Skip to main content
Log in

Prognostic Role of Interim 18-Fluorodeoxyglucose-PET in Diffuse Large B Cell Lymphoma: Experience from a Tertiary Care Centre in North India

  • Original Article
  • Published:
Indian Journal of Hematology and Blood Transfusion Aims and scope Submit manuscript

Abstract

This study was done to investigate the role of Interim 18-FDG-PET/CT (i-PET) in predicting the outcome of Diffuse Large B Cell Lymphoma (DLBCL) patients. The Lymphoma registry data base of the Department of Haematology was reviewed for all newly diagnosed DLBCL patients treated with R-CHOP-21 (n = 63). The PET-CT data of these patients at pre-defined time points (baseline, interim and end of treatment) was systematically collected. The predictive accuracy of i-PET-CT (done after 4 cycles R-CHOP-21 chemotherapy) was analysed to define their prognostic importance. 47 patients were eligible for final analysis in this study. According to Deauville’s criteria 15 patients (31%) were positive on i-PET. The positive predictive value (PPV) of i-PET by DS was 73.3%. At a median follow up of 21 months, DS based i-PET negative and positive cases showed significant differences in 2-year OS (81.2% vs 46.7%, p = 0.007) and PFS (75% vs 26.7%, p = 0.005). Combined analysis of i-PET (by DS) and IPI showed negative predictive value (NPV) of 92.3% in Low IPI while PPV of 76.9% in high IPI subgroup of DLBCL. On a multivariate analysis of all prognostic variables, i-PET was found to be independent prognostic marker predicting outcome in DLBCL patients. i-PET is an independent prognostic marker for outcome in DLBCL patients. Combined analysis of Interim PET along with IPI score at diagnosis improves the predictive accuracy of i-PET (both PPV & NPV) and may guide tailoring of therapy in these patients.

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
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

Data Availability Statement

The data that support the findings of this study are available on request from the corresponding author, Dr. Soniya Nityanand.

References

  1. Fisher SG, Fisher RI (2004) The epidemiology of non-Hodgkin’s lymphoma. Oncogene 23:6524–6534

    Article  CAS  Google Scholar 

  2. Gogia A, Das CK, Kumar L, Sharma A, Sharma MC, Mallick S (2018) Profile of non-Hodgkin lymphoma: an Indian perspective. South Asian J Cancer 7:162–170

    Article  Google Scholar 

  3. Nair R, Arora N, Mallath MK (2016) Epidemiology of Non-Hodgkin’s lymphoma in India. Oncology 91(suppl 1):18–25

    Article  Google Scholar 

  4. Pfreundschuh M, Trümper L, Osterborg A et al (2006) CHOP-like chemotherapy plus rituximab versus CHOP-like chemotherapy alone in young patients with good-prognosis diffuse large-B-cell lymphoma: a randomised controlled trial by the MabThera International Trial (MInT) Group. Lancet Oncol 7(5):379–391

    Article  CAS  Google Scholar 

  5. Habermann TM, Weller EA, Morrison VA et al (2006) Rituximab-CHOP versus CHOP alone or with maintenance rituximab in older patients with diffuse large B-cell lymphoma. J Clin Oncol 24(19):3121–3127. https://doi.org/10.1200/JCO.2005.05.1003

    Article  CAS  PubMed  Google Scholar 

  6. Coiffier B, Thieblemont C, Van Den Neste E et al (2010) Long-term outcome of patients in the LNH-98.5 trial, the first randomized study comparing rituximab-CHOP to standard CHOP chemotherapy in DLBCL patients: a study by the Groupe d’Etudes des Lymphomes de l’Adulte. Blood 116(12):2040–2045. https://doi.org/10.1182/blood-2010-03-276246

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Coiffier B (2005) State-of-the-art therapeutics: diffuse large B-cell lymphoma. J Clin Oncol 23(26):6387–6393. https://doi.org/10.1200/JCO.2005.05.015

    Article  CAS  PubMed  Google Scholar 

  8. Sehn LH, Gascoyne RD (2015) Diffuse large B-cell lymphoma: optimizing outcome in the context of clinical and biologic heterogeneity. Blood 125(1):22–32. https://doi.org/10.1182/blood-2014-05-577189

    Article  CAS  PubMed  Google Scholar 

  9. International Non-Hodgkin’s Lymphoma Prognostic Factors Project (1993) A predictive model for aggressive non-Hodgkin’s lymphoma. N Engl J Med 329(14):987–994. https://doi.org/10.1056/NEJM199309303291402

    Article  Google Scholar 

  10. Zhou Z, Sehn LH, Rademaker AW et al (2014) An enhanced International Prognostic Index (NCCN-IPI) for patients with diffuse large B-cell lymphoma treated in the rituximab era. Blood 123(6):837–842. https://doi.org/10.1182/blood-2013-09-524108

