Original Article

Correlation of Biochemical and FDG PET/CT Responses Following Induction Therapy in Newly Diagnosed Multiple Myeloma: A Prospective Observational Study

Abstract

Background: Multiple myeloma is a heterogeneous malignancy with patchy bone marrow involvement, often leading to discrepancies between biochemical and imaging-based response assessments. Site-specific bone marrow biopsies may miss focal disease, while FDG PET/CT detects metabolically active lesions, and the two approaches offer complementary prognostic value.

Materials and Methods: This prospective study included 44 newly diagnosed multiple myeloma patients. The primary aim was to assess the correlation between biochemical and PET/CT responses at six months post-induction. A secondary objective was to evaluate the impact of PET/CT response on 12-month event-free survival (EFS).

Results: The median age was 55.5 years. At baseline, more than 3 focal lesions and extramedullary disease (EMD) were observed in 61.4% and 34.1% of patients, respectively. After six months of induction therapy, 86.3% achieved at least a very good partial response (≥VGPR) biochemically, but 52.3% remained PET/CT-positive. Baseline >3 focal lesions and EMD significantly predicted persistent PET/CT positivity (p = 0.004). Notably, 50% of patients with ≥VGPR still showed PET/CT-positive findings. At 12 months, 75% of patients who experienced clinical events had been PET/CT-positive at six months, compared with 47.2% of those without events (p = 0.245). The 12-month event-free survival was lower in the PET/CT-positive group (73.9% vs. 90.4%, p = 0.182), though this difference was not statistically significant.

Conclusion: 18-FDG PET/CT can detect residual disease not captured by biochemical markers, highlighting the value of combined assessment in multiple myeloma. Baseline >3 focal lesions and EMD predicted persistent PET/CT positivity. Although PET/CT positivity at six months showed a trend toward worse 12-month EFS, larger studies are needed to confirm its prognostic significance.

