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Correlation between blood magnesium and calcium concentration in patients treated with an anti-EGFR antibody
Journal of Pharmaceutical Health Care and Sciences volume 2, Article number: 23 (2016)
Abstract
Background
Hypomagnesemia is one of the characteristic side effects of the human anti-epidermal growth factor receptor (EGFR) monoclonal antibodies, cetuximab and panitumumab.
The major mechanism of anti-EGFR antibody-related hypomagnesemia is suppression of EGFR-mediated urinary Mg2+ reabsorption in both the renal tubule the intestinal tract.
Since Mg2+ is known to affect blood Ca2+ levels through regulation of parathyroid hormone (PTH) secretion, we investigated the correlation between Ca2+ and Mg2+ concentration in blood.
Methods
Between April 2012 and October 2015, blood Mg2+ and Ca2+ concentrations (albumin corrected value) of 22 colon cancer patients undergoing treatment with either cetuximab or panitumumab at Toyooka Public Hospital were measured simultaneously.
Results
Hypomagnesemia (of all Grades) was reported in 13 of 22 patients. Two patients had hypomagnesemia of severity > Grade 3.
Changes in blood Mg2+ and Ca2+ concentration showed a significant correlation (r2 = 0.7455), which could be expressed using the following equation, Ca2+ concentration = 1.4268 × (Mg2+ concentration) + 7.1126.
Conclusion
Since the early stages of hypomagnesemia produce no characteristic clinical symptoms, it is easily overlooked until it becomes severe.
The investigation results suggest that if low blood Ca2+ concentration (mg/dL) is observed in patients administered anti-EGFR antibodies, early evaluation of blood Mg2+ concentration (mg/dL) and prompt supportive care are required to prevent aggravation of hypomagnesemia.
Background
Cetuximab and panitumumab are anti-epidermal growth factor receptor (EGFR) monoclonal antibodies. Both antibodies are molecular-targeted drugs and their efficacy has been indicated not only in primary treatment, but also in secondary and tertiary treatment of advanced or recurrent colorectal cancer not harboring mutations in the KRAS gene [1].
Various side effects of molecular-targeted agents are known, which are unlikely to occur with a conventional cytotoxic agent. Some of the characteristic side effects of anti-EGFR antibodies include infusion reaction, skin symptoms such as acne-like rash, and electrolyte abnormalities. Of the electrolyte abnormalities, hypomagnesemia is a hidden side effect because it is asymptomatic and progresses slowly despite its high frequency [2].
The causes include inhibition of EGFR-mediated Mg2+ re-absorption from urine in renal tubules, and inhibition of EGFR-mediated Mg2+ absorption in the intestinal tract [3].
Furthermore, Mg2+ has been reported to affect blood Ca2+ level [4] via its in vivo control of parathyroid hormone (PTH) secretion.
Therefore, we examined the correlation between Ca2+ and Mg2+ concentration in patients’ blood.
Methods
Patients
The blood Mg2+ and Ca2+ concentrations (albumin corrected value) of 22 colon cancer patients who received an anti-EGFR antibody (either cetuximab or panitumumab) at our hospital from April 2012 to October 2015 were simultaneously measured. Fourteen of the 22 patients were treated with cetuximab. The remaining 8 patients received panitumumab (Table 1).
Procedures
Mg2+ and Ca2+ concentration in the blood was investigated retrospectively using information from electronic medical records. The severity of Mg2+ and Ca2+ concentration decline (hypomagnesemia/hypocalcemia) was graded according to Common Terminology Criteria for Adverse Events ver4.0 (CTCAE ver4.0 Japanese translation JCOG version).
Magnesium oxide formulations are commonly used as laxatives. Since they are expected to affect Mg2+ concentrations in blood, the incidence of hypomagnesemia was studied for magnesium oxide co-treated and magnesium oxide non-treated groups separately.
Skin toxicity is one of the characteristic side effects of human anti-EGFR monoclonal antibodies. Therefore, the relationship between hypomagnesemia and skin toxicity was investigated. Skin toxicities included pruritus, acneiform dermatitis, skin desquamation, exfoliative dermatitis, paronychia, nail disorder, skin fissures, skin laceration, pruritic rash, pustular rash, skin infection, and skin ulceration. Selected skin toxicities were graded according to Common Terminology Criteria for Adverse Events ver4.0 (CTCAE ver4.0 Japanese translation JCOG version).
