433 RENAL CELL CARCINOMA SURVIVAL Pereverzev
WITH IVC THROMBUS:
RESULTS AND
OF 92 PATIENTS
OUTCOME OF CYTOREDUCTIVE RENAL CELL CARCINOMA
Stief C.. Matuschek I., Kuczyk M.A.. Truss MC..
Shukin Dmitry, llukhin Yuri
Alexeli,
434 LONG-TERM RECURRENT
SURGERY
FOR
iickert S., Jonas U.
Department of Urology, Hannover Medical School, Hannover, Germany Department
of
Urology.
Kharkov’s
Medical
Academy
of
Postgraduate
Education, Kharkov, Ukraine
OBJECTIVES: perioperative
INTRODUCTION
& OBJECTIVES:
Renal cell carcinoma (RCC)
extends into the inferior vena cava in 5.10%
This aim of this retrospective study was to evaluate complications and the long-term follow-up in patients with
recurrent renal cell carcinoma (RCC) after radical nephrectomy.
of cases. We examined the results
and long-term survival of patients after thrombectomy.
MATERIALS
MATERIALS
age of the patients was 64 years (47-80 years), mean follow-up period was 31 months (0.5-149 months). 40 patients presented with local recurrence, I7 with
& METHODS:
& METHODS: Between 1987 and 1999.67 patients which had undergone radical nephrectomy were diagnosed to have recurrent RCC. Mean
From 1977 until 2000. 92 patients underwent
radical nephrectomy including cavatomy and thrombectomy or caval resection. The level of tumour thrombus was assessed preoperatively
by US (65%)
MRI (35%): cavarenal segment of IVC- 19X%, infrahepatic-60.4%, 12.1%,, intrapericardial-3.3%,
atnal thrombus-4.4%.
was 24.6 months (range 3-130).
Mean
and
retrohepaic-
overall follow-up
Mean age was 65 years (range 34-78)
occurred in men in approximately
and
The rate of perioperative mortality was 4.5%.
I year survival for
patients with distant and regional metastases was 3X%, without metastasea-89%. Five-year survival in patients without metastatic lesions was 62%. The survival rate significantly
correlated with the stage of primary tumour and presence
regional and distant metastases. The differences in survival rates of the patients
RESULTS:
I patient died postoperatively and 2 developed renal insufficiency.
22 patients showed various minor complications; these complications had no influence on long-term survival (p=O.62). At the time of follow-up, I7 patients were free of disease, whereas I6 showed evidence of disease. Mean survival period was 46~8 months: 34+8 months in the group of patients with local recurrences, 42+15 months in group with lymph node metastasis, and 76+20 months in the group with contralateral renal metastasis. Mean survival after simple extirpation amounted to 55+11 months and to 25*1 I months after multivisceral extirpation. Mean survival was 63+15 months after complete (RO) and 32+8 months after incomplete (RI) resection of the tumour.
with various level of the thrombus were not demonstrated.
CONCLUSION:
thrombus. 2 other patients had a caval thrombus, 13 an infiltration of the psoas muscle. and I2 an infiltration of various organs. Median survival was estimated using the Kaplan-Meier Analysis.
two thirda of the cases (63 men and 29
women). 26% patients suffered from metaatatic disease at the time of surgery.
RESULTS:
contralateral renal turnours, and 10 with bulky lymph node metastasis. 5 of these patients had infiltration of the vena cava with 2 out of 5 presenting a caval
We believe that extended operation for renal cell carcinoma
are justified in patients without distant and regional metastases at anyone level
CONCLUSION:
Our results show that resection of recurrent RCC can be
of the tumour thrombus. The results of the surgery in this patient are not differed
accomplished with acceptable morbidity. In comparison to the historical database, surgical extirpation of recurrent RCC improved long-term outcome in
from results of the radical operations in patients without tumour invasion in IVC.
these patients.
435 CAPILLARY CHEMOEMBOLISATION IN CASES OF RENAL CELL CARCINOMA - CLINICAL EXPERIENCES OVER THE LAST 8 YEARS Seidensticker Peter’, Rassweiler Jens’ ‘Urology,
Klimkum
‘Radiology,
Klinikum
KurTidem
Markus’,
Heilbronn.
