Background:
The technique of partial nephrectomy for managing
renal cancers is well recognized, but guidelines regarding indications for
its use are not generally accepted.
Methods: The authors review the indications
for partial nephrectomy in various clinical situations, and they include
their own experience to clarify the utility of the technique.
Results: Intraoperative renal ultrasound
and helical computed tomography can assist the surgeon in technical decisions.
Partial nephrectomy is considered when nephrectomy would render the patient
anephric and dependent on dialysis.
Conclusions: The technical and operative advances in partial nephrectomy
make the approach increasingly attractive for patients with kidney cancer
in a variety of clinical circumstances.
Introduction
Whenever
preservation of functioning renal parenchyma is important, nephron-sparing
surgery substitutes for radical nephrectomy. The first partial nephrectomy
was performed in 1884 by Wells1 for the removal of a perirenal
fibrolipoma. Partial nephrectomy to treat renal malignancy was first described
in 1890 by Czerny.2 In 1950, Vermooten3 reported
that peripherally located, encapsulated renal tumors could be removed
by partial excision of renal tissue. Partial nephrectomy has now become
a standard procedure for appropriately selected patients with renal cell
carcinoma (RCC).
Indications
Nephron-sparing
surgery is indicated for cases in which a radical nephrectomy would render
the patient anephric with a subsequent immediate need for dialysis. Such
cases include synchronous bilateral RCC, tumors in a solitary kidney,
and unilateral tumor with a poorly functioning contralateral kidney (imperative
indications).4 Typical reasons for a solitary organ are prior
removal, renal agenesis, or irreversible impairment from a benign disorder.
Further indications for partial nephrectomy are patients with unilateral
RCC and those with a functioning opposite kidney with an uncertain future
function. The main reasons for the latter condition include artery stenosis,
hydronephrosis, chronic pyelonephritis, and systemic diseases such as
diabetes and hypertension that result in arteriosclerosis and nephron-affecting
impairment. Another indication includes patients with small (4 cm or less
in diameter), unilateral tumors with a healthy contralateral organ (elective
indication).5,6 The ongoing controversy regarding elective
indications is discussed later. Nevertheless, the results of partial nephrectomy
are less satisfactory in patients with larger or multiple localized RCC,
thus leaving radical nephrectomy as the standard therapeutic approach
in these cases.
Preoperative
Considerations and Preparation
The
preoperative evaluation of the patient includes the determination of the
extent and precise location of the tumor mass. Thus, in addition to noninvasive
computed tomography (CT) or magnetic resonance imaging (MRI) and ultrasound
to rule out locally extensive and/or metastatic disease, in some cases
a renal angiogram might be performed to locate the main renal artery and
its branches.7,8 Selective renal venography might be performed
in patients with large or centrally located tumors to evaluate for intrarenal
venous thrombosis secondary to malignancy.9 The latter indicates
a more advanced local tumor stage resulting in an increased surgical complexity.
Renal
scintigraphy is helpful to determine preoperatively the function of the
kidney with tumoral lesion. A tumor-burdened kidney revealing low function
is not an indication for partial nephrectomy if the contralateral organ
shows normal creatinine clearance.4-6
Intraoperative
renal ultrasound is increasingly being used during intrarenal surgery
and has played a role in determining if patients are suitable for partial
vs radical nephrectomy.10 Technical advances in the development
of sonographic instrumentation have made this possible. These advances
include the development of high-frequency multi-Hertz transducers offering
a marked improvement in resolution, the development of miniature, intraoperative
transducers that facilitate access into the surgical field, and the compactness
of current model US machines that allow easy transport and mobility into
the operating room suite. Also, the refinement of color and duplex Doppler
sonography and the addition of power Doppler sonography have made intraoperative
ultrasonography an integral component in the management of patients undergoing
partial nephrectomy.
