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NCCN Clinical Practice Guidelines in Oncology™
Testicular
Cancer
V.1.2010
www.nccn.org
Version 1.2010, 08/28/09 © 2009 National Comprehensive Cancer Network, Inc. All rights reserved. These guidelines and this illustration may not be reproduced in any form without the express written permission of NCCN.
Guidelines Index
Testicular Cancer TOC
Staging, Discussion, References
Practice Guidelines
in Oncology – v.1.2010NCCN
®
NCCN Testicular Cancer Panel Members
Continue
Testicular Cancer
*
† Medical oncology
‡ Hematology/hematology oncology
§ Radiotherapy/Radiation oncology
Diagnostic Radiology
£ Supportive Care including Palliative, Pain
Management, Pastoral care and Oncology social work
Þ Internal medicine
Urology
* Writing committee member
ф
�
NCCN Guidelines Panel Disclosures
Robert J. Motzer, MD/Chair
Memorial Sloan-Kettering Cancer Center
Neeraj Agarwal, MD
Huntsman Cancer Institute at the
University of Utah
Clair Beard, MD
St. Jude Children’s Research
Hospital/University of Tennessee Cancer
Institute
Michael A. Carducci, MD
The Sidney Kimmel Comprehensive
Cancer Center at Johns Hopkins
Sam S. Chang, MD
Vanderbilt-Ingram Cancer Center
Toni K. Choueiri, MD
† Þ
‡
§
†
† £
† Þ
† Þ
Dana-Farber/Brigham and Women’s
Cancer Center
Sam Bhayani, MD
Siteman Cancer Center at Barnes-Jewish
Hospital and Washington University
School of Medicine
Graeme B. Bolger, MD
University of Alabama at Birmingham
Comprehensive Cancer Center
Barry Boston, MD
Dana-Farber/Brigham and Women’s
Cancer Center
�
�
Thomas Olencki, DO
The Ohio State University Comprehensive
Cancer Center - James Cancer Hospital and
Solove Research Institute
Roberto Pili, MD
Roswell Park Cancer Institute
UCSF Helen Diller Family Comprehensive
Cancer Center
Memorial Sloan-Kettering Cancer Center
UNMC Eppley Cancer Center at
The Nebraska Medical Center
‡
†
†
†
†
Bruce G. Redman, DO
University of Michigan Comprehensive Cancer
Center
Cary N. Robertson, MD
Duke Comprehensive Cancer Center
Charles J. Ryan, MD
Lawrence H. Schwartz, MD
Joel Sheinfeld, MD
Memorial Sloan-Kettering Cancer Center
Jue Wang, MD
�
�
�
ф
Robert A. Figlin, MD
City of Hope Comprehensive Cancer Center
Mayer Fishman, MD, PhD
H. Lee Moffitt Cancer Center & Research
Institute
Steven L. Hancock, MD
Stanford Comprehensive Cancer Center
Gary R. Hudes, MD
Fox Chase Cancer Center
Eric Jonasch, MD
The University of Texas M. D. Anderson Cancer
Center
Timothy M. Kuzel, MD
Robert H. Lurie Comprehensive Cancer Center
of Northwestern University
Paul H. Lange, MD
Fred Hutchinson Cancer Research
Center/Seattle Cancer Care Alliance
Ellis G. Levine, MD
Roswell Park Cancer Institute
Kim A. Margolin, MD
Fred Hutchinson Cancer Research
Center/Seattle Cancer Care Alliance
M. Dror Michaelson, MD, PhD
Massachusetts General Hospital Cancer Center
†
† ‡ Þ
§ Þ
† ‡
‡
†
† ‡
†
�
Version 1.2010, 08/28/09 © 2009 National Comprehensive Cancer Network, Inc. All rights reserved. These guidelines and this illustration may not be reproduced in any form without the express written permission of NCCN.
Guidelines Index
Testicular Cancer TOC
Staging, Discussion, References
Practice Guidelines
in Oncology – v.1.2010NCCN
®
This manuscript is being
updated to correspond
with the newly updated
algorithm.
These guidelines are a statement of evidence and consensus of the authors regarding their views of currently accepted approaches to treatment.
Any clinician seeking to apply or consult these guidelines is expected to use independent medical judgment in the context of individual clinical
circumstances to determine any patient’s care or treatment. The National Comprehensive Cancer Network makes no representations or warranties
of any kind, regarding their content use or application and disclaims any responsibility for their application or use in any way. These guidelines are
copyrighted by National Comprehensive Cancer Network. All rights reserved. These guidelines and the illustrations herein may not be reproduced
in any form without the express written permission of NCCN. ©2009.
