ROMbugBio Cancer Anatomy Explorer

Front view

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Anatomical male model, front view
ROMbugBioCancer scorecard

ROMbugBioAbout the data

How to read the explorer

Where the figures come from, what they mean, and what they can't tell you.

Who is SEER?

SEER stands for Surveillance, Epidemiology, and End Results. It is a program of the National Cancer Institute, part of the US National Institutes of Health, and it began collecting data on January 1, 1973, after the National Cancer Act of 1971.

SEER gathers records from population-based cancer registries that now cover about 46% of the US population. For each cancer it records the type, where it started, how far it had spread at diagnosis, the first treatment, and whether the person is still alive in later years. It is the only comprehensive US source that tracks both stage at diagnosis and survival across whole populations, which is why most survival figures in this explorer come from it. Death counts come from the National Center for Health Statistics.

What does 5-year relative survival mean?

It is the share of people with a cancer who are alive five years after diagnosis, compared with people of the same age and sex in the general population. Comparing the two groups removes deaths that would have happened anyway, so the figure reflects the effect of the cancer itself.

A figure of 91% means people with that cancer are, on average, 91% as likely to be alive in five years as similar people without it. It is not the same as a cure rate. Many people live far longer than five years, and some cancers, such as chordoma, can return after five years.

What do localized, regional and distant mean?

SEER groups cancers by how far they had spread when first diagnosed. Localized means the cancer was confined to where it started. Regional means it had grown into nearby tissue or lymph nodes. Distant means it had spread to faraway organs such as the liver, lungs or bones.

These are not the stage 1 to 4 numbers doctors use, which follow the more detailed TNM system. The share of cases diagnosed at each stage shows how often a cancer is caught early.

Why the survival figures look backward

To know who is alive five years after diagnosis, people must have been diagnosed at least five years ago. The most recent figures cover people diagnosed between 2016 and 2022, and some cards use earlier periods where that is the latest published breakdown. Treatments have improved since then, so people diagnosed today may do better than these numbers show.

These are averages across large groups. They cannot predict what will happen to one person, whose outlook also depends on age, overall health, the tumor's biology and how it responds to treatment.

Where the case and death numbers come from

Each January the American Cancer Society projects how many new cases and deaths to expect that year, using registry data and national death records. The 2026 numbers on each card are those estimates. Colon and rectal cancer deaths are reported together because death certificates often record one as the other.

For colon cancer, rectal cancer, chondrosarcoma and chordoma, SEER's own summary pages do not publish survival separately, so those cards use the American Cancer Society's analysis of SEER data. Each card footer names its source and period.

What do trial phases mean?

The live list of recruiting studies comes from ClinicalTrials.gov, the registry run by the US National Library of Medicine. Recruiting means the study is enrolling now.

Phase 1
Tests safety and the right dose of a new treatment in a small group of people.
Phase 2
Checks whether the treatment works against a specific cancer and continues to study safety.
Phase 3
Compares the new treatment with the current standard in hundreds or thousands of people. Results usually decide approval.
Phase 4
Follows an approved treatment in wider use to learn more about long-term benefits and risks.

A listing is not an endorsement and does not mean someone is eligible. The trials that changed care on each card are selected by ROMbug Bio from published results, dated by their key publication.

Using this information

The explorer is for information and education. It is not medical advice. Decisions about screening, diagnosis and treatment should be made with a doctor who knows your situation. Questions about the explorer: support@rombugbio.com.

ROMbugBioResearch tool

NeoAntigen Workbench

From a sequenced tumor to a shortlist worth testing.

How the NeoAntigen Workbench works: files from the sequencing laboratory go in, six processing stages run, and a ranked shortlist with supporting evidence comes out.

The ROMbug Bio NeoAntigen Workbench takes annotated sequencing data from a tumor and a matched normal sample, and ranks the tumor-specific protein fragments most likely to be displayed to the immune system. It supplies a prioritised candidate list, with the supporting computational evidence, to a specialist laboratory, which tests those candidates and determines which, if any, are suitable for vaccine development.

It predicts which fragments are displayed, not which provoke an immune response. That distinction is what the laboratory testing resolves.

Why the ranking matters

Why ranking helps: of 918 candidate fragments measured, 41 provoked a T-cell reaction. Testing at random would take 179 synthesised peptides to find 8 that work; testing the top 20 the software picks finds the same 8.

Every candidate has to be synthesised and exposed to T cells taken from the patient, which is slow and limited by how much blood a patient can give. Ordering the candidates well decides where a laboratory looks first.

Working with us

We are interested in hearing from medical laboratories and research groups working on personalised cancer vaccines. For collaboration enquiries, write to support@rombugbio.com.

Research use only. Not a diagnostic device. The shortlist is a set of hypotheses for laboratory testing, not validated targets, and not a treatment.