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Management of Non
Seminomatous Germ Cell
Tumors of Testis
Dr. Akhil Kapoor
Acharya Tulsi Regional Cancer
Treatment & Research Center, Bikaner
Post Orchiectomy Tests
• Post Orchiectomy Serum Marker Status:
Decides Staging
• Usually performed after 3 weeks of Surgery
• Discuss Sperm Banking in young patients,
preferably before surgery.
• CE CT Abdomen & Pelvis
• A Chest CT is indicated if :
 the abdominopelvic CT shows retroperitoneal
adenopathy or,
 the CXR shows abnormal results.
• Brain MRI and Bone Scan. If clinically indicated.
• No role of PET-CT
Treatment options
Stage dependent treatment options after inguinal
orchiectomy include
• Surveillance,
• Chemotherapy, and
• RPLND.
• Although the timing of the RPLND may vary, most
patients will undergo an RPLND at some point during
treatment.
• Major morbidity with bilateral dissection : Retrograde
ejaculation, resulting in infertility.
• Nerve dissection techniques preserve antegrade
ejaculation in 90% of cases.
Bilateral RPLND
Involves removal of lymphatic tissue extending from:
• Lateral: between both ureters,
• Superior: diaphragmatic crus
• Inferior: bifurcation of the common iliac arteries.
Stage IA, IB (T2 only)
(1) Surveillance,
(2) Nerve-sparing RPLND.
• Cure rate with either approach exceeds 95%.
• With surveillance, up to 30% patients will develop
relapse which must be identified early.
• RPLND is recommended within 4 weeks of a CT
scan and within 7 to 10 days of repeat serum
marker testing to ensure accurate presurgical
staging.
Stage IB (T2 only)
• Vascular invasion is a significant predictor of
relapse when orchiectomy is followed by
surveillance alone.
• Surveillance generally not recommended for T2
disease with vascular invasion due to 50% chance
of relapse.
Post RPLND
• pN0: Surveillance
• pN1: Surveillance (preferred) vs. BEP- 2Cycles
• pN2: BEP- 2Cycles
• pN3: BEP- 3Cycles
F/U during Surveillance
Stage IB
1. Nerve-sparing RPLND, or
2. Primary chemotherapy: BEP for 2 cycles
After primary Chemo,
• Residual mass of 1 cm or greater : Nerve-sparing
RPLND
• Residual mass <1cm: Surveillance vs. RPLND
F/U for Stage IB
Stage IS
Elevated levels of AFP and beta-HCG after
orchiectomy :
• Disseminated nonseminoma
• hepatobiliary disease,
• marijuana use, and
• Hypogonadism.
• After excluding other causes, 3 cycles of BEP
Stage IIA with Normal Markers
1. Nerve-sparing RPLND (Preferred), or
2. BEP 3 Cycles.
• For patients with persistently elevated AFP or HCG
levels, induction chemotherapy.
Post Treatment in Stage IIA
After primary Chemo,
• Residual mass of 1 cm or greater : Nerve-sparing
RPLND
• Residual mass <1cm: Surveillance vs. RPLND
After primary RPLND,
• pN0: Surveillance
• pN1: Surveillance (preferred) vs. BEP- 2Cycles
• pN2: BEP- 2Cycles
• pN3: BEP- 3Cycles
IGCCCG Risk Grouping
For Good Risk Stage IIA-S1, IIB, IIC, IIIA
BEP for 3 cycles
• If CR: Surveillance vs. RPLND
• If Partial response (residual mass with normal
AFP & hCG levels) :
• If Incomplete Response, 2nd line CT
For Intermediate & Poor Risk IIIB & IIIC
BEP 4 Cycles
• If CR: Surveillance vs. RPLND
• If Partial response (residual mass with normal
AFP & hCG levels) :
• If Incomplete Response, 2nd line CT
F/U in Stage II, III Non Seminoma
Comparison of F/U Schedules
Second Line Therapy for Metastatic
Germ Cell Tumors
• Prognostic factors to decide whether patient is a
candidate for conventional dose therapy or high-
dose therapy with stem cell support as a second-
line option.
