Since the average lifespan is Abemaciclib mw currently 78.6 years for males and 85.6 years for females, a rapid increase of elderly patients with colorectal cancer is predicted in this country. Accordingly, it is problematic if elderly patients cannot receive effective chemotherapy simply because of their age, so the establishment of safe and effective standard therapy for elderly Japanese patients is important. In Western countries, however, it is considered

possible to treat the elderly with standard therapy, provided TSA HDAC that the performance status (PS) is good, the function of major organs is maintained, and there are no uncontrolled complications. Goldberg et al. [20] reported that Grade 3/4 neutropenia and thrombocytopenia showed higher rates in elderly patients, but there were no differences of the response rate and safety of FOLFOX therapy between elderly patients over 70 years old and younger patients as a result of meta-analysis. In present study,

the elderly group was defined as patients more than 70 years old to assess the safety and efficacy of mFOLFOX6 therapy. We found that the incidence of Grade 3–4 neutropenia tended to be higher in elderly patients than younger patients, but there was Selleck GNS-1480 no statistical significance (62.5% vs. 28.6%, P = 0.1347). Also, the incidence and severity of other adverse events in this study were generally comparable to those reported in Western countries [20]. The regimen was tolerable and there were no deaths due to toxicity. When setting the dose-reduction criteria and GBA3 the method of administration after occurrence of adverse events, it was decided that the dose of oxaliplatin would not be reduced, and that bolus 5-FU would be deleted due to the possibility that dose-limiting hematological toxicity such as neutropenia (which showed a high incidence in this study) might be caused by rapid intravenous injection of 5-FU [21–23]. After bolus 5-FU was stopped in accordance with the dose-reduction criteria (Table

1) due to grade 4 neutropenia in 3 patients (one younger patient and 2 elderly patients) during this study, treatment could be continued safely until PD occurred. Peripheral neuropathy is a characteristic adverse reaction to oxaliplatin and is the dose-limiting toxicity of this drug. Occurrence of neuropathy is dependent on the total dose of oxaliplatin, and grade 3–4 neuropathy (NCI-CTC criteria) shows an incidence of about 15% when the total dose reaches 750 to 800 mg/m2[24]. The dose-dependent neuropathy caused by oxaliplatin is reversible after suspension/omission of the drug, and treatment using a stop-and-go strategy (with reinstitution of therapy after recovery from toxicity) achieves favorable survival [25] and is well tolerated by elderly patients over 75 years old [26]. In the present study, neuropathy showed a lower incidence than that mentioned above, but there was a similar correlation between the total dose of oxaliplatin and the severity of neuropathy in both the younger and elderly groups (Figure 2).