Table 3.
Pertinent Observations in Current Study | Potential Impact of Observation on Current Practice and Guidelines |
---|---|
The majority (98%) of R/POD is associated with serologic evidence of R/POD |
Serologic follow up may be sufficient to monitor patients |
The majority (85%) of patients with R/POD have asymptomatic R/POD. Symptomatic disease is associated with younger age, poor cytogenetics and shorter PFS and post-R/POD survival |
Younger patients with poor cytogenetics may need closer monitoring |
New proposed criteria for relapse in patients with FLC only disease (Currently there are no IMWG criteria available) |
New criteria using FLC assay could be used to detect relapse even in patients with measurable M spike |
Annual skeletal survey was not useful in any patients to predict R/POD |
Annual skeletal survey is not recommended for routine monitoring |
Urine testing was not useful to predict R/POD except in a few patients in CR |
Routine urine testing is possibly not recommended for routine monitoring |
The association between patterns of paraprotein at diagnosis and relapse is predictable and versatile |
Allows to predict patterns of paraprotein at relapse and mitigates the current IMWG recommendation to “follow patients using the same method” as at diagnosis |
A significant percentage of patients with asymptomatic serologic R/POD actually have occult bone lesions |
Imaging at serologic R/POD is recommended in asymptomatic patients, recommendation that departs from the current IMWG recommendation that “CT, MRI, and PET may be indicated according to clinical circumstances” at R/POD |