In patients
undergoing partial nephrectomy, ultrasound can delineate a tumor in relation
to the hilar anatomy10 and can demarcate the boundary of a
surgical margin,10,11 thereby preserving the maximum amount
of uninvolved parenchyma while still obtaining negative surgical margins.11
Color and power Doppler sonography can identify arteries, veins, and the
urinary collecting system near the potential resection site, and the thickness
of a renal parenchymal margin between tumor and vessel may be estimated.12
Vessels around the tumor are delineated, which facilitates dissection,
and the success of revascularization may be assessed using color Doppler
sonography.10 The presence of tumor thrombus in the renal vein
may be determined.10,12 Additionally, vascular structures (arteries
and veins) may be differentiated from nonvascular structures such as cysts
or a dilated calyx.10,13
Preoperative
indeterminate lesions may be evaluated intraoperatively with ultrasound.10
Lesions extending deep into the parenchyma are better evaluated on intraoperative
sonography10-12 due to the use of higher-frequency transducers
and closer proximity to the mass without interference from intervening
organs and soft tissues. Complex cystic masses thought to be solid are
more clearly delineated. Small lesions that are indeterminate on preoperative
CT are characterized more accurately on intraoperative ultrasound; two
small lesions appearing solid on preoperative CT proved to be a cyst10,13
and an angiomyolipoma11 on intraoperative sonography. Intraoperative
sonography may alter the surgical approach by characterizing a lesion
and defining the location and extent of tumor.10 However, sonography
still cannot distinguish whether a solid mass is benign or malignant.
Accessory
lesions may be identified by intraoperative sonography.10,13
However, lesions may be missed, and those smaller than 5 mm may be beyond
the resolution capacity of ultrasound.10,14 With further improvements
in technology and continued research in the area of sonographic contrast
agents, small lesions may prove to be more readily distinguished from
normal renal parenchyma, and fewer accessory lesions may go undetected.
In addition
to the standard imaging modalities, newer techniques have recently been
proposed in an attempt to assist the surgeon in planning the best approach
to remove the tumor. Helical CT combined with three-dimensional volume
rendering has recently been shown to accurately depict both the renal
parenchyma and the vascular anatomy, thus providing the surgeon with a
three-dimensional depiction of the tumor in relation to the critical components
of the kidney.15
Principles
of Open Surgery in Partial Nephrectomy
Several
surgical techniques are available for performing nephron-sparing surgery
in patients with renal tumors. Description of these techniques, including
performing the incision, exposing the kidneys, and closing the situs,
are described in detail elsewhere.4,16-18 The five main surgical
processes include enucleation of tissue, polar segmental nephrectomy,
wedge resection, major transverse resection, and extracorporeal partial
nephrectomy followed by renal autotransplantation.19 All of
these techniques require steady vascular control and thorough hemostasis,
avoidance of renal ischemia, complete tumor removal with free margins,
and efficient closure of the intrarenal collecting system. Finally, an
adequate postoperative renal function must be maintained since a functioning
renal remnant of at least 20% of one normal kidney is necessary to avoid
end-stage renal failure.19,20 However, it is important not
to compromise the extent of the surgical procedure to preserve renal function
at the expense of an incomplete resection.
Partial
nephrectomy can be performed in most cases in situ, but the extracorporeal
access to the kidney still is effective in special cases.21
Extracorporeal surgery, which might achieve a more convenient approach
to the tumor mass, followed by autotransplantation was first performed
in the 1970s.22-24 Cases that are favorable for bench surgery
are large, hypervascular tumors located centrally in the kidney that can
affect the hilar-collecting system. Disadvantages of bench surgery include
longer operative time due to ureteral and vascular anastomosis and an
increased risk for both temporary and permanent postoperative renal failure.25
Laparoscopic
Approach for Partial Nephrectomy
In
1990, laparoscopic nephrectomy was introduced by Clayman et al.26
Since then, various authors reported on their experiences with an endoscopic
technique for total nephrectomy in patients with RCC.27,28
In 1998, Janetschek et al29 investigated whether laparoscopic
surgery is a suitable technique for partial resection of small renal malignancies.
In seven cases in which procedures could be completed as planned, neither
local recurrence nor metastases were observed during a follow-up of 7
to 35 months. The authors conclude that endoscopic partial nephrectomy
is feasible. However, it remains to be seen if future developments in
laparoscopic technology will facilitate this type of surgical approach
in order to significantly reduce the operation time.
