Liver toxicity during temozolomide chemotherapy caused by Chinese herbs
© Melchardt et al.; licensee BioMed Central Ltd. 2014
Received: 3 January 2014
Accepted: 27 March 2014
Published: 30 March 2014
Complementary and alternative medicine is often used by patients with malignant glioma. Although several interactions of various alternative agents with chemotherapy are known, none has been described for temozolomide so far.
We report the case of severe liver toxicity with jaundice during radiochemotherapy with temozolomide likely due to interaction with a popular Chinese herbal formula after surgery for glioblastoma. After cessation of the herbal formula as well as the chemotherapy liver enzymes slowly normalized. Due to tumor progression the patient was retreated with temozolomide for 5 cycles without toxicity. Because of further progression combination treatment of bevacizumab and irinotecan was started and again no liver toxicity was observed.
We conclude that the observed toxicity with jaundice was probably caused by an interaction of this popular Chinese formula and temozolomide. This is the first report about a relevant interaction of temozolomide and any herbal formula.
KeywordsTemozolomide Chinese herbs Interaction Liver toxicity Hepatitis
Complementary and alternative medicine (CAM) is frequently used by glioblastoma patients  but treating physicians are often left uninformed about its use. These patients are potentially at increased risk for herb-drug interactions resulting in increased toxicity due to higher serum levels of cytostatics on the one hand or undertreatment due to decreased efficacy caused by lower serum levels on the other hand.
A 56 year old female Caucasian patient was diagnosed with a temporal-parietal glioblastoma WHO IV° after further evaluation for cephalea. Complete resection was performed using 5-aminolevulinic acid guided surgery and postoperative magnetic resonance investigation showed a small rest tumor. The patient had a Karnofsky performance status scale of 90% after resection without neurological deficiencies and was referred to our department for further treatment with radiotherapy and temozolomide (TEM). Co-medication consisted of dexamethason 4 mg per day because of edema, pantoprazol, levetiracetam and mirtazapine because of depression. Further medical history consisted of hypertension and recurrent cutaneous herpes infections. Adjuvant concomitant radiochemotherapy (RCT) was started with an absolute dose of 140 mg TEM per day 4 weeks after primary resection. Furthermore, prophylactic valaciclovir was prescribed. Treatment was initially well tolerated and the steroid was tampered. Unfortunately, TEM had to be stopped after 32 days of treatment and 24 fractions of radiotherapy because of grade II° thrombopenia and increasing liver enzymes. Mirtazapine, valaciclovir and pantoprazol were paused and radiotherapy was completed as planned after 30 fractions. Because of further increasing liver enzymes and jaundice (bilirubin: 16.7 mg/dl; AST: 263 U/l; ALT: 585 U/l) the patient was hospitalized and underwent further evaluation including exclusion of viral hepatitis, Epstein-Barr virus or cytomegalovirus-infection, computed tomography scan as well as autoantibody screening to exclude an autoimmune hepatitis. Endoscopic retrograde endoscopy excluded pathology of the biliary or pancreatic ductal system. A negative herpes polymerase chain reaction ruled out systemic herpes infection and levetiracetam was reduced in the absence of seizures with the intention to reduce co-medications.
Unfortunately, a [18 F]-fluorethylenthyrosin positron emission tomography positive residual tumor was detected 2 months after the end of radiotherapy. Therefore, despite normalization of the liver parameters was still pending we decided to restart TEM after repeated briefing of the patient to omit any CAM, because we were convinced that this toxic hepatitis was primarily caused by the addition of this Chinese herbal formula. Thus, TEM with an absolute dose of 250 mg per day for 5 days every 4 weeks was re-introduced, supportive medication with valaciclovir and 500 mg bi-daily levetiracetam remained unchanged. We continued treatment for 5 cycles of TEM without any increase of the liver parameters or any other toxicity except for mild cytopenia. Thereafter the patient did not want to continue treatment despite response, because she desired to undergo further complementary treatment. Unfortunately, 3 months after cessation of therapy symptomatic progression due to large edema was diagnosed and combination treatment of bevacizumab and irinotecan was initiated. No liver toxicity or any other severe side effect was observed after 3 months of treatment.
Liver toxicity is a known but very rare side effect of TEM . Reexpositions to TEM in our patient showed that toxic hepatitis was not causally related to TEM treatment alone or caused by the combination with valaciclovir or levetiracetam. Thus, we conclude that the observed liver toxicity was caused by the concomitant intake of the popular Chinese herbal formula, Bu Zhong Yi Qi Wan, in combination with TEM. Some direct hepatotoxicity by the herbal formula itself seems unlikely, because in traditional Chinese medicine Bu Zhong Yi Qi Wan is thought to be protective to the liver, but cannot be completely ruled out. To exclude an unknown toxic product in the formula we asked for some remnants of this formula, but unfortunately it was totally used up by the patient. Furthermore, the Chinese herbs were recommended by a physician not involved in the management of the patient and probable not familiar with GBM. Due to that we were primarily not aware of this possible interaction and this delayed clarification of this case.
Modified form of the Chinese herbal formula called Bu Zhong Yi Qi Wan
Name and species
Zhi Gan Cao
Rhizoma Atractylodes macrocephala
Radix Angelicae sinensis
Furthermore, liver toxicity due to pantoprazol or mirtazapine seems unlikely, because they were started 6 weeks before the start of RCTX without any toxicity and the overall low incidence of liver toxicity of these drugs.
Nevertheless, while the exact mechanism remains unclear, we still observed a severe liver toxicity with the combination of TEM and a popular Chinese formula, which is not reported up to now in the literature. In face of the frequent use of CAM and Chinese herbs in patients with malignant glioma we want to alert cancer physicians about this possible side effect.
We hope to inspire the discussion about the safety of any herbal formulas in combination with cytotoxic therapies and encourage physicians to seek faithful conversations dealing with the use of CAM in cancer patients. There are several reports on the detrimental effects of CAM on the efficacy of chemotherapeutic agents such as St. John’s wort with irinotecan or imatinib  or ascorbic acid and green tea with bortezomib [8, 9] to name but a few. Therefore, we think that a comprehensive management of our patients should also include education about the risk of interactions with herbal formulas.
We state that patient’s privacy is not compromised by this report and informed consent for publication was obtained.
We thank the patient for her consent for publication of this case report.
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