Differences in patient background between the hypomagnesemia groups and non-hypomagnesemia groups were investigated.
Statistical analysis
Statistical analyses were performed by using the chi-square test for categorical variables and Mann-Whitney’s U test for order variables. The relationship between Mg2+ and Ca2+ concentration in blood was examined using a single regression analysis. Statistical analysis was performed using SPSS® version 11. The significance level of the test was set at 5 %.
Ethical issues
This study was approved by the research ethics committee of Toyooka Public Hospital (No. 102) and was performed according to the Declaration of Helsinki.
The waiver of informed consent from individual patients was approved by the ethics committee. Anonymized data with serial study ID numbers created by the study hospital were used throughout the study.
Results
Patients
Patient characteristics are shown in Table 1. Forty-three patients were treated with anti-EGFR antibodies. Of these, 21 patients were excluded from analysis owing to lack of data on Mg2+ concentration or asynchronous measurement of Ca2+ and Mg2+. Finally, 22 patients were included (17 men and 5 women); the median age was 65 years.
Mg2+ concentration before introducing an anti-EGFR antibody was 2.13 ± 0.22 mg/dL. Eleven patients received magnesium oxide co-treatment and the other 11 did not.
Investigation of incidence frequency
The incidence frequency of hypomagnesemia after the start of anti-EGFR antibody administration was 59.1 % (13 cases). About 18.2 % of the patients (4 cases) had Grade 2 hypomagnesemia, and 9.1 % (2 cases) had Grade 3 hypomagnesemia.
The incidence frequency of hypocalcemia after the start of anti-EGFR antibody administration was 72.7 % (16 cases), with 4.5 % of patients (1 case) having Grade 2 hypocalcemia, and none having hypocalcemia higher than Grade3 (Table 2).
Correlation between Mg2+ and Ca2+ concentration in blood
Statistical analyses were performed using single regression analysis. The results show the trends and a significant correlation (r2 = 0.7455) between serum Mg2+ concentration and serum Ca2+ concentration that fits the following linear equation: Ca concentration = 1.4268 × (Mg concentration + 7.1126) (Fig. 1).
Comparison of the incidence of hypomagnesemia in the presence or absence of oral magnesium oxide co-treatment
During treatment with anti-EGFR antibodies, 11 patients were co-treated with oral magnesium oxide preparation for constipation (group with co-treatment). The incidence of Grade 1 or higher hypomagnesemia in this group was 63.6 % (7 patients). The incidence in the magnesium oxide non-treated group (11 patients) was 54.5 % (6 cases).
No significant difference in incidence of hypomagnesemia was observed between the magnesium oxide co-treated group and the magnesium oxide non-treated group (Fig. 2; p = 0.665 by χ 2 test).
Correlation between severity of skin toxicity and hypomagnesemia
In anti-EGFR antibody-treated patients, the incidence of Grade 0 or 1 skin toxicity was 40.9 % (9 patients) and that of Grade 2 or higher skin toxicity was 59.0 % (13 patients). Magnesium values in each group were 1.80 ± 0.32, and 1.51 ± 0.60 mg/dL. No significant difference was observed (p = 0.53; Table 3).
Comparison of patient characteristics in hypomagnesemia
No significant difference in patient characteristics was observed between patients with and without hypomagnesemia (Table 4).
Discussion
In vivo, approximately 70 % of extracellular Mg2+ is re-absorbed by the ascending limb of the loop of Henle. The rest is re-absorbed in the proximal and distal tubules. Since EGFR is frequently expressed on the surface of the cells within the ascending limb of the loop of Henle, anti-EGFR antibodies such as cetuximab and panitumumab, inhibit EGFR in renal tubular epithelial cells [5]. Consequently, the expression level of the Mg2+ channel, TRPM6 (transient receptor potential member-6) decreases. Thus, Mg2+ transport decreases, resulting in Mg2+ loss in the kidney, which is believed to underlie the pathogenesis of hypomagnesemia [6, 7].
The intermediate aggregate results for a domestic performance survey of the anti-EGFR antibody cetuximab showed that electrolyte abnormalities occurred in 11.6 % patients (cases of Grade 3 or higher abnormalities, 1.6 %; and severe cases, 0.2 %). Of the total 1767 cases, 164 patients (9.3 %) had hypomagnesemia, 35 (2.0 %) had hypocalcemia, and 19 (1.1 %) had hypokalemia.
