
It cannot be emphasized
enough that strict adherence to proper specimen collection and handling
technique is crucial to being able to test a wide range of chemotherapy
drugs and to produce a test result that is accurate and useful.
Proper technique is easy but absolutely essential. It is
heartbreaking when we receive a specimen that cannot be tested due to
improper collection or handling methods.
We always try our very best to salvage such specimens, frequently
laboring for an entire day over a single specimen, but results generally are
disappointing for us and for the physician and patient.
Viable (living), non-contaminated tumor
cells are required. Do
not place specimens in formalin
or other fixative. Please phone
Weisenthal Cancer Group at 714-596-2100 at least two days in advance of
surgery or other biopsy procedure (and preferably sooner) so that we can
provide specimen transport medium, shipping containers, and overnight
shipping labels.
Specimens should be kept cool but not frozen and should be shipped with a
frozen cold pack (-20C but not -70C) on the same day they are collected.
Please read carefully the specific information which is provided below.
Also, please note that while we provide emergency and makeshift
techniques, the use of Weisenthal Cancer Group transport media and materials
is mandatory except in the most extreme circumstances.
.
Optimal Specimen Sources
Suboptimal Specimen Sources
Makeshift Methods
· Substitute materials and techniques – emergency use only
|
Suitable For: |
Quantity |
Special Comment: |
|
Solid Tumor Types |
1 – 2 gm |
Use solid tumor transport
medium. |
|
Hodgkin’s Disease |
1 - 2 gm |
Use hematologic transport
medium. Abundant
Reed-Sternberg cells must be present in specimen. |
|
Non-Hodgkin’s Lymphoma |
1 – 2 gm |
In particular, cytologically positive lymph nodes
produce excellent results however other solid tissues are also
acceptable. Use
hematologic transport medium.
|
Obtain dense, viable tissue.
·
Do not use an electrocautery knife.
·
Do not place the specimen in formalin or other fixative.
·
Avoid contamination.
·
Avoid drying of the specimen.
·
Immediately place the specimen in
fresh transport medium.
·
Seal inner and outer transport vials
securely.
·
Keep the specimen cool.
·
Use a frozen cold pack.
·
Do not freeze the specimen.
·
Do not place the ice pack in a minus 70 freezer - minus 20C is
optimal.
·
Do not use dry ice.
·
Transport the specimen the same day it is collected.
|
Suitable For: |
Quantity |
Special Comment: |
|
Solid Tumor Types |
100 – 1000 ml |
Add heparin to collection
container prior to obtaining fluid. |
|
Hodgkin’s Disease |
100 – 1000 ml |
Add heparin to collection
container prior to obtaining fluid.
Abundant Reed-Sternberg cells must be present in
specimen. |
|
Non-Hodgkin’s Lymphoma |
100 – 1000 ml |
Add heparin to collection container prior to obtaining
fluid. Fluid must
be strongly cytologically positive.
|
Add heparin to the fluid collection container prior to obtaining the fluid. · Use 10 units of heparin per each ml of the collection container’s total capacity. · Do not use containers that could leak or break. · Call Weisenthal Cancer Group in advance for malignant effusion shipping containers and materials. · Do not send fluid from bedside drainage racks. · Keep the specimen cold. · Do not freeze the specimen. · Do not use dry ice for shipping. · Transport the specimen the same day it is collected.
|
Suitable For: |
Quantity |
Special Comment: |
|
- ALL
- ANLL
- CLL
- CML Blast Crisis
- Non-Hodgkin’s Lymphoma
(leukemic phase only)
- Plasma Cell Leukemia
- Hairy Cell Leukemia
|
3 – 7 ml |
Collect the blood in a purple
top tube. Remove the top gently expel into Weisenthal Cancer
Group Hematologic transport medium. |
|
WBC |
Specimen Quantity Required Based
Upon WBC |
|
|
> 10,000 WBC |
10 ml |
|
|
5,000 to 10,000 WBC |
20 ml |
|
|
< 5,000 WBC |
30 ml |
|
Collect the specimen in a purple-top tube. · Remove the top of the tube and pour the blood into Hematologic transport medium. · Seal the inner and outer transport vials securely . · Mix by gentle inversion · Keep the specimen cool. · Use a frozen cold pack. (-20C). · Do not freeze the specimen. · Do not use dry ice for shipping. · Transport specimen the same day it is collected.
|
Suitable For: |
Quantity |
Special Comment: |
|
Non-Hodgkin’s Lymphoma |
0.5 – 1 ml |
Add EDTA to the syringe.
Use Hematologic transport medium. |
|
ALL / ANLL |
0.5 – 1 ml |
Add EDTA to the syringe.
Use Hematologic transport medium. |
|
Multiple Myeloma |
0.5 – 1 ml |
Add EDTA to the syringe.
Use Hematologic transport medium. |
Add EDTA to the syringe prior to obtaining the specimen. · Obtain a “first pull” to assure sufficient blast cells for testing · Gently expel the specimen into fresh Hematologic transport media · Seal inner and outer transport vials securely . · Mix by gentle inversion · Keep the specimen cool. · Use frozen cold pack (-20C). · Do not freeze the specimen. · Do not use dry ice for shipping. · Transport the specimen the same day it is collected.
|
Suitable For: |
Quantity |
Special Comment: |
|
Solid Tumors |
0.5 – 1 gm |
Use Weisenthal Cancer Group
Solid Tumor transport medium.
|
Ten or more passes will be required. · Rinse specimen off the needle between passes into a sterile vessel containing Ringers’ solution (use non-D5 Ringers’). · Pour the rinse liquid, which also contains the specimen, into Weisenthal Cancer Group solid Tumor transport media. · Seal the inner and outer transport vials securely. · Keep the specimen cool. · Use a frozen cold pack (-20C). · Do not freeze the specimen. · Do not use dry ice for shipping. · Transport the specimen the same day it is collected.
|
Suitable For: |
Quantity |
Special Comment: |
|
Fine Needle Aspirate
Fiberoptic Bronchoscopy
Percutaneous Needle Bx
Pre-cultured Cells
|
Do Not Send These Specimens |
Specimens from these sources produce highly substandard assays –
non-evaluable assays, few
drugs, poor technical quality, etc.
|
If one of the above items is the only possible specimen source, please call us first and we will discuss possible alternatives or suggest ways to improve the chances for an assay that is at least partially successful.
Makeshift Methods
– For Emergency Use Only
We emphasize that, in all cases, you should phone us a minimum of two days prior to the biopsy procedure so that we can send proper specimen collection and transport medium and other materials. Our transport medium contains multiple ingredients required to sustain cell viability. In an emergency, other methods and materials could possibly be substituted. However, such methods are not optimal and often produce disappointing results.
If you do not have our materials, please phone us at (714) 596-2100 prior to the surgery or biopsy and we will suggest alternative methods which are appropriate to the specimen and the situation.
Do NOT place the specimen in Formalin. Do NOT place the specimen in normal saline, Do NOT place the specimen in RPMI. Do NOT place the specimen in cell culture or transport media from a different laboratory. If absolutely necessary, hold the specimen UNDER REFRIGERATION in a sterile, closed container in Ringer's solution - cold Ringer's is best if available. Use NON-D5 Ringer's. Do NOT freeze the specimen. Please phone us immediately at (714) 596-2100 for further instructions.
