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High-risk features in primary versus secondary enucleated globes with advanced retinoblastoma: a retrospective histopathological study

Abstract

Purpose

The management of bilateral advanced retinoblastoma (RB) cases is challenging with attempts to use neoadjuvant therapy salvaging of one of the globes. Our aim in this study was to demonstrate the effect of this primary therapy on the histopathological features and risk factors in secondary enucleated compared to primarily enucleated globes with groups D and E RB.

Methods

We retrospectively reviewed all enucleated globes with advanced RB received in the pathology laboratories over a period of 5 years. Patients were divided into two groups: one with primary enucleations and another with at least one secondary enucleated globe, and their demographic and clinical data were analyzed. The enucleated globes in the two groups were analyzed to compare the general histopathological features including tumor seeding, size, differentiation, growth pattern, mitotic figures, and focality. More importantly, high-risk features: choroidal invasion, optic nerve (ON) invasion, iris/anterior chamber invasion, ciliary body invasion, and scleral and extra-scleral extension, as well as the pathological classification of the tumor (pT) according to the American Joint Committee on Cancer 7th edition were also compared between the two groups.

Results

We had a total of 106 enucleated globes (78 primary and 28 secondary enucleations) from 99 patients with advanced RB (73 patients with primarily and 26 with secondarily enucleated globes). Demographic and clinical profiles of patients were similar in both, but the mean interval from presentation to enucleation was significantly longer in the secondary enucleations (P = 0.015). Rare/occasional mitotic figures were observed in secondary enucleations using multivariate analysis (P = 0.003). Primarily enucleated globes had higher risk of tumor seeding (P = 0.020), post-laminar/surgical margin ON invasion (P = 0.001), and massive choroidal invasion (P = 0.028). Half of the secondary enucleated globes had tumors confined to the globes without invasion (pT1) and statistically significant lower tumor classifications (pT1 or pT2a) compared to primary enucleations (P =0.001). However, 18% of the secondarily enucleated globes in 3 patients had unfavorable outcome with RB-related mortality after a period of 1–4 years.

Conclusions

Secondary enucleated globes with advanced RB show favorable histopathological findings mainly less mitosis. These eyes have significantly lower chance for harboring choroidal and ON invasion, thus mostly classified as pT1 or pT2a when compared to primarily enucleated globes. The decision for secondary enucleation was observed to be significantly delayed (8.0 months ± 9.8). Prompt decision for needed enucleation based on the response to primary treatment and careful histopathological examination of enucleated globes are essential to prevent disease-related mortality.

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References

  1. Stiller CA, Parkin DM (1996) Geographic and ethnic variations in the incidence of childhood cancer. Br Med Bull 52:682–703

    CAS  Article  Google Scholar 

  2. Berger AH, Knudson AG, Pandolfi PP (2011) A continuum model for tumour suppression. Nature 476:163–169

    CAS  Article  Google Scholar 

  3. Darwich R, Ghazawi FM, Rahme E et al (2019) Retinoblastoma incidence trends in Canada: a national comprehensive population-based study. J Pediatr Ophthalmol Strabismus 56(2):124–130. https://doi.org/10.3928/01913913-20190128-02

    Article  PubMed  Google Scholar 

  4. Yahaya JJ, Rugwizangoga B, Mremi A, Munema A (2019) Clinicopathological findings of retinoblastoma: a 10-year experience from a tertiary hospital in Kampala, Uganda. J Ophthalmol 2019:5829284. https://doi.org/10.1155/2019/5829284eCollection 2019

    Article  PubMed  PubMed Central  Google Scholar 

  5. Abramson DH, Shields CL, Munier FL, Chantada GL (2015) Treatment of retinoblastoma in 2015: agreement and disagreement. JAMA Ophthalmol 133(11):1341–1347. https://doi.org/10.1001/jamaophthalmol.2015.3108

    Article  PubMed  Google Scholar 

  6. Bechrakis NE, Bornfeld N, Schueler A, Coupland SE, Henze G, Foerster MH (1998) Clinicopathologic features of retinoblastoma after primary chemoreduction. Arch Ophthalmol 116(7):887–893. https://doi.org/10.1001/archopht.116.7.887

    CAS  Article  PubMed  Google Scholar 

  7. Brennan RC, Qaddoumi I, Billups CA, Free TL, Haik BG, Rodriguez-Galindo C, Wilson MW (2015) Comparison of high-risk histopathological features in eyes with primary or secondary enucleation for retinoblastoma. Br J Ophthalmol 99:1366–1371

    Article  Google Scholar 

  8. Fabian ID, Stacey AW, Johnson KC, Chowdhury T, Duncan C, Reddy MA, Sagoo MS (2018) Primary enucleation for group D retinoblastoma in the era of systemic and targeted chemotherapy: the price of retaining an eye. Br J Ophthalmol 102:265–271

    Article  Google Scholar 

  9. Alkatan HM, AlQahtani FS, Maktabi AMY (2020) Enucleated globes with advanced retinoblastoma: correlation of histopathological features and reclassification of tumors according to the 8th Edition of the American Joint Commission on Cancer (AJCC). Int Ophthalmol. https://doi.org/10.1007/s10792-020-01342-3

    Article  PubMed  Google Scholar 

  10. Kaliki S, Mittal P, Mohan S, Chattannavar G, Jajapuram SD, Mohamed A, Palkonda VAR (2019) Bilateral advanced (group D or E) intraocular retinoblastoma: outcomes in 72 Asian Indian patients. Eye 33:1297–1304. https://doi.org/10.1038/s41433-019-0409-z

