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Elderberry interaction with pazopanib in a patient with soft‑tissue sarcoma: A case report and literature review

  • Authors:
    • Nikki Agarwal
    • Ankit Mangla
  • View Affiliations

  • Published online on: March 20, 2024     https://doi.org/10.3892/mco.2024.2734
  • Article Number: 36
  • Copyright: © Agarwal et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

Elderberry flower extract is marketed as an herbal supplement with purported benefits in boosting the immune system. The use of elderberry increased during the coronavirus pandemic. However, the interaction of elderberry with cytotoxic medicines has remained elusive. Pazopanib is a multikinase inhibitor approved for patients diagnosed with soft‑tissue sarcoma. The present study reported on the case of a middle‑aged woman diagnosed with localized intermediate‑grade sarcoma of the left sartorius muscle who received neoadjuvant pazopanib with radiation therapy. The patient had no other medical comorbidities and only took over‑the‑counter (OTC) elderberry supplements for numerous years to ‘boost’ her immune system. She started pazopanib at 400 mg per os (PO) daily, which was increased to 800 mg PO daily after a week. By week three on pazopanib, the patient reported intense nausea and a number of loose stools, requiring anti‑nausea medication. By the fourth week on pazopanib, laboratory tests showed grade 3 liver injury, as demonstrated by a fivefold rise in liver enzymes along with severe nausea and loose stools. All medications, including elderberry supplement, were stopped. Within two weeks of stopping all medicines, the liver enzymes started normalizing within two weeks and were normal by the end of four weeks. Pazopanib treatment was resumed without the recurrence of side effect. Pazopanib is metabolized in the liver via the cytochrome P 450 (CYP)3A4 enzyme pathway. Hence, potent inhibitors of CYP3A4 are avoided for concurrent use with pazopanib. Small in vitro studies on elderberry extracts have shown weak inhibition of CYP3A4. However, considering the wide usage of elderberry and the availability of mixed supplements OTC, it is essential to pursue clinical studies in cancer patients to understand the interactions of elderberry extracts with cytotoxic medicines. In this report, the scientific evidence behind the use of elderberry was reviewed and a hypothesis of its interaction with pazopanib was proposed. 

Introduction

Cancer care is complex not only because of the nature of the diagnosis but also due to the toxicity of the treatment. Patients diagnosed with any cancer often suffer from comorbid conditions that bring in a significant risk of drug interactions (1). However, several patients are frequently on supplements (herbal and non-herbal). Patients diagnosed with cancer tend to gravitate towards alternative medicine, primarily because of the purported nontoxic approach (2,3). However, a clear understanding of the merits and flaws is lacking due to a dearth of well-designed clinical trials. The interaction of herbal medicine with several anti-cancer therapies has also remained elusive. Elderberry (Sambucus nigra) is a woody, deciduous shrub that grows across the Americas, Europe, Asia and the South Pacific. Elderberry supplements have become immensely popular in the US, particularly after the coronavirus pandemic (COVID-19) (4,5).

Pazopanib is a multikinase inhibitor of vascular endothelial growth factor receptors, platelet-derived growth factor receptor and c-kit (6). Pazopanib is approved by the US Food and Drug Administration (USFDA) for patients with metastatic renal cell carcinoma and those with metastatic or locally advanced unresectable soft-tissue sarcoma (STS) who experienced progression after chemotherapy (7). Several trials in patients with localized high-risk extremity STS have also explored the utility of administering neoadjuvant pazopanib with preoperative radiation therapy (RT) with mixed results (8,9). The patient presented in the current study was consuming elderberry supplements when she started pazopanib. The current study reports the case of a woman diagnosed with high-risk localized extra-skeletal myxoid chondrosarcoma treated with neoadjuvant pazopanib given concurrently with preoperative RT who had a potential drug-drug interaction with over-the-counter (OTC) elderberry supplement.

