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Apatinib combined with paclitaxel-based chemotherapy in patients with taxane-resistant advanced gastric cancer: a single-arm exploratory study.
Zhao, Shen; Fan, Nanfeng; Li, Hui; Liu, Jie; Huang, Feng; Chen, Yigui; Zhou, Min; Yu, Jiaqing; Lin, Rongbo.
Afiliação
  • Zhao S; Department of Gastrointestinal Medical Oncology, Fujian Cancer Hospital, Fuzhou, Fujian, China.
  • Fan N; Fujian Medical University Cancer Hospital, Fuzhou, Fujian, China.
  • Li H; Fujian Key Laboratory of Translational Cancer Medicine, Fuzhou, Fujian, China.
  • Liu J; Department of Gastrointestinal Medical Oncology, Fujian Cancer Hospital, Fuzhou, Fujian, China.
  • Huang F; Fujian Medical University Cancer Hospital, Fuzhou, Fujian, China.
  • Chen Y; Department of Gastrointestinal Medical Oncology, Fujian Cancer Hospital, Fuzhou, Fujian, China.
  • Zhou M; Fujian Medical University Cancer Hospital, Fuzhou, Fujian, China.
  • Yu J; Department of Gastrointestinal Medical Oncology, Fujian Cancer Hospital, Fuzhou, Fujian, China.
  • Lin R; Fujian Medical University Cancer Hospital, Fuzhou, Fujian, China.
Ann Transl Med ; 8(19): 1233, 2020 Oct.
Article em En | MEDLINE | ID: mdl-33178765
ABSTRACT

BACKGROUND:

Apatinib combined with chemotherapy might be effective and safe for the management of advanced gastric cancer, but the available data are limited. To investigate the efficacy and safety of apatinib in combination with paclitaxel (PTX) alone or POF (PTX, oxaliplatin, and 5-fluorouracil) in patients with taxane-resistant advanced gastric cancer.

METHODS:

Patients with taxane-resistant advanced gastric cancer were enrolled in the single-center, open-labeled, single-arm, exploratory study (ClinicalTrials.gov #NCT02697838). Apatinib was administered at 850 mg po in combination with weekly PTX or the POF regimen. The primary endpoint was the objective response rate (ORR). The secondary endpoints included disease control rate (DCR), progression-free survival (PFS), overall survival (OS), the time to tumor progression (TTP), and safety.

RESULTS:

Twenty participants were recruited from 08/2016 to 01/2018. The duration of the study treatment was 2.07 (0.03-16.2) months. The median follow-up was 24.8 (0.3-26.0) months. The reasons for termination of treatment were disease progression (n=6), adverse events (AEs) (n=5), and patients' will (n=9). The ORR was 11.1% (95% CI 1.4-34.7%) and the DCR was 77.8% (95% CI 52.4-93.6%). The median PFS was 3.5 (95% CI 1.9-5.1) months, the median OS was 4.7 (95% CI 2.0-7.3) months, and the median TTP was 4.2 (95% CI 0.562-7.838) months. All 20 (100%) patients had AEs, 17 (85%) had apatinib treatment-emergent AEs (TEAEs), and 18 (90%) had chemotherapy TEAEs. The main grade 3-4 TEAEs were neutropenia, leukopenia, hypertension, and anemia.

CONCLUSIONS:

This preliminary study suggests that apatinib combined with PTX or POF might be effective and tolerable in patients with chemotherapy-refractory gastric cancer. Studies are necessary to confirm the results. TRIAL REGISTRATION ClinicalTrials.gov #NCT02697838.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Ann Transl Med Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Ann Transl Med Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China