# Reduced‐Dose Bendamustine as a First‐Line Treatment of Follicular Lymphoma Is Associated With Poorer Prognosis

**Authors:** Keisuke Tanaka, Atsushi Takahata, Yuma Noguchi, Keigo Okada, Tatsuya Saito, Junichi Mukae, Yuki Osada, Ken Suzuki, Daisuke Mizuchi, Koh Yamamoto, Takashi Kumagai, Gaku Oshikawa, Takehiko Mori, Shigeo Toyota, Masahide Yamamoto

PMC · DOI: 10.1002/cam4.71702 · Cancer Medicine · 2026-03-08

## TL;DR

Reducing the dose of bendamustine for treating follicular lymphoma is linked to worse patient outcomes, including lower survival and progression-free rates.

## Contribution

This study is the first to show that reduced bendamustine doses in follicular lymphoma correlate with poorer prognosis despite achieving complete remission.

## Key findings

- Dose reduction of bendamustine was associated with significantly worse progression-free survival (PFS) in follicular lymphoma patients.
- Among patients achieving complete remission, those with dose reductions still showed a trend toward poorer 3-year PFS.
- Primary bendamustine-refractory patients had significantly worse overall survival regardless of dose intensity.

## Abstract

The dose of bendamustine used to treat previously untreated follicular lymphoma (FL) is sometimes reduced based on various clinical considerations, but the impact of such dose reductions on outcomes is unclear. We retrospectively analyzed 92 untreated FL patients treated with bendamustine at seven institutions in Japan. Dose reduction was defined as receiving less than 90% of the planned total dose of 1080 mg/m2 over six cycles. Patients with disease progression observed at ≤ 180 days of treatment initiation were defined as primary bendamustine‐refractory (PBR). The 3‐year overall survival (OS) and progression‐free survival (PFS) were 87.1% and 71.8%, respectively. Seven patients were classified as PBR, six of whom received bendamustine at full dose without dose reduction, and they had significantly worse OS with 3‐year OS of 38.1%. We excluded the PBR cases from subsequent analyses of the dose intensity's prognostic significance. The dose‐reduction group had a significantly lower CR rate (93.0% vs. 74.4%, p = 0.032). Similarly, the 3‐year PFS was significantly worse in the dose‐reduction group (86.8% vs. 68.1%, p = 0.005). In univariate and multivariate analyses, dose reduction was associated with inferior PFS. In an analysis limited to patients who completed all six courses, the CR rate was comparable between the two groups, but 3‐year PFS was significantly worse in the dose‐reduction group (86.8% vs. 68.7%, p = 0.041). Furthermore, even among patients who achieved CR, the 3‐year PFS tended to be poorer in the dose‐reduction group (85.7% vs. 72.7%, p = 0.062). These findings suggest that PBR cases are resistant to bendamustine itself regardless of the dose intensity. In contrast, among responders including those who achieved CR, dose reduction was associated with poorer PFS, indicating that maintaining treatment intensity is important for improving prognosis in the treatment of bendamustine‐responsive FL patients.

## Linked entities

- **Chemicals:** bendamustine (PubChem CID 65628)
- **Diseases:** follicular lymphoma (MONDO:0018906)

## Full-text entities

- **Genes:** KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}
- **Diseases:** FL (MESH:D008224), cytopenia (MESH:D006402), death (MESH:D003643), infection (MESH:D007239), lymphoma (MESH:D008223), B-cell lymphoma (MESH:D016393), HT (MESH:D009370), DLBCL (MESH:D016403), lymphopenia (MESH:D008231), malignancies (MESH:D009369), Impaired activities of daily living (MESH:D020773), obesity (MESH:D009765), CR (MESH:D001766)
- **Chemicals:** CHOP (-), obinutuzumab (MESH:C543332), Rituximab (MESH:D000069283), Bendamustine (MESH:D000069461), BR (MESH:D001966)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** M2018-231 — Mus musculus (Mouse), Transformed cell line (CVCL_6553)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12967496/full.md

## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12967496/full.md

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Source: https://tomesphere.com/paper/PMC12967496