Multiple Myeloma an incurable disease, but I have spent the last 25 years in remission using a blend of conventional oncology and evidence-based nutrition, supplementation, and lifestyle therapies from peer-reviewed studies that your oncologist probably hasn't told you about.
Click the orange button to the right to learn more about what you can start doing today.
According to research 20%- 50% of patients with multiple myeloma develop renal disease, most commonly from AKI (acute kidney injury) caused by cast nephropathy. The range is so wide, because of the basis of the definition used.
This is the most common type, resulting from the formation of casts in the kidney tubules due to the binding of free light chains.
Abnormal light chains deposit in the kidney tissue, leading to kidney damage.
Amyloid is an abnormal protein that can deposit in the tissues and organs, including the kidneys, causing damage.
The study linked below explains that novel MM therapies such as velcade/bortizamib and darzalex/daratumumab is effective at both managing the MM that probably caused kidney damage in the first place, leading to normalized kidney function.
While the video above may be helpful in suggesting therapies to help kidney function, I would be remiss if I didn’t mention others such as:
I am a long-term myeloma survivor. Like improvements in MM therapies, diagnostics and oncology care (MM specialists), kidney involvement has now become manageable.
Email me at David.PeopleBeatingCancer@gmail.com with questions about any of the MM CRAB symptoms. I can help.
Hang in there,
David Emerson
“Myeloma cast nephropathy (MCN) is a driver of renal failure in newly diagnosed multiple myeloma (NDMM) and has been historically associated with increased early mortality.
Since patients with moderate to severe renal insufficiency are typically excluded from trials, we performed a retrospective study to characterize modern-era outcomes in MCN. We reviewed 274 consecutive NDMM patients from 2017 to 2023 at an academic center and identified 46 patients (16.8%) with MCN.
Among them, 96% had received bortezomib and 67% anti-CD38+ monoclonal antibody in frontline therapy. As per the International Myeloma Working Group criteria, the renal overall response rate was:
Overall survival (OS) at 6 months did not differ between MCN (100%) and controls (98.2%). At a median follow-up of ~3 years, the mean MCN OS was within 7 months of control (p = 0.039) by equivalence testing.
Most involved free light chain (iFLC) and proteinuria reduction occurred within 1 month of treatment (83.1%, 3.9 g/d, respectively).
In summary, we report excellent 6-month renal recovery without early mortality in MCN patients with modern anti-myeloma therapies. Prospective studies focused on MCN are urgently needed to further improve the renal CR rate.”