
     Of all gynecologic malignancies, ovarian cancer continues to have the
 highest mortality and is the most difficult to diagnose.  In the United States
 female population, ovarian cancer ranks fifth in absolute mortality among 
 cancer related deaths (13,000/yr).  In most reported cases, ovarian cancer, 
 when first diagnosed is in stages III or IV in about 60 to 70% of patients 
 which further complicates treatment of the disease (Barber, 3).     
 
         Early detection in ovarian cancer is hampered by the lack of appropriate 
 tumor markers and clinically, most patients fail to develop significant
 symptoms until they reach advanced stage disease.  The characteristics 
 of ovarian cancer have been studied in primary tumors and in established 
 ovarian tumor cell lines which provide a reproducible source of tumor material.  
 Among the major clinical problems of ovarian cancer, malignant progression,
 rapid emergence of drug resistance, and associated cross-resistance remain 
 unresolved.  Ovarian cancer has a high frequency of metastasis yet generally 
 remains localized within the peritoneal cavity.  Tumor development has been
 associated with aberrant, dysfunctional expression and/or mutation of
 various genes.  This can include oncogene overexpression, amplification or 
 mutation, aberrant tumor suppressor expression or mutation.  Also, subversion 
 of host antitumor immune responses may play a role in the pathogenesis of 
 cancer (Sharp, 77).  
 
         Ovarian clear cell adenocarcinoma was first described by Peham in 1899 as
 "hypernephroma of the ovary" because of its resemblance to renal cell carcinoma.  
 By 1939, Schiller noted a histologic similarity to mesonephric tubules and
 classified these tumors as "mesonephromas."   In 1944, Saphir and Lackner described 
 two cases of "hypernephroid carcinoma of the ovary" and proposed "clear cell"
 adenocarcinoma as an alternative term.  Clear cell tumors of the ovary are now 
 generally considered to be of mullerian and in the genital tract of mullerian origin.  
 A number of examples of clear cell adenocarcinoma have been reported to arise 
 from the epithelium of an endometriotic cyst (Yoonessi, 289).  Occasionally, a renal 
 cell carcinoma metastasizes to the ovary and may be confused with a primary clear 
 cell adenocarcinoma.   
 
         Ovarian clear cell adenocarcinoma (OCCA) has been recognized as a distinct
 histologic entity in the World Health Organization (WHO) classification of ovarian
 tumors since 1973 and is the most lethal ovarian neoplasm  with an overall five year
 survival of only 34% (Kennedy, 342).  Clear cell adenocarcinoma, like most ovarian
 cancers, originates from the ovarian epithelium which is a single layer of cells found on
 the surface of the ovary.   Patients with ovarian clear cell adenocarcinoma are typically
 above the age of 30 with a median of 54 which is similar to that of ovarian epithelial
 cancer in general.  OCCA represents approximately 6% of ovarian cancers and bilateral
 ovarian involvement occurs in less that 50% of patients even in advanced cases.
 
         The association of OCCA and endometriosis is well documented (De La Cuesta,
 243).  This was confirmed by Kennedy et al who encountered histologic or intraoperative 
 evidence of endometriosis in 45% of their study patients.  Transformation
 from endometriosis to clear cell adenocarcinoma has been previously demonstrated in
 sporadic cases but was not observed by Kennedy et al.  Hypercalcemia occurs in a
 significant percentage of patients with OCCA.  Patients with advanced disease are more
 typically affected than patients with nonmetastatic disease.  Patients with OCCA are also
 more likely to have Stage I disease than are patients with ovarian epithelial cancer in
 general (Kennedy, 348).
 
         Histologic grade has been useful as an initial prognostic determinant in some studies
 of epithelial cancers of the ovary.  The grading of ovarian clear cell adenocarcinoma has
 been problematic and is complicated by the multiplicity of histologic patterns found in
 the same tumor.  Similar problems have been found in attempted grading of clear cell
 adenocarcinoma of the endometrium (Disaia, 176).  Despite these problems, tumor
 grading has been attempted but has failed to demonstrate prognostic significance. 
 However, collected data suggest that low mitotic activity and a predominance of clear
 cells may be favorable histologic features (Piver, 136).
 
