# Acute Lymphoblastic Leukemia in a Patient With Advanced Breast Cancer Treated With Cyclin-Dependent Kinase 4/6 Inhibitors and Endocrine Therapy

**Authors:** Ryan E Bailey, Marcela Mazo Canola

PMC · DOI: 10.7759/cureus.69548 · 2024-09-16

## TL;DR

A post-menopausal woman developed leukemia while being treated for breast cancer and was successfully managed with a combined treatment approach.

## Contribution

This case highlights the successful concurrent treatment of breast cancer and leukemia using CDK 4/6 inhibitors and chemotherapy.

## Key findings

- The combined regimen of CDK 4/6 inhibitor + AI and hyperCVAD was well-tolerated.
- The patient remains on treatment with only low-grade fatigue as a side effect.
- Integrated care is essential for managing patients with concurrent hematologic and breast malignancies.

## Abstract

This case shares the case of a post-menopausal woman who develops Philadelphia chromosome-positive B cell acute lymphoblastic leukemia (B-ALL) while receiving treatment for invasive ductal carcinoma (IDC) of the breast. The patient received a cyclin-dependent kinase (CDK) 4/6 inhibitor + aromatase inhibitor (AI) for the IDC; hyperfractionate cyclophosphamide, vincristine sulfate, doxorubicin hydrochloride (Adriamycin), methotrexate, and cytarabine (hyperCVAD), and the steroid hormone dexamethasone were added to treat the B-ALL. HyperCVAD combined with CDK 4/6 inhibitor + AI was very well tolerated. The CDK 4/6 inhibitor and AI were only held once in the treatment course due to adverse effect (AE) intolerance. The patient remains on a CDK 4/6 inhibitor and ponatinib with only low-grade fatigue as an AE. This case underscores the importance of a concurrent approach to managing hematologic and breast malignancies. The combined treatment regimens were effective and well-tolerated. Vigilant follow-up is essential for patients in remission from both malignancies, ensuring effective disease surveillance and treatment management. Integrated care remains pivotal for optimal outcomes.

## Linked entities

- **Chemicals:** cyclophosphamide (PubChem CID 2907), vincristine sulfate (PubChem CID 249332), doxorubicin hydrochloride (PubChem CID 443939), methotrexate (PubChem CID 4112), cytarabine (PubChem CID 6253), dexamethasone (PubChem CID 5743), CDK 4/6 inhibitor (PubChem CID 49765254), ponatinib (PubChem CID 24826799)
- **Diseases:** Acute Lymphoblastic Leukemia (MONDO:0004967), B cell acute lymphoblastic leukemia (MONDO:0004947), invasive ductal carcinoma (MONDO:0004953), breast cancer (MONDO:0004989)

## Full-text entities

- **Diseases:** IDC) of the breast (MESH:D018270), Acute Lymphoblastic Leukemia (MESH:D054198), Breast Cancer (MESH:D001943), B-ALL (MESH:D015456), malignancies (MESH:D009369), fatigue (MESH:D005221), IDC (MESH:D044584)
- **Chemicals:** Adriamycin (MESH:D004317), dexamethasone (MESH:D003907), hyperCVAD (-), vincristine sulfate (MESH:D014750), steroid (MESH:D013256), ponatinib (MESH:C545373), cyclophosphamide (MESH:D003520)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11405092/full.md

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Source: https://tomesphere.com/paper/PMC11405092