R-CHOP appears to be the best first-line treatment for second primary diffuse large B cell lymphoma: a cancer registry study.


Journal

Annals of hematology
ISSN: 1432-0584
Titre abrégé: Ann Hematol
Pays: Germany
ID NLM: 9107334

Informations de publication

Date de publication:
Jul 2020
Historique:
received: 04 12 2019
accepted: 19 05 2020
pubmed: 27 5 2020
medline: 24 7 2020
entrez: 27 5 2020
Statut: ppublish

Résumé

Second primary diffuse large B cell lymphoma (spDLBCL) is defined as a metachronous tumor occurring after a first primary cancer. To date, while R-CHOP is the standard first-line treatment for de novo DLBCL, no available data show that R-CHOP is the optimal treatment for spDLBCL. This exploratory study aimed to investigate treatment of spDLBCL. From 2008 to 2015, the Poitou-Charentes general cancer registry recorded 68 cases of spDLBCL ≤ 80 years old, having received a first-line treatment with either R-CHOP (78%) or other regimens (22%). Patients without R-CHOP have worse overall survival in univariate (HR 2.89 [1.33-6.24], P = 0.007) and multivariate (HR 2.98 [1.34-6.67], P = 0.008) analyses. Patients without R-CHOP more frequently had PS > 1 (67% vs. 28%, P = 0.007) and prior chemotherapy (60% vs. 26%, P = 0.02), which suggests that both of these factors influence a clinician's decision to not use R-CHOP. Prior chemotherapy had no prognostic impact in univariate and multivariate analyses; this result could call into question the risk-benefit balance of not using R-CHOP to prevent toxicity. In our study, one DLBCL out of ten occurred after a first primary cancer, and as regards de novo DLBCL, R-CHOP appeared to be the best first-line treatment. Larger series are needed to confirm these results.

Identifiants

pubmed: 32451709
doi: 10.1007/s00277-020-04100-8
pii: 10.1007/s00277-020-04100-8
doi:

Substances chimiques

Rituximab 4F4X42SYQ6
Vincristine 5J49Q6B70F
Doxorubicin 80168379AG
Cyclophosphamide 8N3DW7272P
Prednisone VB0R961HZT

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1605-1613

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Auteurs

T Systchenko (T)

Poitou-Charentes General Cancer Registry, Université de Poitiers, 6 rue de la Milétrie, 86073, Poitiers Cedex 9, France. tsystchenko@orange.fr.
INSERM CIC 1402, CHU de Poitiers, Poitiers, France. tsystchenko@orange.fr.
Haematology Department, CHU de Poitiers, Poitiers, France. tsystchenko@orange.fr.

G Defossez (G)

Poitou-Charentes General Cancer Registry, Université de Poitiers, 6 rue de la Milétrie, 86073, Poitiers Cedex 9, France.
INSERM CIC 1402, CHU de Poitiers, Poitiers, France.

S Guidez (S)

INSERM CIC 1402, CHU de Poitiers, Poitiers, France.
Haematology Department, CHU de Poitiers, Poitiers, France.

C Laurent (C)

Anatomy-pathology Department, CHU de Toulouse, Réseau Lymphopath, Toulouse, France.

M Puyade (M)

Poitou-Charentes General Cancer Registry, Université de Poitiers, 6 rue de la Milétrie, 86073, Poitiers Cedex 9, France.
INSERM CIC 1402, CHU de Poitiers, Poitiers, France.

C Debiais-Delpech (C)

Anatomy-pathology Department, CHU de Poitiers, Poitiers, France.

B Dreyfus (B)

Haematology Department, CHU de Poitiers, Poitiers, France.

A Machet (A)

Haematology Department, CHU de Poitiers, Poitiers, France.

X Leleu (X)

INSERM CIC 1402, CHU de Poitiers, Poitiers, France.
Haematology Department, CHU de Poitiers, Poitiers, France.

V Delwail (V)

INSERM CIC 1402, CHU de Poitiers, Poitiers, France.
Haematology Department, CHU de Poitiers, Poitiers, France.

P Ingrand (P)

Poitou-Charentes General Cancer Registry, Université de Poitiers, 6 rue de la Milétrie, 86073, Poitiers Cedex 9, France.
INSERM CIC 1402, CHU de Poitiers, Poitiers, France.

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