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Tipos de Cancer / Cáncer del Testículo / Recursos de NCI
National Cancer Institute®
Ultima Vez Modificado: 1 de agosto del 2002
1
UI - 12134704
AU - Kondo T; Wada H; Yata K; Mikami M; Tsujioka T; Suemori S; Suetsugu Y;
TI -
Nakanishi H; Otsuki T; Yamada O; Yawata Y; Morioka M; Tanaka H; Sadahira
Y; Sugihara T
[Seven patients with stage I and II primary testicular lymphoma]
SO - Rinsho Ketsueki 2002 Jun;43(6):473-6
AD - Division of Hematology, Department of Medicine, Kawasaki Medical School.
Seven patients with stage I and II primary testicular lymphoma (PTL)
have been treated since 1990 to the present at Kawasaki Medical School.
All patients, whose median age was 56 yrs, had initially complained of
swelling of the scrotal contents. The lesions were on the right in two
patients, on the left in five, and no patient had bilateral lesions. The
histological diagnosis was diffuse large B-cell type in all patients.
Five patients were classified as Ann Arbor stage I, and two at stage II.
After high-orchiectomy for resection of tumor, two patients received
chemotherapy alone, with a combination of chemotherapy and irradiation
of the contralateral testis in the remaining five. Complete remission
was achieved in all seven patients, but relapse occurred later in one.
As it is recognized that, even in localized stage or low risk group PTL
patients, the relapse rate in the central nervous system (CNS) and
contralateral testis is quite high, chemotherapy, prophylactic CNS
treatment and radiation of the contralateral testis after tumor
resection should be included in the management of PTL.
2
UI - 12115576
AU - Lajer H; Daugaard G; Andersson AM; Skakkebaek NE
TI -
Clinical use of serum TRA-1-60 as tumor marker in patients with germ
cell cancer.
SO - Int J Cancer 2002 Jul 10;100(2):244-6
AD - Department of Oncology, Rigshospitalet, Copenhagen, Denmark.
H.LAJER@rh.dk
TRA-1-60 antigen has been related to the presence of embryonal germ cell
carcinoma (EC) and carcinoma in situ. Our study further investigated the
clinical efficacy of TRA-1-60 as a serum tumor marker for germ cell
cancer in the testis. Three groups of patients with germ cell tumors
were included: Group 1, 34 patients with disseminated disease (24
nonseminomatous germ cell tumors [NSGCT] and 10 seminomatous germ cell
tumors [SGCT]); this group of patients were followed during the course
of chemotherapy with measurements of TRA-1-60, HCG and AFP; Group 2, 28
patients with Stage I NSGCT (22 with embryonal carcinoma [EC]-component
and 6 without EC-component, median follow-up 15 months); and Group 3, 40
patients with Stage I pure SGCT (median follow-up 15 months).
Seventy-eight percent of patients with disseminated EC-positive NSGCT
had increased levels of TRA-1-60 before chemotherapy. After
chemotherapy, levels of TRA-1-60 had dropped significantly (p < 0.01).
Levels of TRA-1-60 did not normalize in 15% of NSGCT and 30% of SGCT
patients after chemotherapy. This was not associated with recurrent
disease. Approximately one-third of patients with Stage I NSGCT had
increased values of TRA-1-60 during follow-up without having a relapse.
Contrary to earlier reports TRA-1-60 is not at present useful as a tumor
marker in patients with germ cell tumors. Although detecting a few early
relapses the rate of false positive elevations in the tumor marker makes
it unreliable in the clinical setting. Our study did confirm that
elevated levels of TRA-1-60 were present in approximately 80% of
patients with disseminated EC-positive NSGCT before start of
chemotherapy and chemotherapy induced a significant decrease in levels
of TRA-1-60. Thus, the TRA-1-60 antigen might still prove clinically
useful provided that the reliability of the assay can be increased.
Copyright 2002 Wiley-Liss, Inc.
3
UI - 2321619
AU - Verreault R; Weiss NS; Hollenbach KA; Strader CH; Daling JR
TI -
Use of electric blankets and risk of testicular cancer.
SO - Am J Epidemiol 1990 May;131(5):759-62
AD - Department of Epidemiology, School of Public Health and Community
Medicine, University of Washington, Seattle.
Electric blankets are an important domestic source of electromagnetic
fields (EMF) because of the relatively high intensity of emission,
prolonged exposure, and intimate contact with the source. In a
case-control study of testicular cancer in western Washington during
1981 to 1984, the relation between EMF exposure from electric blankets
and the occurrence of testicular cancer was examined. The respective
proportions of cases and controls who reported the use of an electric
blanket were almost identical (age-adjusted rate ratio (RR) = 1.0, 95%
confidence interval (CI) 0.7-1.4). Distributions of the duration of use
were also very similar in cases and controls. Compared with controls,
the frequency of use of an electric blanket was slightly lower in men
with seminoma (RR = 0.7, 95% CI 0.5-1.2) and slightly higher among men
with nonseminoma germ cell tumors (RR = 1.4, 95% CI 0.9-2.3). Overall,
the results of this study suggest that increased exposure to EMF from
electric blankets contributes little, if at all, to the risk of
testicular cancer in adult white men.
