Clinical characteristics and outcome of patients over 60 years with Hodgkin lymphoma treated in Switzerland.


Journal

Hematological oncology
ISSN: 1099-1069
Titre abrégé: Hematol Oncol
Pays: England
ID NLM: 8307268

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 21 11 2020
accepted: 06 12 2020
pubmed: 11 12 2020
medline: 22 4 2021
entrez: 10 12 2020
Statut: ppublish

Résumé

Hodgkin lymphoma (HL) in older patients appears to be a different disease compared with younger patients with historically lower survival rates. This is related to a variety of factors, including increased treatment-related toxicity, the presence of comorbidities, and biologic differences. In order to better assess the clinical characteristics, treatment strategies, and outcome of this particular population, we conducted a population-based, retrospective analysis including 269 patients with HL older than 60 years (median age 71 years, range 60-94), treated between 2000 and 2017 in 15 referral centers across Switzerland. Primary endpoints were overall survival (OS), progression-free survival (PFS), and cause-specific survival (CSS). The vast majority of patients were treated with curative intent, either with a combined modality approach (chemotherapy followed by radiation therapy) or with systemic therapy. At a median follow-up of 6.6 years (95% confidence interval [CI], 6.0-7.6), 5-year PFS was 52.2% (95% CI, 46.0-59.2), 5-year OS was 62.5% (95% CI, 56.4-69.2), and 5-year CSS was 85.1.8% (95% CI, 80.3-90.1) for the entire cohort. A significant difference in terms of CSS was observed for patients older than 71 years in comparison to patients aged 60-70 years (hazard ratio 2.6, 1.3-5.0, p = 0.005). Bleomycin-induced lung toxicity (BLT) was documented in 26 patients (17.7%) out of the 147 patients exposed to this compound and was more frequent in patients older than 71 years (15/60, 25%). Outcome of HL pts older than 71 years appeared to decrease substantially in comparison to the younger counterpart. Treatment-related toxicities appeared to be relevant, in particular, BLT. New, potentially less toxic strategies need to be investigated in prospective clinical trials in this particular frail population.

Identifiants

pubmed: 33300135
doi: 10.1002/hon.2830
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

196-204

Subventions

Organisme : Celgene, Roche and Janssen

Informations de copyright

© 2020 John Wiley & Sons Ltd.

Références

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Auteurs

A A Moccia (AA)

Medical Oncology Clinic, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

S Aeppli (S)

Medical Oncology and Hematology Clinic, Kantonsspital St. Gallen, St. Gallen, Switzerland.

S Güsewell (S)

Clinical Trials Unit, Kantonsspital St. Gallen, St. Gallen, Switzerland.

M Bargetzi (M)

Hematology, Kantonsspital Aarau, Aarau, Switzerland.

C Caspar (C)

Medical Oncology and Hematology, Kantonsspital Baden, Baden, Switzerland.

D Brülisauer (D)

Medical Oncology Clinic, Inselspital, University Hospital of Bern, Bern, Switzerland.

M Ebnöther (M)

Medical Oncology and Hematology, Claraspital, Basel, Switzerland.

M Fehr (M)

Medical Oncology and Hematology Clinic, Kantonsspital St. Gallen, St. Gallen, Switzerland.

N Fischer (N)

Medical Oncology and Hematology Clinic, Kantonsspital Winterthur, Winterthur, Switzerland.

G Ghilardi (G)

Hematology Clinic, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

F Krasniqi (F)

Medical Oncology Clinic, University Hospital of Basel, Basel, Switzerland.

N Lang (N)

Medical Oncology Clinic, University Hospital of Geneva, Genève, Switzerland.

U Mey (U)

Medical Oncology and Hematology, Kantonsspital Graubünden, Chur, Switzerland.

W Mingrone (W)

Medical Oncology Clinic, Kantonsspital Olten, Olten, Switzerland.

U Novak (U)

Medical Oncology Clinic, Inselspital, University Hospital of Bern, Bern, Switzerland.

C Pfleger (C)

Medical Oncology and Hematology, Claraspital, Basel, Switzerland.

P Richter (P)

Medical Oncology and Hematology, Kantonsspital Graubünden, Chur, Switzerland.

M Rütti (M)

Internal Medicine Clinic, Spital Wil, Wil, Switzerland.

A Schmidt (A)

Medical Oncology and Hematology Clinic, Stadtspital Triemli, Zürich, Switzerland.

F Stenner (F)

Medical Oncology Clinic, University Hospital of Basel, Basel, Switzerland.

M Voegeli (M)

Medical Oncology and Hematology Clinic, Kantonsspital Baselland, Liestal, Switzerland.

T Zander (T)

Medical Oncology, Luzerner Kantonsspital, Luzern, Switzerland.

E Zucca (E)

Medical Oncology Clinic, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

F Hitz (F)

Medical Oncology and Hematology Clinic, Kantonsspital St. Gallen, St. Gallen, Switzerland.

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