The conditional survival analysis of relapsed DLBCL after autologous transplant: a subgroup analysis of LY.12 and CORAL

Author:

Assouline Sarit1,Li Shen1,Gisselbrecht Christian2,Fogarty Patrick3,Hay Annette4ORCID,van den Neste Eric5,Shepherd Lois E.4,Schmitz Norbert6,Baetz Tara7,Keating Armand8,Robinson Sue9,Seftel Matthew10,Stelitano Caterina11,Djurfeldt Marina S.5,Meyer Ralph12,Chen Bingshu E.5ORCID,Crump Michael8

Affiliation:

1. Lady Davis Institute, Jewish General Hospital, McGill University, Montreal, QC, Canada;

2. Hospital Saint Louis, Paris, France;

3. Lysarc, Hospital Lyon Sud, Pierre-Bénite, France;

4. Canadian Cancer Trials Group, Queens University, Kingston, ON, Canada;

5. Cliniques Universitaires UCL Saint-Luc, Brussels, Belgium;

6. University Hospital Münster, Münster, Germany;

7. Kingston General Hospital, Kingston, ON, Canada;

8. Princess Margaret Hospital, Toronto, ON, Canada;

9. Queen Elizabeth II Health Sciences Centre, Halifax, NS, Canada;

10. CancerCare Manitoba, Winnipeg, MB, Canada;

11. Azienda Ospedaliera Bianchi Melacrino Morelli, Reggio Calabria, Italy; and

12. Juravinski Cancer Center, Hamilton, ON, Canada

Abstract

Abstract The conditional survival of patients after frontline therapy for diffuse large B-cell lymphoma (DLBCL) approaches that of the general population once patients have survived disease free for 2 years. We sought to determine the conditional survival of patients among patients with relapsed de novo DLBCL successfully undergoing an autologous stem-cell transplant (ASCT) after first relapse. A total of 478 patients with de novo DLBCL, relapsed after 1 treatment from the Collaborative Trial in Relapsed Aggressive Lymphoma (CORAL) and LY.12, were included. Patients were followed prospectively after ASCT for a median of 5.3 and 8.2 years, respectively. Individual patient data were analyzed for event-free survival (EFS) and overall survival. Standardized mortality ratios (SMRs) were estimated using French and Canadian life tables. The EFS estimates declined with each year of follow-up after ASCT and were 50.1% (95% confidence interval [CI]: 43.7% to 56.3%) and 43.4% (95% CI: 36.7% to 49.9%) at 5 years in CORAL and LY.12, respectively. The rate of death stabilized once patients achieved at least 4 years of EFS. Compared with the age- and sex-matched population, the SMR was significantly higher until 5 years after ASCT, when values were no longer statistically significant. Patients undergoing ASCT for relapsed DLBCL continue to have a higher rate of death at least until they have survived event free for 5 years. These observations can help to determine endpoints for future clinical trials in this population and for patient counseling. This trial was registered at www.clinicaltrials.gov as #NCT00078949.

Publisher

American Society of Hematology

Subject

Hematology

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