4
UI - 8452131
AU - Wertheimer N; Leeper E
TI -
Re: "Use of electric blankets and risk of testicular cancer" and "Use of
electric blankets and risk of postmenopausal breast cancer".
SO - Am J Epidemiol 1993 Jan 15;137(2):252-7
5
UI - 12095560
AU - Chan JL; Kabeto MU; Oldread AE; Paisley KL; Bennett JE; Sandler HM;
TI -
Smith DC; Hayman JA
The use of preferences to measure the benefit of adjuvant radiation
therapy for stage I seminoma.
SO - Int J Radiat Oncol Biol Phys 2002 Jul 15;53(4):934-41
AD - Department of Radiation Oncology, University of Michigan Health System,
Ann Arbor, MI, USA. chanj@umich.edu
PURPOSE: In Stage I seminoma, treatment with radiation therapy (RT)
after radical inguinal orchiectomy reduces the likelihood of relapse by
15%, but does not improve survival, thus making quality of life an
important outcome measure. The purpose of this study was to use
utilities to assess the quality of life benefits associated with
adjuvant RT in this setting. MATERIALS AND METHODS: One hundred healthy
men were interviewed using a utility assessment tool. Utilities for five
health states were measured using the standard gamble technique: (A)
adjuvant RT with 5% recurrence risk; (B) recurrence after RT, salvaged
with chemotherapy; (C) orchiectomy alone with 20% recurrence risk; (D)
recurrence after orchiectomy alone, salvaged with RT; and (E) recurrence
after orchiectomy alone, salvaged with chemotherapy. RESULTS: The median
age was 25. Utilities were highest for nonrecurrent health states, and
lowest for recurrence salvaged with chemotherapy. All differences in
utilities between health states were significant, except between states
A and C and B and E. Variability in utilities was not explained by the
sociodemographic factors examined. CONCLUSIONS: Our results suggest that
healthy males do not value the 15% reduction in recurrence risk
achievable with adjuvant RT. However, they do predict that an actual
recurrence, especially one requiring salvage chemotherapy, will lead to
significant decline in quality of life. We intend to use these utilities
to further evaluate the cost-effectiveness of RT in this setting.
6
UI - 12146015
AU - Kawai K
TI -
[Long-term side effects of chemotherapy for testicular cancer]
SO - Gan To Kagaku Ryoho 2002 Jul;29(7):1300-5
AD - Dept. of Urology, Institute of Clinical Medicine, University of Tsukuba.
Since the advent of cisplatin-based chemotherapy in the 1970s, a
majority of metastatic testicular cancer patients have been cured with
chemotherapy and surgery. The high curability of testicular cancer,
along with the young age of afflicted patients, can result in patients
living for many years after the chemotherapy. Thus, the assessment of
late effects of chemotherapy is clinically important in testicular
cancer patients. This article summarizes the literature regarding the
long-term side effects, and reviews approaches to the amelioration of
these side effects.
7
UI - 12137835
AU - Steiner H; Holtl L; Wirtenberger W; Berger AP; Bartsch G; Hobisch A
TI -
Long-term experience with carboplatin monotherapy for clinical stage I
seminoma: a retrospective single-center study.
SO - Urology 2002 Aug;60(2):324-8
AD - Department of Urology, University of Innsbruck, Innsbruck, Austria.
OBJECTIVES: To evaluate the long-term oncologic efficacy and morbidity
of carboplatin monotherapy, which was introduced at our department 11
years ago for the treatment of Stage I seminoma. Radiotherapy is the
standard treatment of patients with clinical Stage I seminoma.
Carboplatin has been advocated as a treatment alternative to avoid the
late side effects of radiotherapy and the high recurrence rate of
108 patients received two adjuvant cycles of single-agent carboplatin
(400 mg/m2 body surface on days 1 and 22) 2 weeks after high inguinal
orchiectomy. To assess for myelosuppression, complete blood counts were
performed at least once a week until the nadir occurred after the second
treatment cycle. RESULTS: During a mean follow-up period of 59.8 months
(range 6 to 134), 2 patients (1.85%) developed a recurrence
(retroperitoneal tumor) within the first year. Both patients received
cisplatin-based salvage chemotherapy. At last follow-up, all patients
were alive without any evidence of disease. Carboplatin treatment was
well tolerated by all patients and was associated with only mild
gastrointestinal side effects. Leukopenia was noted in 32 patients
(29.6%); 21 (19.4%) of these patients had World Health Organization
(WHO) grade 1, 8 (7.4%) had grade 2, 3 (2.8%) had grade 3, and none had
grade 4. No patient developed neutropenic fever. Thrombocytopenia was
observed in 48 patients (44.4%); of these patients, 38 (35.2%) had WHO
grade 1, 5 (4.6%) had grade 2, 2 (1.9%) had grade 3, and 3 (2.8%) had
grade 4. CONCLUSIONS: From an oncologic standpoint, two cycles of
carboplatin monotherapy was highly effective and very well tolerated by
all patients.
8
UI - 12131326
AU - Nagarajan M; Marshall RJ; Cook P; O'Rourke S; Mathew J
TI -
Symptomatic renal metastasis of a testicular seminoma mimicking
pelvicaliceal transitional cell carcinoma.