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. National comprehensive Cancer network guidelines for Non Hodgkin’s Lymphoma version 2.2020. Accessed 20 May 2020

  12. Safar V, Dupuis J, Itti E et al (2012) Interim [18F]fluorodeoxyglucose positron emission tomography scan in diffuse large B-cell lymphoma treated with anthracycline-based chemotherapy plus rituximab. J Clin Oncol 30(2):184–190. https://doi.org/10.1200/JCO.2011.38.2648

    Article  CAS  PubMed  Google Scholar 

  13. Rekowski J, Hüttmann A, Schmitz C, et al. (2020) Interim PET evaluation in diffuse large B-cell lymphoma employing published recommendations: comparison of the Deauville 5-point scale and the ΔSUVmax method [published online ahead of print, 2020 May 8]. J Nucl Med jnumed.120.244145. https://doi.org/10.2967/jnumed.120.244145

  14. Vitolo U, Chiappella A, Bellò M, Passera R, Botto B, Castellano G et al (2010) The outcome of patients with difuse large B-Cell lymphoma (DLBCL) treated with Rituximab-CHOP (R-CHOP) is not predicted by 18-FDG-Positron Emission Tomography/Computerized Tomography (PET) performed at intermediate in-course evaluation, but only by PET assessed at the end of therapy. Blood 116:2819

    Article  Google Scholar 

  15. Thomas A, Gingrich RD, Smith BJ et al (2010) 18-Fluoro-deoxyglucose positron emission tomography report interpretation as predictor of outcome in diffuse large B-cell lymphoma including analysis of “indeterminate” reports. Leuk Lymphoma 51(3):439–446. https://doi.org/10.3109/10428190903560198

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Moskowitz CH, Zelenetz A, Schoder H (2010) An update on the role of interim restaging FDG-PET in patients with diffuse large B-cell lymphoma and Hodgkin lymphoma. J Natl Compr Canc Netw 8(3):347–352. https://doi.org/10.6004/jnccn.2010.0023

    Article  PubMed  Google Scholar 

  17. Adams HJA, Kwee TC (2017) An evidence-based review on the value of interim FDG-PET in assessing response to therapy in lymphoma. Semin Oncol 44(6):404–419. https://doi.org/10.1053/j.seminoncol.2018.01.005

    Article  PubMed  Google Scholar 

  18. Moskowitz CH, Schöder H, Teruya-Feldstein J et al (2010) Risk-adapted dose-dense immunochemotherapy determined by interim FDG-PET in Advanced-stage diffuse large B-Cell lymphoma. J Clin Oncol 28(11):1896–1903. https://doi.org/10.1200/JCO.2009.26.5942

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Nols N, Mounier N, Bouazza S et al (2014) Quantitative and qualitative analysis of metabolic response at interim positron emission tomography scan combined with International Prognostic Index is highly predictive of outcome in diffuse large B-cell lymphoma. Leuk Lymphoma 55(4):773–780. https://doi.org/10.3109/10428194.2013.831848

    Article  CAS  PubMed  Google Scholar 

  20. Yim SK, Yhim HY, Han YH et al (2019) Early risk stratification for diffuse large B-cell lymphoma integrating interim Deauville score and International Prognostic Index. Ann Hematol 98(12):2739–2748. https://doi.org/10.1007/s00277-019-03834-4

    Article  CAS  PubMed  Google Scholar 

  21. Swerdlow SH, Campo E, Pileri SA et al (2016) The 2016 revision of the World Health Organization classification of lymphoid neoplasms. Blood 127(20):2375–2390. https://doi.org/10.1182/blood-2016-01-643569

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Barrington SF, Mikhaeel NG, Kostakoglu L, et al. Role of imaging in the staging and response assessment of lymphoma: consensus of the International Conference on Malignant Lymphomas Imaging Working Group [published correction appears in J Clin Oncol. 2016 Jul 20;34(21):2562]. J Clin Oncol. 2014;32(27):3048‐3058. https://doi.org/10.1200/JCO.2013.53.5229

  23. Mikhaeel NG, Smith D, Dunn JT et al (2016) Combination of baseline metabolic tumour volume and early response on PET/CT improves progression-free survival prediction in DLBCL. Eur J Nucl Med Mol Imag 43(7):1209–1219. https://doi.org/10.1007/s00259-016-3315-7

    Article  CAS  Google Scholar 

  24. Kitajima K, Okada M, Yoshihara K et al (2019) Predictive value of interim FDG-PET/CT findings in patients with diffuse large B-cell lymphoma treated with R-CHOP. Oncotarget 10(52):5403–5411. https://doi.org/10.18632/oncotarget.27103

    Article  PubMed  PubMed Central  Google Scholar 

  25. Han EJ, Joo Hyun O, Yoon H et al (2016) FDG PET/CT response in diffuse large B-cell lymphoma: reader variability and association with clinical outcome. Medicine (Baltimore) 95(39):e4983. https://doi.org/10.1097/MD.0000000000004983

