

There is more discipline available to malignancy patients than what one attention squad can keep up with. New diagnostics, treatments, trials, and suppliers keep emerging, and whenever norm of attention runs out, patients are normally remaining to fig out what alternatively power be imaginable on their own.
Future of Cancer Care Today (FCCT) helps malignancy patients and their families connect the dots. Our PhD-led squad surfaces diagnostic and care options applicable to a patient's case, including those beyond norm of care, and finds vetted suppliers and providers who activity beyond norm protocols. FCCT does not substitute doctors or create care decisions. We create playbooks and curate resources to assistance families ask improved questions, so they can stroll into the next conversation alongside a fuller picture.
Free for patients.
Important to know.
Future of Cancer Care Today is not a medicinal provider. We do not diagnose, prescribe, or straightforward treatment. We provision a non-clinical assistance tier focused on information, education, and decision support, intended to complement your association alongside your attention team. Some materials may be generated alongside the assistance of synthetic intellect and have to be reviewed alongside your medicinal providers before notifying any attention decisions. All decisions concerning your attention pertain to you and your doctor.
A curated build of suppliers, clinicians, and investigation groups we have encountered through our work.
Listings are informational only. FCCT does not endorse, certify, or authority these suppliers, and inclusion does not connote a referral or recommendation. Please verify particulars immediately alongside the provider and conversation any next steps alongside the patient’s attention team.
SUPPLIERS AND CARE PROVIDERS
updated regularly
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Services that maintain a patient's tumor tissue at biopsy or operation for forthcoming testing, including therapies that may not yet be at the period of collection.
SpeciCare (US). Patient-orderable.
StoreMyTumor (US, Europe). Patient-orderable.
Kernis Health (US). Patient-orderable. Even One Ventures company.
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Tests that analyze the molecular features of a tumor, including mutations, cistron expression, proteins, and biomarkers, to assistance acknowledge possible care targets. Usually performed on biopsy or surgical tissue.
Tempus (US). Physician-ordered.
Caris Life Sciences (US). Physician-ordered.
Foundation Medicine (US). Accepts global patients. Physician-ordered.
Boston Gene (US). Also includes immune microenvironment analysis. Accepts global patients. Physician-ordered.
Noetik (US). Whole-exome sequencing, spatial profiling, and IHC alongside raw data returned to the patient. Collaborate alongside patients.
Valius Sciences (US). Maximalist diagnostics adding single-cell and proteomic profiling. Patient-orderable. Even One Ventures company.
Protean BioDiagnostics (US). Comprehensive precision oncology evaluation alongside tolerant consultation. Patient accessible, physician-ordered.
Belay Diagnostics (US). CSF-based genomic profiling for brain and spinal cord tumors, helpful whenever tissue biopsy is risky or unavailable. Physician-ordered.
CNSide Diagnostics (US). CSF circulating tumor division grasp alongside molecular profiling for leptomeningeal disease, frequently detecting cases that accepted cytology misses. Physician-ordered.
RGCC International (Worldwide). Blood-based circulating tumor division molecular profiling for care guidance. Patient or physician-ordered.
Navignostics (Switzerland). Spatial single-cell proteomic tumor inspection from a sole FFPE section. Physician-ordered through early-access partner program.
BC Cancer Personalized Oncogenomics Program (Canada). Referral pathway in Canada.
CeGaT (Germany). Tumor-normal difference alongside patient-specific neoantigen identification. Physician-ordered.
OncoDNA (Belgium). Physician-ordered.
Hartwig Medical Foundation (Netherlands). Referral through participating Dutch hospitals.
Vicinity Bio(Germany). Ultra-high-plex spatial proteomic tissue imaging alongside AI-driven pathology reports and biomarker-based therapy guidance. Physician-ordered.
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Tests that develop a patient’s tumor cells or tumor models in the lab and disclose them to malignancy narcotics to measure which treatments may display activity.
Travera (US). Live-cell screening including immunotherapies. Physician-ordered.
First Ascent Biomedical (US). Live-cell medication reply throughout 150+ FDA-approved therapies. Physician-ordered.
Kiyatec(US). Ex vivo 3D medication reply evaluation focused on ovarian, breast, glioblastoma, and rare tumors. Physician-ordered.
Cure-First (US). Nonprofit offering organoid generation and medication screening of 47+ anticancer agents drawn from a 200+ medication library. Patient-accessible.
