Skip to main content

Advertisement

Log in

Occurrence of non-central nervous system cancers during postoperative follow-up of patients who underwent surgery for a WHO grade II glioma: implications for therapeutic management

  • Case Study
  • Published:
Journal of Neuro-Oncology Aims and scope Submit manuscript

Abstract

Purpose

Survival is currently prolonged in WHO grade II glioma (GIIG). Although exceptionally described, long-term survivors may develop second primary cancers outside the central nervous system (CNS). Here, a consecutive series explored the association between non-CNS cancers (nCNSc) and GIIG in patients who underwent glioma resection.

Methods

Inclusion criteria were adult patients operated for a GIIG who experienced nCNSc following cerebral surgery.

Results

Nineteen patients developed nCNSc after GIIG removal (median time 7.3 years, range 0.6–17.3 years), including breast cancers (n = 6), hematological cancers (n = 2), liposarcomas (n = 2), lung cancers (n = 2), kidney cancers (n = 2), cardia cancers (n = 2), bladder cancer (n = 1), prostate cancer (n = 1) and melanoma (n = 1). The mean extent of GIIG resection was 91.68 ± 6.39%, with no permanent neurological deficit. Fifteen oligodendrogliomas and 4 IDH-mutated astrocytomas were diagnosed. Adjuvant treatment was administrated in 12 patients before nCNSc onset. Moreover, 5 patients underwent reoperation. The median follow-up from initial GIIG surgery was 9.4 years (range 2.3–19.9 years). Nine patients (47%) died in this period. The 7 patients who deceased from the second tumor were significantly older at nCNSc diagnosis than the 2 patients who died from the glioma (p = 0.022), with a longer time between GIIG surgery and the occurrence of nCNSc (p = 0.046).

Conclusion

This is the first study investigating the combination between GIIG and nCNSc. Because GIIG patients are living longer, the risk to experience second neoplasm and to die from it is increasing, especially in older patients. Such data may be helpful for tailoring the therapeutic strategy in neurooncological patients developing several cancers.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

Data availability statement

Data that were used in the present study are available from the corresponding author upon request.

References

  1. Rigau V, Zouaoui S, Mathieu-Daudé H, Darlix A, Maran A, Trétarre B et al (2011) French brain tumor database: 5-year histological results on 25 756 cases. Brain Pathol 21(6):633–644

    Article  PubMed  PubMed Central  Google Scholar 

  2. Duffau H (2017) Diffuse Low-Grade Gliomas in Adults, 2nd edn. Springer International Publishing, New York

    Book  Google Scholar 

  3. Pignatti F, van den Bent M, Curran D, Debruyne C, Sylvester R, Therasse P et al (2002) European Organization for Research and Treatment of Cancer Brain Tumor Cooperative Group; European Organization for Research and Treatment of Cancer Radiotherapy Cooperative Group. Prognostic factors for survival in adult patients with cerebral low-grade glioma. J Clin Oncol 20(8):2076–2084

    Article  PubMed  Google Scholar 

  4. Hamdan N, Duffau H (2021) Extending the multistage surgical strategy for recurrent initially low-grade gliomas: functional and oncological outcomes in 31 consecutive patients who underwent a third resection under awake mapping. J Neurosurg 136(4):1035–1044

    Article  PubMed  Google Scholar 

  5. Obara T, Blonski M, Brzenczek C, Mézières S, Gaudeau Y, Pouget C et al (2020) Adult diffuse low-grade gliomas: 35-year experience at the Nancy france neurooncology unit. Front Oncol 10:574679

    Article  PubMed  PubMed Central  Google Scholar 

  6. Lemaitre AL, Herbet G, Ng S, Moritz-Gasser S, Duffau H (2022) Cognitive preservation following awake mapping-based neurosurgery for low-grade gliomas: a longitudinal, within-patient design study. Neuro Oncol 24(5):781–793

