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


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
12 05 2020
Historique:
received: 10 02 2020
accepted: 18 03 2020
entrez: 13 5 2020
pubmed: 13 5 2020
medline: 15 5 2021
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 32396614
pii: S2473-9529(20)31333-1
doi: 10.1182/bloodadvances.2020001646
pmc: PMC7218426
doi:

Banques de données

ClinicalTrials.gov
['NCT00078949']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2011-2017

Informations de copyright

© 2020 by The American Society of Hematology.

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Auteurs

Sarit Assouline (S)

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

Shen Li (S)

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

Christian Gisselbrecht (C)

Hospital Saint Louis, Paris, France.

Patrick Fogarty (P)

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

Annette Hay (A)

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

Eric van den Neste (E)

Cliniques Universitaires UCL Saint-Luc, Brussels, Belgium.

Lois E Shepherd (LE)

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

Norbert Schmitz (N)

University Hospital Münster, Münster, Germany.

Tara Baetz (T)

Kingston General Hospital, Kingston, ON, Canada.

Armand Keating (A)

Princess Margaret Hospital, Toronto, ON, Canada.

Sue Robinson (S)

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

Matthew Seftel (M)

CancerCare Manitoba, Winnipeg, MB, Canada.

Caterina Stelitano (C)

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

Marina S Djurfeldt (MS)

Cliniques Universitaires UCL Saint-Luc, Brussels, Belgium.

Ralph Meyer (R)

Juravinski Cancer Center, Hamilton, ON, Canada.

Bingshu E Chen (BE)

Cliniques Universitaires UCL Saint-Luc, Brussels, Belgium.

Michael Crump (M)

Princess Margaret Hospital, Toronto, ON, Canada.

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Classifications MeSH