Case report

A 65-year-old woman presented to urgent care of University Hospitals Cleveland Medical Center (Cleveland, Ohio) in February 2022 with a lump on her left thigh, which had grown slowly over the last six months. MRI of the femur showed a 13x7.4x7.2 cm mass in the left sartorius, abutting the adjacent neuro-vascular bundle. The patient was seen by an orthopedic oncologist and had a core needle biopsy, which read as unclassified pleomorphic spindle-shaped sarcoma (intermediate grade, 18 mitoses per 10 high-power fields, and no necrosis). The chest CT scan did not show any metastasis. The case was discussed by the multidisciplinary tumor board. The patient was referred to radiation oncology for preoperative radiation and to medical oncology for discussion of neoadjuvant pazopanib. At the first visit to medical oncology, the patient did not report any comorbidities. The patient reported taking an elderberry supplement (quantity unspecified) since the beginning of the COVID-19 pandemic in 2020. The clinical exam was significant for an ~15 cm long and 8 cm wide hard, immobile mass on the anterior part of the left thigh. The mass was not tender and the skin over the mass could be pinched. No regional lymphadenopathy or organomegaly was noted on the clinical exam. The rest of the systemic exam was unremarkable. The vital signs on the initial visit were within normal limits. Laboratory tests on the first visit were also within normal limits (Table I).

Table I

Relevant laboratory tests at various time-points.

Table I

Relevant laboratory tests at various time-points.

Parameter (normal range)Day 0Day 7Day 28Day 35Day 49
Blood count     
     Hemoglobin, (12.0-16.0) g/dl13.312.913.413.112.8
     WBC, (4.4-11.3) x103/Ul7.15.34.34.05.9
     Platelets, (150-450) x103/Ul322276257210308
Liver enzymes     
     AST, (9-39) IU/l172318710423
     ALT, (7-45) IU/l141722814230
     LDH, (84-246) IU/l178245278200161
Infections     
     Hepatitis B AgNDNDNegNDND
     Hepatitis B core AbNDNDNegNDND
     Hepatitis CNDNDNegNDND
     HIVNDNDNegNDND

[i] Ab, antibody; Ag, antigen; ALT, alanine transaminase; AST, aspartate transaminase; HIV, human immunodeficiency virus, IU, international units; ND, not determined; LDH, lactate dehydrogenase; WBC, white blood cells; Neg, negative.

The patient started treatment with pazopanib at 400 mg per os (PO) daily for a week, and it was then increased to 800 mg PO daily. However, by the second week on the full dose of pazopanib, the patient started noticing increased nausea and occasional loose stools. The nausea kept getting worse over the ensuing weeks. By week four on pazopanib, the patient's alanine transferase (ALT) and aspartate transaminase (AST) levels had risen by 4-5-fold. At this time, further investigation was performed with blood tests. The patient tested negative for hepatitis B and C and human immunodeficiency virus. Ultrasound examination of the liver was also unremarkable. At this point, treatment with pazopanib was stopped temporarily and all medicines and supplements taken by the patient were reviewed. The patient was taking a calcium supplement and multivitamins apart from the elderberry supplement, which was permanently discontinued. Soon after stopping all medicines, the patient felt better as her nausea and occasional loose stools resolved within days. The patient's liver enzymes exhibited a downward trend over the next seven days and normalized by the end of the second week on their own. Since the patient's radiation treatment was still ongoing, pazopanib was resumed at 400 mg PO daily, which was administered for another two weeks. The patient reported no GI upset this time and her liver enzymes remained normal. As for RT, the patient received a total of 50 Gy of external beam radiation to the left thigh mass in 25 fractions over 5 weeks. The RT started in the third week of pazopanib and ended in the eighth week. The timeline of events is depicted in Fig. 1. Four weeks after the completion of RT, the patient underwent surgery. The surgical specimen was from a R0 resection and had 85% pathologic necrosis. At two years post-surgery, the patient has no evidence of cancer recurrence.