    Article  CAS  Google Scholar 

  26. Kim J, Song YS, Lee JS, Lee WW, Kim SE (2018) Risk stratification of diffuse large B-cell lymphoma with interim PET-CT based on different cutoff Deauville scores. Leuk Lymphoma 59(2):340–347. https://doi.org/10.1080/10428194.2017.1339877

    Article  PubMed  Google Scholar 

  27. Pregno P, Chiappella A, Bellò M et al (2012) Interim 18-FDG-PET/CT failed to predict the outcome in diffuse large B-cell lymphoma patients treated at the diagnosis with rituximab-CHOP. Blood 119(9):2066–2073. https://doi.org/10.1182/blood-2011-06-359943

    Article  CAS  PubMed  Google Scholar 

  28. Schöder H, Zelenetz AD, Hamlin P et al (2016) Prospective study of 3’-Deoxy-3’-18F-Fluorothymidine PET for early interim response assessment in advanced-stage B-cell lymphoma. J Nucl Med 57(5):728–734. https://doi.org/10.2967/jnumed.115.166769

    Article  CAS  PubMed  Google Scholar 

  29. Lazarovici J, Terroir M, Arfi-Rouche J et al (2017) Poor predictive value of positive interim FDG-PET/CT in primary mediastinal large B-cell lymphoma. Eur J Nucl Med Mol Imag 44(12):2018–2024. https://doi.org/10.1007/s00259-017-3758-5

    Article  Google Scholar 

  30. Casasnovas RO, Ysebaert L, Thieblemont C et al (2017) FDG-PET-driven consolidation strategy in diffuse large B-cell lymphoma: final results of a randomized phase 2 study. Blood 130(11):1315–1326. https://doi.org/10.1182/blood-2017-02-766691

    Article  CAS  PubMed  Google Scholar 

  31. Lamy T, Damaj G, Gyan E et al (2014) R-CHOP with or without radiotherapy in non-bulky limitedstage diffuse large B cell lymphoma (DLBCL): preliminary results of the prospective randomized phase III 02–03 trial from the Lysa/Goelams Group [abstract]. Blood 124:393

    Article  Google Scholar 

  32. Duehrsen U, Huttmann A, Mller S et al (2014) Positron emission tomography (PET) guided therapy of aggressive lymphomas–a randomized controlled trial comparing different treatment approaches based on interim PET results (PETAL Trial). Blood 124:391

    Article  Google Scholar 

  33. Spaepen K, Stroobants S, Dupont P et al (2002) Early restaging positron emission tomography with (18)F-fluorodeoxyglucose predicts outcome in patients with aggressive non-Hodgkin’s lymphoma. Ann Oncol 13(9):1356–1363. https://doi.org/10.1093/annonc/mdf256

    Article  CAS  PubMed  Google Scholar 

  34. Itti E, Lin C, Dupuis J et al (2009) Prognostic value of interim 18F-FDG PET in patients with diffuse large B-cell lymphoma: SUV-based assessment at 4 cycles of chemotherapy. J Nucl Med 50:527–533

    Article  Google Scholar 

Download references

Acknowledgements

The study was carried out in Sanjay Gandhi post Graduate Institute of Medical Sciences, Lucknow. We acknowledge the contribution of clinical hematologist Dr Rajesh Kashyap for recruitment of patients. We also acknowledge the significant contribution of haematopathologists, Dr Ruchi Gupta, Dr. Dinesh Chandra and Dr. Manish Kumar Singh. We also acknowledge all clinical & lab hematology senior residents, and nursing staff without whom this study was impossible.

Author information

Authors and Affiliations

Authors

Contributions

S.K., A.G. conceived the project and prepared the research methodology, R.C, M.O., collected data, K.R. interpreted histopathology results, A.G., S.N. interpreted results and wrote the manuscript.

Corresponding author

Correspondence to Soniya Nityanand.

Ethics declarations

Conflict of interest

The authors declare that there is no conflict of interests regarding the publication of this paper.

Ethics Approval Statement

The study has been approved by Institution Ethics Committee (IEC No. 2017–189-IMP-113).

Patient Consent Statement

Written informed consent has been taken from all patients included in the study.

Additional information

Publisher's Note

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

Permission to reproduce material from other sources: This is the original research and all figures, diagrams, schemes, tables and text in this manuscript are our own, original, unpublished work.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kumar, S., Gupta, A., Ora, M. et al. Prognostic Role of Interim 18-Fluorodeoxyglucose-PET in Diffuse Large B Cell Lymphoma: Experience from a Tertiary Care Centre in North India. Indian J Hematol Blood Transfus 38, 211–222 (2022). https://doi.org/10.1007/s12288-021-01441-w

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12288-021-01441-w

Keywords

Navigation