Favorable prognostic factors to conventional dose
second-line chemotherapy include:
• testicular primary site,
• prior complete response to first-line therapy,
• low levels of post- orchiectomy serum tumor
markers, and
• low-volume disease
Conventional Dose CT
High Dose CT
Resistance to High Dose CT
• For patients who do not experience CR to second-
line high-dose therapy, the disease is nearly always
incurable;
• Only exception is the rare patient with elevated
serum tumor markers and a solitary site of
metastasis (usually retroperitoneal) that undergoes
surgical resection.
• Other options are participation in a clinical trial or
best supportive care.
Palliative Chemotherapy
• Gemcitabine with paclitaxel
• Gemcitabine with oxaliplatin
• Gemcitabine with paclitaxel and oxaliplatin
• Oral Etoposide (50mg/sqm)
Summary
Stage IA, IB (T2 only)
(1) Surveillance,
(2) Nerve-sparing RPLND.
Stage IB
1. Nerve-sparing RPLND, or
2. Primary chemotherapy: BEP for 2 cycles
Stage IS
3 cycles of BEP
Stage IIA with Normal Markers
1. Nerve-sparing RPLND (Preferred), or
2. BEP 3 Cycles.
For Good Risk Stage IIA-S1, IIB, IIC, IIIA
BEP 3 Cycles
For Intermediate & Poor Risk IIIB & IIIC
BEP 4 Cycles
After primary Chemo,
• Residual mass of 1 cm or greater : Nerve-sparing
RPLND
• Residual mass <1cm: Surveillance vs. RPLND
After primary RPLND,
• pN0: Surveillance
• pN1: Surveillance (preferred) vs. BEP- 2Cycles
• pN2: BEP- 2Cycles
• pN3: BEP- 3Cycles
THANK
S

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Management of Non Seminomatous Germ cell tumors of Testis (by Dr. Akhil Kapoor)

  • 1. Management of Non Seminomatous Germ Cell Tumors of Testis Dr. Akhil Kapoor Acharya Tulsi Regional Cancer Treatment & Research Center, Bikaner
  • 2. Post Orchiectomy Tests • Post Orchiectomy Serum Marker Status: Decides Staging • Usually performed after 3 weeks of Surgery • Discuss Sperm Banking in young patients, preferably before surgery.
  • 3. • CE CT Abdomen & Pelvis • A Chest CT is indicated if :  the abdominopelvic CT shows retroperitoneal adenopathy or,  the CXR shows abnormal results. • Brain MRI and Bone Scan. If clinically indicated. • No role of PET-CT
  • 4. Treatment options Stage dependent treatment options after inguinal orchiectomy include • Surveillance, • Chemotherapy, and • RPLND. • Although the timing of the RPLND may vary, most patients will undergo an RPLND at some point during treatment. • Major morbidity with bilateral dissection : Retrograde ejaculation, resulting in infertility. • Nerve dissection techniques preserve antegrade ejaculation in 90% of cases.
  • 5. Bilateral RPLND Involves removal of lymphatic tissue extending from: • Lateral: between both ureters, • Superior: diaphragmatic crus • Inferior: bifurcation of the common iliac arteries.
  • 6. Stage IA, IB (T2 only) (1) Surveillance, (2) Nerve-sparing RPLND. • Cure rate with either approach exceeds 95%. • With surveillance, up to 30% patients will develop relapse which must be identified early. • RPLND is recommended within 4 weeks of a CT scan and within 7 to 10 days of repeat serum marker testing to ensure accurate presurgical staging.
  • 7. Stage IB (T2 only) • Vascular invasion is a significant predictor of relapse when orchiectomy is followed by surveillance alone. • Surveillance generally not recommended for T2 disease with vascular invasion due to 50% chance of relapse.