Complications
of Partial Nephrectomy
Numerous
studies regarding nephron-sparing surgery present data on technical and
renal-related complications secondary to the operation (Table 1).30-40
Several studies support the observation that urinary fistula is the major
complication following partial nephrectomy. In a 1994 study by Campbell
et al,39 local or renal-related complications occurred in 78
(30.1%) of 258 partial nephrectomies. In a 1995 study by Polascik and
colleagues,40 complications were reported after 33 (50%) of
66 operations. In both studies, the most common complication was urinary
fistula in 15.2% and 8.9%, respectively. In the study by Campbell et al,
the incidence of fistulae was significantly less for operations performed
after 1988. However, Polascik and colleagues reported no cases of urinary
fistula occurring after 1988. They attribute the observed diminished complication
rates after 1988 to improvements in surgical technique and an increased
incidence of smaller, serendipitously discovered tumors.
| Table
1. Reported Complications Associated With Partial Nephrectomy
|
| Study |
Urinary
Fistula (%) |
Bleeding
(%)
|
Acute
Renal Failure/
Acute Hemodialysis |
Perioperative
Deaths |
Complications
Requiring
Reoperation |
| Marberger
et al, 198130 |
6.5 |
4.3 |
4.3
/ 4.3 |
2.2 |
2.2 |
| Carini
et al, 198831 |
NR |
NR |
8.2
/ 2.8 |
5.6 |
2.8 |
| Petritsch
et al, 199032 |
NR |
NR |
NR
/ 0.8 |
1.7 |
NR
|
| Morgan
and Zincke, 199033 |
3.3 |
1.1 |
NR
/ 1.1 |
2.2 |
NR |
| Provet
et al, 199134 |
NR
|
3.7 |
NR |
NR |
0.6
|
| Thrasher
et al, 19943 |
4.8 |
2.4 |
7.1
/ 2.4 |
4.8 |
2.4 |
| Campbell
et al, 199439 |
15.2 |
1.6 |
10
/ 4.9 |
0.8 |
1.6 |
| Polascik
et al, 199540 |
8.9 |
0 |
1.5
/ 0 |
1.5 |
0
|
|
NR
= not reported
From Polascik TJ, Pound CR, Meng MV, et al. Partial nephrectomy:
technique, complications, and pathological findings. J Urol.
1995;154:1312-1318. Adapted with permission. (http://lww.com)
|
If persistent
flank drainage suggests the development of a urinary cutaneous fistula,
the diagnosis can be confirmed by measuring the creatinine level of the
drainage fluid and detection of indigo carmine in the fluid following
the intravenous application of the dye. However, if the intrarenal urinary
drainage is not obstructed, the fistula will close and resolve spontaneously
after some weeks in most cases. If the drainage is inadequate, chances
are that a urinoma or abscess may develop. After insertion of a new sufficient
percutaneous flank drainage, an intravenous pyelogram or a retrograde
pyelogram should be performed to detect the cause and localization of
the obstructed drainage; this should be followed by the placement of a
ureteral stent. If this approach is impossible, the insertion of a percutaneous
nephrostomy may be performed. A second operation to close the urinary
fistula is rarely necessary.
Besides
urinary fistulae, further complications of partial nephrectomy include
hemorrhage, ureteral obstruction, and renal insufficiency. Postoperative
hemorrhage might be indicated by gross hematuria and/or a decrease in
hemoglobin and hematocrit, and it is often caused by postoperative relaxation
of angiospastic arteries. If self-tamponade occurs, which most likely
takes place in the retroperitoneal space, it might be self-limiting. However,
regularly monitoring vital signs and determining blood chemistry are required.
The patient should stay in bed, and blood transfusions should be given
if indicated. Renal angiograms may be used to localize the bleeding, and
reexploration should not be delayed if conservative measures seem to be
ineffective within the first hours after surgery.
Clots
within the renal collecting system secondary to postoperative bleeding
may cause ureteral obstruction. The obstruction can lead to urine leakage
and the development of fistulae, but most blood clots are resolved spontaneously
by urease-induced lysis. Placement of a ureteral stent may support initial
urinary drainage if the intrarenal collecting system is entirely blocked.
Postoperative
renal insufficiency results from a combination of intraoperative ischemia
and loss of functioning renal parenchyma. The extent of renal insufficiency
varies, and its degree is reflected by the increase of retention parameters
such as creatinine, blood urea, and potassium. Severe renal insufficiency
may require temporary dialysis. If the compensatory hypertrophy of the
remnant kidney tissue cannot compensate for the loss of renal function,
a permanent insufficiency requiring permanent dialysis may result. The
degree of postoperative renal insufficiency is usually mild and can be
treated with adequate transfusion and electrolyte management.