         Risk factors for OCCA and ovarian cancer in general are much less clear than for
 other genital tumors with general agreement on two risk factors: nulliparity and family
 history.  There is a higher frequency of carcinoma in unmarried women and in married
 women with low parity.  Gonadal dysgenesis in children is associated with a higher risk
 of developing ovarian cancer while oral contraceptives are associated with a decreased
 risk.  Genetic and candidate host genes may be altered in susceptible families.  Among
 those currently under investigation is BRCA1 which has been associated with an
 increased susceptibility to breast cancer.  Approximately 30% of ovarian adenocarcinomas 
 express high levels of HER-2/neu oncogene which correlates with a poor prognosis 
 (Altcheck, 375-376).  Mutations in host tumor suppresser gene p53 are found in 50% of 
 ovarian carcinomas.  There also appears to be a racial predilection, as the vast majority 
 of cases are seen in Caucasians (Yoonessi, 295). 
 
      Considerable variation exists in the gross appearance of ovarian clear cell
 adenocarcinomas and they are generally indistinguishable from other epithelial ovarian
 carcinomas.  They could be cystic, solid, soft, or rubbery, and may also contain
 hemorrhagic and mucinous areas (O'Donnell, 250).  Microscopically, clear cell
 carcinomas are characterized by the presence of variable proportions of clear and hobnail
 cells.  The former contain abundant clear cytoplasm with often centrally located nuclei,
 while the latter show clear or pink cytoplasm and bizarre basal nuclei with atypical
 cytoplasmic intraluminal projections.  The cellular arrangement may be tubulo acinar,
 papillary, or solid, with the great majority displaying a mixture of these patterns.  The
 hobnail and clear cells predominate with tubular and solid forms, respectively (Barber,
 214).  
 
         Clear cell adenocarcinoma tissue fixed with alcohol shows a high cytoplasmic
 glycogen content which can be shown by means of special staining techniques. 
 Abundant extracellular and rare intracellular neutral mucin mixed with sulfate and
 carboxyl group is usually present.  The clear cells are recognized histochemically and
 ultrastructurally (short and blunt microvilli, intercellular tight junctions and desmosomes,
 free ribosomes, and lamellar endoplasmic reticulum).  The ultrastructure of hobnail and
 clear cells resemble those of the similar cells seen in clear cell carcinomas of the
 remainder of the female genital tract (O'Brien, 254).  A variation in patterns of histology
 is seen among these tumors and frequently within the same one.
 
         Whether both tubular components with hobnail cells and the solid part with clear cells
 are required to establish a diagnosis or the presence of just one of the patterns is
 sufficient has not been clearly established.  Fortunately, most tumors exhibit a mixture of
 these components.  Benign and borderline counterparts of clear cell ovarian
 adenocarcinomas are theoretical possibilities.  Yoonessi et al reported that nodal
 metastases could be found even when the disease appears to be grossly limited to the
 pelvis (Yoonessi, 296).  Examination of retroperitoneal nodes is essential to allow for
 more factual staging and carefully planned adjuvant therapy.
 
         Surgery remains the backbone of treatment and generally consists of removal of the
 uterus, tubes and ovaries, possible partial omentectomy, and nodal biopsies.  The
 effectiveness and value of adjuvant radiotherapy and chemotherapy has not been clearly
 demonstrated.  Therefore, in patients with unilateral encapsulated lesions and
 histologically proven uninvolvement of the contralateral ovary, omentum, and biopsied
 nodes, a case can be made for (a)no adjuvant therapy after complete surgical removal
 and (b) removal of only the diseased ovary in an occasional patient who may be young
 and desirous of preserving her reproductive capacity (Altchek, 97).  In the more adv-
 anced stages, removal of the uterus, ovaries, omentum, and as much tumor as possible
 followed by pelvic radiotherapy (if residual disease is limited to the pelvis) or
 chemotherapy must be considered.  The chemotherapeutic regimens generally involve
 adriamycin, alkylating agents, and cisPlatinum containing combinations (Barber, 442).
 
         OCCA is of epithelial origin and often contains mixtures of other epithelial tumors
 such as serous, mucinous, and endometrioid.  Clear cell adenocarcinoma is characterized
 by large epithelial cells with abundant cytoplasm.  Because these tumors sometimes
 occur in association with endometriosis or endometrioid carcinoma of the ovary and
 resemble clear cell carcinoma of the endometrium, they are now thought to be of
 mullerian duct origin and variants of endometrioid adenocarcinoma.  Clear cell tumors of
 the ovary can be predominantly solid or cystic.  In the solid neoplasm, the clear cells are
 arranged in sheets or tubules.  In the cystic form, the neoplastic cells line the spaces. 
 Five-year survival is approximately 50% when these tumors are confined to the ovaries,
 but these tumors tend to be aggressive and spread beyond the ovary which tends to make
 5-year survival highly unlikely (Altchek, 416).
 
