Tissue Cryopreservation

Why Cryopreserve?

1. Protect future testing options when the therapeutic plan changes.

Cancer treatment is increasingly iterative—progression, resistance, and guideline updates often prompt additional testing. Cryopreservation helps retain the highest-value tissue state for future assays, including those that are hard to run (or less reliable) on FFPE due to fixation-related changes and variable preanalytics. (PMC)

2. Enable RNA-forward and multi-omics pathways with stronger sample integrity.

FFPE RNA quality can be highly variable; fragmentation and chemical modifications are common and can limit some transcriptomic workflows. Fresh-frozen/viable preservation can reduce these constraints and support modern “omics” strategies as they become clinically available. (PMC)

3. Preserve tumor heterogeneity for advanced research and single-cell analysis.

Single-cell and multi-omics approaches depend on preserving biologic complexity. Multiple studies show that viable cryopreservation can retain cellular diversity and produce high-quality single-cell data suitable for deep profiling—supporting biomarker discovery and trial matching. (PMC)

4. Standardize preanalytic variables—reduce “silent failure” risk.

Clinicians know the downstream reality: cold ischemia time, fixation duration, and processing variability can materially affect molecular readouts. A cryopreservation pathway can be implemented alongside standard FFPE, with controlled handling steps designed to protect downstream analytic performance. (ASCO Publications)

5. Improve clinical trial readiness.

Trials increasingly specify biomarker requirements (and sometimes fresh/viable tissue preferences). Preserving viable tissue can reduce re-biopsy pressure and accelerate eligibility workflows when trial opportunities emerge. (Trial requirements vary by protocol; SpeciCare supports protocol-based collection planning.) (PMC)

Optional “clinician callout box”:

Cryopreservation is additive, not disruptive. Most cases maintain standard diagnostic FFPE workflows; cryopreservation is an adjunct pathway designed for future testing optionality and trial enablement.

Why Cryopreserve?

1. Protect future testing options when the therapeutic plan changes.

Cancer treatment is increasingly iterative—progression, resistance, and guideline updates often prompt additional testing. Cryopreservation helps retain the highest-value tissue state for future assays, including those that are hard to run (or less reliable) on FFPE due to fixation-related changes and variable preanalytics. (PMC)

2. Enable RNA-forward and multi-omics pathways with stronger sample integrity.

FFPE RNA quality can be highly variable; fragmentation and chemical modifications are common and can limit some transcriptomic workflows. Fresh-frozen/viable preservation can reduce these constraints and support modern “omics” strategies as they become clinically available. (PMC)

3. Preserve tumor heterogeneity for advanced research and single-cell analysis.

Single-cell and multi-omics approaches depend on preserving biologic complexity. Multiple studies show that viable cryopreservation can retain cellular diversity and produce high-quality single-cell data suitable for deep profiling—supporting biomarker discovery and trial matching. (PMC)

4. Standardize preanalytic variables—reduce “silent failure” risk.

Clinicians know the downstream reality: cold ischemia time, fixation duration, and processing variability can materially affect molecular readouts. A cryopreservation pathway can be implemented alongside standard FFPE, with controlled handling steps designed to protect downstream analytic performance. (ASCO Publications)

5. Improve clinical trial readiness.

Trials increasingly specify biomarker requirements (and sometimes fresh/viable tissue preferences). Preserving viable tissue can reduce re-biopsy pressure and accelerate eligibility workflows when trial opportunities emerge. (Trial requirements vary by protocol; SpeciCare supports protocol-based collection planning.) (PMC)

Optional “clinician callout box”:

Cryopreservation is additive, not disruptive. Most cases maintain standard diagnostic FFPE workflows; cryopreservation is an adjunct pathway designed for future testing optionality and trial enablement.

The process SpeciCare makes it easy

Below is a standard clinical workflow pattern designed to align with common pathology and procedural environments. (Your team can adjust details to match your exact kit + logistics.)

Step 1 — Identify candidate cases

Common triggers:

  • high likelihood of systemic therapy, targeted therapy, or immunotherapy consideration
  • advanced/metastatic disease, suspected aggressive biology, or anticipated resistance monitoring
  • patients likely to seek clinical trials or tertiary opinions
  • limited tissue scenarios (where preserving optionality matters most)

Step 2 — Order the kit + specimen plan

SpeciCare provides a kit and a collection plan that clarifies:

  • specimen type and minimum recommended volume (biopsy cores, surgical tissue, fluids when applicable)
  • labeling + chain-of-custody requirements
  • transport conditions and timing windows

 

Step 3 — Coordinate with pathology (preanalytic stewardship)

Preanalytics remain critical. Professional guidance emphasizes minimizing cold ischemia and controlling processing variables for biomarker fidelity. SpeciCare’s workflow is built to reduce variability while coexisting with standard fixation requirements. (College of American Pathologists)

Step 4 — Collect and transfer to the cryopreservation pathway

Specimen is placed into the SpeciCare-prescribed containment/medium and prepared for cold-chain transport per kit instructions.

 

 

 

 

 

 

Step 5 — Ship under validated conditions

Courier pickup and tracking. (If you have a preferred courier or institutional shipping SOP, SpeciCare can align to it.)

Step 6 — Receive, triage, and quality control

Specimen is accessioned, documented, and evaluated for:
  • tissue adequacy for downstream testing pathways
  • viability/handling quality checks where applicable
  • storage readiness, including controlled processes consistent with biobanking best practices (PMC)

Step 7 — Store and enable future testing

Tissue is stored for future use in:

  • ex-vivo testing workflows (tumor response testing / organoid-style platforms, when feasible)
  • genomic or transcriptomic profiling
  • immuno-oncology biomarker pathways
  • trial protocol-specific testing and research partnerships

How to order Requesting cryopreservation (clinician workflow)

Option A — “Standard” ordering (fastest)

  1. Submit the SpeciCare order form (clinic or pathology)
  2. Receive kit + collection guide
  3. SpeciCare coordinates pickup and confirms receipt
  4. You receive confirmation + specimen status

Option B — “Protocol-first” ordering (clinical trials / research)

  1. Provide trial/protocol requirements (biomarkers, tissue type, timing)
  2. SpeciCare maps collection + shipping to protocol language
  3. Tissue is handled to support both standard care and protocol needs, as allowed

Option C — “Pathology liaison” ordering (hands-off)

  1. Introduce SpeciCare to your lab manager/pathology contact
  2. SpeciCare trains the team, confirms supplies, and provides quick-reference SOPs

 

 

Need help right now? Call SpeciCare. We can coordinate directly with pathology, surgery centers, and hospital receiving.