Annals of Saudi Medicine (Mar 2024)

Improved long-term survival rate in the responders to bortezomib, cyclophosphamide, dexamethasone induction therapy in a transplant-eligible cohort of predominantly middle-age multiple myeloma patients

  • Ahmed Kotb Abdrabou,
  • Fahad Al Sharif,
  • Riad El Fakih,
  • Hazaa Al Zahrani,
  • Ruah Al Yamany,
  • Mostafa Saleh,
  • Saud Alhayli,
  • Zakia Al Somali,
  • Ahmad Alotaibi,
  • AlFadel AlShaibani,
  • Farah Deeba,
  • Maryam Asif,
  • Syed Ahmed Osman Ali Ahmed,
  • Feras Al Fraih,
  • Marwan Shaheen,
  • Ali Alahmari,
  • Walid Rasheed,
  • Naeem Arshad Chaudhri,
  • Fahad Al Mohareb,
  • Mahmoud Aljurf,
  • Amr Hanbali

DOI
https://doi.org/10.5144/0256-4947.2024.93
Journal volume & issue
Vol. 44, no. 2
pp. 93 – 103

Abstract

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BACKGROUND: Multiple myeloma (MM) represents the second most common hematologic malignancy (15%). Induction with bortezomib, cyclophosphamide, and dexamthasone VCd (d: low dose dexamthasone) regimen is widely used due to its high effectiveness, low toxicity and good tolerability, particularly with renal impairment. Real-world data on the use of VCD in clinical practice is lacking. OBJECTIVES: Evaluate the real-world experience of the VCD regimen DESIGN: Retrospective SETTING: Tumor registry database of tertiary cancer care center PATIENTS AND METHODS: Newly diagnosed MM patients who received VCD induction and underwent autologous stem cell transplant (ASCT) from July 2007 to July 2020 MAIN OUTCOME MEASURES: Response evaluation, progression-free survival (PFS) and overall survival (OS). SAMPLE SIZE: 87 patients RESULTS: Of 102 patients who started induction with VCd, 87 patients experienced a partial response or more overall response rate of 85%). The median age of these 87 patients at diagnosis was 52 years, of which 29.9% presented with renal impairment and 60.3% of patients had stage 2 by the Revised International Staging System (R-ISS). Patients with a standard cytogenetic risk achieved a better response compared to those with a poor cytogenetic risk (P=.044). The post-induction response rates were 6.9% stringent complete remission (sCR), 35% complete remission (CR); 41.4% very good partial response (VGPR), and 16.1% partial response (PR), respectively; the response rates became greater for sCR and CR post-transplantation at day 100 with 16.1% sCR, 35.6% CR, 32.2% VGPR and 16.1% PR, respectively. The median PFS was 49 months and 5 years OS was 84%. PFS was better in patients who achieved sCR vs PR (83 vs 35 months, P=.037). High LDH, high-risk cytogenetic and stage 3 R-ISS showed a worse median PFS and OS. CONCLUSIONS: VCD induction in newly diagnosed MM is highly effective, convenient, tolerable and affordable regimen, especially in low and middle-income countries with limited resources, also with favorable outcomes and survival. while those who did not respond successfully shifted to VRD or VTD. LIMITATIONS: The usual limitations of a retrospective analysis using registry-level data, no data on quality of life.