Our Technology

The Akesis Gemini 360

The only adaptive radiotherapy machine in Utah. It doesn't just deliver radiation. It sees, adapts, and responds to your cancer in real time.

At 5D Cancer Services in St. George, Utah, we use this technology to deliver treatments that are more precise, more efficient, and produce fewer side effects than conventional radiation — often in as few as 5 sessions.

Why Adaptive Matters

Because cancer doesn't sit still

Tumors change shape, shift position, and shrink during treatment. A plan created on day one may not match reality on day five. Conventional radiation machines treat based on a static plan — delivering radiation to where the tumor was, not where it is. The Gemini 360 solves this by re-imaging and recalculating your treatment plan at every single session.

99%

of radiation machines cannot adapt

They deliver based on a static plan made before treatment begins, regardless of how the tumor changes.

0.3mm

isocenter targeting accuracy

About the width of three human hairs — precision that maximizes tumor dose while sparing healthy tissue.

5

sessions for many cancers

Compared to 20–45 treatments over 5–9 weeks with conventional radiation therapy.

Your Treatment Journey

How a treatment session works

Each session follows the same adaptive process — from imaging to delivery, everything is optimized for your cancer that day.

Step 01

Consultation & Planning

Our physicians and staff review your diagnosis, imaging, and pathology to determine if adaptive radiotherapy is right for you. A personalized treatment plan is created based on your specific cancer type and location.

Step 02

Real-Time 3D Imaging

Before each session, the Gemini 360 captures a full 3D image of your tumor using cone-beam CT (CBCT) and kV/kV imaging. This shows exactly where the tumor is today — not where it was last week.

Step 03

Plan Adaptation

The system automatically compares today's image to the original plan and recalculates the treatment in real time. If your tumor has shifted, shrunk, or changed shape, the plan adapts accordingly.

Step 04

Precision Delivery

Radiation is delivered with 0.3mm isocenter accuracy — about the width of three human hairs. The system targets your tumor precisely while sparing surrounding healthy tissue.

Step 05

Treatment Complete

Many cancers are treated in as few as 5 sessions over one week, compared to 20–45 treatments over 5–9 weeks with conventional radiation. Most patients continue normal activities throughout treatment.

Technical Specifications

Built for precision

The Gemini 360 pairs a high-energy LINAC with onboard CBCT imaging in a single ring gantry — enabling adaptive treatments like dose painting, grid irradiation, and simultaneous multi-target therapy.

0.3mm
Isocenter Accuracy

Sub-millimeter targeting precision

1400 cGy/min
Maximum Dose Rate

Faster delivery, shorter sessions

40 x 40 cm
Field Size

Treats small brain tumors to large complex cancers

CBCT + kV/kV
Imaging

Real-time 3D imaging before every session

Automated
Tracking

Skull tracking with less than 1mm accuracy

Workflow

Online vs offline adaptive

Adaptive radiotherapy comes in two flavors. The Gemini360RT delivers online adaptive treatment — your plan is recalculated against today's anatomy, on the couch, before the beam fires.

Offline adaptive

Replan between sessions

After one or more fractions, the team reviews recent imaging, redesigns the plan offline, and treats the patient on the new plan at a later visit. It improves on a static plan, but it cannot react to today's anatomy.

Online adaptive — what we deliver

Replan at the moment of treatment

The Gemini360RT acquires a CBCT in treatment position, the system recalculates the plan against today's anatomy, the physician approves the adapted plan, and treatment is delivered — all in one visit, before you get up.

AI-assisted contouring & replanning

What makes online adaptation practical is automation. Deep-learning models propose tumor and organ contours on the daily CBCT in seconds, the system recalculates dose against today's anatomy in minutes, and independent QA runs in the background. The physician reviews and approves — but the team no longer needs to start a fresh plan from scratch every fraction. That is how the Gemini360RT compresses what used to take hours into a single, on-couch session.

Read the full evidence-based explainer
See the difference

Traditional vs. Adaptive Radiotherapy

Here's how the Akesis Gemini 360 compares to conventional radiation treatment.

0

treatments
Traditional max

0

sessions
Adaptive minimum

0x

faster
Time to complete

FeatureTraditionalAdaptive
Treatment sessions20–45 treatmentsAs few as 5 sessions
Treatment duration5–9 weeks1 week or less
Real-time 3D imagingCBCT + kV/kV imaging
Automated tumor trackingSkull tracking with ≤1mm accuracy
Adapts to tumor changes
Targeting precisionStandard margins0.3mm isocenter accuracy
Side effectsMore commonSignificantly reduced
Akesis Gemini 360 treatment room
FDA Cleared Technology

Safe, proven, and FDA cleared.

We understand that trusting a new treatment approach is a big decision. The Akesis Gemini 360 has received both FDA 510(k) clearance and Premarket Approval, along with FDA Breakthrough Device Designation. It has been thoroughly reviewed and authorized by the U.S. Food and Drug Administration for safety and effectiveness. This isn't experimental. It's the next generation of radiation treatment, and it's here now.

What does FDA clearance mean?

FDA 510(k) clearance means the device has been reviewed by the FDA and determined to be substantially equivalent to other legally marketed devices. It must meet safety standards, performance benchmarks, and quality controls before it can be used to treat patients.

Explore the clinical data

FDA 510(k) Clearance & Premarket Approval

The Akesis Gemini 360 has received both U.S. FDA 510(k) clearance and Premarket Approval, meeting the most rigorous safety and effectiveness standards required for medical devices in the United States.

FDA Breakthrough Device Designation

The Gemini 360 earned FDA Breakthrough Device Designation — a status reserved for technologies that offer significant advantages over existing treatments for life-threatening conditions.

First U.S. patient treated December 2025

The first U.S. patient was treated with the Gemini 360 on December 16, 2025, at Advanced Radiation Centers of New York in Lake Success, NY — marking a new era in integrated radiotherapy.

Board-certified team

Every treatment is planned and supervised by our physicians and staff — board-certified radiation oncology professionals with over 30 years of combined clinical experience.

Conditions treated with adaptive radiotherapy

The Gemini 360's large 40x40 cm field and adaptive workflow make it effective for a wide range of cancers and benign conditions.

Take the next step

There is no time for cancer.

You deserve the most advanced care available. Schedule a consultation with our physicians and staff today to discuss your treatment options.

1308 E 900 South, Unit B, St. George, UT 84790

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No Time for Cancer billboard — Instead of 6+ weeks, treat your cancer in 5 days