Table of Contents
NCCN Testicular Cancer Panel Members
Workup, Primary Treatment and Pathologic Diagnosis (TEST-1
Seminoma: Postdiagnostic Workup and Clinical Stage (TEST-2
Stage IA, IB (TEST-3
Stage IIA, IIB (TEST-3
Stage IIC, III (TEST-3
Nonseminoma: Postdiagnostic Work-up and Clinical Stage (TEST-5
Stage IA, IB, IS (TEST-6
Stage IIA, IIB (TEST-7
Postchemotherapy Management (TEST-8
Postsurgical Management (TEST-9
Stage IIC, IIIA, IIIB, IIIC, and Brain Metastases (TEST-10
Follow-up for Nonseminoma (TEST-11
)
)
)
)
)
)
)
)
)
)
)
)
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Stage IS (TEST-3
Recurrence and Second Line Therapy (TEST-12
Risk Classification (TEST-A
Primary Chemotherapy Regimens for Germ Cell Tumors (TEST-B
Second Line or Subsequent Chemotherapy Regimens for Metastatic Germ
Cell Tumors (TEST-C
)
)
)
)
)
Summary of Guidelines Updates
For help using these
documents, please click here
Staging
Discussion
References
Clinical Trials:
Categories of Evidence and
Consensus:
NCCN
The
believes that the best management
for any cancer patient is in a clinical
trial. Participation in clinical trials is
especially encouraged.
To find clinical trials online at NCCN
member institutions,
All recommendations
are Category 2A unless otherwise
specified.
See
NCCN
click here:
nccn.org/clinical_trials/physician.html
NCCN Categories of Evidence
and Consensus
Testicular Cancer
Guidelines Index
Print the Testicular Cancer Guidelines
Version 1.2010, 08/28/09 © 2009 National Comprehensive Cancer Network, Inc. All rights reserved. These guidelines and this illustration may not be reproduced in any form without the express written permission of NCCN.
Guidelines Index
Testicular Cancer TOC
Staging, Discussion, References
Practice Guidelines
in Oncology – v.1.2010NCCN
®
Note: All recommendations are category 2A unless otherwise indicated.
Clinical Trials: NCCN believes that the best management of any cancer patient is in a clinical trial. Participation in clinical trials is especially encouraged.
UPDATES
Summary of the Guidelines updates
Summary of changes in the 1.2010 version of the Testicular Cancer Guidelines from the 2.2009 version include:
Seminoma
�
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Residual mass, positive PET scan, “salvage therapy’ was clarified as “second line chemotherapy”.
Follow-up abdominal/pelvic CT interval was clarified as “4 mo post surgery, then as indicated”.
Surveillance after complete response to chemotherapy and/or RPLND and months between abdominal/pelvic CT:
For 6 + years, the interval between CT scans was changed from “12- 24 mo” to “as clinically indicated”.
Previous footnote was modified as, “CT scans apply only to patients treated with chemotherapy . For patients
who are post RPLND, a postoperative baseline CT scan is recommended
” and moved under surveillance for clarification.
Second line therapy for favorable prognosis, “high-dose chemotherapy” was added as a treatment option.
Second line therapy, incomplete response or relapse, “high-dose chemotherapy” was modified by adding “if not
previously given” to preferred.
:
High-dose chemotherapy regimens were added to the page.
�
� alone
and additional CT scans as clinically
indicated
Nonseminoma, “post-orchiectomy” was added to markers for clarification for each risk status
TEST-4
TEST-11
TEST-12
TEST-A
TEST-C
Nonseminoma
Testicular Cancer
Version 1.2010, 08/28/09 © 2009 National Comprehensive Cancer Network, Inc. All rights reserved. These guidelines and this illustration may not be reproduced in any form without the express written permission of NCCN.
Guidelines Index
Testicular Cancer TOC
Staging, Discussion, References
Practice Guidelines
in Oncology – v.1.2010NCCN
®
Note: All recommendations are category 2A unless otherwise indicated.
Clinical Trials: NCCN believes that the best management of any cancer patient is in a clinical trial. Participation in clinical trials is especially encouraged.
WORKUP PRIMARY TREATMENT PATHOLOGIC DIAGNOSIS
a
b
Quantitative analysis of beta subunit.
