Sarcoma is 100 diseases pretending to be one. We treat the one you have.
Sarcoma comes in many forms — our needle-based treatment is tuned to yours, for disease that has spread or stopped responding.
Personalized
Minimally invasive
Immune-activating
Outpatient
In plain terms
What we do, in three paragraphs.


Histology-driven re-engagement.
Individual results vary. These outcomes represent specific patient cases and are not guaranteed for all patients.
Treatment options by stage.
Find your diagnosis below to see what standard care offers, where we add to it, and what role our approach plays.
Destroy the tumor, then teach your immune system to finish the job.
Why this approach for sarcoma?

Treats tumors near critical structures
Retroperitoneum, extremity, chest wall, viscera — non-thermal PEF allows treatment near major vessels and nerves.

Converts “cold” subtypes into “hot” targets
Leiomyosarcoma, synovial, and GIST are cold to checkpoint monotherapy. Ablation + intratumoral immunotherapy addresses the root cause.

Aims for systemic response
The investigational goal is to determine whether treating one tumor can stimulate immune activity at untreated sites in the lung, liver, and elsewhere.
Histology-aware intratumoral cocktails.
“Sarcoma is 100 diseases pretending to be one. The right intratumoral combination for a leiomyosarcoma isn’t the same as for a synovial sarcoma. We tune the immune amplification to the histology.”
— Dr. Jason R. Williams

Extending pembrolizumab activity
For UPS / DDLPS / ASPS / Kaposi, intratumoral OX40 / CD40 + CpG is a rational priming strategy to extend and re-engage checkpoint response.

Synovial sarcoma antigens
Cancer-testis antigens (MAGE-A4 / NY-ESO-1) are conserved across synovial sarcoma — ablation antigen release can engage broader responses beyond TCR therapy.

Leiomyosarcoma cold conversion
LMS is one of the most immune-cold subtypes — ablation + intratumoral immunotherapy addresses the cold microenvironment directly.
“Sarcoma histology drives immunotherapy choice. We pick the intratumoral therapies based on that subtype’s immune biology — not one-size-fits-all.” — Dr. Williams
Beyond the procedure: whole-patient support.
We optimize your entire system for the best possible response — and coordinate with the team you already have.
Gut microbiome optimization
Diet, probiotics, and related therapies to support a stronger immunotherapy response.
Off-label protocols
Strategic use of repurposed medications to enhance immune response.
Personalized cocktails
Multi-agent immunotherapy tailored to your specific cancer.
Oncologist coordination
We work alongside your current chemo and radiation team.
Your path to treatment.
Case review
We review your imaging and pathology with subtype, IHC, and mutation profile (NTRK, EWSR1, SS18-SSX, KIT).
Protocol design
A histology-aware personalized intratumoral cocktail.
Procedure week
Image-guided PEF or cryoablation + intratumoral immunotherapy. Outpatient.
Follow-up
Imaging at 6–8 weeks, coordination with your home sarcoma team.
Procedure ~1 hour
Recovery ~2 hours
All outpatient
Is this right for you?
You may be a candidate if:
It may not be suitable if:
Each case is individually evaluated by Dr. Williams’ team.
Innovation for sarcoma.
Multi-agent intratumoral protocols
The AblationVax concept.
Combination protocols reported
Yervoy / Opdivo / CpG / PV-10 combinations.
Histology-aware PEF + intratumoral protocols
For cold sarcoma subtypes.
There is more ahead. Take the next step with confidence.
Complimentary evaluation.
Dr. Williams’ team will personally review your case and imaging — no cost, no obligation.
Or email info@williamscancerinstitute.com
Beverly Hills · San Jose del Cabo · Mexico City — most patients complete treatment in one week



