# Treatment of Follicular Lymphoma With CHOP and Anti-CD20 Therapy: 15-Year Follow-Up of the SWOG S0016 Trial

**Authors:** Mazyar Shadman, Michael LeBlanc, Lisa Rimsza, John P. Leonard, Sonali M. Smith, Hongli Li, Jonathan W. Friedberg

PMC · DOI: 10.1001/jamaoncol.2026.0042 · JAMA Oncology · 2026-02-26

## TL;DR

A 15-year follow-up of a clinical trial shows that some patients with advanced-stage follicular lymphoma may be cured with CHOP-based chemoimmunotherapy.

## Contribution

This study provides long-term evidence that follicular lymphoma may be curable, challenging prior assumptions about its incurability.

## Key findings

- The 15-year overall survival rate was 70%, with a cure rate estimated at 42%.
- Relapse rates declined significantly over time, from 6.8% in the first 5 years to 0.6% between years 15 and 20.
- CHOP-RIT showed superior 15-year progression-free survival compared to R-CHOP.

## Abstract

Is advanced-stage follicular lymphoma (FL) curable with standard chemoimmunotherapy treatment?

In this secondary analysis of the SWOG S0016 trial of 531 individuals with FL, the overall 15-year overall survival was 70%, and cure modeling estimated an overall cure rate of 42%. The median follow-up was 15.5 years, and the rate of relapse declined substantially over time, from 6.8% during the first 5 years to 0.6% between 15 and 20 years.

The findings represent a major paradigm shift in the understanding and approach to FL, with broad implications for initial patient discussions, clinical care, and research strategies involving patients with FL.

Follicular lymphoma (FL) has historically been regarded as incurable, with patients experiencing late relapses after initial chemoimmunotherapy treatment.

To provide 15-year follow-up data from the SWOG S0016 trial that evaluated the potential for long-term remission and cure following chemoimmunotherapy with cyclophosphamide, hydroxydaunorubicin/doxorubicin, oncovin, and prednisone/prednisolone (CHOP)–based regimens.

This multicenter, intergroup study was conducted at academic and community practice locations throughout the US and enrolled patients with untreated, advanced-stage FL. Cure modeling, which involves estimating the proportion of patients cured of the disease, was conducted by incorporating background mortality rates to estimate the proportion of patients cured of FL during the S0016 trial. Patients were enrolled between May 2001 and October 2008 and followed up for a median (IQR) of 15.5 (13.6-16.9) years. The 15-year analysis was conducted in June 2025.

Patients were randomized to receive either rituximab plus CHOP (R-CHOP) or CHOP followed by radioimmunotherapy (CHOP-RIT).

The main outcomes were 15-year progression free survival (PFS) and overall survival (OS). Secondary outcomes included cure modeling.

A total of 531 eligible patients (242 female patients [46%]; median [IQR] age, 53 [45-61] years) were included in the final analysis (267 [50%] received R-CHOP and 264 [50%] CHOP-RIT). The overall 15-year OS was 70%, with no significant difference between treatment arms, and the 15-year PFS was 40% (95% CI, 36.0%-44.7%). CHOP-RIT demonstrated superior 15-year PFS (47% vs 34%; P = .004) compared with R-CHOP. Cure modeling estimated an overall cure rate of 42%, with the highest cure rates observed in patients with low Follicular Lymphoma International Prognostic Index scores and normal β2 microglobulin levels. The rate of relapse declined substantially over time, from 6.8% during the first 5 years to 0.6% between 15 to 20 years.

The results of this secondary analysis suggest that a subset of patients with advanced-stage FL can achieve cure with CHOP-based chemoimmunotherapy, as relapse rates decline over time. This finding represents a paradigm shift in the understanding of and approach to FL, with implications for initial patient discussions and future research strategies.

ClinicalTrials.gov Identifier: NCT00006721

This secondary analysis examines 15-year follow-up data from a randomized clinical trial to evaluate the potential for long-term remission and cure for follicular lymphoma following chemoimmunotherapy with cyclophosphamide, hydroxydaunorubicin/doxorubicin, oncovin, and prednisone/prednisolone (CHOP)–based regimens.

## Linked entities

- **Proteins:** MS4A1 (membrane spanning 4-domains A1)
- **Chemicals:** cyclophosphamide (PubChem CID 2907), hydroxydaunorubicin (PubChem CID 31703), doxorubicin (PubChem CID 31703), oncovin (PubChem CID 249332), prednisone (PubChem CID 5865), prednisolone (PubChem CID 5755)
- **Diseases:** follicular lymphoma (MONDO:0018906)

## Full-text entities

- **Genes:** HLA-G (major histocompatibility complex, class I, G) [NCBI Gene 3135] {aka MHC-G}, KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}
- **Diseases:** FL (MESH:D008224)
- **Chemicals:** prednisone (MESH:D011241), rituximab (MESH:D000069283), doxorubicin (MESH:D004317), prednisolone (MESH:D011239), CHOP (-), cyclophosphamide (MESH:D003520), oncovin (MESH:D014750)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12947078/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12947078/full.md

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Source: https://tomesphere.com/paper/PMC12947078