Postoperative
Follow-up
Surveillance
for recurrence of the malignancy, particularly local recurrence, is critical
in patient follow-up. Table 2 presents data from recent studies indicating
a 1.2% to 9% incidence of local recurrent malignancy.25,33,36,41-45
Surveillance for recurrence should be performed at six-month intervals
over a period of at least four years and at yearly intervals thereafter.
Surveillance includes biochemical liver and renal function studies, chest
radiographs, and abdominal ultrasound. The most accurate tool for detecting
local recurrence remains CT scanning. If local recurrence has been detected
and metastases have been ruled out, the patient may be considered for
secondary surgical treatment.46 A second partial nephrectomy
might be feasible for some patients, but if technically not possible,
Novick19 suggests that total nephrectomy with initiation of
chronic dialysis and subsequent renal allotransplantation is an alternative.
However, Zincke and Ghavamian47 cite emerging data suggesting
that the problem of local recurrence is not that of a poorly performed
surgical procedure but rather of multifocality. Multifocality seems to
be increased in the presence of papillary tumors and possibly also in
those patients who have evidence of neovascularity in their malignancies.48,49
Current data suggest that the incidence of satellite tumors is high when
the primary tumor has vascular invasion. Moreover, those results suggest
that satellite lesions are overlooked in 40% of patients who undergo partial
nephrectomy.50 Again, these data underline the importance of
careful long-term follow-up.
| Table
2. Studies Evaluating the Incidence of Local Recurrent Malignancy
|
| Study
|
Number
of Patients |
Local
Tumor Recurrence |
5-Year Cancer-Specific Survival |
| Novick
et al, 198925 |
100 |
9.0% |
Not
reported |
| Morgan
and Zincke, 199033 |
104 |
5.8% |
89% |
| Steinbach
et al, 199236 |
121 |
4.1% |
90% |
| Licht
et al, 199441 |
216 |
4.2% |
87% |
| Herr,
199942 |
70 |
1.4% |
97%* |
| Dechet
et al, 19994 |
171 |
1.2% |
99.3%** |
| Filipas
et al, 199944 |
201 |
1.9% |
98%
|
| Hafez
and Novick, 199945 |
485 |
3.2% |
92%
|
|
*
10-yr survival
** 15-yr survival
|
Long-term
Renal Function After Partial Nephrectomy
Recent
data show that patients with a remnant solitary kidney are at higher risk
for developing glomerular hyperfiltration resulting in increased risk
for proteinuria, glomerular damage, and impaired renal function.51-53
A statistically significant association was found between more proteinuria
and lesser amount of remnant renal parenchyma. Renal biopsies in patients
with moderate to severe proteinuria detected focal segmental or even global
glomerulosclerosis. The development of proteinuria is a common early indication
of structural or functional renal impairment. Thus, the postoperative
follow-up should include monitoring of 24-hour urinary protein concentration
and glomerular filtration rate. Patients presenting with proteinuria of
higher than 150 mg/day should be treated with a low-protein diet. Converting
enzyme inhibitor drugs should also be prescribed since these agents suggest
a beneficial effect on preventing glomerulopathy induced by loss of renal
parenchyma.54,55
Partial
Nephrectomy vs Radical Nephrectomy With Subsequent Treatments
Controversies
arise from the point of view that patients would receive better treatment
if they underwent radical nephrectomy with subsequent dialysis or renal
transplantation. The majority of patients receiving partial nephrectomy
are between the fifth and seventh decade of life, and few of them are
eligible for allotransplantation because of concurrent pulmonary and/or
heart diseases.56,57 In his 1983 study, Penn58 reported
an overall 32% incidence of recurrent RCC in patients who underwent dialysis
and transplantation. Only those who received an allograft after a four-year
observation period remained recurrence-free within the reported follow-up
interval. With the additional waiting period due to organ shortage, patients
after total nephrectomy likely face subsequent dialysis for a long period
of time. The five-year survival time for dialysis patients in their fifth
or sixth decade of life is only approximately 40% (Table 3 - Please see
print copy of journal for this table.).59 If the patients finally
undergo renal transplantation, 80% to 85% of them will show a functioning
graft at the end of the first year; that percentage declines to less than
60% after five years.60 These data strongly suggest that nephron-sparing
surgery is the better choice for treatment for appropriately selected
patients.