    Article  PubMed  Google Scholar 

  7. Ng S, Herbet G, Moritz-Gasser S, Duffau H (2020) Return to work following surgery for incidental diffuse low-grade glioma: a prospective series with 74 patients. Neurosurgery 87:720–729

    Article  PubMed  Google Scholar 

  8. Scarbrough PM, Akushevich I, Wrensch M, Il’yasova D (2014) Exploring the association between melanoma and glioma risks. Ann Epidemiol 24(6):469–474

    Article  PubMed  PubMed Central  Google Scholar 

  9. Scheurer ME, Etzel CJ, Liu M, Barnholtz-Sloan J, Wiklund F, Tavelin B et al (2010) Familial aggregation of glioma: a pooled analysis. Am J Epidemiol 172:1099–1107

    Article  PubMed  PubMed Central  Google Scholar 

  10. Kim JY, Jackman JG, Woodring S, McSherry F, Herndon JE, Desjardins A et al (2019) Second primary cancers in long-term survivors of glioblastoma. Neurooncol Pract 6(5):386–391

    PubMed  PubMed Central  Google Scholar 

  11. Tabouret E, Barrié M, Vicier C, Goncalves A, Chinot O, Viens P et al (2012) Association of carcinoid tumor and low grade glioma. World J Surg Oncol 10:236

    Article  PubMed  PubMed Central  Google Scholar 

  12. Louis DN, Perry A, Wesseling P, Brat DJ, Cree IA, Figarella-Branger D et al (2021) The 2021 WHO classification of tumors of the central nervous system: a summary. Neuro Oncol 23:1231–1251

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. De Witt Hamer PC, Robles SG, Zwinderman AH, Duffau H, Berger MS (2012) Impact of intraoperative stimulation brain mapping on glioma surgery outcome: a meta-analysis. J Clin Oncol 30(20):2559–2565

    Article  PubMed  Google Scholar 

  14. Duffau H (2021) New philosophy, clinical pearls, and methods for intraoperative cognition mapping and monitoring “à la carte” in brain tumor patients. Neurosurgery 88(5):919–930

    Article  PubMed  Google Scholar 

  15. Duffau H, Ng S, Lemaitre AL, Moritz-Gasser S, Herbet G (2022) Constant multi-tasking with time constraint to preserve across-network dynamics throughout awake surgery for low-grade glioma: a necessary step to enable patients resuming an active life. Front Oncol 12:924762

    Article  PubMed  PubMed Central  Google Scholar 

  16. Mandonnet E, Delattre JY, Tanguy ML, Swanson KR, Carpentier AF, Duffau H et al (2003) Continuous growth of mean tumor diameter in a subset of grade II gliomas. Ann Neurol 53:524–528

    Article  PubMed  Google Scholar 

  17. Duffau H, Taillandier L (2015) New concepts in the management of diffuse low-grade glioma: proposal of a multistage and individualized therapeutic approach. Neuro Oncol 17:332–342

    CAS  PubMed  Google Scholar 

  18. O’Brien MM, Donaldson SS, Balise RR, Whittemore AS, Link MP (2010) Second malignant neoplasms in survivors of pediatric Hodgkin’s lymphoma treated with low-dose radiation and chemotherapy. J Clin Oncol 28(7):1232–1239

    Article  PubMed  PubMed Central  Google Scholar 

  19. Grantzau T, Mellemkjær L, Overgaard J (2013) Second primary cancers after adjuvant radiotherapy in early breast cancer patients: a national population based study under the Danish breast cancer cooperative group (DBCG). Radiother Oncol 106(1):42–49

    Article  PubMed  Google Scholar 

  20. Momota H, Narita Y, Miyakita Y, Shibui S (2013) Secondary hematological malignancies associated with temozolomide in patients with glioma. Neuro Oncol 15(10):1445–1450

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Sharma A, Gupta D, Mohanti BK, Thulkar S, Dwary A, Goyal S et al (2009) Non-Hodgkin lymphoma following temozolomide. Pediatr Blood Cancer 53(4):661–662