1. Rajkumar SV, Dimopoulos MA, Palumbo A, et al. International myeloma working group updated criteria for the diagnosis of multiple myeloma. Lancet Oncol. 2014; 15(12):e538-48.
2. Siegel RL, Giaquinto AN, Jemal A. Cancer statistics, 2024. CA Cancer J Clin. 2024; 74(1):12-49.
3. Kyle RA, Rajkumar SV. Multiple myeloma. N Engl J Med. 2004, 351(18):1860-73.
4. Resnick D, Kransdorf MJ. Plasma cell dyscrasias. In: Resnick D, Kransdorf MJ, editors. Bone and Joint Imaging. 3rd ed. Philadelphia: Elsevier Saunders; 2004. pp: 1101-20.
5. Collins CD. Multiple myeloma. Cancer Imaging. 2004, 4 Spec No A(Spec No A):S47-53.
6. Singh J, Fairbairn KJ, Williams C, et al. Expert radiological review of skeletal surveys identifies additional abnormalities in 23% of cases: further evidence for the value of myeloma multi-disciplinary teams in the accurate staging and treatment of myeloma patients. Br J Haematol. 2007, 137(2):172-3.
7. Wahlin A, Holm J, Osterman G, et al. Evaluation of serial bone X-ray examination in multiple myeloma. Acta Med Scand. 1982;12(6): 385-7.
8. Ludwig H, Frühwald F, Tscholakoff D, et al. Magnetic resonance imaging of the spine in multiple myeloma. Lancet. 1987; 2(8555):364-6.
9. Ghanem N, Lohrmann C, Engelhardt M, et al. Whole-body MRI in the detection of bone marrow infiltration in patients with plasma cell neoplasms in comparison to the radiological skeletal survey. Eur Radiol. 2006, 16(5):1005-14.
10. Baur-Melnyk A, Buhmann S, Becker C, et al. Whole-body MRI versus whole-body MDCT for staging of multiple myeloma. AJR Am J Roentgenol. 2008; 190(4):1097-104.
11. Baur-Melnyk A, Buhmann S, Dürr HR, et al. Role of MRI for the diagnosis and prognosis of multiple myeloma. Eur J Radiol. 2005; 55(1):56-63.
12. Joffe J, Williams MP, Cherryman GR, et al. Magnetic resonance imaging in myeloma. Lancet. 1988; 1(8595):1162-3.
13. Nosàs-Garcia S, Moehler T, Wasser K, et al. Dynamic contrast-enhanced MRI for assessing the disease activity of multiple myeloma: a comparative study with histology and clinical markers. J Magn Reson Imaging. 2005, 22(1):154-62.
14. Therneau TM, Kyle RA, Melton LJ III, et al. Incidence of monoclonal gammopathy of undetermined significance and estimation of duration before first clinical recognition. Mayo Clin Proc. 2012, 87(11):1071-1079.
15. Kumar S, Paiva B, Anderson KC, et al. International Myeloma Working Group consensus criteria for response and minimal residual disease assessment in multiple myeloma. Lancet Oncol. 2016; 17(8):e328-e346.
16. Sundaram S, Driscoll J, Fernandez-Ulloa M, et al. FDG PET imaging in multiple myeloma: implications for response assessments in clinical trials. Am J Nucl Med Mol Imaging. 2018; 8(6): 421-7.
17. Kaur P, Shah BS, Baja P. Multiple myeloma: a clinical and pathological profile. Gulf J Oncolog. 2014; 1(16):14-20.
18. Gupta P, Kochupillai V, Singh S, Berry M, Kumar L, Sundaram KR. A twelve year study of multiple myeloma at the All India Institute of Medical Sciences, New Delhi, India. Indian J Med Paediatr Oncol. 1995;16(2):108.
19. Kumar L, Vikram P, Kochupillai V. Recent advances in the mangement of multiple myeloma. Natl Med J India. 2006, 19(2):80-9.
20. Costa LJ, Brill IK, Omel J, et al. Recent trends in multiple myeloma incidence and survival by age, race, and ethnicity in the United States. Blood Adv. 2017;1(4): 282-287.
21. Zamagni E, Patriarca F, Nanni C, et al. Prognostic relevance of 18-F FDG PET/CT in newly diagnosed multiple myeloma patients treated with up-front autologous transplantation. Blood. 2011, 118(23):5989-95.
22. Sachpekidis C, Merz M, Raab MS, et al. The prognostic significance of [18F]FDG PET/CT in multiple myeloma according to novel interpretation criteria (IMPeTUs). EJNMMI Res. 2021; 11(1):100.
23. Kumar SK, Jacobus SJ, Cohen AD, et al. Carfilzomib or bortezomib in combination with lenalidomide and dexamethasone for patients with newly diagnosed multiple myeloma without intention for immediate autologous stem-cell transplantation (ENDURANCE): a multicentre, open-label, phase 3, randomised, controlled trial. Lancet Oncol. 2020; 21(10):1317-1330.
24. Sonneveld P, Dimopoulos MA, Boccadoro M, et al. Daratumumab, bortezomib, lenalidomide, and dexamethasone for multiple myeloma. N Engl J Med. 2024; 390(4):301-13.
25. Charalampous C, Goel U, Broski SM, et al. Utility of PET/CT in assessing early treatment response in patients with newly diagnosed multiple myeloma. Blood Adv. 2022; 6(9):2763-72.
26. Nørgaard JN, Abildgaard N, Lysén A, et al. Intensifying treatment in PET-positive multiple myeloma patients after upfront autologous stem cell transplantation. Leukemia. 2023; 37(10):2107-14.
27. Davies FE, Rosenthal A, Rasche L, et al. Treatment to suppression of focal lesions on positron emission tomography-computed tomography is a therapeutic goal in newly diagnosed multiple myeloma. Haematologica. 2018; 103(6):1047-53.
28. Zamagni E, Tacchetti P, Cavo M. Imaging in multiple myeloma: How? When?. Blood. 2019; 133(7): 644-651.
29. Zamagni E, Nanni C, Mancuso K, et al. PET/CT improves the definition of complete response and allows to detect otherwise unidentifiable skeletal progression in multiple myeloma. Clin Cancer Res. 2015; 21(19):4384-90.
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IssueVol 20 No 2 (2026) QRcode
SectionOriginal Article(s)
Keywords
Multiple myeloma; Biochemical response; FDG PET/CT scan; Focal lesion; Extramedullary

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How to Cite
1.
Sharma H, Kumar P, Nayan N, Kumar R, Seth T, Dhawan R, Dass J, Aggarwal M, Viswanathan G, Chauhan R, Mahapatra M. Correlation of Biochemical and FDG PET/CT Responses Following Induction Therapy in Newly Diagnosed Multiple Myeloma: A Prospective Observational Study. Int J Hematol Oncol Stem Cell Res. 2026;20(2):159-173.