SageMedic (US). Physician-ordered live-cell functional medication evaluation for firm tumors, including rare cancers and cancers of unidentified primary, using 3D microtumors to measure tumor-cell killing, growth inhibition, and drug-combination activity.
KYAN Technologies (Singapore/US).Live-cell functional precision medication using proprietary AI to measure and position 1,500+ personalized medication combinations. Physician-ordered.
CanCertain (UK). 3D cell-culture medication evaluation on tumor cells from blood-based circulating tumor cells, compatible alongside immunotherapy testing. Patient or physician-ordered.
2cureX (Denmark). Through hospitals in Denmark, Germany, Sweden, and the UK. Physician-ordered.
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Blood-based tests that detect tumor DNA or another cancer-related signals to detect sickness complete time, including residual disease, recurrence, and care response.
Adaptive Biotechnologies (US). FDA-cleared MRD test, for B-cell malignancies (multiple myeloma, B-ALL, CLL, DLBCL). Physician-ordered.
BillionToOne (US). Tissue-free care monitoring and genomic profiling. Physician-ordered.
Caris Life Sciences (US). AI-enabled whole-exome and transcriptome lifeblood assay. Physician-ordered.
Foundation Medicine (US). Tumor-informed ctDNA monitoring developed alongside Natera. Physician-ordered.
Guardant Health (US). Tissue-free MRD and therapy reply monitoring. Physician-ordered.
Labcorp (US). Tumor-informed MRD throughout firm tumors, launched January 2026. Physician-ordered.
Natera (US). Tumor-informed personalized ctDNA assay for firm tumors. Physician-ordered.
NeoGenomics (US). Personalized MRD throughout firm tumors. Physician-ordered.
Personalis (US). Whole-genome tumor-informed MRD. Physician-ordered.
Quest Diagnostics (US). Tumor-informed ctDNA test alongside bounds of finding at 0.0006%. Physician-ordered.
Tempus (US). MRD and recurrence monitoring, powered by Personalis NeXT Personal Dx via partnership. Physician-ordered.
Veracyte (US). Whole-genome MRD for muscle-invasive bladder malignancy (coming in H1 2026; acquired from C2i Genomics). Physician-ordered.
Belay Diagnostics (US). CSF-based monitoring of chief and metastatic brain and spinal cord tumors, including detecting recurrence and distinguishing pseudoprogression from true progression. Physician-ordered.
CNSide Diagnostics (US). Longitudinal CSF monitoring of leptomeningeal sickness through circulating tumor division quantification and tracking of molecular markers. Physician-ordered.
RGCC International (Worldwide). Blood-based circulating tumor division counts complete period for monitoring sickness action and care response. Patient or physician-ordered.
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Tests that characterize a patient’s immune scheme and its communication alongside cancer, including immune-cell types, immune activity, and T-cell or B-cell patterns that may communicate immunotherapy discussions.
Personalis (US). Combines tumor sequencing alongside neoantigen prediction, TCR repertoire, and immune division composition. Physician-ordered.
Adaptive Biotechnologies (US). FDA-cleared minimal residual sickness assay for B-cell malignancies (multiple myeloma, ALL, CLL, DLBCL). Physician-ordered.
Arden Bio (US). Adds biology-matched immune therapy recommendations alongside tumor microenvironment profiling. Patient-orderable. Even One Ventures company.
Pathfinder Oncology (US). Bespoke immune profiling and inspection as part of personalized treatment-pathway activity for advanced cancer, led by William Hoos. Patient-accessible.
Navignostics (Switzerland). Spatial single-cell proteomic profiling of tumor-immune division interactions from a sole FFPE section. Physician-ordered through early-access partner program.
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Therapies that train the immune scheme to acknowledge and assault tumor-specific proteins. Most malignancy vaccines today are lone accessible through medicinal test enrollment. The exceptions are mostly on the peptide side: a fistful of clinics and programs can provision personalized peptide vaccines to patients who do not meet requirements for trials, during personalized mRNA vaccines remain nearly entirely confined to sponsor-run trials. Practically, this method a peptide vaccine is additional obtainable today.
Jaime Leandro Foundation (US). Personalized peptide vaccines through FDA Expanded Access (compassionate use) whenever no test is available. Patient-orderable.
Invoke Bio (US). Modality-agnostic neoantigen scheme (peptide, DNA, mRNA). Patient-orderable.
CeCurio (Germany). Personalized peptide vaccines through CeGaT collaboration, alongside real-world endurance data in glioblastoma. Patient-bookable in Germany.
