Testis Cancer Flashcards
(46 cards)
What is typical finding on scrotal ultrasound of a patient with testicular cancer.
Hypoechoic mass w/ vascular flow (occasionally without)
What are risk factors for testicular cancer? Important in men with testicular microlithiasis.
Hx of UDT, familial hx of testicular cancer, personal hx of testicular cancer, prior dx of GCNIS
What happens if indeterminate lesion (< 1 cm, non palpable), and normal tumor markers?
Repeat U/S in 6-8 weeks.
Counsel patient, can offer continued surveillance, orchiectomy, TSS with intra op frozen.
Only antibiotics if signs of infection.
Where is the spermatic cord supposed to be ligated on a radical orchiectomy?
At the internal inguinal ring.
What to be discussed with patient prior to orchiectomy?
sperm cryopreservation, hypogonadism, and TESTICULAR PROSTHESIS
What to counsel patient on scrotal violation?
Higher chance of LOCALIZED recurrence (2.5%) - rarely do adjuvant tx such as excision of scar or radiation tx.
What are indications for a partial orchiectomy?
Small lesion < 2cm.
Non palpable. Normal STM. These may be 50% benign.
Contraindication to radical, such as solitary testis, or bilateral lesions.
Need to discuss with patient what to do if GCT is found.
If GCNIS - must sample area outside lesion. Then discuss with patient closer surveillance.
Higher chance for local recurrence ~20%.
Need to discuss testicular atrophy, sub fertility and hypogonadism
Is a person with testicular cancer have a higher chance of CA in contralateral testes? What are some risk factors?
YES
Risk factors - younger age of diagnosis, testicular atrophy, UDT
What is management for patient with GCNIS
SDM
50% chance of developing GCT
Surveillance - if wishes fertility or testosterone production is important
Orchiectomy
Radiation - but will cause hypogonadism and subfertility, and still small risk of developing GCT
Give me the TNM-S staging for testicular CA
Tis - GCNIS
T1 - within testis, no LVI, w/in TA
T2 - outsides testis (TUNICA VAGINALIS), LVI,
T3 - spermatic cord involvment
T4 - scrotal wall involvement
N0 - no nodes
N1 - < 2 cm
N2 - 2-5 cm
N3 - > 5cm
M0 - no mets
M1a - pulm mets, non-RP LN
M2a - visceral mets
S0 - normal
S1 - one is above normal
S2 - one is “intermediate” above normal
S3 - one is “poor” above normal
Give me staging for testicular CA
stage IA - testis, no LVI
stage IB - testis, w/ LVI
Stage IIA - LN, < 2cm
Stage IIB - LN, 2-5cm
stage IIB - LN > 5cm
Stage IIIA - pulm
Stage IIIB - pulm but elevated STM
Stage IIIC - PULM OR non pulm or S3 elevated STM
When is good, intermediate, and poor risk used?
For chemotherapy purposes.
Good - BEP x 3, EP x 4
Intermediate or Poor - BEP x 4
Break down risk for sem vs non sem
Sem:
Good risk - pulm mets, normal AFP, other STM can be anything
Int risk - non-pulm visceral mets, normal AFP, other STM can be anything
Non-sem
Good risk - no non-pulm mets, AFP < 1000, BHCG < 5000, LDH < 1.5x
Int risk - no non-pulm mets, AFP 1-10k, BHCG 5k - 50000, LHD 1.5x - 10x
Poor - non-pulm mets, AFP > 10k, BHCG > 50K, LDH > 10x
Can you make decision based off a borderline AFP or HCG (w/in 3x of normal)?
No - must continue to trend
What is metastatic workup?
CT A/P W/ IV contrast (or MRI), with some chest imaging
When should treatment decisions be made?
Within 10 days of HCG or AFP levels, as well as 4 weeks of imaging.
Who are usual consultants for testicular CA?
med onc, rad onc, pathology, radiology
What happens if you have equivocal imaging (not CLEAR) and STM are normal?
repeat imaging in 6-8 weeks. BE SURE.
What is treatment option for sem - stage IIA or stage IIB LN </= 3 cm?
SDM - XRT (dog leg field) or BEP x 3 / EP x 4
If toxicity of XRT and chemo are concern – then can offer RPLND
What are long term effects of chemo and radiation?
cardiotoxicity, GI toxicity, hematologic toxicity, secondary malignancy
infertility, peripheral neuropathy, high-pitch hearing loss, cardiovascular disease, and secondary malignancies
What is treatment for sem - stage IIB LN > 3
Chemo - BEP x 3 / EP x 4
What is treatment for non sem with any elevated STM?
Chemo - according to risk status
What is treatment for non sem - stage IA?
Preferred - surveillance (relapse rate - ~20%)
Option - RPLND vs BEP x 1
Risk factors for relapse is embryonal or LVI
What is treatment for non sem - stage IB?
Surveillance vs RPLND vs BEP 1-2x (relapse rate is ~50%)