SO - J Urol 2002 Aug;168(2):634-5
AD - Department of Urology, Royal Cornwall Hospital, Truro, Cornwall, United
Kingdom.
9
UI - 12131327
AU - Kausch I; Galle J; Buttner H; Bohle A; Jocham D
TI -
Leiomyo-adenomatoid tumor of the epididymis.
SO - J Urol 2002 Aug;168(2):636
AD - Department of Urology, Medical University of Lubeck, Lubeck, Germany.
10
UI - 12131337
AU - Steinberg GD; Rinker-Schaeffer CW; Sokoloff MH; Brendler CB
TI -
Highlights of the Society of Urologic Oncology meeting, June 2, 2001.
SO - J Urol 2002 Aug;168(2):653-9
AD - Section of Urology, Department of Surgery, Pritzker School of Medicine,
University of Chicago Hospitals, Chicago, Illinois, USA.
11
UI - 12146055
AU - Reis-Filho JS; Schmitt FC; Soares MF; Figueiredo TM; Fillus-Neto J
TI -
Fine needle aspiration cytology of paratesticular rhabdomyosarcoma
mimicking a testicular germ cell tumor.
SO - Acta Cytol 2002 Jul-Aug;46(4):787-9
12
UI - 12040227
AU - Rudberg L; Carlsson M; Nilsson S; Wikblad K
TI -
Self-perceived physical, psychologic, and general symptoms in survivors
of testicular cancer 3 to 13 years after treatment.
SO - Cancer Nurs 2002 Jun;25(3):187-95
AD - Hogskolan Dalarna, Health and Caring Sciences, Falun, Sweden. lru@du.se
Due to the large group of patients with advanced testicular cancer now
being cured, it is important to identify the men who are at risk of
deteriorated health.The purposes of this study were: (1) to delineate
and compare frequency of self-perceived physical, psychologic, and
general symptoms in men treated for testicular cancer with those of a
general population sample and (2) to compare self-perceived physical,
psychologic, and general symptoms in relation to secondary Raynaud
phenomena, sexual dysfunction, infertility, and self-perceived
attractiveness in different treatment modalities. The subjects were 277
survivors of testicular cancer (M = 42.2 years) who had completed a
self-reported questionnaire (75.5% response rate). A population survey
comprising 392 men was used as a comparison group (M = 45 years).The
result demonstrated that although survivors of testicular cancer as a
group reported significantly less frequency of backache, leg pain,
cough, and eye problems than did the general population sample, they
described that they significantly more often felt cold. Men reporting
secondary Raynaud phenomena, infertility, and/or feeling less attractive
had experienced significantly more self-perceived symptoms. Oncologist
nurses could play an important role in psychologic counseling for those
men.
13
UI - 12077948
AU - Thomas L
TI -
'Keep your eye on the ball! is aimed at ensuring football players and
supporters are aware of testicular cancer'.
SO - Nurs Stand 2002 Jun 5-11;16(38):25
14
UI - 11885993
AU - Fizazi K; Chen I; Logothetis CJ
TI -
Germ-cell tumor survivors: the price for cure.
SO - Ann Oncol 2002 Feb;13(2):187-9
15
UI - 11885998
AU - Fossa SD; Aass N; Winderen M; Bormer OP; Olsen DR
TI -
Long-term renal function after treatment for malignant germ-cell
tumours.
SO - Ann Oncol 2002 Feb;13(2):222-8
AD - Department of Medical Oncology and Radiotherapy, The Norwegian Radium
Hospital, Oslo. s.d.fossa@klinmed.uio.no
OBJECTIVE: To evaluate prospectively renal function in patients with
malignant germ-cell tumours (MGCTs) >10 years after retroperitoneal
lymph node dissection alone (RPLND), radiotherapy alone (RAD) or
different schedules of cisplatin-based chemotherapy with or without
surgery/radiotherapy (CHEM). PATIENTS AND METHODS: In 85 patients, three
groups were identified: RPLND, 14; RAD, 18; CHEM, 53, with subdivision
of the latter group according to the cumulative cisplatin dose or the
additional use of radiotherapy. Renal function was determined by
131Iodine Hippuran clearance or 99m DTPA glomerular filtration rate, and
was assessed before treatment and four times during 14 years of
follow-up. A value of <70% of the upper limit of the normal range
identified impaired renal function. RESULTS: Twenty-five patients
displayed long-term impaired renal function, 23 of them from the RAD or
CHEM group. In the RAD group, renal function decreased by 8%, whereas a
14% reduction of renal function was observed in the CHEM group. In the
CHEM group the cumulative dose of cisplatin, and in the RAD group the
age at treatment, were associated with impairment of renal function.
Combining all patients, age at treatment and the type of treatment were
associated with impaired renal function. CONCLUSIONS: In 20-30% of the
patients with germ-cell tumour, standard radiotherapy and chemotherapy
strategies are followed by long-term subclinical impaired renal
function. These findings support current intentions to avoid
overtreatment with these treatment modalities.
16
UI - 11885999
AU - Strumberg D; Brugge S; Korn MW; Koeppen S; Ranft J; Scheiber G; Reiners
TI -
C; Mockel C; Seeber S; Scheulen ME
Evaluation of long-term toxicity in patients after cisplatin-based
chemotherapy for non-seminomatous testicular cancer.
