CancerFax
Cancer Knowledge Hub β€” Expert-reviewed insights

Cancer insights that inform better decisions

Step-by-step guides, research summaries, and treatment overviews β€” reviewed by oncology navigators and written clearly for patients, families, and caregivers.

From newly diagnosed to relapsed and refractory β€” we publish what patients actually need to understand their options.

Reviewed by oncology navigators Updated regularly 50+ countries reached Clinically grounded
What you'll find here

Insights built for complex decisions

CancerFax Insights exists because cancer patients face decisions that are genuinely hard β€” not because of lack of will, but because the information landscape is fragmented, fast-moving, and often written for clinicians, not families.

Every insight published here is reviewed by our oncology navigation team before it goes live. We focus on the questions patients actually ask us: What is this treatment? Who qualifies? What should I prepare? What should I ask my doctor?

Use the search and filters below to find what's most relevant to your situation.

Cancer insights library

Browse the full library

Search, filter, and explore all published insights β€” by cancer type, treatment category, clinical trial readiness, or stage of your journey.

Search across cancer types, treatments, mutations, drugs, and trials

Topic

8 of 8 insights

Precision Oncology

Precision Oncology

Limitations of Genomic Testing

The limitations of NGS testing are real and worth understanding. They do not cancel the clinical value -- they define the conditions under which results should be interpreted. Standard DNA panels may miss gene fusions better detected by RNA sequencing. A single biopsy samples one region at one timepoint. Liquid biopsy has reduced sensitivity in low-shedding tumours. A negative result means not detected -- not definitively absent.

Precision Oncology

Precision Oncology

NGS Testing Cost Worldwide

Comprehensive genomic profiling list prices in the US range from $3,000-$7,500. Medicare covers comprehensive NGS for advanced solid tumours under a National Coverage Determination. Most testing laboratories (Foundation Medicine, Guardant Health, Tempus) have patient assistance programmes that reduce or eliminate cost based on financial need. Prior authorization denials are frequently overturned on appeal.

Precision Oncology

Precision Oncology

NGS Testing for Rare Cancers

Rare cancer patients who have been told that limited options exist should know: the question precision oncology asks is not whether your cancer type has a matched drug, but whether your tumour carries a molecular feature that has a matched drug regardless of cancer type. Tumour-agnostic approvals (MSI-H, NTRK fusions, TMB-high, RET fusions) apply to any solid tumour carrying the feature.

Precision Oncology

Precision Oncology

Questions to Ask About NGS Testing

The questions worth asking about NGS results differ by what is being decided. Before the results appointment: is the testing picture complete (comprehensive NGS, TMB, MSI, RNA sequencing)? During the results appointment: which findings are Tier I? Is there an FDA-approved drug? A tumour-agnostic approval? Currently enrolling basket trials? After: should this case go to a molecular tumour board?

Targeted Therapy

Targeted Therapy

Targeted Therapy for Lung Cancer (EGFR, ALK)

EGFR mutations are found in 10-15% of NSCLC in Western populations and up to 50% in East Asia. ALK rearrangements in 3-5%. Osimertinib is the preferred first-line EGFR inhibitor with median PFS of 18-20 months and strong CNS activity. Lorlatinib achieves median PFS exceeding 4 years in ALK-rearranged NSCLC. Comprehensive NGS testing before any systemic treatment is global standard of care.

Stage 4 Cancer

Stage 4 Cancer

Targeted Therapy for Stage 4 Cancer

Targeted therapy for stage 4 cancer requires a molecular target to be present. Comprehensive NGS testing before first-line treatment identifies which options apply. In molecularly matched patients, response rates, depth of response, and duration frequently exceed chemotherapy. Some EGFR-mutated stage 4 NSCLC patients on osimertinib have been disease-free at five years.

Precision Oncology

Precision Oncology

What Is NGS Testing?

NGS (next-generation sequencing) sequences hundreds of cancer-relevant genes simultaneously from a single tumour sample, replacing the old approach of testing one gene at a time. A comprehensive panel test returns results in 2-3 weeks, covers all established targetable alterations, and also assesses TMB and MSI for immunotherapy eligibility.

Precision Oncology

Precision Oncology

When Should Patients Do NGS Testing?

Earlier is almost always better for comprehensive genomic profiling in advanced cancer. Many targeted therapy approvals are first-line standards -- the molecularly matched therapy is the best initial treatment, not the rescue option after chemotherapy fails. Testing before first-line treatment is finalized means results are available when they can change the first decision.

By cancer type

Insights by cancer type

Find content specific to your diagnosis β€” from treatment overviews to clinical trial access and second opinion guidance.

Clinical trial access

Access to trials unavailable at home

CancerFax connects patients with clinical trials in China, India, and leading global centres β€” including phase I and II trials closed to international enrolment through standard channels.

500+

active clinical trials across China, India, and leading global centres

40+

cancer types with current advanced therapy access pathways

12+

years of patient navigation experience in cross-border oncology

A note from the CancerFax team

Why we publish independently

CancerFax Insights is editorially independent of the hospitals, pharmaceutical companies, and treatment centres we work with. Our navigation team writes what patients need to hear β€” not what any institution wants them to read.

That means we tell patients when a treatment is likely out of reach, when a clinical trial has closed, and when the evidence for a new therapy is still thin. We believe informed patients make better decisions and have better outcomes β€” even when the honest answer is harder to hear.

β€” CancerFax oncology navigation team

Questions

About CancerFax Insights

How our content is produced, reviewed, and how to use it effectively.

What kind of insights does CancerFax publish?
CancerFax publishes expert-reviewed, patient-facing content covering advanced cancer treatments, clinical trials, precision oncology, international care pathways, and caregiver guidance. Every insight is reviewed by our oncology navigation team before publication.
Are these insights written for patients or medical professionals?
Our insights are written primarily for patients, families, and caregivers β€” but are clinically grounded enough to be a useful reference for healthcare professionals. We aim for clarity without oversimplification.
How often is content updated?
Insights are reviewed and updated regularly, especially when new clinical data or trial results change the standard of care. The last review date is shown on each article.
Can I use these insights to make treatment decisions?
Our insights are educational β€” they help you understand options, ask better questions, and prepare for medical consultations. They do not replace the advice of your treating oncologist. If you need structured guidance for your specific case, our navigation team can help.
How do I find insights relevant to my cancer type?
Use the search bar above to filter by cancer type, treatment name, mutation, or stage. You can also browse by topic category using the filter pills, or use the cancer type tags in the sidebar.
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Every navigation request is reviewed by a qualified oncology professional. We do not recommend treatments without reviewing your medical records.