CancerCareE — Independent Patient Information & Introduction Platform $0 patient fees — Always Vetted institutions across multiple destinations | info@cancercaree.com | 🏥 Explore Hospitals 📋 Explore Options
For Physicians — Oncology Access Intelligence for Referring Physicians | CancerCareE
CancerCareE — Independent Patient Information & Introduction Platform $0 patient fees — Always Vetted institutions across multiple destinations | info@cancercaree.com | 🏥 Explore Hospitals 📋 Explore Options

When Standard Oncology Pathways Reach Their Limit

An independent, evidence-based intelligence platform helping physicians navigate advanced treatment options for patients who have exhausted standard care — across 8 countries and 200+ partner institutions.

"بیمارم درمان استاندارد را تمام کرده. حالا چه؟"
"بیمارم در کشور ما واجد شرایط نیست. کجا باید رفت؟"
"نمی‌دانم کدام کشور بهترین گزینه را دارد. چه کسی می‌تواند کمک کند؟"
CancerCareE provides structured pathway intelligence — not marketing, not opinions.
200+
Partner Institutions
700+
Active CAR‑T Trials (China)
48–72h
Tumor Board Response
$0
Cost for Physicians

The Reality Check

Myth: "A medical coordination company will manage your patient's treatment and guarantee a cure."
Reality: We provide the logistical roadmap, cost transparency, and hospital introductions. You and your licensed physician colleagues make all medical decisions. We do not guarantee outcomes, we never collect sensitive medical data on this website, and our role ends once you are directly connected to the partner center.

Clinical Decision Support

Three Clinical Decision Support Services

Structured, evidence-based intelligence for referring physicians — at no cost.

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Treatment Pathway Navigation

Identify Next-Step Treatment Options

When local guidelines have been exhausted, we map the patient's molecular profile, prior treatments, and clinical status to available therapies across our global network.

  • Matches cases to available institutions
  • Country-specific access conditions
  • Transparent cost estimates from multiple centers
  • Travel, visa, accommodation logistics
  • Referring physician oversight maintained
  • Post-treatment continuity coordination
Request Pathway Navigation
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International Tumor Board

Independent Multi-Specialist Review

Submit de-identified cases for evaluation by 2–3 independent specialist oncologists. Structured consensus recommendation with PubMed citations within 48–72 hours.

  • 2–3 independent specialist opinions per case
  • Consensus-based methodology (reduced bias)
  • Structured recommendation document
  • Clinical trial eligibility assessment
  • Multi-country treatment landscape view
  • Optional physician-to-physician consultation
Learn About Tumor Board Review
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Global Trial Intelligence

Identify Trial Options Across Countries

Real-time intelligence on clinical trial availability, feasibility, eligibility, and enrollment conditions — including one of the world's largest CAR-T trial ecosystems.

  • 700+ CAR-T trials in China alone
  • Trials across 8 countries
  • Eligibility criteria matching
  • Real-time slot availability verification
  • Next-generation constructs (dual-target, allogeneic)
  • Enrollment coordination support
Explore Trial Intelligence
Clinical Expertise

Areas of Highest Expertise

Our global network covers a wide range of therapeutic modalities, targets, and cancer types.

Therapeutic Modalities

  • CAR‑T Cell Therapy (CD19, BCMA, CD22, dual-target)
  • Bispecific Antibodies (CD3/CD20, BCMA/CD3)
  • TIL Therapy
  • Gamma Delta T‑Cell Therapy
  • NK Cell Therapy
  • Antibody-Drug Conjugates (ADCs)
  • Checkpoint Inhibitors & Combinations
  • Personalized Cancer Vaccines

Rare & Emerging Targets

  • GPC3 (Hepatocellular Carcinoma)
  • Claudin18.2 (Gastric, Pancreatic)
  • Mesothelin (Mesothelioma, Ovarian)
  • GD2 (Neuroblastoma, Sarcoma)
  • EGFRvIII (Glioblastoma)
  • MUC1, MUC16 (Ovarian, Pancreatic)
  • NY-ESO-1 (Sarcoma, Melanoma)
  • MAGE-A4 (Multiple Solid Tumors)

Cancer Types

  • DLBCL, ALL, AML, Multiple Myeloma
  • Mantle Cell Lymphoma, Follicular Lymphoma
  • Lung Cancer (NSCLC & SCLC)
  • Pancreatic Cancer
  • Gastric / Gastroesophageal Cancer
  • Liver Cancer (HCC)
  • Colorectal Cancer
  • Glioblastoma
  • Triple‑Negative Breast Cancer
  • Sarcoma & Rare Solid Tumors
Information Quality

Google / PubMed vs CancerCareE

What you can find through literature search — and what we provide that you cannot easily collect yourself.

Google / PubMed

  • Published clinical trial data (often years old)
  • Single-center outcomes
  • Regulatory approvals (time‑lagged)
  • Abstract‑level information only
  • No real‑time slot availability
  • No logistical feasibility data
  • Patient advocacy content

CancerCareE

  • Aggregated real‑world outcomes (anonymized)
  • Multi‑center, multi‑country data
  • Regulatory conditions — country‑specific
  • Full protocol and access conditions
  • Real‑time manufacturing slot verification
  • Visas, accommodation, language support
  • Independent, evidence‑based intelligence
Real‑World Intelligence

Intelligence You Cannot Easily Collect Yourself

Data that is not available in PubMed, clinical trial registries, or hospital websites.

