Our approach combining
LITT + LTSL-Dox
Helpful Context: some definitions
Normal Body Temperature: 37°C/98.6°F
LITT: Laser Interstitial Thermal Therapy is a minimally invasive surgical technique that uses a small laser (central ablation 50°C-80°C, to peripheral hyperthermia 43°C - 45°C) to heat and destroy tumors and unhealthy tissue guided by MRI with near realtime heat thermometry.
LTSL- Dox: Low Temperature Sensitive Liposome Doxorubicin (also called LTLD, and commercially branded as Thermodox) is a special kind of liposome, that encapsulates the anti-cancer drug, doxorubicin, and releases the drug when warmed to just 41°-42°C.
HT: Hyperthermia is warming any tissue, especially cancers, to temperatures above body temperature i.e., from about 100°F/40°C to about 113 °F/45°C https://www.cancer.gov/about-cancer/treatment/types/hyperthermia .
NOTE: LITT is primarily a central-tumor ablative-technology but can also warm peripheral regions of the tumor to these lower hyperthermic temperatures that could release Doxorubicin from intravenously administered LTSL-Dox.
Our Clinical Rationale and Underlying Science
Our Clinical Rationale
"if the whole tumor can be heated, the whole tumor can be treated"
Confocal fluorescent video microscope video of LTSL-Dox injected via the rat tail vein by Manzoor et al (3), and viewed in the micrcoscope window chamber, showing 20 minutes of observation in 20 seconds of video time
Microscopic images of the tumor vasculature in a window chamber by Chen et al, (4) showing the tumor blood vessels before a 1hr treatment with LTSL-Dox + heat, and 24hrs after the treatment, when all the blood vessels had been shut down and all that was left was a small thrombosis.
Summary of Preclinical Underlying Science
LTSL-Dox cures 11/11 mice
As described in more detail in the later page on "Introducing LTSL-Dox", the first time we tried it in a mouse study, LTSL-Dox cured 11/11 tumors out to 60 days (1), with just a singler dose and warming the tumors for just 1 hr
LTSL-Dox + HT: Dox is delivered throughout whole tumor in 20 mins
Here is a video of a tumor implanted in a microscopic rat window chamber warmed to 42°C showing how the LTSL-Dox liposomes (green) release their doxorubicin (red) throughout the whole tumor in only 20 minutes of warming (2). Every cell is not only loaded with doxorubicin, and doxorubicin is in the nucleus of every cell where it kills the cancer.
LTSL-Dox + HT: shuts down tumor blood vessels in 24 hrs
And the black and white images from Chen et al (3), show that because dox is also delivered into the blood vessel wall cells (endothelial and pericytes) the blood vessels are shut down within 24 hrs after the 1 hr treatment.
This is why we say: “the only way to get a drug throughout a whole tumor is to release the drug in the blood vessels of the tumor”
(1) Needham, D., et al., A new temperature-sensitive liposome for use with mild hyperthermia: Characterization and testing in a human tumor xenograft model. Cancer Research, 2000. 60(5): p. 1197-1201.
(3) Chen, Q., et al., Tumor microvascular permeability is a key determinant for antivascular effects of doxorubicin encapsulated in a temperature sensitive liposome. International Journal of Hyperthermia, 2008. 24(6): p. 475-482
LITT + LTSL-Dox and What We Envision
Laser Interstitial Thermal Therapy could be combined with an intravenous infusion of LTSL-Dox at an already established dose of 50mg/m^2. Since the in tact LTSL-Dox liposome only has a relatively short half-life of ~1.5 hrs, it is essential for the tumor to be concurrently warmed to target temperature of 41-42°C or the infusion started within a few minutes of starting LITT in the MRI suite.
The goal is to capture the most "Area Under the Curve" for the plasma LTSL-Dox. Shown below is the Mean Plasma Concentration of total doxorubicin vs time in subjects (with liver malignancies undergoing RFA (n = 6) (Wood et al. 2012) (1).
"Could LITT + LTSL-Dox work?"
As we were discussing the LTSL-Dox technology and what we had done over the years, Kate asked the question, "Could LITT plus LTSL-Dox work?" i.e., could LITT plus LTSL-Dox, that could release its drug in the imposible-to-remove peripheral, and known-to-be-invasive regions, provide additional advantages beyond LITT alone?
As we show below, in the core of the irradiated area, there is virtually instantaneous irreversible cell destruction at temperatures > 60 °C, Then, there is a dynamic thermal reaction (48–60 °C), but it is the tissue margins that may only suffer reversible cell damage and it is the periphery that becomes a region with a high rate of relapses.