Northwest Biotherapeutics (US, UK). Personalized autologous dendritic division vaccine for glioblastoma and another firm tumors in medicinal trials.
Immunocine (Mexico). Personalized dendritic division therapy at a Cancun medicinal center for patients alongside phase IV firm tumors who do not meet requirements for US trials. Patient-bookable, self-pay.
Diakonos Oncology (US). Patient-derived dendritic division therapy alongside trials underway in glioblastoma, pancreatic and melanoma. Trial enrollment.
Elicio Therapeutics (US). Lymph-node-targeted peptide vaccine against average KRAS mutations, in Phase 2 for pancreatic cancer. Trial enrollment.
UbiVac (US). Off-the-shelf vaccine targeting proteins from non-coding genome regions, alongside RNAseq-based screening for mark expression. Clinical-stage alongside fine data in caput and neck cancer. Trial enrollment.
Moderna (US). Personalized mRNA neoantigen vaccines. Trial enrollment.
Houston Methodist Center for RNA Therapeutics (US). Academic mRNA vaccine program led by Dr. John Cooke. Trial enrollment as studies open.
BioNTech (Germany). Personalized mRNA neoantigen vaccines. Trial enrollment.
IO Biotech (Denmark). Off-the-shelf peptide vaccine targeting IDO and PD-L1. Trial enrollment.
Echo (US). Personalized mRNA vaccines designed and manufactured for idiosyncratic patients. Patient-orderable. Even One Ventures company.
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Therapies that use engineered immune cells (CAR-T, TCR-T), tumor-infiltrating lymphocytes (TIL), or antibodies to mark cancer. Most are accessed through medicinal test enrollment; FDA-approved exceptions noted below.
Iovance (US). First FDA-approved TIL therapy for advanced melanoma, alongside multiple others in trials. Available at authorized care centers in the US.
UCSF Cancer Immunotherapy Program (US). Standard-of-care CAR-T for B-cell lifeblood cancers and multiple myeloma; trials in firm tumors. Referral through oncology consult.
Stanford Center for Cancer Cell Therapy (US). Standard-of-care CAR-T for B-cell lymphoma; trials in melanoma, firm tumors, and inoperable brainstem gliomas, including pediatric DIPG. Referral through oncology consult.
Memorial Sloan Kettering Cellular Therapeutics Center (US). Standard-of-care CAR-T for lifeblood cancers and trials in firm tumors. Referral through oncology consult.
CARTx Therapeutics (US). A Nationwide Children’s Hospital spin-off evolving affordable, off-the-shelf CAR γδT division therapies for firm tumors and lifeblood cancers using fit donor-derived polyclonal gamma-delta T cells.
Immatics (Germany). Engineered TCR-T targeting PRAME, expressed throughout many firm tumors. Trial enrollment.
DKFZ Heidelberg (Germany). Heidelberg cellular therapy hub operating TCR-T, CAR-T, and bispecifics alongside on-site GMP cleanrooms. Dirk Jäger group; referral pathway in Germany.
Ranata Therapeutics (US). Patient-specific antibodies and T-cell engagers designed against an idiosyncratic patient's malignancy division exterior targets. Patient-orderable. Even One Ventures company.
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Engineered viruses that selectively infect and demolish tumor cells during triggering an immune response. Access is currently via medicinal test enrollment.
Replimune (US, UK). Engineered HSV-1 oncolytic microorganism alongside BLA under FDA assessment for advanced melanoma; broader pipeline includes liver and another firm tumors. Trial enrollment in the meantime.
CG Oncology (US). Selective oncolytic adenovirus for BCG-unresponsive non-muscle invasive bladder cancer. BLA filing expected. Trial enrollment.
EpicentRx (US). Oncolytic adenovirus armed alongside a TGF-β trap (AdAPT-001), in trials throughout multiple firm tumors. Trial enrollment.
Candel Therapeutics (US). Adenoviral oncolytic blended alongside valacyclovir, alongside trials in prostate cancer, pancreatic cancer, and NSCLC. Trial enrollment.
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Services that assistance patients and physicians acknowledge applicable open medicinal trials. Most use AI-driven matching against medicinal records or indication profiles.
Picnic Health (US). Patient-accessible.
Massive Bio (US). Patient-accessible.
Antidote (US, UK). Patient-accessible.