Partial
Nephrectomy for Patients Presenting With von Hippel-Lindau Disease
The
von Hippel-Lindau syndrome is the most common cause of familial renal
cancer characterized by hemangioblastomas of the central nervous system,
retinal angiomas, pheochromocytoma, epididymal cystadenomas, and pancreatic
and renal cysts and carcinomas.61-63 Because individuals affected
with this autosomal dominant hereditary disorder might develop multiple
bilateral tumors throughout their lives,64 the nephron-sparing
surgical approach to this group of patients has always been controversial.
RCC will develop in 45% of all patients with von Hippel-Lindau disease.65-67
The disease is nearly always bilateral, the presenting lesions are usually
small and frequently low grade. Furthermore, the renal cysts in von Hippel-Lindau
disease contain either frank carcinoma or a lining of hyperplastic clear
cells representing incipient cancer.68,69 Therefore, all patients
with von Hippel-Lindau disease who undergo partial nephrectomy or enucleation
for RCC should also have all other solid and cystic renal lesions excised
to ensure complete tumor removal.17
Partial nephrectomy for von Hippel-Lindau disease has been supported argumentatively
by Taylor70 and by the surgical and clinical experience of
several other authors.71-73 The latest study by Persad et al74
supports the preceding series that nephron-sparing surgery can provide
effective initial treatment for those patients. The surgery should be
accompanied by close follow-up, since most of the patients will eventually
develop local recurrent malignancies. Studies with a long-term follow-up
of patients with von Hippel-Lindau disease have shown that some patients
can remain free of renal malignancies for more than five years.66,73,75
However, other authors presented data showing development of metastasis
following partial nephrectomy.71 Walther et al72
suggest from these series that it might be possible to select patients
with fewer aggressive manifestations of renal neoplasm and who show low
grade, low stage, and smaller renal lesions. Using their own screening
criteria that focused on early localized disease and low grade, they found
that none of their patients with a lesion of 3 cm or greater developed
metastatic disease over their short-term follow-up. It remains to be seen
if the results of his long-term follow-up support the excellent long-term
survival data reported by Steinbach et al73 in 1995. They reported
5- and 10-year cancer specific survival rates of 100% and 81%, respectively.
They concluded from their data that nephron-sparing surgery, if technically
feasible, can preserve renal function for an extended interval without
compromising cancer-free survival in most patients. However, patients
treated in this manner should be advised of the importance of close postoperative
surveillance and the probable need for repeat renal surgery, since the
malignancy will recur locally in most patients. If bilateral nephrectomy
becomes necessary, the data from Steinbach et al suggest that renal transplantation
can provide satisfactory replacement therapy for end-stage renal disease
in patients with von Hippel-Lindau syndrome.
Partial
Nephrectomy for Advanced RCC
Although
data have been gathered since the early 1980s on the feasibility of nephron-sparing
surgery for advanced RCC, the indications for partial nephrectomy in those
patients are still indistinct and not well defined.
Starting
in 1981, Marberger et al30 reported on three patients with
Robson stage IV disease and four patients with lymphatic involvement who
underwent partial nephrectomy. All of the first three patients died within
the following 43 weeks, and three of the latter four patients died shortly
after surgery. Similarly, in 1986, Bazeed et al76 reported
that two patients presenting with stage IV cancer died shortly after operation.
In their 1989 study, Novick et al25 presented a 42% five-year
cancer-specific survival rate for six patients with resected metastases.
In a 1990 report from Morgan and Zincke,33 four of six patients
with stage IV disease died due to the development of metastases. Finally,
in the same year, Angermeier et al9 reviewed nine patients
with venous involvement in a solitary functioning kidney. Four patients
died of metastatic RCC, two of them additionally showing local recurrence
in the remnant kidney.
In summary,
these data suggest poor survival outcome for partial nephrectomy in patients
with advanced RCC. The limiting factor is clearly the high incidence of
recurrent malignancy.