The results of cetuximab post-marketing all-patient surveillance as of July 2010 showed that among the 4345 total cases, 40 (0.9 %) exhibited decreased blood Mg2+, which is considerably smaller than that observed in Phase II clinical trials in Japan (51.3 %).
Since serum Mg2+ levels are not routinely measured at many facilities, the ability to detect hypomagnesemia may vary.
This varied capability can be considered a possible reason for the frequency gap between these two reaction reports. In vivo, Mg2+ participates in activation of enzymes, peripheral nerve regulation of muscle relaxation, and bone formation. Mg2+ also plays a particularly important role as a cofactor required for the catalytic activity of enzymes involved in intracellular metabolism. Although mild Mg2+ decrease is usually asymptomatic, as hypomagnesemia progresses, tetany, tremors, seizures, muscle weakening and other neuromuscular symptoms, psychiatric symptoms, cardiovascular symptoms such as severe arrhythmia, and other electrolyte abnormalities occur as complications [8]. Since hypomagnesemia is difficult to detect from subjective symptoms in its early stages, few complaints have been reported. Therefore, regular measurement of serum Mg2+ level is needed.
In this study, the effect of administration of magnesium oxide preparations in combination with an anti-EGFR antibody was also analyzed. In the group administered magnesium oxide preparations, although hypomagnesemia improvement occurred, no relation was observed between magnesium oxide administration and hypomagnesemia improvement. Since oral magnesium oxide preparations are only weakly absorbed in the intestinal tract and are excreted by absorbing moisture from the intestine, the lack of correlation could be attributed to its low oral bioavailability.
In addition, skin toxicity such as acne-like rash and paronychia with anti-EGFR antibody treatment, can lead to early discontinuation of treatment. But Anti-EGFR antibody drugs have been reported to have a marked therapeutic effect in patients who exhibit skin toxicities. Using the data in the present study, we investigated the correlation between skin toxicity and electrolyte disturbances. We also looked for correlations between patient characteristics and electrolyte disturbances, but were unable to discover a significant correlation. Since all patients are routinely and thoroughly screened for skin toxicity symptoms, we consider any effect of skin toxicities on electrolyte imbalances (or vice versa) to be slight.
Since an anti-EGFR antibody can now be used as the primary treatment, cases of chronic administration are increasing. Further, in cases where hypomagnesemia has been reported, prolonged treatment with cetuximab is currently required because of its marked therapeutic effect8). It has been reported that in the elderly and in patients with high pre-treatment serum Mg2+ levels, the risk of developing hypomagnesemia is high, and the frequency of severe hypomagnesemia increases if anti-EGFR drug administration exceeds 6 months [9]. Nakamoto et al. reported that since recovery from severe hypomagnesemia is poor even if supplemental Mg2+ is administered, withdrawal of anti-EGFR antibodies was situationally required. To prevent severe hypomagnesemia, prompt initiation of supportive care should also be required [10].
Hypercalcemia has been reported in about 20–30 % of cancer patients. In patients with malignant tumors, bone destruction and tumor cell expansion associated with bone metastasis lead to the production of PTH-related peptides, which eventually result in the development of hypercalcemia. Since onset is often sudden, blood Ca2+ concentration is regularly measured.
Hypercalcemia is typically associated with bone metastasis. Although all patients were at stage IV, a significant correlation between magnesium and calcium concentrations in bone metastatic cancer patients was not observed. ALP is a bone metastasis marker. A significant difference in changes in ALP levels was not observed between the hypercalcemia group and the non- hypercalcemia group (data not shown).
Ca2+ is a major regulator of PTH secretion, and Mg2+ regulates PTH secretion as well. Lack of intracellular Mg2+ is known to suppress PTH secretion, which may result in reduction of serum PTH and Ca2+ levels. Therefore, in patients with hypomagnesemia due to administration of anti-EGFR antibodies, hypocalcemia could be concurrent [4].
Since a correlation between Ca2+ and Mg2+ concentration in patients treated with an anti-EGFR antibody was indicated in this investigation, it is suggested that prompt evaluation of blood Mg2+ concentration is required to avoid incidence of hypomagnesemia, especially when reduction in blood Ca2+ concentration is detected.
