Dose increase by 50%
(6 mg q 2 weeks) of Trastuzumab led to … Discussion We present a case of HER2-positive metastatic gastric cancer that required a higher than standard dose of trastuzumab to achieve a response to therapy. Standard breast cancer dosing of trastuzumab on a 3-week schedule is 8 mg/kg load followed by 6 mg/kg q 3 weeks, or on a weekly schedule (4 mg/kg load, 2 mg/kg q week) (1). Our patient was treated with FOLFOX chemotherapy every two weeks, and thus Inhibitors,research,lifescience,medical received an appropriate proportional trastuzumab dose (6 mg/kg load, 4 mg/kg q 2 weeks). The patient progressed very quickly following initiation of therapy (after 3 treatments), and subsequently responded immediately following an increase in trastuzumab dose to 6 mg/kg q 2 weeks (i.e., 50% dose increase in maintenance). This response was
noted without a change in the FOLFOX cytotoxic therapy, suggesting that the initial administered Inhibitors,research,lifescience,medical dose of trastuzumab was insufficient for treatment response; more specifically, the patient required a higher dose of trastuzumab to achieve a response to therapy. The observation that our patient responded to a higher dose of trastuzumab than routinely administered suggests that some patients with HER2-positive gastric cancer may be underdosed. It is suggested that gastric cancer patients may have a higher renal clearance of trastuzumab than patients with HER2-positive Inhibitors,research,lifescience,medical Inhibitors,research,lifescience,medical breast cancer. Bruno and colleagues (4) determined the steady state pharmacokinetics of trastuzumab in patients with metastatic breast cancer. On the weekly trastuzumab schedule, trastuzumab clearance is 0.231 L/day (for a median body weight of 68 kg) with a corresponding elimination half-life of approximately 3 weeks. On the every 3-week schedule in metastatic breast cancer, the trastuzumab pharmacokinetics is very similar (1). In contrast, the pharmacokinetic
Inhibitors,research,lifescience,medical profile of trastuzumab reported from the ToGA study in patients with metastatic gastric cancer demonstrate a higher clearance is 0.378 L/day (~70% higher), with a corresponding elimination half-life of approximately only 2 weeks (Roche, Inc 2011) (Table 1) (5). This suggests that the current “standard” dosing of trastuzumab in almost metastatic gastric cancer may be grossly underdosed by nearly 50%, and that higher trastuzumab doses may be necessary in some patients for maximum efficacy. Table 1 Pharmacokinetics of trastuzumab (Herceptin) in breast cancer vs. metastatic gastric cancer In breast cancer, it has been shown that patients with four or more metastatic sites of disease have faster clearance, independent of HER-2 see more extracellular domain levels (4). Trastuzumab elimination appears to depend on serum levels of circulating HER-2 extracellular domains, which can be cleaved from the surfaces of cancer cells by matrix metalloproteinase.