This includes seminoma histology with elevated AFP.
Suspicious
testicular
mass
Seminoma
(AFP negative; may have
elevated beta-hCG)
Nonseminomatous
germ cell tumorb
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Discuss sperm banking
Radical inguinal orchiectomy
Consider open inguinal biopsy
of contralateral testis if:
Suspicious ultrasound for
intratesticular abnormalities
Cryptorchid testis
Marked atrophy
�
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H&P
Alpha-fetoprotein (AFP)
beta-hCG
Chemistry profile
Chest x-ray
Optional:
Testicular ultrasound
a
LDH
�
See
Postdiagnostic
Workup and
Clinical Stage
(TEST-2)
See
Postdiagnostic
Workup and
Clinical Stage
(TEST-5)
TEST-1
Testicular Cancer
Version 1.2010, 08/28/09 © 2009 National Comprehensive Cancer Network, Inc. All rights reserved. These guidelines and this illustration may not be reproduced in any form without the express written permission of NCCN.
Guidelines Index
Testicular Cancer TOC
Staging, Discussion, References
Practice Guidelines
in Oncology – v.1.2010NCCN
®
Note: All recommendations are category 2A unless otherwise indicated.
Clinical Trials: NCCN believes that the best management of any cancer patient is in a clinical trial. Participation in clinical trials is especially encouraged.
PATHOLOGIC DIAGNOSIS POSTDIAGNOSTIC WORKUP CLINICAL STAGE
Seminoma
(AFP negative ; may
have elevated beta-hCG)
c
d
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Abdominal/pelvic CT
Chest CT if:
Positive abdominal CT
or abnormal chest x-ray
Repeat beta-hCG, LDH,
AFP (if elevated
preoperatively)
Brain MRI, if clinically
indicated
Bone scan, if clinically
indicated
Discuss sperm banking
�
e
Stage
IA, IB
Stage
IIA, IIB
Stage
IIC, III
See Primary Treatment
and Follow-up (TEST-3)
See Primary Treatment
and Follow-up (TEST-3)
See Primary Treatment
and Follow-up (TEST-3)
c
d
e
Mediastinal seminoma should be treated as good risk nonseminomatous germ cell tumor with
etoposide/cisplatin for 4 cycles or bleomycin/etoposide/cisplatin for 3 cycles.
If positive, treat as nonseminoma.
Elevated values should be followed with repeated determination to allow precise staging.
TEST-2
Testicular Cancer
Seminoma
Stage
IS
See Primary Treatment
and Follow-up (TEST-3)
Version 1.2010, 08/28/09 © 2009 National Comprehensive Cancer Network, Inc. All rights reserved. These guidelines and this illustration may not be reproduced in any form without the express written permission of NCCN.
Guidelines Index
Testicular Cancer TOC
Staging, Discussion, References
Practice Guidelines
in Oncology – v.1.2010NCCN
®
Note: All recommendations are category 2A unless otherwise indicated.
Clinical Trials: NCCN believes that the best management of any cancer patient is in a clinical trial. Participation in clinical trials is especially encouraged.
CLINICAL
STAGE
Stage
IA, IB
Stage
IIA, IIB
RT: Infradiaphragmatic (35-40 Gy) to include
para-aortic and ipsilateral iliac nodes
Consider p
EP for 4 cycles for selected stage IIB patients
rimary chemotherapy:g
FOLLOW-UPPRIMARY TREATMENT
Surveillance if:
Horseshoe or pelvic kidney
Inflammatory bowel disease
Prior RT
Consider surveillance if: (category 2B)
T1 or T2 histology in selected patients
committed to long-term follow-up
or
Single agent carboplatin
(AUC=7 x 1 cycle or AUC=7 x 2 cycles)
(category 1)
(category 1)
or
RT: Infradiaphragmatic (20-30 Gy) to
include para-aortic ± ipsilateral iliac
nodes (category 1)
�
�
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H&P + chest x-ray, AFP, beta-hCG, LDH:
every 3-4 mo for year 1,
every 6 mo for year 2, then annually
Pelvic CT annually for 3 years (for
patients status post only para-aortic RT)
�
�
H&P + chest x-ray
for year 4, then annually
Abdominal CT at month 4 of year 1
, AFP, beta-hCG, LDH:
every 3-4 mo for years 1-3,
every 6 mo
�
�
H&P, AFP, beta-hCG, LDH:
every 3-4 mo for years 1-3,
every 6 mo for years 4-7, then annually
Abdominal/pelvic CT at each visit, chest
x-ray at alternative visits (up to 10 y)
TEST-3
Recurrence, treat
according to extent of
disease at relapse
Recurrence, treat
according to extent of
disease at relapse
Recurrence, treat
according to extent of
disease at relapse
See Post Chemotherapy Management
and Follow-up (TEST-4)
fSee Risk Classification (TEST-A
See Primary Chemotherapy Regimens for Germ Cell Tumors (TEST-B
)
)
.
