Early thrombocytopenia predicts longer time‑to‑treatment discontinuation in trastuzumab emtansine treatment.

adverse event breast cancer survival thrombocytopenia trastuzumab emtansine

Journal

Oncology letters
ISSN: 1792-1082
Titre abrégé: Oncol Lett
Pays: Greece
ID NLM: 101531236

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 10 11 2022
accepted: 22 09 2023
medline: 6 11 2023
pubmed: 6 11 2023
entrez: 6 11 2023
Statut: epublish

Résumé

Thrombocytopenia is a characteristic adverse event of trastuzumab emtansine (T-DM1), one of the essential treatment options for human epithelial growth factor receptor 2 (HER2)-positive breast cancer. The present study investigated the predictive value of thrombocytopenia for time-to-treatment discontinuation (TTD) in patients receiving T-DM1 for advanced-stage HER2-positive breast cancer. The present observational study enrolled 138 patients who received T-DM1 at six oncology centers from January 2016 to December 2021. Univariate and multivariate Cox regression analyses were performed to determine the factors affecting TTD. The median age of patients was 50 years (range, 26-83). The median number of T-DM1 cycles was 9 (range, 2-58), the overall response rate was 50.0% and the disease control rate was 69.6%. At a median follow-up time of 19.3 months, the median TTD was 9.5 months [95% confidence interval (CI), 7.3-11.7], and the median overall survival was 28.2 months (95% CI, 19.2-37.2). Thrombocytopenia during treatment was observed in 39% of all patients, and 66.7% of these patients experienced early thrombocytopenia (in the first four treatment cycles). Multivariate analysis revealed that the independent factors for TTD were hormone receptor status [hazard ratio (HR), 1.837; 95% CI, 1.249-2.701; P=0.002], Eastern Cooperative Oncology Group performance status score (HR, 3.269; 95% CI, 1.788-5.976; P<0.001) and thrombocytopenia during treatment (HR, 0.297; 95% CI, 0.198-0.446; P<0.001). Patients with early thrombocytopenia had a significantly longer TTD of 17.3 months (95% CI, 11.8-22.8) compared with 7.6 months (95% CI, 5.8-9.4) for patients without early thrombocytopenia (P<0.001). The results of the present study indicated that patients with early thrombocytopenia had improved survival outcomes compared with those without. Thus, maximum benefit from T-DM1 treatment may be achieved by confirming the predictive role of thrombocytopenia in T-DM1 treatment in prospective studies and large-scale cohorts.

Identifiants

pubmed: 37927419
doi: 10.3892/ol.2023.14110
pii: OL-26-6-14110
pmc: PMC10623092
doi:

Types de publication

Journal Article

Langues

eng

Pagination

523

Informations de copyright

Copyright © 2023, Spandidos Publications.

Déclaration de conflit d'intérêts

The authors declare that they have no competing interests.

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Auteurs

Ahmet Bilgehan Sahin (AB)

Department of Medical Oncology, School of Medicine, Usak University, Usak 64100, Turkey.

Burcu Caner (B)

Department of Medical Oncology, Atatürk City Hospital, Altieylul, Balıkesir 10100, Turkey.

Birol Ocak (B)

Department of Medical Oncology, School of Medicine, Uludag University, Nilufer, Bursa 16059, Turkey.

Ahmet Gulmez (A)

Department of Medical Oncology, School of Medicine, Inonu University, Battalgazi, Malatya 44280, Turkey.

Buket Hamitoglu (B)

Department of Medical Oncology, School of Medicine, Dokuz Eylul University, Konak, İzmir 35210, Turkey.

Erdem Cubukcu (E)

Department of Medical Oncology, School of Medicine, Uludag University, Nilufer, Bursa 16059, Turkey.

Adem Deligonul (A)

Department of Medical Oncology, School of Medicine, Uludag University, Nilufer, Bursa 16059, Turkey.

Sibel Oyucu Orhan (SO)

Department of Medical Oncology, School of Medicine, Uludag University, Nilufer, Bursa 16059, Turkey.

Mustafa Canhoroz (M)

Department of Medical Oncology, Bursa Medicana Hospital, Nilufer, Bursa 16110, Turkey.

Hikmet Utku Odman (HU)

Department of Medical Oncology, School of Medicine, Uludag University, Nilufer, Bursa 16059, Turkey.

Isil Somali (I)

Department of Medical Oncology, School of Medicine, Dokuz Eylul University, Konak, İzmir 35210, Turkey.

Gokhan Ocakoglu (G)

Department of Biostatistics, School of Medicine, Uludag University, Nilufer, Bursa 16059, Turkey.

Turkkan Evrensel (T)

Department of Medical Oncology, School of Medicine, Uludag University, Nilufer, Bursa 16059, Turkey.

Classifications MeSH