    Article  PubMed  PubMed Central  Google Scholar 

  11. Gallie BL, Budning A, DeBoer G, Thiessen JJ, Koren G, Verjee Z, Ling V, Chan HS (1996) Chemotherapy with focal therapy can cure intraocular retinoblastoma without radiotherapy. Arch Ophthalmol 114:1321–1328

    CAS  Article  Google Scholar 

  12. Murphree AL, Villablanca JG, Deegan WF, Sato JK, Malogolowkin M, Fisher A, Parker R, Reed E, Gomer CJ (1996) Chemotherapy plus local treatment in the management of intraocular retinoblastoma. Arch Ophthalmol 114:1348–1356

    CAS  Article  Google Scholar 

  13. Shields CL, DePotter P, Himelstein BP, Meadows AT, Maris JM (1996) Chemoreduction in the initial management of intraocular retinoblastoma. Arch Ophthalmol 114:1330–1338

    CAS  Article  Google Scholar 

  14. Wahdan M, Shaleel A, El Zomor H, El Baz H (2018) Outcome of unilateral intraocular retinoblastoma. Egypt J Hospital Med 73(9):7412–7417. https://doi.org/10.12816/ejhm.2018.18581

    Article  Google Scholar 

  15. Jain M, Rojanaporn D, Chawla B, Sundar G, Gopal L, Khetan V (2019) Retinoblastoma in Asia. Eye (Lond) 1:87–96. https://doi.org/10.1038/s41433-018-0244-7

    Article  Google Scholar 

  16. Chawla B, Hasan F, Azad R, Seth R, Upadhyay AD, Pathy S, Pandey RM (2015) Clinical presentation and survival of retinoblastoma in Indian children. Br J Ophthalmol 100:172–178

    Article  Google Scholar 

  17. Singh U, Katoch D, Kaur S, Dogra MR, Bansal D, Kapoor R (2018) Retinoblastoma: a sixteen-year review of the presentation, treatment, and outcome from a tertiary care institute in Northern India. Ocul Oncol Pathol 4:23–32

    Article  Google Scholar 

  18. Shah PK, Narendran V, Kalpana N (2015) Outcomes of intra-and extraocular retinoblastomas from a single institute in South India. Ophthalmic Genet 36:248–250

    Article  Google Scholar 

  19. Fabian ID, Stacey AW, Chowdhury T, Duncan C, Karaa EK, Scheimberg I, Reddy MA, Sagoo MS (2017) High-risk histopathology features in primary and secondary enucleated international intraocular retinoblastoma classification group D eyes. Ophthalmology 124(6):851–858. https://doi.org/10.1016/j.ophtha.2017.01.048

    Article  PubMed  Google Scholar 

  20. Demirci H, Eagle RC, Shields CL, Shields JA (2003) Histopathologic findings in eyes with retinoblastoma treated only with chemoreduction. Arch Ophthalmol 121(8):1125–1131. https://doi.org/10.1001/archopht.121.8.1125

    Article  PubMed  Google Scholar 

  21. Luo C, Deng YP (2013) Retinoblastoma: concerning its initiation and treatment. Int J Ophthalmol 6(3):397–401. https://doi.org/10.3980/j.issn.2222-3959.2013.03.26

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  22. Chawla B, Jain A, Azad R (2013) Conservative treatment modalities in retinoblastoma. Indian J Ophthalmol 61(9):479–485. https://doi.org/10.4103/0301-4738.119424

    Article  PubMed  PubMed Central  Google Scholar 

  23. Schueler AO, Jurklies C, Heimann H, Wieland R, Havers W, Bornfeld N (2003) Thermochemotherapy in hereditary retinoblastoma. Br J Ophthalmol 87(1):90–95. https://doi.org/10.1136/bjo.87.1.90

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  24. Alkofide A, Ayas M, Khafagah Y, Rawashde A, Anas M, Barri M, Siddiqui K, AlMesfer S, Alkatan H (2013) Efficacy of vincristine and carboplatin as chemo-reduction for advanced bilateral retinoblastoma, the Saudi experience. Saudi J Ophthalmol 27(3):193–196. https://doi.org/10.1016/j.sjopt.2013.07.009

    Article  PubMed  PubMed Central  Google Scholar 

  25. Zhao J, Dimaras H, Massey C, Xu X, Huang D, Li B, Chan HS, Gallie BL (2011) Pre-enucleation chemotherapy for eyes severely affected by retinoblastoma masks risk of tumor extension and increases death from metastasis. J Clin Oncol 29:845–851

    Article  Google Scholar 

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Acknowledgements

This work was supported by the College of Medicine Research Center, Deanship of Scientific Research, King Saud University, Riyadh, Saudi Arabia. The authors would like also to thank Ms. Priscilla W. Gikandi (MPH), Research Unit, Department of Ophthalmology, College of Medicine, King Saud University, for her extensive help with the data management and analysis.

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Correspondence to Hind M. Alkatan.

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Ethical statement

This study was prepared in accordance with the ethical standards of the human ethics committee at KKESH and expedited approval as a retrospective study from the HEC/IRB of the Research department in accordance with the Helsinki Declaration (Research project #RP 1941-R). A general informed written consent was taken from the guardians of all cases which includes permission for anonymous use of data for the purpose of publication. The authors have no conflict of interest or financial disclosures in relation to this work. This work did not receive funding from any of the institutions.

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Alkatan, H.M., Al-Dahmash, S.A., Almesfer, S.A. et al. High-risk features in primary versus secondary enucleated globes with advanced retinoblastoma: a retrospective histopathological study. Int Ophthalmol 40, 2875–2887 (2020). https://doi.org/10.1007/s10792-020-01472-8

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Keywords

  • Advanced retinoblastoma
  • Histopathology
  • Choroidal invasion
  • Optic nerve invasion
  • Primary enucleation
  • Secondary enucleation