SO - Ann Oncol 2002 Feb;13(2):229-36
AD - Department of Internal Medicine (Cancer Research), West German Cancer
Center, University of Essen. dirk.strumberg@uni-essen.de
BACKGROUND: Because of the increasing number of long-term survivors of
metastatic testicular germ-cell cancer, a general concern has been
secondary morbidities, especially cardiovascular risk factors. PATIENTS
AND METHODS: Thirty-two patients treated with cisplatin- and
doxorubicin-containing chemotherapy > or = 13 years before the time of
analyses were evaluated for neuro-, oto-, pulmonary-, vascular- and
gonadal toxicity including evaluation of myocardial damage and
cardiovascular risk factors and analysis of microcirculation. RESULTS:
Thirty percent of the patients showed abnormal left ventricle function.
Elevated follicle stimulating hormone (FSH) and luteinising hormone (LH)
levels in 75% of patients were often associated with low testosterone
levels. Elevated total cholesterol levels were found in 82% and higher
triglyceride levels in 44% of patients, most of them were overweight.
About 25% of the patients developed diastolic arterial hypertension
after chemotherapy. Reduced hearing was confirmed in 23% of patients,
especially at frequencies higher than 3000 Hz. Moreover, 53% of patients
presented transient evoked otoacoustic emissions. In 38% of patients
non-symptomatic neuropathy was detected, in 28% symptomatic neuropathy,
and in 6% disabling polyneuropathy. In 80% of patients with neuropathic
symptoms additional morphological and functional abnormalities were
found by nailfold capillary videomicroscopy, compared to only 57% of the
patients without neuropathic symptoms. CONCLUSIONS: Patients cured by
cisplatin-based chemotherapy for metastatic testicular cancer have to be
cognizant of their unfavorable cardiovascular risk profile, that might
be a greater risk than developing a relapse or second malignancy.
17
UI - 11886000
AU - Harvey ML; Geldart TR; Duell R; Mead GM; Tung K
TI -
Routine computerised tomographic scans of the thorax in surveillance of
stage I testicular non-seminomatous germ-cell cancer--a necessary risk?
SO - Ann Oncol 2002 Feb;13(2):237-42
AD - Department of Radiology, Royal South Hants Hospital, Southampton, UK.
BACKGROUND: The standard management approach to stage I testicular
non-seminomatous germ-cell tumours (NSGCT) in the UK is a surveillance
programme with adjuvant bleomycin, etoposide, cisplatin (BEP)
chemotherapy being offered to individuals with high risk disease.
Conventionally, computed tomography (CT) scanning of the thorax has
formed part of the surveillance programme. This paper evaluates the
contribution of routine thoracic CT imaging in the management of this
disease. PATIENTS AND METHODS: We retrospectively reviewed the case
notes of 168 patients with stage I NSGCT referred to the Wessex Medical
Oncology Unit over a period of 13 years (1986-1998). These patients
entered onto a surveillance programme that included serial chest X-ray
follow up rather than thoracic CT. RESULTS: Forty-two out of 168
patients (25%) evaluated suffered relapse during the follow up period.
Eight of 42 patients (19%) relapsed with intrathoracic disease. Seven
out of eight of these patients (87.5%) had at least one other indicator
of disease recurrence (elevated serum marker, abnormal abdominal CT).
One of 42 patients (2.4%) relapsed with isolated intrathoracic disease
with no other indicator of relapse. All patients with intrathoracic
relapse had evidence of disease on chest X-ray. Of the 42 relapsing
patients, 93% could be categorised as having good prognosis metastatic
disease. Seven per cent relapsed with intermediate or poor prognostic
disease; relapse in these patients would not have been detected earlier
with the inclusion of routine thoracic CT. Only one patient has died
giving a cure rate of 98% for relapsing patients. CONCLUSIONS: The
elimination of chest CT did not compromise outcome but significantly
reduced radiation exposure thereby minimising the risk of
radiation-induced secondary malignancy. Continued review of surveillance
programmes is essential if we are to optimise management of this
disease.
18
UI - 11885847
AU - Horvath LG; McCaughan BC; Stockle M; Boyer MJ
TI -
Resection of residual pulmonary masses after chemotherapy in patients
with metastatic non-seminomatous germ cell tumours.
SO - Intern Med J 2002 Mar;32(3):79-83
AD - Department of Medical Oncology, Sydney Cancer Centre, Royal Prince
Alfred Hospital, Sydney University, New South Wales, Australia.
BACKGROUND: Resection of residual post-chemotherapy pulmonary masses in
patients with non-seminomatous germ cell tumours gives therapeutic
benefit and prognostic information. AIM: This study was undertaken to
review the experience of this intervention in a single teaching
hospital. METHODS: The Germ Cell Database of the Sydney Cancer Centre
was searched for all patients who had undergone excision of pulmonary
metastases. These patient records were subsequently reviewed. RESULTS:
Between 1976 and 1999, 15 patients underwent a combined total of 19
thoracotomies for resection of residual tumour mass after
cisplatin-based chemotherapy. The primary tumour histology included
mature teratoma in 47% (7 of 15) of patients. Prior to chemotherapy, 73%
(11 of 15) of patients had elevated serum levels of alpha-fetoprotein
(median 180 ng/mL) and 60% (9 of 15) of patients had elevated beta-human
chorionic gonadotropin (median 672 IU/L). The median length of hospital
stay related to thoracotomy was 7 days. There were two surgical
complications, a prolonged air leak and a residual pleural effusion.
