Prognostic impact of rapid reduction of involved free light chains in multiple myeloma patients under first-line treatment with Bendamustine, Prednisone, and Bortezomib (BPV)
Introduction Light chain involvement is observed in almost every patient (pt) with newly diagnosed multiple myeloma (MM). Owing to a relatively short half-life, rapid reduction in the involved free light chain (iFLC) is of potential prognostic value. Methods This retrospective analysis included 92 p...
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Veröffentlicht in: | Journal of cancer research and clinical oncology 2021-08, Vol.147 (8), p.2349-2359 |
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Sprache: | eng |
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Zusammenfassung: | Introduction
Light chain involvement is observed in almost every patient (pt) with newly diagnosed multiple myeloma (MM). Owing to a relatively short half-life, rapid reduction in the involved free light chain (iFLC) is of potential prognostic value.
Methods
This retrospective analysis included 92 pts with newly diagnosed MM treated with bendamustine, prednisone, and bortezomib (BPV).
Results
After a median number of two (range 1–5) BPV cycles, the majority of pts (
n
= 86; 93%) responded with either sCR (
n
= 21), CR (
n
= 1), nCR (
n
= 25), VGPR (
n
= 20), or PR (
n
= 19). PFS and OS at 48 months were 39% and 67%, respectively. At baseline, 79 out of 92 pts (86%) had iFLC levels above the upper standard level and an abnormal ratio of involved to uninvolved free light chain ≥ 8. In a subgroup analysis of these pts, we evaluated the prognostic importance of an early reduction of the iFLC during the first two BPV cycles. A reduction ≥ 50% of the iFLC on day 8 of the first cycle was observed in 31 of 69 pts. These pts had a significantly better median PFS of 49 months as compared to 20 months in 38 pts with a lower iFLC reduction (
p
= 0.002). In contrast, OS did not differ significantly with a 48 months survival of 77% vs 69% (
p
> 0.05).
Conclusion
These results indicate that a rapid decrease in the iFLC on day 8 is an early prognostic marker for newly diagnosed MM pts undergoing BPV treatment. |
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ISSN: | 0171-5216 1432-1335 |
DOI: | 10.1007/s00432-020-03504-3 |