Discussion

Elderberry has been used in folk medicine to treat cold and flu (10). Historically, various parts of the elderberry plant have been used for specific ailments. A poultice made from the leaves of the elderberry plant has been used to promote healing and relieve joint pains (11). The flower of elderberry has anti-inflammatory and antioxidant properties (11). Hippocrates, in 400 BC, referred to elderberry as his ‘medicine chest’, considering the broad applications of the shrub (12). Two small randomized studies on patients with influenza reported that elderberry use may reduce the duration of symptoms (13-15). The use of elderberry grew exponentially during COVID-19 despite the lack of a demonstrated scientific benefit of the supplement (5). Elderberry supplement is primarily marketed as an herbal dietary supplement that can stimulate the immune system and increase antioxidant levels in the body. However, consuming raw elderberries, leaves and branches may cause severe gastrointestinal (GI) toxicity (16). The clinical use of elderberry in patients diagnosed with cancer is experimental. As with various other herbal supplements, the interaction of elderberry with anti-cancer therapies remains unknown to a large extent.

Several in vitro studies have explored the interaction of various herbal products with cytochrome P450 (CYP) enzymes in the context of non-cancer conditions, such as pregnancy. Several products, including fennel seeds, ginger, horsetails, raspberry leaf, cranberry and black elderberry had varying half-maximal inhibitory concentrations (IC50s) for CYP1A2, CYP2D6 and CYP3A4. Within the CYP family, numerous clinically used medicines are metabolized by CYP3A4 in particular, which is also considered a significant candidate for pharmacokinetic interactions (17). Although several herbs have shown in vitro inhibition of CYP3A4, grapefruit juice and St. John's Wort have proven clinically relevant in vivo interactions with CYP3A4(18). Pazopanib is metabolized in the liver primarily through the CYP3A4 enzyme with a minor contribution from CYP1A2 and CYP2C8(19). Strong inhibitors of CYP3A4 are to be avoided for concurrent use with pazopanib. If it is necessary to administer potent CYP3A4 inhibitors, then the dose of pazopanib should be reduced to 400 mg daily (from the recommended dose of 800 mg PO daily). The USFDA label for pazopanib strictly prohibits the concurrent use of grapefruit juice with pazopanib.

Two studies have reported the in vitro activity of black elderberry against CYP3A4 (18,20) However, Schrøder-Aasen et al (18) only tested Echinacea purpurea, which was part of a commercial product called Sambucus Force (marketed as Elderberry Defense). The authors demonstrated the significant inhibition of CYP3A4 by E. purpurea and drew an inference regarding the activity of S. nigra without performing any dedicated experiments. Langhammer and Nilsen (20) conducted dedicated experiments with S. nigra and reported 100% inhibition of CYP3A4 at high concentrations. Since high concentrations of the herb (S. nigra) were needed to reach the IC50, the authors concluded that S. nigra does not inhibit CYP3A4 in vitro. However, Schrøder-Aasen et al (18) did acknowledge that S. nigra may have inhibitory effects on CYP3A4 at high concentrations. Despite the increasing popularity of elderberry-based products, no other studies have evaluated the metabolic activity of elderberry on CYP3A4, neither in vitro nor in vivo.

STS are a rare group of cancers of mesenchymal origin. Although sarcomas can arise anywhere in the body, the extremities and retroperitoneum are the most common sites of origin (21). Intending to preserve the limb, surgery with perioperative (pre- or post-operative RT) is the treatment of choice in patients with localized sarcoma (22). In the present case, neoadjuvant pazopanib was added to radiation to improve the local control rates based on the results of the PASAART-1 and -2 trials (8). The GI toxicity experienced by the patient soon after starting pazopanib and the resolution of symptoms after stopping elderberry hint towards a possible drug-drug interaction. The patient was able to resume pazopanib without the return of adverse effects when elderberry was no longer consumed. It should be acknowledged that the patient restarted pazopanib at a lower dose. In the phase 1 study of pazopanib, there was a linear growth in the maximum concentration of the drug with increasing doses (the doses were tested from 50 to 2,000 mg). However, there was no linear relationship observed between the dose and the toxicity of pazopanib. Only one patient developed a grade 3 rise in AST levels and was on a dose of 300 mg PO twice a day. Hence, it is unlikely that starting at half the dose of pazopanib prevented the resurgence of the hepatic and GI toxicity (23). Although it may seem that elderberry is a weak inhibitor of CYP3A4, it may lead to significant drug interactions if consumed in high quantities (18).