Pathology of residual pulmonary masses revealed necrosis alone in 37% (7
of 19) of procedures, mature teratoma alone in 32% (6 of 19) of
procedures and viable tumour in 32% (6 of 19) of procedures. Of those
with viable tumour, three achieved long-term complete response (CR), two
died of progressive disease (PD) and one is alive with PD. Of those with
teratoma, two achieved CR and one relapsed. The long-term CR rate was
80% (12 of 15 patients).The median follow up was 10 years (range
0.75-17.5 years). Four patients died, two of PD and two of
cardiovascular disease while in CR. CONCLUSION: At this institution,
thoracotomy for residual pulmonary masses was well tolerated, with a
high cure rate.
19
UI - 12052503
AU - Bianchi NO; Richard SM; Peltomaki P; Bianchi MS
TI -
Mosaic AZF deletions and susceptibility to testicular tumors.
SO - Mutat Res 2002 Jun 19;503(1-2):51-62
AD - Instituto Multidisciplinario de Biologia Celular (IMBICE), La Plata,
Argentina. bianchi@satlink.com
We tested for azoospermia factor (AZF) deletions 17 loci corresponding
to AZF subintervals a-d in 17 cases of testicular tumors occurring in
Finns. While DNA samples from 48 CEPH and 32 Finnish males showed no
deletions, patients with testicular cancer displayed AZF deletion
mosaicisms in various non-tumor tissues (13 cases) and specific deletion
haplotypes in tumor tissues (10 cases). Two of the cases with AZF
deletions were testicular non-Hodgkin lymphomas indicating that
Y-microdeletions appear also in malignancies other than seminoma and
non-seminoma tumors. In good agreement with this assumption, we detected
one AZF deletion in normal cells from 1 of 5 HNPCC cases, heterozygous
for an MLH1 mutation. We propose that AZF deletions occur in early
embryogenesis due to mutations of TSPY, mismatch repair (MMR), or
X-specific genes. Since fathers of testicular, tumor cases did not
exhibit AZF deletions, we assumed they were not carriers of the mutation
inducing AZF deletion-mosaicisms. Therefore, tumor cases should have
received the MMR gene or X mutations via the maternal lineage, or for
the case of TSPY and MMR genes via a sperm carrying a mutation occurred
in the paternal germ-cell line. We consider AZF microdeletions in
non-tumor cells to be part of a broader pattern of chromosome
instability producing susceptibility to testicular tumors. Clonal
transformation and expansion of one of these tumor-susceptible cell
lineages give rise to testicular tumors showing genome anomalies
characteristic of testicular cancers (i12p, LOH and genetic imbalance
for various autosomal regions, Y- and autosomal MSI, specific AZF
deletion haplotypes).
20
UI - 12128117
AU - Incrocci L; Hop WC; Wijnmaalen A; Slob AK
TI -
Treatment outcome, body image, and sexual functioning after orchiectomy
and radiotherapy for Stage I-II testicular seminoma.
SO - Int J Radiat Oncol Biol Phys 2002 Aug 1;53(5):1165-73
AD - Department of Radiation Oncology, Erasmus MC-Daniel den Hoed, Rotterdam,
The Netherlands. incrocci@rtdh.azr.nl
PURPOSE: Orchiectomy followed by infradiaphragmatic irradiation is the
standard treatment for Stage I-II testicular seminoma in The
Netherlands. Because body image and sexual functioning can be affected
by treatment, a retrospective study was carried out to assess treatment
outcome, body image, and changes in sexuality after orchiectomy and
radiotherapy. METHODS AND MATERIALS: The medical charts of 166 patients
with Stage I-II testicular seminoma were reviewed. A questionnaire on
body image and current sexual functioning regarding the frequency and
quality of erections, sexual activity, significance of sex, and changes
in sexuality was sent to 157 patients (at a mean of 51 months after
treatment). RESULTS: Seventy-eight percent (n = 123, mean age 42 years)
completed the questionnaire. During irradiation, almost half of patients
experienced nausea and 19% nausea and vomiting. Only 3 patients had
disease relapse. After treatment, about 20% reported less interest and
pleasure in sex and less sexual activity. Interest in sex, erectile
difficulties, and satisfaction with sexual life did not differ from
age-matched healthy controls. At the time of the survey, 17% of patients
had erectile difficulties, a figure that was significantly higher than
before treatment, but which correlated also with age. Twenty percent
expressed concerns about fertility, and 52% found their body had changed
after treatment. Cancer treatment had negatively influenced sexual life
in 32% of the patients. CONCLUSIONS: Orchiectomy with radiotherapy is an
effective and well-tolerated treatment for Stage I-II testicular
seminoma. Treatment-induced changes in body image and concerns about
fertility were detected, but the sexual problems encountered did not
seem to differ from those of healthy controls, although baseline data
are lacking.
