Early serum TARC reduction predicts prognosis in advanced-stage Hodgkin lymphoma patients treated with a PET-adapted strategy.


Journal

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

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 31 03 2020
revised: 24 06 2020
accepted: 25 06 2020
pubmed: 1 7 2020
medline: 3 11 2020
entrez: 1 7 2020
Statut: ppublish

Résumé

Among patients with advanced-stage classical Hodgkin lymphoma (cHL) receiving ABVD chemotherapy, PET performed after the first two treatment cycles (PET-2) has prognostic value. However, 15% of patients with a negative PET-2 will experience treatment failure. Here we prospectively evaluated serum thymus and activation-regulated chemokine (TARC) levels, to improve risk assessment in patients treated according to HD0607 PET-driven trial (#NCT00795613). In 266 patients with available serum samples, who have agreed to participate in a sub-study for assessment of the role of TARC monitoring, serum TARC levels were measured at baseline and at time of PET-2 by commercially available ELISA test kits. The primary end-point was to evaluate the association between TARC after 2 ABVD cycles and PFS. Median TARC-2 values were significantly higher in PET-2-positive patients compared to PET-2-negative patients (P = .001), and in patients with treatment failure compared to those in continuous CR (P = .01). The 4-year PFS significantly differed between patients with TARC-2 >800 pg/mL vs ≤800 pg/mL (64% vs 86%, P = .0001). Moreover, among PET-2-negative patients, elevated TARC-2 identified those with a worse prognosis (74% vs 89%; P = .01). In multivariable analysis, TARC-2 >800 pg/mL was a significant independent predictor of PFS in the whole study population (HR 2.39, P = .004) and among the PET-2-negative patients (HR 2.49, P = .02). In conclusion, our results indicate that TARC-2 serum levels above 800 pg/mL suggest the need for a stringent follow-up in PET-2-negative patients, and the evaluation of new drugs in PET-2-positive, who will likely fail to respond to intensification with escalated BEACOPP.

Identifiants

pubmed: 32602970
doi: 10.1002/hon.2775
doi:

Substances chimiques

Biomarkers, Tumor 0
CCL17 protein, human 0
Chemokine CCL17 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

501-508

Subventions

Organisme : Michelangelo Foundation

Informations de copyright

© 2020 John Wiley & Sons Ltd.

Références

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Auteurs

Simonetta Viviani (S)

Department of Hemato-Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Arabella Mazzocchi (A)

Immuno-hematology and Transfusion Medicine Service, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Chiara Pavoni (C)

Department of Oncology and Hematology, Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.

Francesca Taverna (F)

Immuno-hematology and Transfusion Medicine Service, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Andrea Rossi (A)

Department of Oncology and Hematology, Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.

Caterina Patti (C)

Division of Hematology 1, Azienda Ospedali Riuniti Villa Sofia-Cervello, Palermo, Italy.

Alessandra Romano (A)

Department of Medical and Surgery Science, Hematology Unit, University of Catania, Catania, Italy.

Livio Trentin (L)

Department of Hematology, University of Padova, Padova, Italy.

Roberto Sorasio (R)

Division of Hematology, Azienda Ospedaliera Santa Croce e Carle, Cuneo, Italy.

Anna Guidetti (A)

Department of Hemato-Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Daniela Gottardi (D)

Division of Hematology, Ospedale Mauriziano Umberto I di Torino, Turin, Italy.

Corrado Tarella (C)

Hemato-Oncology Division, European Institute of Oncology IRCCS, Milan, Italy.
University Department "Scienze della Salute" (DISS), University of Milan, Milan, Italy.

Michele Cimminiello (M)

Divisione Universitaria di Ematologia, Ospedale San Carlo, Potenza, Italy.

Roberta Zanotti (R)

Hematology Unit, Department of Medicine, Azienda Ospedaliera Universitaria Integrata di Verona, Verona, Italy.

Lucia Farina (L)

Department of Hemato-Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Andrés José Maria Ferreri (AJM)

Lymphoma Unit, Department of Onco-Hematology, IRCCS Istituto di Ricovero e Cura a Carattere Scientifico Ospedale San Raffaele, Milan, Italy.

Marina Galbiati (M)

Immuno-hematology and Transfusion Medicine Service, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Paolo Corradini (P)

Department of Hemato-Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Alessandro Massimo Gianni (AM)

Department of Hemato-Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Andrea Gallamini (A)

Division of Hematology, Azienda Ospedaliera Santa Croce e Carle, Cuneo, Italy.

Alessandro Rambaldi (A)

Department of Oncology and Hematology, Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.
Department of Oncology and Hematology, University of Milan, Milan, Italy.

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