de publicación:

Autores de IIS La Fe

Participantes ajenos a IIS La Fe

  • Balaña C
  • Perez P
  • Gallego O
  • Ribalta T
  • Capellades J
  • Gonzalez S
  • Verger E

Grupos

Abstract

Sunitinib is a tyrosine kinase inhibitor with direct anti-tumor and anti-angiogenesis activity targeting VEGFR 1-2, PDGFR alpha-beta, c-kit, bFGF, (CSF-1), FLT3 and RET. The present trial examined the activity of sunitinib in 12 patients with newly diagnosed, non-resectable glioblastoma. Patients (<= 75 years of age with performance status [PS] >= 2 and minimental status [MMS] >= 25) were treated post-biopsy with sunitinib 37.5 mg daily for 8 weeks pre-radiotherapy, during radiotherapy (60 Gy, 6 weeks) and post-radiotherapy until disease progression. The primary endpoints were overall response rate (ORR; RANO criteria) after 8 weeks of sunitinib and patient tolerance. Secondary endpoints were percentage of patients free of neurological deterioration pre-radiotherapy, percentage of patients completing radiotherapy, progression-free survival (PFS), overall survival (OS), and 1-year survival. A Simon 2-stage design (12 -> 20) based on ORR was applied to calculate the number of patients needed to detect at least 10 % response with a error of 0.05 and beta error of 0.10. The trial was closed because it did not meet minimal activity criteria. ORR was 0 % with only 1/12 patients (8.3%) achieving stable disease after sunitinib treatment. No patient showed reduction in gadolinium enhancement. The most frequent G3/4 toxicities were fatigue (24.9 %) and diarrhea (16.6 %); one patient died of a CNS hemorrhage; 10/12 patients (83.3 %) deteriorated neurologically before radiation therapy; median PFS was 7.7 weeks (95 % CI: 7.2-8.2); median OS was 12.8 weeks (95 % CI: 0.5-23.8 weeks); 1-year survival was 0 %. Sunitinib has no activity as monotherapy in glioblastoma, and further investigation of its efficacy in this setting is unwarranted.

Datos de la publicación

ISSN/ISSNe:
1776-2596, 1776-260X

TARGETED ONCOLOGY  SPRINGER

Tipo:
Article
Páginas:
321-329
Factor de Impacto:
1,405 SCImago
Cuartil:
Q1 SCImago

Citas Recibidas en Web of Science: 26

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Keywords

  • Glioblastoma; Sunitinib; Radiotherapy

Campos de estudio

Proyectos asociados

ESTUDIO RETROSPECTIVO DEL MANEJO DE PACIENTES CON CANCER DE PROSTATA HORMONORESISTENTE AVANZADO. ESTUDIO ESPRO.

Investigador Principal: GASPAR REYNES MUNTANER

SAN-DOC-2010-02 . 2011

ENSAYO CLINICO ABIERTO, FASE II DE TRATAMIENTO NEO-ADYUVANTE DE SUNITINIB (SU11248) PREVIO AL TRATAMIENTO CON IRRADIOACION Y CONCOMITANTE A LA MISMA EN PACIENTES CON GLIOBLASTOMA RPA V-VI Y SOLO BIOPSIA

Investigador Principal: GASPAR REYNES MUNTANER

GENOM-008 . 2009

ENSAYO CLÍNICO FASE II PILOTO, ABIERTO, MULTICÉNTRICO Y PROSPECTIVO PARA EVALUAR LA SEGURIDAD Y EFICACIA DE PF299804, UN INHIBIDOR PAN-HER IRREVERSIBLE, EN PACIENTES CON GLIOBLASTOMA RECURRENTE CON AMPLIFICACIÓN DE EGFR O PRESENCIA DE LA MUTACIÓN EGFRVIII .

Investigador Principal: GASPAR REYNES MUNTANER

GEINO-11 . 2012

ENSAYO CLINICO, FASE II ALEATORIZADO DE TRATAMIENTO NEO-ADYUVANTE CON DOS CICLOS DE TEMOZOLOMIDA A DOSIS EXTENDIDAS, PREVIOS AL TRATAMIENTO CON TEMOZOLOMIDA MAS IRRADIACION Y POSTERIOR ADYUVANCIA CON TEMOZOLOMIDA VERSUS MISMO TRATAMIENTO CON BEVACIZUMAB

Investigador Principal: GASPAR REYNES MUNTANER

GENOM-009 . 2010

EVALUACIÓN Y VALIDACIÓN DE LOS FACTORES DE RIESGO DE COMPLICACIONES EN PACIENTES APARENTEMENTE ESTABLES CON NEUTROPENIA FEBRIL Y TUMORES SÓLIDOS.

Investigador Principal: GASPAR REYNES MUNTANER

FINITE-RISK

ESTUDIO POSTAUTORIZACIONAL, MULTICÉNTRICO, OBSERVACIONAL, RETROSPECTIVO PARA EVALUAR LA EFICACIA, SEGURIDAD Y TOLERABILIDAD DE LACOSAMIDA COMO FÁRMACO ANTICONVULSIVANTE EN PACIENTES CON CRISIS SECUNDARIAS A TUMOR CEREBRAL.

Investigador Principal: GASPAR REYNES MUNTANER

FPC-LAC-2013-01

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