21
UI - 12128133
AU - Campostrini F; Gregianin M; Rampin L; Lonardi F; De Lucchi A; Coeli M;
TI -
Gioga G; Prina M; Ferretti G; Povolato M
How iliopelvic lymphoscintigraphy can affect the definition of planning
target volume in radiation therapy of pelvic and testicular tumors.
SO - Int J Radiat Oncol Biol Phys 2002 Aug 1;53(5):1303-13
AD - Department of Radiation Oncology, ASL 21, Legnago General Hospital,
Legnago, Verona, Italy. lradioter@hotmail.com
PURPOSE: External beam radiation therapy (EBRT) of most intrapelvic and
testicular tumors has been generally performed with large fields
encompassing both the primary disease and lymphatic drainage. This study
was carried out to map the pelvic and periaortic lymphatics by means of
iliopelvic lymphoscintigraphy (IPL) in preparation for radiotherapy
70 patients scheduled for EBRT (61 operated on, 52 females, 18 males,
mean age 61, range, 24-80), affected with uterine (43), rectal (11),
testicular (8), anal (4), penile (2), and vulvar (2) cancers were
enrolled in the study. IPL was performed by injection of
99mtechnetium-nanocolloids in the bipedal (70 cases) or bipedal plus
perianal (20 cases) sites. The sensitivity of IPL in mapping the
lymphatic anatomy was evaluated first. Then three radiation oncologists
scored the modifications induced by IPL on the planning target volume
(PTV) which had been previously delineated only on the basis of bony
landmarks. The original fields were classified "inadequate" if they
failed to match the new PTV by more than 1 cm. RESULTS: IPL sensitivity
in showing the inguinal, external iliac, common, and periaortic
lymphatics was 100%, 90%, 80%, and 70% in anterior-posterior (A-P)
projections, and 100%, 80%, 70%, and 60% in lateral projections
respectively. For the presacral and hypogastric ones the sensitivity was
40%. When compared with bony landmarks, IPL changed the delineation of
PTV in 24 of 70 A-P P-A fields (34%) and 22 of 58 (38%) lateral fields.
Furthermore, 8/12 (67%) lymphadenectomies resulted in being incomplete.
No IPL-related toxicity was observed. CONCLUSION: IPL is a safe,
inexpensive (cost: 100 Euros), and effective method to map the lymphatic
chains. In the A-P scintigrams these structures were detected in 85%
(70-100%) of the patients referred for total pelvis irradiation, and
this figure could be higher in subjects not operated on. IPL can also
give a reliable evaluation of the lymphadenectomies in order to schedule
the proper treatments after surgery. Finally, IPL may change the
conventional PTV for pelvic irradiation in about 36% (34-38%) of the
cases; therefore, the fields should be tailored more around the
lymphatic landmarks than the bony landmarks.
22
UI - 12010239
AU - Sanchez D; Zudaire JJ; Fernandez JM; Lopez J; Arocena J; Sanz G; Gimenez
TI -
M; Rosell D; Robles JE; Berian JM
18F-fluoro-2-deoxyglucose-positron emission tomography in the evaluation
of nonseminomatous germ cell tumours at relapse.
SO - BJU Int 2002 Jun;89(9):912-6
AD - Department of Urology, Facultad di Medicina, Clinica Universitaria,
Universidad de Navarra, Pamplona, Spain.
OBJECTIVES: To compare the performance of
18F-fluoro-2-deoxyglucose-positron emission tomography (FDG-PET) and
computed tomography (CT) in the follow-up of nonseminomatous germ cell
tumours (NSGCT) in the retroperitoneum. PATIENTS AND METHODS: FDG-PET
was used 25 times in 15 patients diagnosed with NSGCT. At the time of
diagnosis five patients each were in stage I, II and III. Five patients
had pure embryonal carcinoma, two had yolk sac tumours, one
choriocarcinoma and seven had mixed tumours. RESULTS: Eleven patients
either presented with retroperitoneal disease or this did not disappear
after chemotherapy. The results of both examinations coincided in 18
cases and were contradictory in the other seven, the difference being
statistically significant (P=0.042). CONCLUSION: In these patients
FDG-PET detected the retroperitoneal relapse of NSGCT, in advanced
stages treated with surgery plus chemotherapy, earlier than did CT; it
also detected the presence of mature teratoma in residual
retroperitoneal masses more accurately than CT. More extensive trials
are needed before making conclusions about FDG-PET imaging as a routine
method for NSGCT.
23
UI - 12151969
AU - Sarid DL; Ron IG; Avinoach I; Sperber F; Inbar MJ
TI -
Spontaneous regression of retroperitoneal metastases from a primary pure
anaplastic seminoma: a case report.
SO - Am J Clin Oncol 2002 Aug;25(4):380-2
AD - Department of Oncology, Tel Aviv Sourasky Medical Center and Sackler
Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Spontaneous regression of pure seminoma metastases is a rare phenomenon,
with only a few cases reported to date. To the best of our knowledge,
this is the first report of regression of anaplastic pure seminoma
metastases located in the retroperitoneum. We present a 27-year-old man,
a marihuana smoker, with metastatic pure anaplastic seminoma in the high
retroperitoneal lymph nodes. After orchiectomy, his metastases regressed
with no medication. Several mechanisms are suggested to explain this
phenomenon, which still remains elusive.
