1887
6 The Anbar 2nd International Medical Conference (AIMCO 2022)
  • ISSN: 1999-7086
  • EISSN: 1999-7094

Abstract

Multiple myeloma (MM) is a clonal proliferation of malignant plasma cells that results in the production of a monoclonal paraprotein with a light or heavy chain that is seen in the urine and/or serum. The ultimate goal of the MM therapy is the achievement of complete response (CR). The aim of this study is to evaluate the efficacy of the commonly used therapeutic protocols of MM utilized at the National Center of Hematology in Baghdad, Iraq.

Fifty-two patients with MM were enrolled consecutively for a cross-sectional study between July 2015 and May 2022 at one of Iraq’s major hematology institutions, the National Center of Hematology, Mustansiriyah University. The enrolled patients were evaluated for the overall response rate (ORR), which constitutes CR, very good partial response, and partial response, in comparison to non-response (NR), which constitutes stable disease and progressive disease. Responses to the main MM triple therapeutic regimens used in Iraq, VCD, VRD, and VTD, were evaluated. These regimens are composed of cyclophosphamide (C), bortezomib (V), thalidomide (T), lenalidomide (R), and dexamethasone (D). According to its availability, subsequent autologous stem cell transplantation (ASCT) was performed for some patients.

Of the 52 enrolled patients, 50 (96.2%) were assessed at a median follow-up time of 60.5 months. The mean ± SD age of the enrolled patients was 61.5 ± 11.0 years, and the male-to-female ratio was 3:2. However, two patients (3.8%) died before the end of the follow-up. The most common features the patients presented with were bone pain and/or backache in 67.3% of the patients, followed by lower limb weakness and mass (1.9% each). The radiological changes include osteolytic lesions in 34.6% and vertebral wedging in 15.4% of the patients. The most frequent laboratory findings were anemia (69.2%), with hemoglobin levels of 10.0 ± 1.5g/dL, detection of IgG-kappa paraprotein (51.9 %), and high levels of serum calcium in 23.1% (11.7 ± 1.1mg/dL) and serum creatinine in 21.2% (3.3 ± 1.5mg/dL) of the patients. ORR was 88.5%, while NR was reported in 11.5% of the patients. The outcomes were stratified according to the treatment used. It was found that ORR showed statistically significant differences and the VRD group demonstrated the best ( < 000.1). Twenty-one (40.4%) patients underwent subsequent ASCT, and the ORR showed non-significant differences compared to that when patients did not undergo transplantation ( > 0.05).

In this study, VRD was the most effective protocol with a better ORR. In addition, the age of the patients presenting with MM in Iraq was less than in western countries. Also, most of the patients were presented with bone lesions, and IgG was the predominant type of myeloma paraproteins.

Loading

Article metrics loading...

/content/journals/10.5339/jemtac.2022.aimco.6
2022-12-06
2024-05-04
Loading full text...

Full text loading...

/deliver/fulltext/jemtac/2022/6/jemtac.2022.aimco.6.html?itemId=/content/journals/10.5339/jemtac.2022.aimco.6&mimeType=html&fmt=ahah

