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First-line panitumumab plus capecitabine for the treatment of older patients with wild-type RAS metastatic colorectal cancer. The phase II, PANEL study.
Méndez Méndez, José Carlos; Salgado Fernández, Mercedes; de la Cámara Gómez, Juan; Pellón Augusto, Mari Luz; Covela Rua, Marta; Quintero Aldana, Guillermo; Fernández Montes, Ana; Reboredo López, Margarida; Valladares Ayerbes, Manuel; Jorge Fernández, Mónica; González Villarroel, Paula; Romero Reinoso, Carlos; Ramos Vázquez, Manuel.
Afiliação
  • Méndez Méndez JC; Cancer Centre of Galicia, A Coruña, Spain. Electronic address: jcmendez.m@gmail.com.
  • Salgado Fernández M; University Hospital Complex of Ourense, Ourense, Spain.
  • de la Cámara Gómez J; University Hospital Complex of Ferrol, Ferrol, Spain.
  • Pellón Augusto ML; University Hospital Complex of Ferrol, Ferrol, Spain.
  • Covela Rua M; Lucus Augus University Hospital, Lugo, Spain.
  • Quintero Aldana G; Lucus Augus University Hospital, Lugo, Spain.
  • Fernández Montes A; University Hospital Complex of Ourense, Ourense, Spain.
  • Reboredo López M; University Hospital Complex of A Coruña, A Coruña, Spain.
  • Valladares Ayerbes M; Virgen del Rocío University Hospital, Sevilla, Spain.
  • Jorge Fernández M; Álvaro Cunqueiro University Hospital Complex, Vigo, Spain.
  • González Villarroel P; Álvaro Cunqueiro University Hospital Complex, Vigo, Spain.
  • Romero Reinoso C; Povisa Hospital, Vigo, Spain.
  • Ramos Vázquez M; Cancer Centre of Galicia, A Coruña, Spain.
J Geriatr Oncol ; 11(8): 1263-1267, 2020 11.
Article em En | MEDLINE | ID: mdl-32580916
ABSTRACT

BACKGROUND:

Despite the high morbidity and mortality of metastatic colorectal cancer (mCRC) in older patients, they have been underrepresented in clinical trials and their optimal treatment is yet to be determined. This open-label phase II study evaluated the benefits of panitumumab and capecitabine as a first-line chemotherapy regimen in older patients with wild-type [WT] RAS mCRC. PATIENTS AND

METHODS:

Patients (≥70 years; ECOG≤2) received 3-week cycles of panitumumab (9 mg/kg on day 1) plus capecitabine (850 mg/m2 twice daily on days 1-14) until disease progression or unacceptable toxicity. Response was evaluated every 9 weeks according to RECIST_1.1. Outcome measures were objective response rate (ORR), duration of response (DoR), time to response (TTR), progression (TTP) and treatment failure (TTF), progression-free survival (PFS), overall survival (OS), and safety.

RESULTS:

Twenty-seven patients (11 women; median age 78 years; ECOG 0 [26%], 1 [67%], 2 [7%]) were evaluated. Median follow-up was 17.7 months. Confirmed ORR (95%CI) was 44.4% (25.7-63.2), with 25.9% of patients achieving at least stable disease. Median (95%CI) DoR was 8.7 (5.5-10.4) months, and median TTR was 2.2 (1.9-2.8) months. Median TTP was 9.6 (4.8-11.5) months, with a median TTF of 5.2 (2.8-7.2) months. The median PFS was 7.5 (4.4-10.4) months, and the median OS was 23.7 (7.4-27.5) months. Seventeen (63%) patients reported panitumumab and/or capecitabine-related adverse events grade 3-4, with skin toxicity (18.5%) being the most common. Two (7.4%) deaths were treatment-related.

CONCLUSION:

This study suggests that panitumumab plus capecitabine is a safe and effective regimen in older patients with WT RAS mCRC.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Limite: Aged / Female / Humans Idioma: En Revista: J Geriatr Oncol Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Limite: Aged / Female / Humans Idioma: En Revista: J Geriatr Oncol Ano de publicação: 2020 Tipo de documento: Article