With LITT + LTSL-Dox, while central and medium zones can still have their effects, the goals of the procedure shift to optimal warming of the tumor, especially at the periphery to 42°C. For the right sized tumor (up to 3 cm), LTSL-Dox could, in principle, 'clean up' the remaining tumor cells when the margins are warmed by LITT. Is this where LTSL-Dox could help eradicate this all-important peripheral cell zone.
Minimally invasive to patient, maximally invasive to tumor
Possible tumor warming scenario for LITT + LTSL-Dox
Brain Cancer and LITT
While surgical resection does provide some enhancement of OS, not all tumors are amenable to conventional surgical resection. Even with resection, recurrence is the norm. Data to the left shows, GBM median survival times as a function of age (3).
The Brain Cancer Problem
According to the Central Brain Tumor Registry of the United States (CBTRUS) (1), the most commonly occurring malignant brain and other CNS histopathology was glioblastoma (14.2% of all tumors and 50.1% of all malignant tumors). Unfortunately, even with the best available treatments, patients inevitably progress and die from the disease. As reported by Mohamed et al, (2) and references therein, "Despite the initiation of aggressive treatment along with extensive surgery, concurrent radiation and adjuvant temozolomide, the median survival time of adult patients remains around 10 months and up to 14 months in patients receiving combined treatment with radiotherapy" And... "Only 3% to 5% of patients survive more than three years, and reports of survival exceeding five years are sporadic".
See also the edited 21-chapter book by Steven De Vleeschouwer, entitled "Glioblastoma".
(1) Ostrom, Q.T., et al., CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2015–2019. Neuro-Oncology, 2022. 24(Supplement_5): p. v1-v95.
(2) Mohammed, S., M. Dinesan, and T. Ajayakumar, Survival and quality of life analysis in glioblastoma multiforme with adjuvant chemoradiotherapy: a retrospective study. Rep Pract Oncol Radiother, 2022. 27(6): p. 1026-1036.
(3) Gorlia, T., et al., New prognostic factors and calculators for outcome prediction in patients with recurrent glioblastoma: a pooled analysis of EORTC Brain Tumour Group phase I and II clinical trials. Eur J Cancer, 2012. 48(8): p. 1176-84.
As described at Atlanta Health, Magnetic resonance imaging (MRI) is used to guide a small probe with a side firing laser (below) that delivers precisely controlled heat to destroy brain cancer tissue.
An Improved Solution: Laser Interstitial Thermal Therapy (LITT)
As discussed by de Groot et al, (1)"LITT offers a therapeutic alternative for patients with newly diagnosed and recurrent glioblastoma for whom conventional, open surgical approaches are not deemed optimal, whether due to surgical risk or patient preference". And, as pioneered by Sloan et al (2), the NeuroBlate system with its gas-cooled, side-firing laser probe (image to the left), represents new technology for delivering laser interstitial thermal therapy, allowing controlled thermal ablation of deep hemispheric rGBM. It provides patients with a minimally invasive surgical option for recurrent brain tumors, (as well as radiation necrosis and certain types of epilepsy).
Ablation temperatures right next to the probe (central zone where early liquefactive necrosis occurs) ranges between 50 °C and 80 °C. And then the temperature drops off, as the inverse square law, (so 1/radius^2) down to body temperature (3) . In this peripheral region, where temperatures can be between 43 °C and 45 °C for more than 10 min, the cancer cells are sensitized to chemotherapy and radiation therapy, but not necessarily killed.
Thermal Damage Threshold (TDT) lines. Image from Kamath et al 2019, (7) , during laser ablation, demonstrating tumor volume (constructed manually on Monteris® [Plymouth, Minnesota] proprietary software at the time of surgery) and yellow and blue thermal damage threshold (TDT) lines (derived from real-time MR thermometry).
LITT Nevertheless has Limitations...
As also reported in the paper by de Groot et al (1), while studies have demonstrated strong safety data for LITT there is variable efficacy in subgroups of patients. "In 29 new and 60 recurrent grade 4 glioblastoma patients the median overall survival (OS) was 9.73 months for newly diagnosed patients and median post-procedure survival was 8.97 months for recurrent patients".
Despite median physician-estimated extent of ablation of 91%-99%, tumors still progressed. The infiltrated cancer cells for GBM tumors make it difficult for surgeons to surgically and completely resect the whole tumor or to fully ablate with LITT. In the picture shown to the left from Kamath et al, (2) in their phase 1 trial testing times and temperatures, there are areas outside of the yellow Thermal Damage Threshold (TDT) line that miss the pink border outlining the tumor. It’s these external margins that cause the GBM tumors to grow back so consistently in patients.