                 Some debate continues as to whether clear cell or mesonephroid carcinoma is a
 separate clinicopathological entity with its own distinctive biologic behavior and natural
 history or a histologic variant of endometrioid carcinoma.  In an effort to characterize
 clear cell adenocarcinoma, Jenison et al compared these tumors to the most common of
 the epithelial malignancies, the serous adenocarcinoma (SA).  Histologically determined
 endometriosis was strikingly more common among patients with OCCA than with SA. 
 Other observations by Jenison et al suggest that the biologic behavior of clear cell
 adenocarcinoma differs from that of SA.  They found Stage I tumors in 50% of the
 observed patient population as well as a lower incidence of bilaterality in OCCA
 (Jenison, 67-69).  Additionally, it appears that OCCA is characteristically larger than
 SA, possibly explaining the greater frequency of symptoms and signs at presentation.  
 
 Risk Factors
         There is controversy regarding talc use causing ovarian cancer.  Until recently, most
 talc powders were contaminated with asbestos.  Conceptually, talcum powder on the
 perineum could reach the ovaries by absorption through the cervix or vagina.  Since
 talcum powders are no longer contaminated with asbestos, the risk is probably no longer
 important (Barber, 200).  The high fat content of whole milk, butter, and meat products
 has been implicated with an increased risk for ovarian cancer in general. 
  
         The Centers for Disease Control compared 546 women with ovarian cancer to 4,228
 controls and reported that for women 20 to 54 years of age, the use of oral
 contraceptives reduced the risk of ovarian cancer by 40% and the risk of ovarian cancer
 decreased as the duration of oral contraceptive use increased.  Even the use of oral
 contraceptives for three months decreased the risk.  The protective effect of oral
 contraceptives is to reduce the relative risk to 0.6 or to decrease the incidence of disease
 by 40%.  There is a decreased risk as high as 40% for women who have had four or
 more children as compared to nulliparous women.  There is an increase in the incidence
 of ovarian cancer among nulliparous women and a decrease with increasing parity.  The
 "incessant ovulation theory" proposes that continuous ovulation causes repeated trauma
 to the ovary leading to the development of ovarian cancer.  Incidentally, having two or
 more abortions compared to never having had an abortion decreases one's risk of
 developing ovarian cancer by 30% (Coppleson, 25-28).
         
  Etiology
         It is commonly accepted that cancer results from a series of genetic alterations that
 disrupt normal cellular growth and differentiation.  It has been proposed that genetic
 changes causing cancer occur in two categories of normal cellular genes, proto-
 oncogenes and tumor suppressor genes.  Genetic changes in proto-oncogenes facilitate
 the transformation of a normal cell to a malignant cell by production of an altered or
 overexpressed gene product.  Such genetic changes include mutation, translocation, or
 amplification of proto-oncogenes  Tumor suppressor genes are proposed to prevent
 cancer.  Inactivation or loss of these genes contributes to development of cancer by the
 lack of a functional gene product.  This may require mutations in both alleles of a tumor
 suppressor gene.  These genes function as regulatory inhibitors of cell proliferation, such
 as a DNA transcription factor, or a cell adhesion molecule.  Loss of these functions
 could result in abnormal cell division or gene expression, or increased ability of cells in
 tissues to detach.  Cancer such as OCCA most likely results from the dynamic interaction
 of several genetically altered proto-oncogenes and tumor suppressor genes (Piver, 64-
 67).
 
         Until recently, there was little evidence that the origin of ovarian was genetic.  Before
 1970, familial ovarian cancer had been reported in only five families.  A familial cancer
 registry was established at Roswell Park Cancer Institute in 1981 to document the
 number of cases occurring in the United States and to study the mode of inheritance.  If
 a genetic autosomal dominant transmission of the disease can be established, counseling
 for prophylactic oophorectomy at an appropriate age may lead to a decrease in the death
 rate from ovarian cancer in such families. 
 