24
UI - 12163388
AU - Takayama H; Takakuwa T; Tsujimoto Y; Tani Y; Nonomura N; Okuyama A;
TI -
Nagata S; Aozasa K
Frequent Fas gene mutations in testicular germ cell tumors.
SO - Am J Pathol 2002 Aug;161(2):635-41
AD - Department of Pathology, Osaka University Medical School, Suita, Osaka,
Japan.
The Fas (Apo-1/CD95)/Fas ligand (L) system is involved in cell death
signaling, and has been suggested to be important for the regulation of
germ cell apoptosis in the testis. Mutations of the Fas gene may result
in accumulation of germ cells and thus might contribute to testicular
carcinogenesis. The open reading frame of Fas cDNA was examined in 24
cases of testicular germ cell tumors (TGCTs), comprised of 19 pure
histological type (15 seminomas, 3 embryonal carcinomas, 1 immature
teratoma) and 5 mixed-type tumors. Mutations of the Fas gene were found
in nine (37.5%) of these cases. Each lesion with a homogeneous
histological picture was selectively microdissected using a laser
capture microdissection method: samples consisted of 18 lesions from
seminomas, 7 embryonal carcinomas, 4 immature teratomas, 2
choriocarcinomas, and 1 from a yolk sac tumor. Microdissected genomic
DNA was examined to determine which mutations were derived from which
kind of histological lesion. Eleven mutations were detected in 10 TGCT
lesions from nine cases, but none were found in benign lesions. All were
point mutations, and eight missense mutations occurred in exon 9
encoding the core protein of the death domain essential for apoptotic
signal transduction. Three were silent mutations. Mutations were found
in the seminoma (27.8%) and embryonal carcinoma lesions (62.5%), but
none were found in the one yolk sac tumor, two choriocarcinomas, or four
immature teratoma lesions. Each seminoma and embryonal carcinoma lesion
found in the same case had a different type of Fas mutation from the
others. Mouse T-cell lymphoma cells transfected with missense mutated
genes were resistant to apoptosis induced by anti-Fas antibody,
indicating these to be loss-of-function mutations. These findings
suggested a role of Fas gene mutations in the pathogenesis of TGCTs.
25
UI - 11888046
AU - Lechner L; Oenema A; de NJ
TI -
Testicular self-examination (TSE) among Dutch young men aged 15-19:
determinants of the intention to practice TSE.
SO - Health Educ Res 2002 Feb;17(1):73-84
AD - Department of Social Science, Open University The Netherlands.
The present study analyzed what determinants are important to describe
and explain the intention of testicular self-examination (TSE) for young
men aged 15-19 attending senior high school (response rate 80%, n =
274). The questionnaire assessed determinants, including knowledge,
attitude (positive and negative consequences, anticipated regret, and
moral obligation), social influence (social norm, social support and
modeling) and self-efficacy. Knowledge of testicular cancer and TSE was
very low. Only 2% of the subjects reported regularly performing TSE.
After hearing of TSE (through the questionnaire), 41% of all young men
had a positive intention to start performing TSE regularly. The various
intention groups (positive, neutral and negative) differed significantly
on almost all of the determinants. Multiple regression analysis showed
that young men who where anxious about TSE and those who were not
anxious had different determinants explaining the variance in the
intention to perform TSE regularly (R2 = 41-57%). Differences in
determinants of intention between young men who are anxious about TSE
and young men who are not can be used to design health education
interventions that may therefore be more effective for these different
subgroups.
26
UI - 12063007
AU - Classen J; Souchon R; Hehr T; Bamberg M
TI -
Radiotherapy for early stages testicular seminoma: patterns of care
study in Germany.
SO - Radiother Oncol 2002 May;63(2):179-86
AD - Department of Radiation Oncology, Tubingen University,
Hoppe-Seyler-Strasse 3, D-72076, Tubingen, Germany.
BACKGROUND AND PURPOSE: To evaluate compliance of radiotherapeutic
departments with 1997 German consensus guidelines for staging and
treatment of testicular cancer patients. MATERIAL AND METHODS: A
questionnaire was mailed to all departments of radiotherapy in Germany
as identified by the data-base of the German Society for Radiation
Oncology (DEGRO). The questionnaire was analysed with particular respect
to institutional characteristics, frequency of seminoma patients treated
per year, treatment techniques, and institutional compliance with
consensus guidelines. RESULTS: Fifty-six institutions (39%) returned the
questionnaire, 46% of which fully complied with consensus guidelines
concerning staging requirements. A minimum workup with computed
tomography (CT) of abdomen and pelvis, X-ray or CT of the chest and
tumour markers was mandatory in 87.5% of the departments. Compliance
with the recommended treatment schedule was high in stage I with less
than 5% major violations of recommended dose prescription or target
volume definition. In stage IIA/B, however, 22.6 and 10.2% of the
departments showed major deviations from either standardised treatment
target volumes or total doses of irradiation, respectively. CONCLUSIONS:
Compliance with consensus recommendations in German departments for
radiotherapy is satisfactory in many institutions. However, major
deviations from treatment guidelines were observed in stage II disease
indicating the need for continuous improvement in the quality of
testicular cancer patient management.
