Long-term trastuzumab (Herceptin®) treatment in a continuation study of patients with HER2-positive breast cancer or HER2-positive gastric cancer

被引:21
作者
Mueller, Volkmar [1 ]
Clemens, Michael [2 ,7 ]
Jassem, Jacek [3 ]
Al-Sakaff, Nedal [4 ]
Auclair, Petra [4 ]
Nuesch, Eveline [4 ]
Holloway, Debbie [4 ]
Shing, Mona [5 ]
Bang, Yung-Jue [6 ]
机构
[1] Univ Med Ctr Hamburg Eppendorf, Dept Gynecol, Martinistr 52, D-20246 Hamburg, Germany
[2] Klinikum Mutterhaus Borromaerinnen gGmbH, Innere Med I, Feldstr 16, D-54290 Trier, Germany
[3] Med Univ Gdansk, Dept Oncol & Radiotherapy, M Sklodowskiej Curie 3A, PL-80210 Gdansk, Poland
[4] F Hoffmann La Roche Ltd, Grenzacherstr 124, CH-4070 Basel, Switzerland
[5] Genentech Inc, Global Pharma Dev, 1 DNA Way, San Francisco, CA 94080 USA
[6] Seoul Natl Univ, Coll Med, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea
[7] CaritasKlinikum Saarbrucken, Rheinstr 2, D-66113 Saarbrucken, Germany
关键词
Herceptin; Trastuzumab; Breast cancer; Gastric cancer; HER2-positive; MONOCLONAL-ANTIBODY; PHASE-II; EFFICACY; SAFETY; TRIAL; CHEMOTHERAPY; THERAPY; PLUS; HER2;
D O I
10.1186/s12885-018-4183-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Trastuzumab (Herceptin (R) [H]) is the standard of care for HER2-positive locally advanced/metastatic breast cancer and gastric/gastroesophageal junction (GEJ) cancer. However, there is a paucity of data available on long-term H treatment of patients. The Rollover Protocol (ROP) Study was conducted to report safety data for patients with HER2-positive locally advanced/metastatic breast and gastric/GEJ cancer who have received long-term H therapy (>= 5 years and >= 3 years for breast and gastric/GEJ cancer, respectively). Methods: The ROP Study was a single-arm, multicenter, international continuation trial of H in patients who had previously completed a global Roche-sponsored trial with H therapy, had stable disease, and were receiving H at the end of the lead-in trial. Patients with chronic heart failure during the lead-in trial could be included following a risk-benefit analysis. The primary objectives were to provide H therapy to patients with HER2-overexpressing locally advanced/metastatic breast or gastric/GEJ cancer at the end of the lead-in study, and to follow the long-term outcomes and long-term overall safety in these patients. Results: Twenty-five of 69 patients enrolled in the ROP Study received long-term H therapy (19 breast cancer and 6 gastric/GEJ cancer). The median duration of H treatment for patients with breast cancer was 8 years 7 months, and 5 years 2 months for patients with gastric/GEJ cancer. The cardiac status of the patients remained stable over time, with no serious cardiac adverse events or marked changes in left ventricular ejection fraction (LVEF). The median overall worst LVEF measurement was 57.0%, and no patients experienced an LVEF of < 45% (range 47-63%). There were no serious adverse events related to study treatment. Conclusions: These results suggest that H has an acceptable safety profile and was well tolerated in patients who received long-term H therapy (>= 5 years and >= 3 years for breast and gastric/GEJ cancer, respectively). Further investigation and reporting of long-term H therapy would be valuable.
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页数:6
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