  • 8. Post RPLND • pN0: Surveillance • pN1: Surveillance (preferred) vs. BEP- 2Cycles • pN2: BEP- 2Cycles • pN3: BEP- 3Cycles
  • 10. Stage IB 1. Nerve-sparing RPLND, or 2. Primary chemotherapy: BEP for 2 cycles After primary Chemo, • Residual mass of 1 cm or greater : Nerve-sparing RPLND • Residual mass <1cm: Surveillance vs. RPLND
  • 12. Stage IS Elevated levels of AFP and beta-HCG after orchiectomy : • Disseminated nonseminoma • hepatobiliary disease, • marijuana use, and • Hypogonadism. • After excluding other causes, 3 cycles of BEP
  • 13. Stage IIA with Normal Markers 1. Nerve-sparing RPLND (Preferred), or 2. BEP 3 Cycles. • For patients with persistently elevated AFP or HCG levels, induction chemotherapy.
  • 14. Post Treatment in Stage IIA After primary Chemo, • Residual mass of 1 cm or greater : Nerve-sparing RPLND • Residual mass <1cm: Surveillance vs. RPLND After primary RPLND, • pN0: Surveillance • pN1: Surveillance (preferred) vs. BEP- 2Cycles • pN2: BEP- 2Cycles • pN3: BEP- 3Cycles
  • 16. For Good Risk Stage IIA-S1, IIB, IIC, IIIA BEP for 3 cycles • If CR: Surveillance vs. RPLND • If Partial response (residual mass with normal AFP & hCG levels) : • If Incomplete Response, 2nd line CT
  • 17. For Intermediate & Poor Risk IIIB & IIIC BEP 4 Cycles • If CR: Surveillance vs. RPLND • If Partial response (residual mass with normal AFP & hCG levels) : • If Incomplete Response, 2nd line CT
  • 18. F/U in Stage II, III Non Seminoma
  • 19. Comparison of F/U Schedules
  • 20. Second Line Therapy for Metastatic Germ Cell Tumors • Prognostic factors to decide whether patient is a candidate for conventional dose therapy or high- dose therapy with stem cell support as a second- line option. Favorable prognostic factors to conventional dose second-line chemotherapy include: • testicular primary site, • prior complete response to first-line therapy, • low levels of post- orchiectomy serum tumor markers, and • low-volume disease
  • 23. Resistance to High Dose CT • For patients who do not experience CR to second- line high-dose therapy, the disease is nearly always incurable; • Only exception is the rare patient with elevated serum tumor markers and a solitary site of metastasis (usually retroperitoneal) that undergoes surgical resection. • Other options are participation in a clinical trial or best supportive care.
  • 24. Palliative Chemotherapy • Gemcitabine with paclitaxel • Gemcitabine with oxaliplatin • Gemcitabine with paclitaxel and oxaliplatin • Oral Etoposide (50mg/sqm)
  • 25. Summary Stage IA, IB (T2 only) (1) Surveillance, (2) Nerve-sparing RPLND. Stage IB 1. Nerve-sparing RPLND, or 2. Primary chemotherapy: BEP for 2 cycles Stage IS 3 cycles of BEP
  • 26. Stage IIA with Normal Markers 1. Nerve-sparing RPLND (Preferred), or 2. BEP 3 Cycles. For Good Risk Stage IIA-S1, IIB, IIC, IIIA BEP 3 Cycles For Intermediate & Poor Risk IIIB & IIIC BEP 4 Cycles
  • 27. After primary Chemo, • Residual mass of 1 cm or greater : Nerve-sparing RPLND • Residual mass <1cm: Surveillance vs. RPLND After primary RPLND, • pN0: Surveillance • pN1: Surveillance (preferred) vs. BEP- 2Cycles • pN2: BEP- 2Cycles • pN3: BEP- 3Cycles