References

  1. Alant J, Pool R, Thomson J, Moodley V. The diagnosis and investigation of multiple myeloma in 2018. Arch Clin Pathol J. 2018; 1:(1):2–6.
    [Google Scholar]
  2. Gerecke C, Fuhrmann S, Strifler S, Schmidt-Hieber M, Einsele H, Knop S. The diagnosis and treatment of multiple myeloma. Dtsch Arztebl Int. 2016; 113:(27–28):470–6. doi: 10.3238/arztebl.2016.0470.
    [Google Scholar]
  3. Bergstrom DJ, Kotb R, Louzada ML, Sutherland HJ, Tavoularis S, Venner CP. Consensus guidelines on the diag-nosis of multiple myeloma and related disorders. Recommendations of the Myeloma Canada Research Network Con-sensus Guideline Consortium. Clin Lymphoma Myeloma Leuk. 2020; 20:(7):e352–67. doi: 10.1016/j.clml.2020.01.017.
    [Google Scholar]
  4. Rajkumar SV, Kumar S. Multiple myeloma: Diagnosis and treatment. Mayo Clin Proc. 2016 Jan; 91:(1):101–19. doi: 10.1016/j.mayocp.2015.11.007.
    [Google Scholar]
  5. Mitsiades N, Mitsiades CS, Poulaki V, Chauhan D, Richardson PG, Hideshima T. Apoptotic signaling induced by immunomodulatory thalidomide analogs in human multiple myeloma cells: therapeutic implications. Blood. 2002; 99:(12):4525–30. doi: 10.1182/blood.v99.12.4525.
    [Google Scholar]
  6. Hideshima T, Mitsiades C, Akiyama M, Hayashi T, Chauhan D, Richardson P. Molecular mechanisms mediating antimyeloma activity of proteasome inhibitor PS-341. Blood. 2003; 101::1530–4. doi: 10.1182/blood-2002-08-2543.
    [Google Scholar]
  7. Attal M, Lauwers-Cances V, Hulin C, Leleu X, Caillot D, Escoffre M, et al. Lenalidomide, bortezomib, and dexamethasone with transplantation for myeloma. N Engl J Med. 2017; 376::1311–20. doi: 10.1056/NEJMoa1611750.
    [Google Scholar]
  8. Durie BG, Hoering A, Abidi MH, Rajkumar SV, Epstein J, Kahanic SP. Bortezomib with lenalidomide and dexamethasone versus lenalidomide and dexamethasone alone in patients with newly diagnosed myeloma without intent for immediate autologous stem-cell transplant (SWOG S0777): a randomised, open-label, phase 3 trial. Lancet. 2017; 389::519–27. doi: 10.1016/S0140-6736(16)31594-X.
    [Google Scholar]
  9. Kumar SK, Rajkumar SV, Dispenzieri A, Lacy MQ, Hayman SR, Buadi FK. Improved survival in multiple myeloma and the impact of novel therapies. Blood. 2009; 111:(5):2516–20. doi: 10.1182/blood-2007-10-116129.
    [Google Scholar]
  10. Pozzi S, Marcheselli L, Bari A, Liardo EV, Marcheselli R, Luminari S. Survival of multiple myeloma patients in the era of novel therapies confirms the improvement in patients younger than 75 years: a popu-lated based analysis. Br J Haematol. 2013; 163:(1):40–6. doi: 10.1111/bjh.12465.
    [Google Scholar]
  11. Kapoor P, Ramakrishnan V, Rajkumar SV. Bortezomib combination therapy in multiple myeloma. Seminars in Hematology. 2012; 49:(3):228–42. doi: 10.1053/j.seminhematol.2012.04.010.
    [Google Scholar]
  12. Padala SA., Barsouk A, Barsouk A, Rawla P, Vakiti A, Kolhe R. Epidemiology, staging, and management of multi-ple myeloma. Med Sci (Basel). 2021 Jan 20; 9:(1):3. doi: 10.3390/medsci9010003.
    [Google Scholar]
  13. Mjali A, Al Baroodi BNH. Some facts about cancers in Karbala province of Iraq, 2012–2020. Asian Pac J Cancer Care. 2020 Jun 7; 5:(2):67–9. doi: 10.31557/apjcc.2020.5.2.67–69.
    [Google Scholar]
  14. Kyle RA, Gertz MA, Witzig TE, Lust JA, Lacy MQ, Dispenzieri A, et al. Review of 1027 patients with newly diag-nosed multiple myeloma. Mayo Clin Proc. 2003; 78:(1):21–33. doi: 10.4065/78.1.21.
    [Google Scholar]
  15. Zagouri F, Kastritis E, Zomas A. Hypercalcemia remains an adverse prognostic factor for newly diagnosed multiple myeloma patients in the era of novel antimyeloma therapies. Eur J Haematol. 2017; 99::409–14. doi: 10.1111/ejh.12923.
    [Google Scholar]
  16. Badi AI, Al-Allawi NA, Yassin AK, Safar BM, Abdulla BK, Shamoon RP. Health-related quality of life in multiple myeloma in Kurdistan Iraq. Iraqi J Hematol. 2020; 9::101–6. doi: 10.4103/ijh.ijh_22_20.
    [Google Scholar]
  17. João C, Costa C, Coelho I, Vergueiro MJ, Ferreira M, Silva MG. Long-term survival in multiple myeloma. Clinical Case Reports. 2014; 2:(5):173–9. doi: 10.1002/ccr3.76.
    [Google Scholar]
  18. Chakraborty R, Muchtar E, Kumar S, Buadi F.K., Dingli D, Dispenzieri A, et al. The impact of induction regimen on transplant outcome in newly diagnosed multiple myeloma in the era of novel agents. Bone Marrow Transplant. 2017 Jan; 52:(1):34–40. doi: 10.1038/bmt.2016.214.
    [Google Scholar]
  19. Attal M, Lauwers-Cances V, Hulin C, Leleu X, Caillot D, Escoffre M. Lenalidomide, bortezomib, and dexame-thasone with transplantation for myeloma. N Engl J Med. 2017; 376:(14):1311–20. doi: 10.1056/NEJMoa1611750.
    [Google Scholar]
  20. Kumar L, Chellapuram SK, Sahoo R, Gupta R. VRd versus VCd as induction therapy for newly diagnosed multi-ple myeloma: A Phase III, randomized study. Clin Lymphoma Myeloma Leuk. 2019; 19:(10);e361. doi: 10.1016/j.clml.2019.09.597.
    [Google Scholar]
  21. Al Hamed R, Bazarbachi AH, Malard F, Harousseau JL, Mohty M. Current status of autologous stem cell trans-plantation for multiple myeloma. Blood Cancer J. 2019 Apr 8; 9::44. doi: 10.1038/s41408-019-0205-9.
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journals/10.5339/jemtac.2022.aimco.6
Loading
/content/journals/10.5339/jemtac.2022.aimco.6
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error