TY - JOUR
T1 - Effects of metformin versus placebo on vitamin B12 metabolism in non-diabetic breast cancer patients in CCTG MA.32
AU - From the CCTG, Alliance, SWOG, ECOG, NSABP Cooperative Groups
AU - Lohmann, Ana Elisa
AU - Liebman, Mira F.
AU - Brien, William
AU - Parulekar, Wendy R.
AU - Gelmon, Karen A.
AU - Shepherd, Lois E.
AU - Ligibel, Jennifer A.
AU - Hershman, Dawn L.
AU - Rastogi, Priya
AU - Mayer, Ingrid A.
AU - Hobday, Timothy J.
AU - Lemieux, Julie
AU - Thompson, Alastair Mark
AU - Pritchard, Kathleen I.
AU - Whelan, Timothy Joseph
AU - Mukherjee, Som D.
AU - Chalchal, Haji I.
AU - Bernstein, Vanessa
AU - Stambolic, Vuk
AU - Chen, Bingshu E.
AU - Goodwin, Pamela Jean
N1 - Funding Information:
The MA.32 Study was supported by Canadian Cancer Society Research Institute (CCSRI) (Grant #021039), National Institute of Health (NIH) (Grant #CA180863), Canadian Breast Cancer Foundation (CBCF), Breast Cancer Research Foundation (US), and Apotex (in kind donation of placebo and metformin).
Funding Information:
Dr. Lohmann’s work was supported by Hold’Em for Life Translating Discoveries into Breast Cancer Cures (Canada). Dr. Stambolic’s work was supported by the Canadian Institutes of Health Research (CIHR), Canadian Cancer Society Research Institute (CCSRI), and Hold’Em for Life Translating Discoveries into Breast Cancer Cures (Canada). Dr. Goodwin’s work was supported by The Breast Cancer Research Foundation (United States) and Hold’Em for Life Translating Discoveries into Breast Cancer Cures (Canada).
Publisher Copyright:
© 2017, Springer Science+Business Media New York.
PY - 2017/7/1
Y1 - 2017/7/1
N2 - Background: Metformin is associated with low levels of vitamin B12 (VitB12) in patients with diabetes. The CCTG/MA.32 trial investigates the effects of metformin vs placebo on breast cancer (BC) outcomes in non-diabetic high-risk BC patients. We analyzed VitB12 at baseline and after 6 months of metformin (versus placebo) in the first 492 patients with paired blood samples. Methods: VitB12 was analyzed centrally in baseline and 6-month fasting plasma. Levels <181 pmol/L were considered deficient, 181–221 pmol/L borderline, and ≥222 pmol/L sufficient. Methylmalonic acid (MMA) and homocysteine (HC) were assayed in those with VitB12 levels <222 pmol/L. Statistical analyses used Spearman’s rank correlation coefficients and Wilcoxon signed-rank test for continuous variables and Chi-square test for categorical variables. Results: 237 patients received metformin and 255 received placebo; median (inter quartile range) baseline VitB12 levels were 390 (290, 552) and 370 (290, 552) pmol/L in the metformin and placebo arms, respectively (p = 0.97). At 6 months, the median levels were 320 (244, 419) in the metformin versus 380 (286, 546) pmol/L in the placebo arm (p = 0.0001). At baseline, 15 patients (11 metformin and 4 placebo) had VitB12 <181 pmol/L, and at 6 months, 18 patients (15 metformin and 3 placebo) (p = 0.004). Median hemoglobin was similar at baseline, metformin, 130 g/L (124–137), and placebo arms, 131 g/L (124–137) (p = 0.38), and at 6 months, metformin, 131 g/L (91–162), and 131 g/L (106–169) in placebo group (p = 0.11). Of the 74 subjects with vitamin B12 <222 pmol/L at either time point (45 metformin, 29 placebo), at baseline MMA was normal in all patients and two had elevated HC (>15μmol/L). At 6 months, one patient (metformin) had MMA >0.4μmol/L and 3 (2 metformin, 1 placebo) had HC > 15μmol/L. Conclusions: There was an increased rate of biochemical VitB12 deficiency after 6 months of metformin; this was not associated with anemia. Further research will investigate VitB12 levels in all subjects at baseline and at 6 and 60 months.
AB - Background: Metformin is associated with low levels of vitamin B12 (VitB12) in patients with diabetes. The CCTG/MA.32 trial investigates the effects of metformin vs placebo on breast cancer (BC) outcomes in non-diabetic high-risk BC patients. We analyzed VitB12 at baseline and after 6 months of metformin (versus placebo) in the first 492 patients with paired blood samples. Methods: VitB12 was analyzed centrally in baseline and 6-month fasting plasma. Levels <181 pmol/L were considered deficient, 181–221 pmol/L borderline, and ≥222 pmol/L sufficient. Methylmalonic acid (MMA) and homocysteine (HC) were assayed in those with VitB12 levels <222 pmol/L. Statistical analyses used Spearman’s rank correlation coefficients and Wilcoxon signed-rank test for continuous variables and Chi-square test for categorical variables. Results: 237 patients received metformin and 255 received placebo; median (inter quartile range) baseline VitB12 levels were 390 (290, 552) and 370 (290, 552) pmol/L in the metformin and placebo arms, respectively (p = 0.97). At 6 months, the median levels were 320 (244, 419) in the metformin versus 380 (286, 546) pmol/L in the placebo arm (p = 0.0001). At baseline, 15 patients (11 metformin and 4 placebo) had VitB12 <181 pmol/L, and at 6 months, 18 patients (15 metformin and 3 placebo) (p = 0.004). Median hemoglobin was similar at baseline, metformin, 130 g/L (124–137), and placebo arms, 131 g/L (124–137) (p = 0.38), and at 6 months, metformin, 131 g/L (91–162), and 131 g/L (106–169) in placebo group (p = 0.11). Of the 74 subjects with vitamin B12 <222 pmol/L at either time point (45 metformin, 29 placebo), at baseline MMA was normal in all patients and two had elevated HC (>15μmol/L). At 6 months, one patient (metformin) had MMA >0.4μmol/L and 3 (2 metformin, 1 placebo) had HC > 15μmol/L. Conclusions: There was an increased rate of biochemical VitB12 deficiency after 6 months of metformin; this was not associated with anemia. Further research will investigate VitB12 levels in all subjects at baseline and at 6 and 60 months.
KW - Anemia
KW - Breast cancer
KW - Homocysteine
KW - Megaloblastic anemia
KW - Metformin
KW - Methylmalonic acid
KW - Vitamin B12
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U2 - 10.1007/s10549-017-4265-x
DO - 10.1007/s10549-017-4265-x
M3 - Article
C2 - 28447237
AN - SCOPUS:85018320413
SN - 0167-6806
VL - 164
SP - 371
EP - 378
JO - Breast Cancer Research and Treatment
JF - Breast Cancer Research and Treatment
IS - 2
ER -