Real-World Outcome Data: Aggregated, anonymized response rates, PFS, adverse event profiles
Waiting Time & Manufacturing Slots: Actual vein-to-vein timelines across centers
Country-Specific Availability: Regulatory and administrative conditions
Travel & Logistics Feasibility: Visa, accommodation, language support
Hospital & Program Experience: Volume and experience data per therapy
Trial Slot Availability: Real-time enrollment slot verification
This intelligence is aggregated from partner institutions, updated regularly, and presented without bias. We do not claim outcomes — we document what exists.
Real Cases

Case Stories

Three documented cases demonstrating how pathway intelligence works in practice.

Case 1: Relapsed DLBCL After Second-Line Therapy

52-year-old male · Refractory to R‑CHOP and R‑ICE

Prior Therapies: R‑CHOP ×6, R‑ICE ×3 — progressive disease

Molecular Finding: CD19‑positive, adequate organ function

Review Outcome: Dual‑target CD19/CD22 CAR‑T study (Shanghai)

Center: Academic medical center, 14‑day vein‑to‑vein time

Outcome: CR at Day 28. MRD‑negative at 6‑month follow‑up.

Case 2: Advanced HCC with GPC3 Expression

64-year-old female · Progressed on sorafenib and lenvatinib

Prior Therapies: Sorafenib → progression at 4 months. Lenvatinib → progression at 6 months

Molecular Finding: GPC3‑positive by IHC. Child‑Pugh A. ECOG 1.

Review Outcome: GPC3‑targeted CAR‑T phase I/II study

Selected Country: China — GPC3 CAR‑T not available in home country

Outcome: Enrollment within 10 days. Stable disease at first assessment.

Case 3: Metastatic Gastric Cancer — CLDN18.2 Positive

58-year-old male · CLDN18.2 positive · Third-line setting

Prior Therapies: FOLFOX → progression. Ramucirumab + paclitaxel → progression

Molecular Finding: Claudin18.2 (IHC 2+, >70% tumor cells). HER2‑negative. MSI‑stable.

Review Outcome: Claudin18.2‑targeted CAR‑T clinical study

Selected Center: Beijing — one of world's most experienced in CLDN18.2 CAR‑T

Outcome: PR at Day 28 with significant symptomatic improvement.
All cases are de‑identified. Outcomes shown are real but individual results vary. We do not claim these outcomes are typical.
Global Access

Why China Matters for Advanced Cell Therapy

Documented facts about one of the world's largest clinical trial ecosystems.

World's Largest CAR‑T Trial Ecosystem — 700+ active trials
Fast Manufacturing — 14–21 days vein‑to‑vein
Dual‑Target & Next‑Generation CAR‑T Development
Early Access to Novel Solid Tumor Targets
High‑Volume Centers with therapy‑specific experience
Regulatory & Quality Framework — NMPA, ICH‑GCP

Counter‑Signal: What China Is Not

We do not promote China as the only destination. We document access conditions across all 8 countries in our network. China is not a "cheap alternative" — it is a high‑volume clinical trial ecosystem with 700+ active studies.

  • Not every therapy is available in China
  • Not every patient is eligible for Chinese trials
  • We do not claim China is "the best" — we document what exists
Data Protection

Security & Data Protection

We take data security and patient privacy seriously.

End‑to‑End Encryption256‑bit SSL. Files encrypted at rest and in transit.
De‑Identified SubmissionsNo PII shared without explicit consent.
Role‑Based AccessMFA required. Only authorized personnel can view cases.
Complete Audit TrailsAll access logged and auditable.
HIPAA‑Aligned & GDPR‑ReadyBAA available. European data protection compliant.
PHI Not Stored Longer Than NecessarySecure deletion after case closure.
Transparency

How Is This Service Funded?

CancerCareE is completely free for physicians and patients to use for information and introduction services.

After a patient is introduced to a partner institution, CancerCareE may receive a fixed referral fee from the partner center.

This fee is not performance‑based and does not influence which center is suggested. Our recommendations are based on clinical trial availability, hospital accreditation, and treatment protocols.

Eligibility

Who Can Use This Service?

Eligible Physicians

  • Board‑certified oncologists (medical, radiation, surgical)
  • Board‑certified hematologists
  • Active, unrestricted medical license
  • Verified institutional affiliation
  • Specialists in cellular therapy or immunotherapy
  • Physicians treating rare or complex cancers
  • Academic researchers in oncology
  • Clinical trial investigators

Not Eligible

  • Non‑licensed practitioners
  • Physicians with restricted or suspended licenses
  • Alternative medicine providers without oncology certification
  • Unverified institutional affiliations
  • Commercial entities seeking patient data
  • Individuals misrepresenting credentials
All physicians are verified through license checks, board certification verification, and institutional affiliation validation before case review begins.
Getting Started

How to Get Started

A simple, structured process for referring physicians.

1

Submit Credentials

Complete physician verification form

2

Verification

License, board certification, affiliation validation (24‑48h)

3

Submit Patient Case

Upload de‑identified case for review

4

Receive Recommendation

Structured pathway within 48‑72h

Global Network

Our Global Network

Partner institutions across 8 countries, each with therapy-specific experience.

🇨🇳China80+
🇮🇳India40+
🇹🇷Turkey30+
🇰🇷South Korea25+
🇺🇸USA25+
🇩🇪Germany20+
🇸🇬Singapore15+

Network continuously expanding. Data current as of August 2026.

Questions

Frequently Asked Questions

Ready to Explore Options for Your Patient?

Get independent, evidence-based pathway intelligence for your patient — at no cost.