Partial
nephrectomy for advanced RCC will probably become more significant in
the light of novel systemic therapeutic approaches to RCC, especially
adoptive immunotherapy and gene therapy.77,78
Partial
Nephrectomy for Patients With Normal Contralateral Kidney
The
decision to perform nephron-sparing surgery in patients with RCC and with
normal contralateral kidney is again driven by the desire to preserve
renal tissue, particularly in cases presenting with small, peripherally
located tumors, often incidentally detected. An increase in incidentally
detected tumors is due to the widespread use of ultrasound and CT in most
fields of clinical medicine.79,80 The majority of those incidental
tumors show a low pathologic stage.81-84 However, Novick19
notes that radical nephrectomy is still considered the definitive form
of surgical treatment due to (1) the low risk of a metachronous contralateral
RCC (1% to 2%), (2) a local tumor recurrence rate of approximately 5%
after partial nephrectomy,47-49 and (3) occasional cases of
unsuspected multicentricity that would not be treated by partial nephrectomy.
Moreover, in favor of total nephrectomy, he refers to long-term follow-up
studies on living, related kidney donors who proved a low risk of contralateral
kidney renal loss in individuals with one kidney. On the other hand, Novick
reports on several studies presenting excellent results with partial nephrectomy
for a selected group of patients. Table 4 summarizes some of the data.31-35,42-44,76,85-87
Local recurrence was reported in only one study in which two patients
were successfully treated with repeat surgical excision.85
In recent years, it has become clear that the tumor size is of great significance
for the clinical outcome of these patients.79,88 Also, it is
generally accepted that nephron-sparing surgery should be performed only
if the tumor lesion has a diameter of less than 4 cm; otherwise, total
nephrectomy is recommendable. Wunderlich and colleagues79 in
their 1998 autopsy study suggests that nephron-sparing surgery might be
advisable in patients with RCC that is 2-cm or less in diameter if there
is an imperative indication in cases of RCC larger than 2 cm. However,
the establishment of the benchmark of 4 cm has led to a recent proposal
to subdivide the 1997 TNM staging criteria for T1 lesions into T1a (less
than 4 cm) and T1b (greater than 4 cm).50
| Table
4. Outcomes in Selected Studies on Partial Nephrectomy
|
| Study |
Number
of
Patients |
Disease-
Specific
Survival (%) |
Mean
Follow-up
(mos) |
Mean
Tumor Size
(cm)* |
Local
Tumor
Recurrence
(%) |
| Bazeed
et al, 198676 |
23 |
100 |
35 |
8
3 |
.3
0 |
| Carini
et al, 198831 |
10 |
90 |
29 |
9
3 |
5
0 |
| Brisset
et al, 198986 |
15 |
100 |
40 |
3.0
- 5.5 |
0
|
| Morgan
and Zincke, 199033 |
20 |
100 |
45.6 |
3.1 |
0 |
| Petritsch
et al, 199032 |
52 |
96 |
60 |
NR
|
NR
|
| Van
Poppel et al, 199135 |
21 |
95 |
41.2 |
3.2 |
0 |
| Selli
et al, 199187 |
20 |
90 |
2
- 31 |
<3.5 |
0 |
| Provet
at al, 199134 |
19 |
100 |
35 |
2.6 |
0
|
| Steinbach
et al, 199185 |
61 |
90 |
36 |
3.2 |
3.3 |
| Herr,
199942 |
70 |
97 |
10
yrs |
3.0 |
1.4
|
| Dechet
et al, 199943 |
171 |
99.3 |
5.6
yrs |
2.6 |
1.2
|
| Filipas
et al, 199944 |
201 |
98 |
4.2
yrs |
3.3 |
1.9 |
|
NR
= not reported
From Licht MR, Novick AC. Nephron sparing surgery for renal cell
carcinoma. J Urol. 1993;149:1-7. Updated with permission.
(http://lww.com)
|
Partial
Nephrectomy for Patients With Synchronous Bilateral RCC
In
1952, Krumbach and Ansell89 reported for the first time a partial
and radical nephrectomy for synchronous bilateral RCC without metastatic
lesions. Generally, the intent is to preserve the highest possible amount
of renal parenchyma for patients presenting with bilateral synchronous
malignancies. Total nephrectomy with subsequent separate contralateral
partial nephrectomy should be performed only if one kidney is extensively
affected by RCC. On the other hand, if the patient presents with a very
low tumor burden on one side, a bilateral surgical approach may be performed
in one operating session, thus reducing perioperative risks and mortality.