    Article  PubMed  Google Scholar 

  22. Su YW, Chang MC, Chiang MF, Hsieh RK (2005) Treatment-related myelodysplastic syndrome after temozolomide for recurrent high-grade glioma. J Neurooncol 71(3):315–318

    Article  PubMed  Google Scholar 

  23. Chamberlain MC, Raizer J (2009) Extended exposure to alkylator chemotherapy: delayed appearance of myelodysplasia. J Neurooncol 93(2):229–232

    Article  CAS  PubMed  Google Scholar 

  24. Vega-Stromberg T (2003) Chemotherapy-induced secondary malignancies. J Infus Nurs 26(6):353–361

    Article  PubMed  Google Scholar 

  25. Lu G, Li J, Wang S, Pu J, Sun H, Wei Z et al (2018) The fluctuating incidence, improved survival of patients with breast cancer, and disparities by age, race, and socioeconomic status by decade, 1981–2010. Cancer Manag Res 10:4899–4914

    Article  PubMed  PubMed Central  Google Scholar 

  26. Molenaar WM, de Leij L, Trojanowski JQ (1991) Neuroectodermal tumors of the peripheral and the central nervous system share neuroendocrine N-CAM-related antigens with small cell lung carcinomas. Acta Neuropathol 83:46–54

    Article  CAS  PubMed  Google Scholar 

  27. Anbazhagan R, Tihan T, Bornman DM, Johnston JC, Saltz JH, Weigering A et al (1999) Classification of small cell lung cancer and pulmonary carcinoid by gene expression profils. Cancer Res 59(20):5119–5122

    CAS  PubMed  Google Scholar 

  28. Zhang Y, Wei H, Tang K, Lin D, Zhang C, Mi Y et al (2012) Mutation analysis of isocitrate dehydrogenase in acute lymphoblastic leukemia. Genet Test Mol Biomarkers 16(8):991–995

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Maharjan U, Kauppila JH (2022) Survival trends in gastric cancer patients between 1987 and 2016: a population-based cohort study in Finland. Gastric Cancer 25(6):989–1001

    Article  PubMed  PubMed Central  Google Scholar 

  30. International CLL-IPI working group (2016) An international prognostic index for patients with chronic lymphocytic leukaemia (CLL-IPI): a meta-analysis of individual patient data. Lancet Oncol 17(6):779–790

    Article  Google Scholar 

  31. Zhang L, Wu B, Zha Z, Qu W, Zhao H, Yuan J (2019) Clinicopathological factors in bladder cancer for cancer-specific survival outcomes following radical cystectomy: a systematic review and meta-analysis. BMC Cancer 19(1):716

    Article  PubMed  PubMed Central  Google Scholar 

  32. Tie H, Luo J, Shi R, Li Z, Chen D, Wu Q (2021) Characteristics and prognosis of synchronous multiple primary lung cancer after surgical treatment: A systematic review and meta-analysis of current evidence. Cancer Med 10(2):507–520

    Article  PubMed  Google Scholar 

Download references

Funding

The author declares that no financial support was received during the preparation of this manuscript.

Author information

Authors and Affiliations

Authors

Contributions

Author contributions to the study and manuscript preparation include the following: Conception and design: HD. Acquisition of data: HD. Analysis and interpretation of data: HD. Drafting the article: HD. Critically revising the article: HD. Reviewed submitted version of manuscript: HD. Approved the final version of the manuscript: HD. Study supervision: HD.

Corresponding author

Correspondence to Hugues Duffau.

Ethics declarations

Competing interests

The author has no competing financial or nonfinancial interests to disclose.

Prior presentations

None.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Duffau, H. Occurrence of non-central nervous system cancers during postoperative follow-up of patients who underwent surgery for a WHO grade II glioma: implications for therapeutic management. J Neurooncol 162, 237–244 (2023). https://doi.org/10.1007/s11060-023-04288-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11060-023-04288-5

Keywords

Navigation