Author:

Gregor Adams, PhD | Director, Scientific Development

Date:

July 2019

Acute lymphoblastic leukemia (ALL) is a cancer of the lymphoid lineage characterized by the development of increased numbers of immature lymphocytes. ALL is a relatively rare cancer, representing less than 0.5% of all cancers in the United States, with the American Cancer Society estimating approximately 5,930 new cases and 1,500 deaths from ALL in the United States for 2019. However, the fact that ALL is the most common childhood cancer makes it of interest to researchers. The risk for developing ALL is highest in children younger than 5 years of age. This risk then declines slowly until the mid-20s before it begins to rise again after age 50. While most cases of ALL occur in children, most deaths from ALL occur in adults. Standard therapies for ALL include the use of aggressive or long-term chemotherapy. These treatment regimens result in 90% of children surviving after five years. However, this drops to around 40% of adult patients remaining disease free. Due to this relapse rate in ALL, other treatment options have been sought.

Use of CAR T Cell Therapy for B-cell ALL

One such treatment option for B-cell ALL is chimeric antigen receptor (CAR) T cell immunotherapy directed against the CD19 protein. The first FDA-approved CAR T cell therapy was Kymriah (tisagenlecleucel), which was approved on August 30, 2017 for the treatment of pediatric or young adult (up to 25 years of age) relapsed or refractory B-cell ALL. This novel therapeutic approach currently results in an overall response rate of 81% at three months and a durable remission rate of 59% at 12 months, thereby providing a potentially curative option for patients who otherwise had relapsed after, or are refractory to, standard treatment regimens.

While these response rates in a relapsed or refractory patient population are very impressive, accumulating experience demonstrates that remissions may not be complete in a significant number of patients. There are multiple potential explanations for the partial remissions including poor persistence and function of the engineered T cell population due to exposure to multiple rounds of chemotherapy or other toxic agents. In addition, relapse due to loss or modulation of the target antigen on the malignant cell population has been observed. Various strategies are being employed to overcome these limitations of CAR T cell therapy, including dual targeting approaches to additional antigens on the cell surface of the leukemic cells. However, a continued effort into understanding the overall biology of CAR T cell function in a given indication will be critical to realizing the full potential of this novel treatment approach and the development of the next generation of therapies.

NALM6-Luc-mCh-Puro as a Model for B-cell ALL

Robust and reliable preclinical animal models are essential for the effective screening and selection of candidate CAR T therapies for clinical use. MI Bioresearch is optimally positioned to provide these models. In 2003, we became the first contract research organization (CRO) to offer in vivo bioluminescence imaging, which is a critical component of studies aimed at determining the efficacy of CAR T cells in hematologic malignancies. We have also made significant efforts to increase our knowledge and experience of preclinical in vivo studies for CAR T cell products to further drug development in this therapeutic space—having run over 200 studies for more than 24 different clients. Details can be found on our adoptive cell therapy page.

Recently we have expanded our portfolio through the establishment in-house of the NALM6-Luc-mCh-Puro model in NSG mice as a model for ALL. This tumor line was established from the ALL of a 19-year-old male. Similar to the growth kinetics of other well established B-cell malignancy models, such as our Raji-Luc model, the growth of the NALM6-Luc-mCh-Puro tumor cells in 6-7 week old female NSG mice is very robust and reproducible at low cell inocula and demonstrates tumor doubling times in the range of 1 to 1.3 days (Figure 1).

Figure for NALM6-Luc-mCh-Puro Model Spotlight Figure 1: Mean Tumor Burden.
Fig. 1: Growth kinetics for NALM6-Luc-mCh-Puro in NSG mice.

This tumor growth rate results in rapid death in untreated animals, with a median survival time of 24 days (Figure 2). While hind limb paralysis was observed in mice at advanced stages of disease, necropsy findings found evidence of several small nodules in the brain in the majority of euthanized animals. This is of particular interest given the known central nervous system (CNS) disease involvement which is observed in most patients with ALL.

Figure for 2019_0709 - NALM6-Luc-mCh-Puro Model Spotlight Figure 2: Percent Survival.
Fig. 2: NALM6-Luc-mCh-Puro median survival plot.

This model provides yet another tool for the preclinical development of therapies directed against B-cell malignancies, particularly in indications aimed at the treatment of ALL. Contact MI Bioresearch for your next ALL study or other B-cell malignancy related study.

 

Image of Gregor Adams, PhD - Director, Scientific DevelopmentAbout the Author: Dr. Gregor Adams has extensive experience overseeing in vivo pharmacology aimed at bringing a variety of CAR-T and TCR therapies from preclinical efforts into clinical development. His background is in cell therapy with an emphasis on the interaction of hematopoietic stem cells with their microenvironment. Previous to joining MI Bioresearch, he headed preclinical in vivo studies at Kite Pharma for the development of all chimeric antigen receptor and engineered T cell receptor-based therapies. Dr. Adams received his Ph.D. from Imperial College School of Medicine in London, United Kingdom where his thesis focused on the development of a gene therapy for HIV-1 infection.

MODEL SPOTLIGHT | Modeling Human Acute Lymphoblastic Leukemia – Using the NALM6-Luc-mCh-Puro Model for the Development of CAR T Cell Therapies (PDF Version)

MODEL SPOTLIGHT | Modeling Human Acute Lymphoblastic Leukemia – Using the NALM6-Luc-mCh-Puro Model for the Development of CAR T Cell Therapies (PDF Version)