ClinicalTrials.gov (US). Official US authorities register of medicinal trials worldwide; the underlying data origin most matching tools diagram from. Patient-accessible.
myTomorrows (Netherlands). Trial finding affirmative expanded admission program (compassionate use) coordination, supported by tolerant navigators. Active in nearly 50 countries. Patient-accessible.
Klineo (France). European test coverage. Patient-accessible.
EU Clinical Trials Information System (CTIS) (EU). Official European Medicines Agency repository of medicinal trials in EU associate states. Patient-accessible.
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Patient navigation services, AI-driven tools, and attention coordination resources to assistance patients and families comprehend their disease, discover care options, and oversee attention complete time.
Cancer Commons (US). PhD-led navigation affirmative an N-of-1 site-less observational study matching off-guideline FDA-approved narcotics through the patient's own oncologist. Patient-accessible.
Center for Metabolic Oncology (US). Physician-led metabolic health optimization custom for malignancy prevention, care support, survivorship, and surgical recover. Combines exercise, nutrition, sleep, stress, and ketogenic interventions as adjuncts to norm care. Led by Dr. Mark Kelley for cancer. Patient bookable.
Galen (US). AI-driven individual aide for malignancy patients covering test finding, lab interpretation, project management, coverage coordination. Patient-accessible.
OpenCancerAI (US). Open malignancy infrastructure and AI to decrease data asymmetry for patients. Patient-accessible.
Pathfinder Oncology (US). High-touch personalized treatment-pathway concierge assistance for advanced cancer. Patient-accessible.
Patient Advocators (US). Multi-disciplinary personal tolerant assistance resolute offering expert referrals, care navigation, and insurance/cost coordination throughout malignancy and another complex conditions. Patient-accessible.
Private Health Management (US). High-touch tolerant guidance, expert access, second opinions, and attention coordination. Patient-accessible.
Sagely Health (US). Led by oncologist Jason Sager, MD, Sagely Health helps malignancy patients and families create awareness of evolving science, medicinal trials, and treatment-access pathways. It offers a free, HIPAA-compliant medicinal test report, affirmative affordable individualized consultation alongside expert research, oncologist oversight, and tolerant protagonist support. Patient-accessible.
Outperform Cancer (US). Patient-built instructional website and podcast aggregating investigation on malignancy vaccines, exercise oncology, dietary interventions, and another adjunctive strategies. Patient-accessible.
NAVEXIO(US, Canada, Global). High-touch precision oncology navigation and consulting combining molecular diagnostics expertise, medicinal test and medication admission navigation. Patient-accessible.
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Physicians and centers known for taking complex cases, considering off-guideline options, and supporting patients exploring beyond norm of care.
Asthra Health (US). Outside medicinal opinion for complex malignancy cases. Patient-bookable.
Sarcoma Oncology Center (US). Sarcoma-focused second opinions, medicinal trials, and multimodal care planning. Patient-bookable.
Private Medical (US). Private Medical takes complex cases alongside notice to overlooked medicinal angles. Patient-bookable.
Gustave Roussy (France). Europe's largest thorough malignancy center, alongside a powerful precision oncology program, ample Phase I trials portfolio, and global referral pathway.
Docrates Cancer Center (Finland). Private malignancy center in Helsinki serving global patients, offering unified diagnostics, treatment, and follow-up under a individual attention squad model. Patient-bookable internationally.
SELF-SERVE PLAYBOOKS
updated regularly
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Find open-minded physicians
What to appearance for, and what to ask, whenever seeking an oncologist consenting to think beyond norm protocols.
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Assemble your tumor board
How to build a small collection of expert perspectives on your case, including who to contain and how to run a session.
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Tips for medication admission advocacy
A applicable walkthrough of expanded access, Right to Try, and medicinal test pathways, alongside what tends to activity and what tends to backfire.
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Bridging to a medicinal trial
How to extend the timing gap between sickness progression and a medicinal test that hasn't yet opened, through expanded access, Right to Try, and state-level frameworks akin Montana SB535.
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Preserving your tumor tissue
What tissue conservation makes imaginable and how to commencement the conversation alongside your attention team.
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Comprehensive tumor diagnostics
What thorough profiling can add beyond a norm panel and how it fits into decisions at diagnosis, recurrence, and following treatment.
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Therapeutic ladder template
A template for organizing care options and questions to conversation alongside your attention team.
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Personalized malignancy vaccines
What personalized malignancy vaccines are, what published studies display so far, how patients admission them, and questions to conversation alongside your attention team.