.g
Stage
IIC, III
Primary chemotherapy:
EP for 4 cycles (category 1)
or
BEP for 3 cycles (category 1)
g
Good riskf
Intermediate
riskf
Primary chemotherapy:g
BEP for 4 cycles (category 1)
See Post Chemotherapy Management
and Follow-up (TEST-4)
EP = Etoposide/cisplatin
BEP = Bleomycin/etoposide/cisplatin
Testicular Cancer
Seminoma
Stage
IS
RT: Infradiaphragmatic (25-30 Gy) to
include para-aortic ± ipsilateral iliac nodes
or
Version 1.2010, 08/28/09 © 2009 National Comprehensive Cancer Network, Inc. All rights reserved. These guidelines and this illustration may not be reproduced in any form without the express written permission of NCCN.
Guidelines Index
Testicular Cancer TOC
Staging, Discussion, References
Practice Guidelines
in Oncology – v.1.2010NCCN
®
FOLLOW-UP
�
�
�
H&P + chest x-ray
every 2 mo for
for
for year 4,
then annually
Abdominal/pelvic CT
4 mo post surgery,
then as indicated
PET scan as
clinically indicated
,
AFP, beta-hCG, LDH:
year 1
every 3 mo year 2,
every 4 mo for year 3,
every 6 mo Recurrence,
See Second
line Therapy
(TEST-12)
TEST-4
Note: All recommendations are category 2A unless otherwise indicated.
Clinical Trials: NCCN believes that the best management of any cancer patient is in a clinical trial. Participation in clinical trials is especially encouraged.
Residual mass
(nodes > 3 cm
on CT)
Residual mass
(nodes 3 cm
on CT)
�
Progressive
disease (growing
mass or rising
markers)h
Surveillance
or
Surgery
or
RT
(category 2B)
(category 2B)
See Second line Therapy for
nonseminoma (TEST-12)
�
�
Chest, abdominal,
pelvic CT scan
Serum tumor
markers
No residual
mass and
normal
markersh
Residual
mass and
normal
markersh
Surveillance
Consider surgery
with biopsy
or
Biopsy and
second line
chemotherapy
or
RT (category 2B)
i
PET scan
(preferred)
Positive
Negative Surveillance
PET scan
not feasible
hFor persistent elevated beta-hCG which is not rising, repeat serial markers, testosterone suppression test and consider a PET scan
iSee Second Line or Subsequent Chemotherapy Regimens for Metastatic Germ Cell Tumors (TEST-C).
STAGE IIB, IIC, III AFTER PRIMARY
TREATMENT WITH CHEMOTHERAPY
Surveillance
Testicular Cancer
Seminoma
POST
CHEMOTHERAPY
MANAGEMENT
Version 1.2010, 08/28/09 © 2009 National Comprehensive Cancer Network, Inc. All rights reserved. These guidelines and this illustration may not be reproduced in any form without the express written permission of NCCN.
Guidelines Index
Testicular Cancer TOC
Staging, Discussion, References
Practice Guidelines
in Oncology – v.1.2010NCCN
®
Note: All recommendations are category 2A unless otherwise indicated.
Clinical Trials: NCCN believes that the best management of any cancer patient is in a clinical trial. Participation in clinical trials is especially encouraged.
PATHOLOGIC DIAGNOSIS
Nonseminomatous
germ cell tumorb
POSTDIAGNOSTIC WORKUP
b
j
This includes seminoma histology with elevated AFP.
Treatment may be initiated prior to histology for patients with rising markers and a deteriorating clinical situation.
eElevated values should be followed with repeated determination to allow precise staging.
