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Chemotherapy-Induced Myelosuppression in Esophageal Cancer Patients: Risks and Suggestions for Its Management

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Summary

Objective

The influential factors of chemotherapy-induced myelosuppression in esophageal cancer in central China are unclear. This study aimed to investigate the effect of commonly used chemotherapy regimens on the incidence of myelosuppression in clinical treatment of esophageal cancer.

Methods

In this retrospective study, 624 patients with esophageal cancer who received six different chemotherapy regimens between 2013 and 2020 at our institute were included. Chemotherapy consisted of lobaplatin, 5-fluorouracil (5-F), lobaplatin and 5-F, nedaplatin, nedaplatin and paclitaxel (PTX), cisplatin and PTX. Multivariable logistic regression analysis was used to explore the risk of myelosuppression among the six different chemotherapy regimens.

Results

Compared with lobaplatin group, the incidence of myelosuppression in patients treated with chemotherapy regimens of lobaplatin and 5-F, nedaplatin, nedaplatin and PTX and cisplatin and PTX were significantly ameliorated. The dose of lobaplatin was significantly reduced (P=0.007) when lobaplatin was combined with 5-F, and the combination could significantly reduce the risk of myelosuppression (P=0.022). Furthermore, chemotherapeutic regimens, the dose of platinum, hemoglobin and uric acid levels, age, sex, total bilirubin and immune-enhancing drugs were found to be strong predictors of developing myelosuppression.

Conclusion

Targeted preventive interventions that enhance immune function, reduce uric acid levels and choose combined medication during chemotherapy should be implemented for high-risk patients to reduce the occurrence of myelosuppression. In addition, the dose of lobaplatin should be adjusted when combined with other chemotherapy drugs to reduce the incidence of myelosuppression.

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References

  1. Allemani C, Matsuda T, Di Carlo V, et al. Global surveillance of trends in cancer survival 2000-14 (CONCORD-3): analysis of individual records for 37513025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries. Lancet (London, England), 2018,391(10125):1023–1075

    Article  Google Scholar 

  2. Bollschweiler E, Plum P, Monig SP, et al. Current and future treatment options for esophageal cancer in the elderly. Expert Opin Pharmacother, 2017,18(10):1001–1010

    Article  CAS  Google Scholar 

  3. Pickens A, Orringer MB. Geographical distribution and racial disparity in esophageal cancer. Ann Thorac Surg, 2003,76(4):S1367–1369

    Article  Google Scholar 

  4. Bosetti C, Levi F, Ferlay J, et al. Trends in oesophageal cancer incidence and mortality in Europe. Int J Cancer, 2008,122(5):1118–1129

    Article  CAS  Google Scholar 

  5. Lordick F, Mariette C, Haustermans K, et al. Oesophageal cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann oncol, 2016,27 (suppl 5):v50–v57

    Article  CAS  Google Scholar 

  6. Ajani JA, J.S. Barthel JS, Bentrem DJ, et al. Esophageal and esophagogastric junction cancers. J Natl Compr Canc Netw, 2011,9(8):830–887

    Article  Google Scholar 

  7. Watanabe M, Otake R, Kozuki R, et al. Recent progress in multidisciplinary treatment for patients with esophageal cancer. Surg Today, 2020,50(1):12–20

    Article  Google Scholar 

  8. Fatehi Hassanabad A, Chehade R, Breadner D, et al. Esophageal carcinoma: Towards targeted therapies. Cell Oncol (Dordr), 2020,43(2):195–209

    Article  Google Scholar 

  9. Carr C, Ng J, Wigmore T. The side effects of chemotherapeutic agents. Curr Anaesth Crit Care, 2008,19(2):70–79

    Article  Google Scholar 

  10. Crawford J, Dale DC, Lyman GH. Chemotherapy-induced neutropenia: risks, consequences, and new directions for its management. Cancer, 2004,100(2):228–237

    Article  Google Scholar 

  11. Groopman JE, Itri LM. Chemotherapy-induced anemia in adults: incidence and treatment. J Natl Cancer Inst, 1999,91(19):1616–1634

    Article  CAS  Google Scholar 

  12. Kuter DJ. Managing thrombocytopenia associated with cancer chemotherapy. Oncology, 2015,29(4):282–294

    PubMed  Google Scholar 

  13. Barreto JN, McCullough KB, Ice LL, et al. Antineoplastic agents and the associated myelosuppressive effects: a review. J Pharm Pract, 2014,27(5):440–446

    Article  Google Scholar 

  14. Taylor SJ, Duyvestyn JM, Dagger SA, et al. Preventing chemotherapy-induced myelosuppression by repurposing the FLT3 inhibitor quizartinib. Sci Transl Med, 2017,9(402):eaam8060

    Article  Google Scholar 

  15. Yin WJ, Yi YH, Guan XF, et al. Preprocedural Prediction Model for Contrast-Induced Nephropathy Patients. J Am Heart Assoc, 2017,6(2):e004498

