Macrocytosis with sunitinib: Canadian data
Wednesday, May 26, 2010
From: Renal Adenocarcinoma Digest (RADAR)
A Canadian retrospective single-centre review of advanced RCC patients reports that macrocytosis occurred in 21 of 43 patients (48.8%) during sunitinib treatment (Price et al. Curr Oncol 2010; 17: 30-33; free full text
here). Macrocytosis was defined as an increase in RBC mean corpuscular volume (MCV) > upper limit of normal (ULN).
Patients received sunitinib for a median of 5 cycles (30 weeks); 79% received >3 cycles. Macrocytosis occurred after a median of 3 cycles (17 weeks) of sunitinib and was not observed in the 9 patients who received < 2 cycles of sunitinib. Among the 22 patients who did not develop macrocytosis, there was a trend to increasing MCV with sunitinib, although 3 patients had received RBC transfusions and/or iron supplementation that could have contributed to an increase in MCV.
Nine of 21 patients (42.8%) had anemia when macrocytosis was detected, while another 9 (42.8%) subsequently developed anemia.
Other causes of macrocytosis (medications, vitamin B12 or folate deficiency, comorbidities) did not appear to contribute to the high incidence of macrocytosis.
There have been several previous reports of sunitinib-associated macrocytosis (Schallier et al. Anticancer Res 2009; 29: 5225-5228;
www.ncbi.nlm.nih.gov/pubmed/20044640. Rini et al. Cancer 2008; 113: 1309-1314; free full text
here. Billemont et al. N Engl J Med 2007; 357: 1351-1352; no abstract available. Gillessen et al. N Engl J Med 2007; 356: 2330-2331; no abstract available). The mechanisms by which macrocytosis occurs in patients treated with sunitinib or imatinib have not been determined.
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