Therapy‐related acute lymphoblastic leukaemia in women with antecedent breast cancer

Author:

Pourhassan Hoda1ORCID,Zhang Jianying2,Tinajero Jose3,Pullarkat Vinod1,Agrawal Vaibhav1,Koller Paul1ORCID,Al Malki Monzr1ORCID,Aribi Ahmed1ORCID,Salhotra Amandeep1ORCID,Sandhu Karamjeet1,Ali Haris1,Stein Anthony1,Marcucci Guido1,Forman Stephen1,Aldoss Ibrahim1ORCID

Affiliation:

1. Department of Hematology and Hematopoietic Cell Transplantation City of Hope National Medical Center Duarte California USA

2. Division of Biostatistics, Department of Computational and Quantitative Medicine City of Hope National Medical Center Duarte California USA

3. Pharmacy City of Hope National Medical Center Duarte California USA

Abstract

SummaryTherapy‐related acute lymphoblastic leukaemia (tr‐ALL) is a disease entity attributed to previous exposure to chemotherapy and/or radiation for antecedent malignancy. There is observed female predominance for tr‐ALL, likely due to high prevalence and excellent curable rate for non‐metastatic breast cancer as well as the frequent use of carcinogenic agents as part of adjuvant therapy. Here, we reviewed 37 women with diagnosis of ALL following breast cancer treatment with focus on cytogenetic categorization. Philadelphia chromosome positivity (Ph+), KMT2A alterations and other cytogenetic change groups were observed in 32%, 22% and 46% of patients respectively. Median overall survival (OS) and relapse‐free survival (RFS) were 19.4 and 12.9 months, overall while both OS and RFS were superior in tr‐ALL with Ph+ disease compared to KMT2Ar and other cytogenetics respectively. Seventeen (45.9%) patients underwent consolidative allogeneic haematopoietic cell transplantation (alloHCT) in CR1 out of which 4 (24%) relapsed following transplant. Both OS and RFS were superior in the KMT2Ar cytogenetics group following alloHCT. Ph chromosome represents the largest genetic entity of tr‐ALL following breast cancer therapy, and it may be associated with superior survival outcomes while KMT2Ar may be associated with poorer outcomes that can perhaps be mitigated by alloHSCT.

Publisher

Wiley

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