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Discontinuation of first-line bevacizumab in metastatic colorectal cancer: the BEAWARE Italian Observational Study.
Lonardi, Sara; Nasti, Guglielmo; Fagnani, Daniele; Gemma, Donatello; Ciuffreda, Libero; Granetto, Cristina; Lucchesi, Sara; Ballestrero, Alberto; Biglietto, Maria; Proserpio, Ilaria; Bergamo, Francesca; Proietti, Emanuela; Tonini, Giuseppe.
Afiliación
  • Lonardi S; 1 UOC Oncologia Medica 1, Istituto Oncologico Veneto-IRCCS, Padova, Italy.
  • Nasti G; 2 Divisione di Oncologia Medica, Istituto Nazionale per lo Studio e la Cura dei Tumori "Fondazione Giovanni Pascale"-IRCCS, Naples, Italy.
  • Fagnani D; 3 UOC Oncologia, ASST Vimercate, Italy.
  • Gemma D; 4 UOC Oncologia Medica, ASL Frosinone, Italy.
  • Ciuffreda L; 5 UOC Oncologia Medica 1, AOU Città Della Salute e Della Scienza, Torino, Italy.
  • Granetto C; 6 UOC Oncologia Medica, AO Santa Croce e Carle, Cuneo, Italy.
  • Lucchesi S; 7 UO Oncologia Medica, Ospedale Felice Lotti, Pontedera, Italy.
  • Ballestrero A; 8 DIMI Università di Genova e Ospedale Policlinico San Martino, Genova, Italy.
  • Biglietto M; 9 UO Oncologia, A.O.R.N. 'A Cardarelli,' Napoli, Italy.
  • Proserpio I; 10 UO Oncologia Medica, ASST Sette Laghi, Varese, Italy.
  • Bergamo F; 1 UOC Oncologia Medica 1, Istituto Oncologico Veneto-IRCCS, Padova, Italy.
  • Proietti E; 11 Roche SpA Medical Affairs and CO, Monza, Italy.
  • Tonini G; 12 OUC Oncologia, Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Tumori ; 105(3): 243-252, 2019 Jun.
Article en En | MEDLINE | ID: mdl-30857495
ABSTRACT

AIMS:

BEAWARE investigated the pattern of first-line bevacizumab early interruption in the Italian real-world setting of metastatic colorectal cancer.

METHODS:

A total of 386 patients were followed for 15 months after first-line chemotherapy + bevacizumab start. The rate of bevacizumab interruption for progression or adverse drug reactions (ADRs) constituted the primary endpoint.

RESULTS:

A total of 78.2% of patients interrupted bevacizumab 56.6% for progression, 7.3% for ADRs, and 36.1% for other reasons. Median treatment duration was 6.7, 2.5, and 4.6 months, respectively. Median progression-free survival was 10.3 months; however, 35.8% of patients were not progressed and were thus censored at the data cutoff of 15 months, while 21.8% were still receiving bevacizumab. Patients discontinuing for progression/ADRs more frequently had metastases in >1 site (p = .0001), and a shorter median progression-free survival (6.9 vs 13.9 months, p < .0001).

CONCLUSIONS:

In Italy, first-line bevacizumab is interrupted mainly for progression, only 7.3% due to adverse events, and about one third of cases for other reasons. In clinical practice, the attitude to treat until progression as per guidelines might be implemented. ClinicalTrials.gov Identifier NCT01609075.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Inhibidores de la Angiogénesis / Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos / Bevacizumab Tipo de estudio: Guideline / Observational_studies / Prognostic_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Tumori Año: 2019 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Inhibidores de la Angiogénesis / Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos / Bevacizumab Tipo de estudio: Guideline / Observational_studies / Prognostic_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Tumori Año: 2019 Tipo del documento: Article País de afiliación: Italia