# Concurrent Immunoglobulin Light Chain and Transthyretin Cardiac Amyloidosis Patient Treated With Daratumumab and Tafamidis: A Case Report

**Authors:** Taiki Nishihara, Yawara Kawano, Masayoshi Tasaki, Ayuko Naito, Hiromichi Yuki, Yasuhiro Nagayoshi, Seiji Takashio, Nao Nishimura, Mitsuharu Ueda, Kenichi Tsujita, Jun‐Ichirou Yasunaga

PMC · DOI: 10.1002/jha2.70122 · EJHaem · 2025-08-13

## TL;DR

A 75-year-old man with two rare heart conditions was successfully treated with a combination of daratumumab and tafamidis.

## Contribution

This case report presents a rare instance of concurrent AL and ATTRwt cardiac amyloidosis treated with a sequential therapy approach.

## Key findings

- The patient had both AL and ATTRwt amyloid deposits confirmed by immunohistochemistry and mass spectrometry.
- Treatment with daratumumab followed by tafamidis was safe and effective for the patient.
- The case highlights the importance of accurate amyloid typing for effective treatment.

## Abstract

Immunoglobulin light chain (AL) and wild‐type transthyretin (ATTRwt) amyloidosis, while sharing similar clinical presentations, require distinct treatments. We report a rare case of a 75‐year‐old man with heart failure diagnosed with concurrent AL and ATTRwt cardiac amyloidosis. Immunohistochemistry and liquid chromatography‐tandem mass spectrometry confirmed both AL and ATTR amyloid deposits in the heart. The patient was safely and effectively treated with daratumumab‐based chemotherapy followed by tafamidis. This case underscores the necessity of precise amyloid typing for tailored therapy, suggesting sequential daratumumab and tafamidis as a viable strategy for this complex overlap.

Trial Registration: The authors have confirmed clinical trial registration is not needed for this submission.

## Linked entities

- **Chemicals:** tafamidis (PubChem CID 11001318)
- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** TNNT2 (troponin T2, cardiac type) [NCBI Gene 7139] {aka CMD1D, CMH2, CMPD2, LVNC6, RCM3, TnTC}, TTR (transthyretin) [NCBI Gene 7276] {aka AMYLD1, ATTR, CTS, CTS1, HEL111, HsT2651}, CD38 (CD38 molecule) [NCBI Gene 952] {aka ADPRC 1, ADPRC1, cADPR1}
- **Diseases:** diastolic dysfunction (MESH:D018487), Amyloid cardiomyopathy (MESH:D009202), toxicities (MESH:D064420), edema (MESH:D004487), pleural effusion (MESH:D010996), AF (MESH:D001281), cardiac toxicity (MESH:D066126), ATTRwt amyloidosis (MESH:D000686), shortness of breath (MESH:D004417), amyloid (MESH:C000718787), AL (MESH:D009101), HF (MESH:D006333), fatigue (MESH:D005221), AL (MESH:D000075363), function (MESH:D003291), cardiac (MESH:D006331), pulmonary congestion (MESH:D001261), ATTR amyloidosis (MESH:C567782), carpal tunnel syndrome (MESH:D002349)
- **Chemicals:** Tafamidis (MESH:C547076), pyrophosphate (MESH:C107241), dexamethasone (MESH:D003907), bortezomib (MESH:D000069286), cyclophosphamide (MESH:D003520), DaraCyBorD (-), Daratumumab (MESH:C556306), 99mTc (MESH:D013667)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12345594/full.md

## References

14 references — full list in the complete paper: https://tomesphere.com/paper/PMC12345594/full.md

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Source: https://tomesphere.com/paper/PMC12345594