
It cannot be emphasized enough that strict
adherence to proper specimen collection and handling technique is critical
to being able to test a wide range of chemotherapy drugs and to produce a
test result which 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.
Optimal Specimen Sources
Suboptimal Specimen Sources
Makeshift Methods
·
Substitute materials and
techniques – For 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 specimen in formalin or other fixative.
·
Avoid contamination.
·
Avoid drying of the specimen.
·
Immediately place the specimen in
fresh Weisenthal Cancer Group transport medium.
·
Seal inner and outer transport vials
securely.
· Keep specimen cool.
·
Use a frozen cold pack.
·
Do not freeze the specimen.
·
Do not place ice pack in minus 70 freezer (minus 40 is acceptable).
·
Do not use dry ice.
·
Transport 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 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 cool. · Use a frozen cold pack. · 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: |
|
- ALL - ANLL - CLL - CML Blast Crisis - Non-Hodgkin’s Lymphoma
(leukemic phase only) - Plasma Cell Leukemia - Hairy Cell Leukemia |
3 – 7 ml |
Add
preservative-free heparin to a syringe or collect the specimen
in a purple top tube. Remove needle and gently expel into
Weisenthal Cancer Group Hematologic transport medium. |
|
WBC |
Additional Quantity Required Based Upon
WBC |
|
|
> 10,000 WBC |
10ml |
|
|
5,000 to 10,000 WBC |
20ml |
|
|
< 5,000 WBC |
30ml |
|
Add
preservative-free heparin to a syringe or collect the specimen in a
purple-top tube.
·
Remove the needle after collection to avoid shearing the cells.
·
Gently expel the specimen into fresh Hematologic transport media
·
If a tube is used for collection, remove the top and pour the blood
into Hematologic transport medium.
· Seal inner and outer
transport vials securely .
·
Mix by gentle inversion
·
Keep the specimen cool.
·
Use frozen cold pack.
·
Do not freeze 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 preservative-free
heparin 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
preservative-free heparin 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.
·
Do not freeze 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 the specimen off of the needle between passes into a clean
vessel containing Ringers’s solution (use non-D5 Ringer’s).
· 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.
·
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 generally do not produce quality results – few drugs,
poor technical quality, etc.
|
If one of the above is the only possible
specimen source, please call us first and we will discuss whether or not it
is worth attempting, explore possible alternatives, or suggest ways to
improve the chances for an assay that is at least partially successful.
Alternative 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 before 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 avaliable. Use NON-D5 Ringer's.
Do NOT freeze the specimen. Please phone us at (714) 596-2100 for
further instructions.