27
UI - 12125389
AU - Nori F; Settimi L; Figa-Talamanca I
TI -
[Testicular tumors in Italy: historical trends, geographic differences,
and etiological hypotheses]
SO - Epidemiol Prev 2002 Mar-Apr;26(2):76-81
AD - Dipartimento di biologia animale e dell'uomo, Universita degli studi La
Sapienza, Roma.
Testicular cancer is a rare tumour. Its incidence has been increasing in
many parts of the world during the last decades. This cancer has an
unusual age distribution with one peak in incidence in young adults
(aged 20-39) and a second peak in over 60. On the basis of the Italian
Bureau of Statistics, mortality rate was higher in northern regions of
the country compared to southern ones, up to the beginning of the
1980's. However, the progressive decline in mortality in all regions
eliminated the geographical differences in recent years. Incidence rates
obtained from the existing cancer Registries, confirm a strong
geographical gradient, with higher rates in the North (ex. 5.1/100,000
in Parma in 1988-92) than in the South (ex. 1.1/100,000 in Ragusa in
1988-92). The comparison between incidence rates of two recent periods
(1983-87 and 1988-92), showed an increase in most of the provinces for
which data were available. The age distribution curve showed that
testicular cancer occurs after puberty, with a peak in incidence among
30-34 year olds, and after the age of 60. These observations suggest the
possible causative role of some environmental exposures. Epidemiological
studies have found an association between some occupational exposures in
industrial and agricultural settings and testicular cancer. Moreover
some studies have found an association between parental occupation and
testicular cancer in the offspring. However, the aetiology of testicular
cancer is still poorly understood.
28
UI - 12173328
AU - Tu SM; Reyes A; Maa A; Bhowmick D; Pisters LL; Pettaway CA; Lin SH;
TI -
Troncoso P; Logothetis CJ
Prostate carcinoma with testicular or penile metastases. Clinical,
pathologic, and immunohistochemical features.
SO - Cancer 2002 May 15;94(10):2610-7
AD - Department of Genitourinary Medical Oncology, University of Texas M. D.
Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA.
stu@notes.mdacc.tmc.edu
BACKGROUND: Despite the proximity, prostate carcinoma seldom
metastasizes to the penis or testis. METHODS: In the current study, the
authors retrospectively examined the clinical history of 12 patients
with prostate carcinoma and testicular or penile metastases. Pathologic
review and immunohistochemical staining were performed on tumors from
eight of these patients. RESULTS: Patients with prostate carcinoma and
testicular or penile metastasis responded to androgen ablative therapy
(median duration, 33 months). They were predisposed to developing
persistent or recurrent urinary symptoms and visceral metastases. Six of
9 evaluable patients had elevated serum carcinoembryonic antigen levels
(> 6 ng/mL), whereas 2 of 10 patients had low or undetectable serum
prostate specific antigen levels (< 4 ng/mL). In seven of the eight
patients for whom specimens were available, the tumors were found to
contain histologic features that were compatible with a diagnosis of
ductal or endometrioid adenocarcinoma of the prostate. CONCLUSIONS:
Patients with prostate carcinoma and testicular or penile metastases
have unique clinical and pathologic characteristics. Many of these
patients' tumors are compatible with a subtype of prostate carcinoma
known as ductal adenocarcinoma. Further studies need to be performed to
elucidate the biologic basis of the various histologic subtypes of
prostate carcinoma.
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Calcium Leucovorin, Citrovorum Factor, Folinic Acid
Cladribine (2-CDA, Leustatin®)
Cyclophosphamide (Cytoxan®, Neosar®, Endoxan®)
Cyclosporine (Neoral®, Sandimmune®, Restasis®, Gengraf®)
Cytarabine (Cytosar-U®, Ara-C)
Irinotecan (Camptosar®, CPT-11)
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Leucovorin (Calcium Leucovorin, Citrovorum Factor, Folinic Acid)
Leuprolide Acetate (Lupron®, Lupron Depot®, Eligard®, Prostap®, Viadur®) - For Men
Leuprolide Acetate (Lupron®, Lupron Depot®, Eligard®, Prostap®, Viadur®) - For Women
Lupron®, Lupron Depot®, Eligard®, Prostap®, Viadur®
Lupron®, Lupron Depot®, Eligard®, Prostap®, Viadur®
Busulfan (Myleran®, Busulfex®)
Intravesicular Mitomycin (Mutamycin®, Mitomycin-C, given into the bladder)
Mechlorethamine (Mustargen®, Nitrogen Mustard)
mechlorethamine, mustine, Mustargen®
Megestrol (Megace®, Megace-ES®)
Mercaptopurine (Purinethol®, 6-MP)
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Mexate®, Folex®, Rheumatrex®, Amethopterin, MTX
Mitomycin (Mutamycin®, Mitomycin-C)
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Morphine Sulfate (MS Contin®, Avinza®, Kadian®, Oramorph SR®)
MS Contin®, Avinza®, Kadian®, Oramorph SR®
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Nitrogen mustard (mechlorethamine, mustine, Mustargen®)
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