Conclusions
In conclusion, the investigation results suggest that if low blood Ca2+ concentration (mg/dL) is observed in patients administered anti-EGFR antibodies, early evaluation of blood Mg2+ concentration (mg/dL) and prompt supportive care are required to prevent aggravation of hypomagnesemia. Changes in blood Mg2+ and Ca2+ concentration showed a significant correlation (r2 = 0.74555), which could be expressed by the following equation: Ca2+ concentration = 1.4268 × (Mg concentration) + 7.1126. Since there is no characteristic clinical symptom in early stages of hypomagnesemia, it is easily overlooked until it becomes severe. Since the correlation between Ca2+ and Mg2+ concentration in patients treated with an anti-EGFR antibody was indicated in this investigation, it is suggested that prompt evaluation of blood Mg2+ concentration is required to avoid an incidence of hypomagnesemia, especially when reduction in blood Ca2+ concentration is detected.
Abbreviations
- ALP:
-
Alkaline phosphatase
- CTCAE ver4.0:
-
Common terminology criteria for adverse events ver4.0
- EGFR:
-
Human anti-epidermal growth factor receptor
- PTH:
-
Parathyroid hormone
- TRPM6:
-
Transient receptor potential member-6
References
Cunningham D, Humblet Y, Siena S, Khayat D, Bleiberg H, Santoro A, et al. Cetuximab monotherapy and cetuximab plus irinotecan-refractory metastatic colorectal cancer. N Eng J Med. 2004;351:337–45.
Fakih MG, Wilding G, Lombardo J. Cetuximab-induced hypomagnesemia in patients with colorectal cancer. Clin Colorectal Cancer. 2006;6:152–6.
Tejpar S, Piessevaux H, Claes K, Hoenderop JG, Verslype C, Van Cutsem E. Magnesium wasting associated with epidermal-growth-factor receptor-targeting antibodies in colorectal cancer. A prospective study. Lancet Oncol. 2007;8:387–94.
Tahara H, Nishizawa Y. Hypomagnesemia and hypoparathyroidism. Clinical Calcium. 2007;17:1200–4.
Groenestege WM, Thebault S, van der Wijst J, van den Berg D, Janssen R, Tejpar S, et al. Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia. J Clin Invest. 2007;117:2260–7.
Wagner CA. Disorders of renal magnesium handling explain renal magnesium transport. J Nephrol. 2007;20:507–10.
Schlingmann KP, Waldegger S, Konrad M, Chubanov V, Gudermann T. TRPM6 and TRPM7-Gatekeepers of human magnesium metabolism. Biochim Biophys Acta. 2007;1772:813–21.
Vincenzi B, Santini D, Galluzzo S, Russo A, Fulfaro F, Silletta M, et al. Early magnesium reduction in advanced colorectal cancer patients treated with cetuximab plus irinotecan as predictive factor of efficacy and outcome. Clin Cancer Res. 2008;14:4219–24.
Fakih M. Management of anti-EGFR-targeting monoclonal antibody-induced hypomagnesemia. Oncology. 2008;22:74–6.
Nakamoto E, Kawakami K, Imada H. Retrospective investigation on cetuximab-induced hypomagnesemia; incidence, time of onset, and management. Jpn J Pharm Health Care Sci. 2011;37:403–9.
Acknowledgement
We are grateful to the staff of the Hyogo University of Health Sciences, Toyooka Public Hospital, Japan.
Funding
There are no funding sources for this report.
Availability of data and materials
Data used in this report will not be shared owing to the risk of identifying an individual, although most patients’ data are presented in the main paper.
Authors’ contributions
TT, TO, KN, KI and DK designed the research. TT, TO, KN, and DK analyzed the data. TT, ST, HU, and MM participated in interpretation of the results. All authors have read and approved the final manuscript.
Competing interests
The authors declare that they have no competing interests.
Consent for publication
Written informed consent was obtained from all subjects for publication of this report and accompanying images. A copy of the written consent is available for review upon request.
Ethics approval and consent to participate
This study was approved by the research ethics committee of Toyooka Public Hospital (No. 102) and was performed according to the Declaration of Helsinki. The waiver of informed consent from individual patients was approved by the ethics committee. Anonymized data with serial study ID numbers created by the study hospital were used throughout the study.
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Tsujii, T., Ogaki, T., Nakae, K. et al. Correlation between blood magnesium and calcium concentration in patients treated with an anti-EGFR antibody. J Pharm Health Care Sci 2, 23 (2016). https://doi.org/10.1186/s40780-016-0060-9
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DOI: https://doi.org/10.1186/s40780-016-0060-9
Keywords
- Hypomagnesemia
- Calcium
- EGFR-targeting antibodies
- Cetuximab
- Panitumumab