    Article  Google Scholar 

  16. Epstein RS, Aapro MS, Basu Roy UK, et al. Patient Burden and Real-World Management of Chemotherapy-Induced Myelosuppression: Results from an Online Survey of Patients with Solid Tumors. Adv Ther, 2020,37(8):3606–3618

    Article  Google Scholar 

  17. Grading standard for acute and subacute toxicity of anticancer drugs (WHO standard), Cancer, 1992,(3):254

  18. Saggam A, Kale P, Shengule S, et al. Ayurveda-based Botanicals as Therapeutic Adjuvants in Paclitaxel-induced Myelosuppression. Front Pharmacol, 2022,13: 835616

    Article  CAS  Google Scholar 

  19. Zheng Y, Li Y, Liu X, et al. Multicentre Comparison of the Toxicity and Effectiveness of Lobaplatin-Based Versus Cisplatin-Based Adjuvant Chemotherapy in Oesophageal Carcinoma. Front Oncol, 2021,11:668140

    Article  Google Scholar 

  20. Park MH, Jung IK, Min WK, et al. Neuropeptide Y improves cisplatin-induced bone marrow dysfunction without blocking chemotherapeutic efficacy in a cancer mouse model. BMB reports, 2017,50(8):417–422

    Article  CAS  Google Scholar 

  21. Javarappa KK, D. Tsallos D, Heckman CA. A Multiplexed Screening Assay to Evaluate Chemotherapy-Induced Myelosuppression Using Healthy Peripheral Blood and Bone Marrow. SLAS Discov, 2018,23(7):687–696

    Article  CAS  Google Scholar 

  22. Reddel CJ, Tan CW, Chen VM. Thrombin Generation and Cancer: Contributors and Consequences. Cancers, 2019,11(1):100

    Article  CAS  Google Scholar 

  23. Sun W, Ren H, Gao CT, et al. Clinical and Prognostic Significance of Coagulation Assays in Pancreatic Cancer Patients With Absence of Venous Thromboembolism. American J Clin Oncol, 2015,38(6):550–556

    Article  CAS  Google Scholar 

  24. Bestari MB, Agustanti N. Obstructive jaundice due to pancreatic metastasis from non-small cell lung cancer. Acta medica Indonesiana, 2013,45(3):216–219

    PubMed  Google Scholar 

  25. Wang XB, Wu DJ, Chen WP, et al. Impact of radiotherapy on immunological parameters, levels of inflammatory factors, and clinical prognosis in patients with esophageal cancer. J Radiat Res, 2019,60(3):353–363

    Article  CAS  Google Scholar 

  26. Bhat S, Coleman HG, Yousef F, et al. Risk of malignant progression in Barrett’s esophagus patients: results from a large population-based study. J Natl Cancer Inst, 2011,103(13):1049–1057

    Article  Google Scholar 

  27. Huang FL, Yu SJ. Esophageal cancer: Risk factors, genetic association, and treatment. Asian J Surg, 2018, 41(3):210–215

    Article  Google Scholar 

  28. Cook MB, Chow WH, Devesa SS. Oesophageal cancer incidence in the United States by race, sex, and histologic type, 1977–2005. Brit J Cancer, 2009,101(5):855–859

    Article  CAS  Google Scholar 

  29. Ohira M, Kubo N, Yamashita Y, et al. Impact of Chemoradiation-induced Myelosuppression on Prognosis of Patients with Locally Advanced Esophageal Cancer After Chemoradiotherapy Followed by Esophagectomy. Anticancer Res, 2015,35(9):4889–4895

    PubMed  Google Scholar 

  30. Ojima T, Nakamori M, Nakamura M, et al. Phase I/II study of divided-dose docetaxel, cisplatin and fluorouracil for patients with recurrent or metastatic squamous cell carcinoma of the esophagus. Dis Esophagus, 2017,30(2):1–7

    CAS  PubMed  Google Scholar 

  31. Lan YQ, Wu RP, Huang XB, et al. Paclitaxel, oxaliplatin, 5-fluorouracil and leucovorin combination chemotherapy in patients with recurrent or metastatic gastric cancer. Tumori, 2018,104(1):22–29

    Article  CAS  Google Scholar 

  32. J. Liu, Z. Wang, Wu K, et al. Paclitaxel or 5-fluorouracil/esophageal stent combinations as a novel approach for the treatment of esophageal cancer. Biomaterials, 2015,53:592–599

    Article  CAS  Google Scholar 

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Correspondence to Zi-ming Zheng or Yu Zhang.

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Conflict of Interest Statement

The authors declare no conflicts of interest.

The present research was supported by a grant from the National Key R&D Programmes (NKPs) of China (No. 2017YFC0909900).

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Zhang, Ql., Wu, Tt., Han, Y. et al. Chemotherapy-Induced Myelosuppression in Esophageal Cancer Patients: Risks and Suggestions for Its Management. CURR MED SCI 42, 530–537 (2022). https://doi.org/10.1007/s11596-022-2587-3

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  • DOI: https://doi.org/10.1007/s11596-022-2587-3

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