# Assessment of Predictive Factors That Shorten Duration of Treatment in Patients With Multiple Myeloma Using AI: Real-World Longitudinal Study Using Data From Medical Data Vision Claims Database

**Authors:** Hiroshi Handa, Tadao Ishida, Shuji Ozaki, Shinsuke Iida, Kittima Wattanakamolkul, Chika Sakai, Kenichi Kato, David Bin-Chia Wu, DaeYoung Yu, Shota Nemoto, Yasuho Yamashita, Takuma Shibahara

PMC · DOI: 10.2196/75586 · JMIR Cancer · 2026-02-19

## TL;DR

This study uses AI to identify factors that shorten treatment duration in Japanese patients with multiple myeloma using real-world data.

## Contribution

The study introduces an explainable deep learning model to predict treatment duration in multiple myeloma patients using real-world claims data.

## Key findings

- The PWL model achieved AUC scores of 0.61, 0.64, and 0.66 for predicting treatment duration at 3, 6, and 12 months.
- Patients in certain clusters had higher comorbidity scores and lower prediction probabilities for longer treatment duration.
- Use of immunomodulatory drugs and aspirin was significantly associated with meeting predicted treatment duration thresholds.

## Abstract

With the availability of newer therapies, the duration of therapy (DoT) shortens with each increasing line of treatment in Japanese patients with multiple myeloma (MM).

This study aimed to identify factors that shorten DoT in patients with MM using a machine learning (ML) procedure from the Medical Data Vision (MDV) database.

This nationwide, retrospective observational real-world study was conducted using anonymized patient data from the MDV claims database from 2003 to 2022. Patients (≥18 y) with transplant-ineligible newly diagnosed MM (continued first line therapy), or relapsed or refractory MM (continued second or third line therapies) were included. To identify important predictive factors, an explainable deep learning model was created using 647 extracted variables (continuous, binary, and nominal categorical) from the MDV database, and the extracted data were used to train ML algorithms to build point-wise linear (PWL) models for predicting DoT. Predictive performance of the PWL model was compared with the elastic net (regularized logistic regression) and the extreme gradient boosting models, and calculated by area under the curve and evaluated by 10-fold double cross-validation. A clustering analysis (k-means method) of 4848 individual samples assessed the relationship between each sample and DoT (3, 6, and 12 months). The characteristics of clusters and sample features belonging to each cluster during and after treatment were studied.

Overall, 2762 (4848 individual samples) patients were evaluated (mean age 69.6, SD 11.8 years; 1450/2762, 52.5% male). The area under the curve score of the PWL model to predict DoT at 3, 6, and 12 months was 0.61, 0.64, and 0.66, respectively. Based on the similarity of coefficients of regression models, samples were categorized into 2 clusters (clusters A and B) at DoT of 3 months, 3 clusters (clusters A, B, and C) at 6 months, and 12 months (clusters A, B, and C). Cluster B versus cluster A (at 3 months) and cluster C versus cluster A and B (at 6 and 12 months) had a significantly (P<.01) higher pretreatment Charlson Comorbidity Index. They also showed a lower median of prediction probability. At 3 months in cluster B and at 6 and 12 months in cluster C, the use of immunomodulatory drugs for MM treatment was significantly higher in patients who met predicted DoT at each threshold versus those who did not. Additionally, the use of aspirin was significantly higher in cluster B and cluster C at 3 and 6 months, respectively.

Applying ML techniques using the PWL model yielded efficient results to understand trends associated with treatment and characteristics of Japanese patients with MM whose DoT were shortened. The study demonstrated that patients’ disease status and management-related factors, including use of immunomodulatory drugs and management of thromboprophylaxis, may be associated with DoT length.

## Linked entities

- **Chemicals:** aspirin (PubChem CID 2244)
- **Diseases:** multiple myeloma (MONDO:0009693)

## Full-text entities

- **Genes:** DLD (dihydrolipoamide dehydrogenase) [NCBI Gene 1738] {aka DLDD, DLDH, E3, GCSL, LAD, OGDC-E3}
- **Diseases:** GERD (MESH:D005764), Comorbidity (MESH:D004194), pain (MESH:D010146), MM (MESH:D009101), Cancer (MESH:D009369), pneumonia (MESH:D011014), purine and pyrimidine metabolism disorders (MESH:D011686), hematologic neoplasm (MESH:D019337), CCI (MESH:C566784), thrombotic (MESH:D013927), death (MESH:D003643), extramedullary disease (MESH:D023981), hypertension (MESH:D006973), plasmacytomas (MESH:D010954), DoT (MESH:D016609), toxicity (MESH:D064420), T2DM (MESH:D003924), bowel dysfunction (MESH:D015212), depression (MESH:D003866)
- **Chemicals:** pomalidomide (MESH:C467566), aspirin (MESH:D001241), panobinostat (MESH:D000077767), bortezomib (MESH:D000069286), carfilzomib (MESH:C524865), thalidomide (MESH:D013792), MDV (-), isatuximab (MESH:C000599209), elotuzumab (MESH:C546027), lenalidomide (MESH:D000077269), daratumumab (MESH:C556306), ixazomib (MESH:C548400)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12963979/full.md

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Source: https://tomesphere.com/paper/PMC12963979