In all other cases of synchronous bilateral RCC, the kidney that is less
tumor-burdened should be removed first.14
The
UCLA Experience on Partial Nephrectomy for Renal Cell Cancer
We
recently reviewed our experience with nephron-sparing surgery vs radical
nephrectomy from 1987 to 1998 and evaluated the efficacy of all partial
nephrectomies performed during that time period (Fig 1).90
A total of 163 patients undergoing nephron-sparing surgery were matched
with 125 patients undergoing radical nephrectomy (Table 5). Patients were
followed for a period of 10 to 160 months (mean follow-up time of 74 months)
during which tumor recurrence, metastasis, and patient deaths were recorded.
 |
| Fig
1. Number of patients who had a partial nephrectomy from 1987
to 1998: UCLA experience. |
| Table
5. Patient Characteristics and Outcomes: Partial vs Radical
Nephrectomy |
| |
Partial
Nephrectomy |
Radical
Nephrectomy |
| Number
of Patients |
163
|
125
|
| Median
Age (range |
62.4
(34-86)
|
61.5 (32-81)
|
| Men/Women
(%) |
54
/ 46
|
60 / 40
|
| Category: |
T1* |
132
(81%)
|
79
(63.2%)
|
| |
T2* |
18
(11%
|
30
(24%)
|
| |
T3* |
12
(7.4%)
|
16
(12.8%)
|
| |
T4* |
(0.6%)
|
0
|
| Medium
Months Follow-up (range) |
57
(10-160
|
55
(12-113)
|
| Cancer-Specific
Survival Rate (%) |
98
|
91.2
|
|
*
Based on 1997 TNM classification.
|
Twenty patients in
the partial nephrectomy arm died. Two patients died of an acute myocardial
infarction one day postoperatively, and one patient died of pneumonia
five days postoperatively. Seven patients died free of disease. Of the
10 cancer deaths, seven were secondary to metastatic disease and three
were due to local recurrence. The overall crude survival rate of patients
treated with nephron-sparing surgery was 92%, and the disease-free survival
rate was 98%.
The
overall cancer-specific survival rate of patients treated with radical
nephrectomy was 91.2% vs 98% for partial nephrectomies performed during
the same time period. The survival rate of patients undergoing radical
nephrectomy for T1 RCC was 100% based on the 1997 TNM staging system.
The Kaplan-Meier cancer-specific survival curves in Figs 2 and 3 are based
on the 1997 staging system. There was no statistical difference in survival
in patients with T1 lesions who were treated with partial or radical nephrectomy
(P=0.219).
 |
| Fig
2. Kaplan-Meier disease-specific survival plots by 1997 TNM
staging classification for patients who had a partial vs radical nephrectomy
from 1987 to 1997 (operative deaths excluded in each group). |
 |
| Fig
3. Kaplan-Meier survival plots method by 1997 TNM staging classification.
There was a difference in survival between T2-3 patients with partial
nephrectomy and any other T1. |
In contrast, the survival
rates of patients who underwent radical nephrectomy with T2-3 RCC lesions
were 91.4% compared with 66% of patients who underwent partial nephrectomy.
Survival of patients with RCC lesions greater than T1 receiving partial
nephrectomy was significantly lower than survival of patients with lesions
greater than T1 receiving radical nephrectomies as well as those with
T1 lesions receiving either type of surgery (P=0.001) (Fig 3).
Our
data indicate and underscore that radical nephrectomy and nephron-sparing
surgery provide equally effective curative treatment for patients who
present with a single, small, clearly localized RCC (T1 tumors). Following
nephron-sparing surgery for localized RCC, cancer-free survival is significantly
better in patients with tumors less than 4 cm in size compared to patients
with larger tumors. The results of partial nephrectomy are less satisfactory
in patients with greater than T1 tumors.
Conclusions
Partial
nephrectomy provides effective therapy for patients presenting with RCC
and thus has been established as an accepted therapeutic approach and
surgical procedure. However, its future importance as a therapeutic option
for the control of localized kidney tumor depends on the use of the appropriate
diagnostic inventory that leads to the correct indication and proper patient
selection. Moreover, surgical skills and operative detail will affect
postoperative complications and tumor recurrence.
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From the Department
of Urology at the University of California, Los Angeles School of Medicine,
Los Angeles, Calif.
Address
reprint requests to Arie S. Belldegrun, MD, UCLA School of Medicine, Department
of Urology, 10833 Le Conte Avenue, Room 66-118CHS, Box 951738, Los Angeles,
CA 90095-1738.
No
significant relationship exists between the authors and the companies/organizations
whose products or services may be referenced in this article.
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