University
Heilbronn,
University
Schulze
of
Michael’,
Heidelberg,
Prager Peter’,
Heilbronn,
of Heidelberg,
Heilbronn,
Germany, Germany
shown,
that
of the procedure.
with
capillary
chemoembolisation
could
In this paper,
significantly
we want
increase
the
to focus on our clinical
ablative
used: to 7.5 ml EthibloY IO mg MitomycinC were mixed. Capillary propagation of embolic agent was guaranteed by preinjection of 40% glucose (=30% of the embolisation volume). Embolisation volume was estimated by contrast dye perfualon of the kidney. Between 1994 and 2001, 24 patients with renal cell carcinoma and the
temporary
(N=l7,
deficiency)
or absolute
postinfarction,
insufficiency)
Ethibloc”“/Mitomycin inclusions,
preceding
inoperability were
(n=7,
treated
with
C at our department.
perfusion,
tumour
size).
tumour vena
and
surgery.
cava
capillary Follow-up in
cardio-pulmonary
thrombus,
cases
cardiomyopathia.
chemoembolisation included
CT-scan
of
subsequent
I7
of
nephrectomy
in
the
cases.
Incomplete
(n=7) was mostly caused by underembolisation. Signs of a postembolic syndrome, i.e. pain, fever. hypertension and leukocytoais. here observed in 4 cases
occlusion
underembolised)
‘Department
of Interventional
‘Department
of IMR,
and can be prevented
by achieving
complete
de Jode Michael*,
Vale
Justin’,
Gedroyc
MRI,
St Marys
Hospital,
London,
United
St Marys Hospital, London, United Kingdom,
of Urology, St Marys Hospital, London, United Kingdom
INTRODUCTION
& OBJECTIVES:
To test the hypothesis that MR.guided
laser thermal ablation of inoperable renal tumours is a safe, tolerable, feasible procedure which produces significant tumour necrosis.
& METHODS:
Nine
patients (age range 56-81
years) with
malignant renal turnours underwent percutaneous laser thermal ablation (LTA) under MR guidance in a OST open magnet. Real-time colour thermal mapping monitored tumour ablation, follow-up was with gadolinium-enhanced weeks and (where appropriate)
4 monthly postprocedure
MRI at 6
intervals. Tumour
volume and percentage (c/r) viable tumour pre- and postablation (assessed by % enhancement of entire tumour volume) were compared.
RESULTS:
Average period of follow-up was 16.9 months after first ablation
(range 3-32 months). Mean pre-treatment tumour diameter was 4.3 cm (mean tumour volume 32 cm’).
seen
R&a*,
using (air bubble
of the specimen.
RESULTS: Complete tumour necrosis was
(all
Joarder
OF RENAL TUMOURS
Wladyslaw’
MATERIAL
MATERIAL & METHODS: As occlusive agent Ethibloc”” (Ethicon, Hamburg) was
histopathology
Elizabeth’.
ABLATION
experience
this technique.
cerebral
Dick
LASER THERMAL
Kingdom, ‘Department
INTRODUCTION & OBJECTIVES: Embolisation as a treatment for renal cell malignancy is a subject of controversial discussion. Open or laparoscopic radical nephrectomy should undoubtedly be the method of choice for operable renal turnours. Nevertheless elimination of a tumour-bearing kidney by embolisation of the renal artery is a minimal invasive alternative in selected cases. In earlier studies, we have efficacy
436 MR-GUIDED
arterial
occlusion.
Tumour progression after embolisation wab shown in 3 01.7 cases.
Average tumour size did not change. Average
%
enhancing tumour significantly decreased from an average of 73.7% preablation to 29.5%
postablation
(p
Signed Ranks Test). No patient
demonstrated further tumour growth locally. TIW
real time themal maps of
ablated tissue dimensions correlated closely with gadolinium-enhanced
follow-
up MRIs. There were two minor and one major complication.
CONCLUSIONS: ml/IO
mg)
Capillary
as occluding
agent
chemoembolisation is an cffcctive.
with
selected number of patlents with renal cell carcinoma realized. lrcatment.
Indications Due
Ethibloc’“/Mltomycin
minimal
invasive
if nephrectomy
are temporary
and absolute
inoperability
to the completeness
of the organ
necrosis.
syndrome has been ohuerved.
treatment
only
can
(7.5
for a not be
an well
as palliative
a mild
postrmbolic
CONCLUSIONS:
In patients unsuitable for surgery, MR guided laser thermal
ablation of renal tumours is safe, (with a complication rate comparable with other percutaneous techniques) feasible. (being well produces
significant
reduction
European
in viable
tumour
size.
Urology Supplements
tolerated
by the patient)
by an average
1 (2002)
and
of 45.5%.
No. 1, pp. 111