Director, Patient Connections
Bayli DiVita Dean, Ph.D.
Bayli is a researcher and discipline communicator dedicated to improving the lives of those diagnosed alongside cancer. She developed her ability in malignancy immunotherapy investigation at the University of Florida and in translating complex specialized findings into accessible tongue during her period at the American Brain Tumor Association. Bayli was additionally a chap at the National Institutes of Health, Office of the Director, through the American Association for the Advancement of Science Science and Technology Policy Fellowship, anywhere she addressed guideline needs connected to incorporating the community into medicinal investigation and bioethical issues. Inspired by her mother's assessment alongside metastatic colon cancer, she now applies her caregiving, scientific, and communication ability to provision data and compassion to clients of FCCT.

Associate, Patient Information
Donnia Robins, MSc.
Donnia is a researcher alongside training in chemistry, community health, and pharmaceutical sciences. Before joining FCCT, she was an Early Stage Researcher in the AGePOP consortium, an EU Horizon 2020 program focused on medicines for particular populations, including older adults. At FCCT, Donnia supports tolerant case research, asset mapping, and preparedness of instructional materials for patients.

Patient-First Data and Tissue Release
One position authorization US patients can use to petition or straightforward the publish of records, imaging, test data, and accessible tissue to recipients they choose.
We invitation patients, and the organizations that create or clasp their data or tissue, to use the publish and portion feedback on how it plant in practice. This volition assistance us create the form clearer, easier to process, and additional productive for everyone involved.
Why This Form Is Needed
Patients can normally get medicinal notes and summary reports. Obtaining the underlying materials can be additional difficult. These may contain first imaging files, pathology materials, sequencing files, lab data, and accessible tissue. They may be needed for a second opinion, additional testing, medicinal test evaluation, or research.
What the Form Does
- Identifies who is authorizing the publish and anywhere the materials are held. The form includes the patient’s information, the authority of any individual representative, and multiple releasing institutions and departments.
- Defines the records and data covered. This includes medicinal and billing records; laboratory, pathology, and imaging reports; first imaging files; digital health data exports; genomic and lab reports; raw data files; and connected assay and inspection information. The authority covers all dates.
- Includes accessible tissue and another specimens. Covered materials contain pathology slides and tissue blocks, as fine as blood, plasma, serum, skeletal marrow, and another biologic materials.
- Addresses delicate data separately. The tolerant must first the categories they authorize for release, including familial or genomic, HIV/AIDS-related, mental health, and reproductive or intimate health information. Psychotherapy notes are excluded. Substance use disturbance records covered by 42 C.F.R. Part 2 necessitate distinct consent.
- Defines who may obtain the materials. The authority covers stated healthcare, laboratory, data exchange, and investigation recipients, as fine as another individual or institution identified by the patient. The recipient may inform the releasing institution anywhere to dispatch the materials.
- Creates a position authorization. Once the form is on file, an authorized recipient may petition covered materials without obtaining a new tolerant signature for all request. The authority remains productive for up to 99 years unless the tolerant revokes it or applicable law requires an before expiration.
- Explains the limits of releasing bodily materials. Tissue and another specimens can be released lone whenever they remain accessible and publish is permitted. Materials that were abandoned or not preserved cannot be recovered. A publish may additionally decrease what remains for forthcoming attention or testing.
- Includes norm authority terms. These location purpose, expiration, revocation, imaginable re-disclosure, voluntariness, permitted fees, the correct to a copy, governing law, and signatures. The form is intended to fulfill HIPAA authority requirements under 45 C.F.R. § 164.508.
Requests remain topic to applicable law, availability, and organizational policy. The form covers the publish of the materials. Later use or sharing by the recipient may necessitate a distinct agreement.
Email feedback to: [email protected]
Materials move immediately from the holder to the tolerant or chosen recipient. FCCT does not obtain or shop data or tissue and does not provision lawful or medicinal advice.
Work alongside us.
If our activity could be helpful to you or your community, delight attain out. There is no disbursal to patients or families for our help.
Patients and Caregivers
Whether you are newly diagnosed, facing progression, or trying to fig out what comes next, we may be capable to assistance you think additional plainly concerning the way ahead.
Clinicians, Researchers, Partners
If you are operating in diagnostics, therapeutics, personalized medicine, or health technology, and accept patients need improved assistance navigating complexity, let's conversation concerning how our activity could complement yours.