Since the patient of the present study was receiving treatment with curative intent in the neoadjuvant setting, a detailed workup (including liver biopsy, CYP3A4 activity, pazopanib levels, etc.) for proving the drug-drug interaction was deemed as time-consuming and not in the best interest of the patient. Furthermore, the transaminitis and GI toxicity resolved within two weeks, which would have made further testing futile. However, based on the timeline and sequence of events, there may have been a significant drug-drug interaction. The present report aims to highlight the importance of understanding the interaction (both beneficial and detrimental) between herbal supplements and cytotoxic medicines. In vivo mouse experiments have shown the activity of elderberry in breast, bladder and ovarian cancer (24). It is thought that elderberry flower exerts its medicinal effect due to the abundance of polyphenolic compounds contained in it, primarily flavonols, phenolic acid and anthocyanins. In preclinical experiments, rutin, the most common polyphenol in elderberry flowers, affected the viability of neuroblastoma, leukemia and breast cancer cells (24). However, the lack of data demonstrating clinical activity limits the interpretability of the preclinical results. The oncology community is only beginning to realize the importance of integrative oncology. There is an inevitable shift in our perception and acceptance of traditional medicine, including herbal medicine. However, the supplement market is not strictly regulated. The USFDA regulates dietary supplements under the Federal Food, Drug and Cosmetic Act as amended by the Dietary Supplement Health and Education Act from 1994. Under the provisions of this act, dietary supplements do not need any prior approval and the safety of the product is determined primarily through post-market surveillance (25). Considering the complexity of cancer care and the rise in consumption of herbal supplements, it becomes prudent to conduct clinical trials in a controlled setting to determine clinical interactions between allopathic and traditional medicines.

In conclusion, the present study signifies the importance of understanding the potential drug interactions between herbal products and cytotoxic drugs in cancer patients. This report also emphasizes the importance of diligently reconciling the medicine list, including OTC herbal supplements, which often go underreported. More studies are needed to understand the in vitro and in vivo activity of herbal supplements and their potential impact on cancer care.

Acknowledgements

Not applicable.

Funding

Funding: No funding was received.

Availability of data and materials

The data generated in the present study are included in the figures and/or tables of this article.

Authors' contributions

NA and AM wrote the manuscript and researched the references. NA conceived the study and prepared the tables and figures. AM provided expert opinions. Both authors have read and approved the final version of the manuscript. Both authors have confirmed the authenticity of the raw data.

Ethics approval and consent to participate

The case report was exempted from review by the Institutional Review Board at the Case Western Reserve University School of Medicine (Cleveland, USA).

Patient consent for publication

The patient provided consent for the publication of her data.

Competing interests

The authors declare that they have no competing interests.

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Spandidos Publications style
Agarwal N and Mangla A: Elderberry interaction with pazopanib in a patient with soft‑tissue sarcoma: A case report and literature review. Mol Clin Oncol 20: 36, 2024.
APA
Agarwal, N., & Mangla, A. (2024). Elderberry interaction with pazopanib in a patient with soft‑tissue sarcoma: A case report and literature review. Molecular and Clinical Oncology, 20, 36. https://doi.org/10.3892/mco.2024.2734
MLA
Agarwal, N., Mangla, A."Elderberry interaction with pazopanib in a patient with soft‑tissue sarcoma: A case report and literature review". Molecular and Clinical Oncology 20.5 (2024): 36.
Chicago
Agarwal, N., Mangla, A."Elderberry interaction with pazopanib in a patient with soft‑tissue sarcoma: A case report and literature review". Molecular and Clinical Oncology 20, no. 5 (2024): 36. https://doi.org/10.3892/mco.2024.2734