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Bendamustine and rituximab treatment for Waldenström macroglobulinemia with renal AL amyloidosis shows hematologic responseNew treatment approach shows promise for rare blood cancer

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Key Takeaway
Note that while bendamustine and rituximab can improve hematologic status in WM, it requires monitoring for infection.

This case report describes the management of a 71-year-old woman diagnosed with Waldenström macroglobulinemia and renal AL amyloidosis. The patient received a bendamustine plus rituximab (BR) regimen, which resulted in a partial hematologic response and improvement of proteinuria.

Specific laboratory improvements included serum IgM levels decreasing from 23.7 g/L to 7.1 g/L and urine protein excretion decreasing from 18.2 g/d to 15.0 g/d. However, the patient experienced a severe pulmonary infection leading to death. The authors note that while BR is a reasonable first-line treatment for these conditions, it requires vigilant monitoring for severe infections.

A significant limitation of this evidence is that it is based on a single case report. Therefore, the results cannot be generalized to the broader population of patients with Waldenström macroglobulinemia. The report emphasizes the necessity of routine serum and urine monoclonal free light chain testing in these patients.

How this fits prior evidence

This case report addresses a gap in managing concurrent Waldenström macroglobulinemia and renal AL amyloidosis. While prior coverage notes that rituximab-resistant primary membranous nephropathy may be treated with CAR-T or bispecific engagers, this case highlights the use of bendamustine plus rituximab for patients with specific monoclonal gammopathies.

Living with both a rare blood cancer called Waldenström macroglobulinemia and a kidney condition known as renal AL amyloidosis is incredibly difficult. These conditions can impact how the body functions and manage waste. In one case, a 71-year-old woman received a combination of two drugs: bendamustine and rituximab.

The treatment led to a partial response in her blood counts and an improvement in her protein levels in her urine. Specifically, her serum IgM levels dropped from 23.7 g/L to 7.1 g/L, and her daily urine protein excretion decreased from 18.2 g/d to 15.0 g/d. These numbers suggest the treatment was effective at managing her specific condition.

While the results were positive for her blood and kidney markers, the treatment came with a serious risk. The patient suffered a severe pulmonary infection that led to her death. Because this is based on just one person's experience, we cannot know how many others would have the same outcome. It highlights that while these drugs are a reasonable first choice, doctors must watch very closely for infections.

What this means for you:
A drug combination showed promise for rare blood cancer but carries a risk of severe infection.

Common questions

What drugs were used to treat the patient?

The patient was treated with a combination of two medications: bendamustine and rituximab. This specific regimen is considered a reasonable first-line treatment for patients with Waldenström macroglobulinemia, though it requires very close monitoring because it can lead to severe infections.

What were the results of the treatment?

The patient showed a partial response in her blood and an improvement in her urine protein. Her serum IgM levels dropped from 23.7 g/L to 7.1 g/L, and her daily urine protein excretion decreased from 18.2 g/d to 15.0 g/d.

Is this treatment safe for everyone?

Because this report is based on only one patient, we cannot know if it is safe or effective for everyone. The patient in this case unfortunately died from a severe pulmonary infection after starting the treatment, highlighting the need for careful medical supervision.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedJun 2026
View Original Abstract ↓
Waldenström macroglobulinemia (WM) is a rare indolent B-cell lymphoma, characterized by lymphoplasmacytic infiltration of bone marrow and the existence of monoclonal IgM in circulation. Renal AL amyloidosis is an uncommon complication of WM, and its treatment is an enormous challenge to clinicians. This report describes a 71-year-old woman who presented with a 10-month history of recurrent bilateral lower extremity edema and a progressive fatigue. Physical and laboratory examinations revealed serum monoclonal IgMλ, nephrotic syndrome, moderate anemia and mild enlargement of bilateral inguinal superficial lymph nodes. Bone marrow aspiration demonstrated clonal lymphoplasmacytic infiltration, lymph node biopsy was consistent with lymphoplasmacytic lymphoma, and peripheral blood testing confirmed the presence of the MYD88L265P mutation. Renal biopsy confirmed the diagnosis of renal AL amyloidosis, evidenced by Congo red-positive amorphous deposits with λ light chain restriction in glomeruli, interstitium, and small arterial walls. Following multidisciplinary consultation, the patient was treated with the bendamustine plus rituximab (BR) regimen. After three cycles, the patient achieved partial hematologic response (serum IgM levels decreased from 23.7 g/L to 7.1 g/L) with slight improvement of proteinuria (urine protein excretion decreased from 18.2 g/d to 15.0 g/d). However, during the subsequent treatment, the patient developed a severe pulmonary infection that led to death. This case underscores two critical points: First, patients with WM should be routinely tested for serum and urine monoclonal free light chains, as they can exist in WM at a high proportion and can independently induce monoclonal gammopathy-associated renal diseases, including renal amyloidosis. Second, for WM patients with renal AL amyloidosis, choosing BR regimen as the first-line treatment is reasonable. However, during the treatment process, it is essential to closely monitor and actively prevent the adverse effects of this regimen, particularly severe infections which may have fatal consequences.
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