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Table 1 Clinical characteristics of MM patients

From: Post-exposure prophylaxis with sotrovimab for Omicron (B.1.1.529) SARS-CoV-2 variant during the aplastic phase of autologous stem cell transplantation

 

N° (%)

(N = 15)

Age at transplant, (years)

 Median (range)

58 (43–70)

Gender

 Male

9 (60)

 Female

6 (40)

Paraprotein isotype

 IgG/κ

7 (47)

 IgG/λ

3 (20)

 IgA/κ

1(7)

 Light chain/κ

2 (13)

 Light chain/λ

1 (7)

 Nonsecretory

1 (7)

Frontline MM therapy

 VTD

14 (93)

 VCD

1 (7)

Stem Cells Mobilization procedure

 G-CSF steady-state

10 (67)

 Vinorelbine-Cyclophosphamide

2 (13)

 High-dose Cyclophosphamide

3 (20)

Total CD34 + cells yield (× 106/kg)

 Median (range)

4.54 (2.6–8.4)

High-dose conditioning (Melphalan 200 mg/m2)

 Total mg.s of Mel delivered (median, range)

376 (278–430)

Total CD34 + cells infused (× 106/kg)

 Median (range)

2.9 (2.4–4.7)

Hemogram at day 0 [median (range)]

 ANC × 109/L

4.0 (3.7–6.4)

 Platelets × 109/L

220 (123–310)

 ALC × 109/L

0.2 (0.0–0.5)

Hemocomponents support up to discharge

 RBC units transfused (median, range)

0 (0–3)

 Platelet units transfused (median, range)

1 (0–3)

Transplant-related Toxicity (G1-G2)*

 Febrile neutropenia

2 (13)

 Fever of unknown origin

3 (20)

 Microbiologically documented infection

2 (13)

 Mucositis

7 (47)

 Diarrhoea

6 (40)

 Other adverse events

1 (7)

  1. *N° of patients experiencing G1-G2 events. Toxicity was assessed using Common Terminology Criteria for Adverse Events version 4.0. MM, multiple myeloma; VTD, bortezomib, thalidomide, dexamethasone; VCD, bortezomib, cyclophosphamide, dexamethasone