�
�
�
�
�
�
Abdominal/pelvic CT
Chest CT if:
Abnormal abdominal CT
Abnormal chest x-ray
Repeat beta-hCG, LDH, AFP
Brain MRI, if clinically
indicated
Bone scan, if clinically
indicated
Discuss sperm banking
�
�
e
CLINICAL STAGEj
Stage IA, IB, IS:
See Primary
Treatment (TEST-6)
Stage IIA, IIB:
See
Treatment (TEST-7
Primary
)
Stage IIC, IIIA, IIIB, IIIC,
and brain metastasis:
See Treatment
(TEST-10
Primary
)
TEST-5
Testicular Cancer
Nonseminoma
Version 1.2010, 08/28/09 © 2009 National Comprehensive Cancer Network, Inc. All rights reserved. These guidelines and this illustration may not be reproduced in any form without the express written permission of NCCN.
Guidelines Index
Testicular Cancer TOC
Staging, Discussion, References
Practice Guidelines
in Oncology – v.1.2010NCCN
®
Note: All recommendations are category 2A unless otherwise indicated.
Clinical Trials: NCCN believes that the best management of any cancer patient is in a clinical trial. Participation in clinical trials is especially encouraged.
CLINICAL STAGE
Stage IA
Surveillance
(in compliant patients)
or
Open nerve-sparing RPLNDk
Stage IB
Open nerve-sparing RPLND
or
Primary chemotherapy:
BEP for 2 cycles (category 2B)
or
Surveillance (only if T2,
compliant patients [category 2B])
k
g
The EP and BEP chemotherapy regimens have
shown survival advantage in randomized clinical
trials and may be considered as category 1
compared with other chemotherapy regimens.
EP = Etoposide/cisplatin
BEP = Bleomycin/etoposide/cisplatin
TEST-6
See Follow-up for
Nonseminoma (TEST-11)
See Follow-up for
Nonseminoma (TEST-11)
Stage IS
Persistent
marker
elevation
Primary chemotherapy:
EP for 4 cycles or
BEP for 3 cycles
g
See Postchemotherapy
Management (TEST-8)
See Postchemotherapy
Management (TEST-8)
See Postsurgical
Management (TEST-9)
See Postsurgical
Management (TEST-9)
Testicular Cancer
Nonseminoma
g
k
.
Retroperitoneal lymph node dissection (RPLND) is recommended within 4 weeks of CT scan and 7-10 days of markers (category 2B).
See Primary Chemotherapy Regimens for Germ Cell Tumors (TEST-B)
PRIMARY TREATMENT
Version 1.2010, 08/28/09 © 2009 National Comprehensive Cancer Network, Inc. All rights reserved. These guidelines and this illustration may not be reproduced in any form without the express written permission of NCCN.
Guidelines Index
Testicular Cancer TOC
Staging, Discussion, References
Practice Guidelines
in Oncology – v.1.2010NCCN
®
Note: All recommendations are category 2A unless otherwise indicated.
Clinical Trials: NCCN believes that the best management of any cancer patient is in a clinical trial. Participation in clinical trials is especially encouraged.
CLINICAL STAGE PRIMARY TREATMENT
Stage IIA
Markers negative
Persistent marker
elevation
Open nerve-sparing RPLND
or
Primary chemotherapy (category 2B):
EP for 4 cycles or BEP for 3 cycles
k
g
Primary chemotherapy:
EP for 4 cycles or BEP for 3 cycles
g
TEST-7
See Postchemotherapy
Management (TEST-8)
The EP and BEP chemotherapy regimens have
shown survival advantage in randomized clinical
trials and may be considered as category 1
compared with other chemotherapy regimens.
EP = Etoposide/cisplatin
BEP = Bleomycin/etoposide/cisplatin
See Postchemotherapy
Management (TEST-8)
See Postsurgical
Management (TEST-9)
Stage IIB
Markers negative
Persistent marker
elevation
Lymph node metastases,
within lymphatic drainage
sites (landing zone positive)
Multifocal symptomatic lymph
node metastases with
aberrant lymphatic drainage
Primary chemotherapy:
EP for 4 cycles or BEP for 3 cycles
g
Primary chemotherapy:
EP for 4 cycles or BEP for 3 cycles
g
Open nerve-sparing RPLND
or
Primary chemotherapy:
EP for 4 cycles or BEP for 3 cycles
k
g
See
Postchemotherapy
Management
(TEST-8)
See Postsurgical
Management (TEST-9)
g .
kRetroperitoneal lymph node dissection (RPLND) is recommended within 4 weeks of CT scan and 7-10 days of markers (category 2B).
See Primary Chemotherapy Regimens for Germ Cell Tumors (TEST-B)
Testicular Cancer
Nonseminoma
Version 1.2010, 08/28/09 © 2009 National Compreh
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