         The registry at Roswell Park reported 201 cases of ovarian cancer in 94 families in
 1984.  From 1981 through 1991, 820 families and 2946 cases had been observed. 
 Familial ovarian cancer is not a rare occurrence and may account for 2 to 5% of all cases
 of ovarian cancer.  Three conditions that are associated with familial ovarian cancer are
 (1) site specific, the most common form, which is restricted to ovarian cancer, and (2)
 breast/ovarian cancer with clustering of ovarian and breast cases in extended pedigrees
 (Altchek, 229-230). One characteristic of inherited ovarian cancer is that it occurs at a
 significantly younger age than the non-inherited form.  
 
         Cytogenetic investigations of sporadic (non-inherited) ovarian tumors have revealed
 frequent alterations of chromosomes 1,3,6, and 11.  Many proto-oncogenes have been
 mapped to these chromosomes, and deletions of segments of chromosomes (particularly
 3p and 6q) in some tumors is consistent with a role for loss of tumor suppressor genes. 
 Recently, a genetic linkage study of familial breast/ovary cancer suggested linkage of
 disease susceptibility with the RH blood group locus on chromosome 1p.  
 
         Allele loss involving chromosomes 3p and 6q as well as chromosomes 11p, 13q, and 
 17 have been frequently observed in ovarian cancers.  Besides allele loss, point mutations
 have been identified in the tumor suppressor gene p53 located on chromosome17p13. 
 Deletions of chromosome 17q have been reported in sporadic ovarian tumors suggesting
 a general involvement of this region in ovarian tumor biology.  Allelic loss of MYB and
 ESR genes map on chromosome 6q near the provisional locus for FUCA2, the locus for
 a-L-fucosidase in serum.  Low activity of a-L-fucosidase in serum is more prevalent in
 ovarian cancer patients.  This suggests that deficiency of a-L-fucosidase activity in serum
 may be a hereditary condition associated with increased risk for developing ovarian
 cancer.  This together with cytogenetic data of losses of 6q and the allelic losses at 6q
 point to the potential importance of chromosome 6q in hereditary ovarian cancer
 (Altchek, 208-212).
 
         Activation of normal proto-oncogenes by either mutation, translocation, or gene
 amplification to produce altered or overexpressed products is believed to play an
 important role in the development of ovarian tumors.  Activation of several proto-
 oncogenes (particularly K-RAS, H-RAS, c-MYC, and HER-2/neu) occurs in ovarian
 tumors.  However, the significance remains to be determined.  It is controversial as to
 whether overexpression of the HER-2/neu gene in ovarian cancer is associated with poor
 prognosis.  In addition to studying proto-oncogenes in tumors, it may be beneficial to
 investigate proto-oncogenes in germ-line DNA from members of families with histories
 of ovarian cancer (Barber, 323-324).  It is questionable whether inheritance or rare
 alleles of the H-RAS proto-oncogene may be linked to susceptibility to ovarian cancers.
         
 Diagnosis and Treatment
         The early diagnosis of ovarian cancer is a matter of chance and not a triumph of
 scientific approach.  In most cases, the finding of a pelvic mass is the only available
 method of diagnosis, with the exception of functioning tumors which may manifest
 endocrine even with minimal ovarian enlargement.  Symptomatology includes vague
 abdominal discomfort, dyspepsia, increased flatulence, sense of bloating, particularly
 after ingesting food, mild digestive disturbances, and pelvic unrest which may be present
 for several months before diagnosis (Sharp, 161-163).
 
         There are a great number of imaging techniques that are available.  Ultrasounds,
 particularly vaginal ultrasound, has increased the rate of pick-up of early lesions,
 particularly when the color Doppler method is used.  Unfortunately, vaginal sonography
 and CA 125 have had an increasing number of false positive examinations.  Pelvic
 findings are often minimal and not helpful in making a diagnosis.  However, combined
 with a high index of suspicion, this may alert the physician to the diagnosis.
 
 These pelvic signs include:
         Mass in the ovarian area
         Relative immobility due to fixation of adhesions
         Irregularity of the tumor
         Shotty consistency with increased firmness
         Tumors in the cul-de-sac described as a handful of knuckles
         Relative insensitivity of the mass
         Increasing size under  observation
         Bilaterality (70% for ovarian carcinoma versus 5% for benign cases) (Barber, 136)
 
         Tumor markers have been particularly useful in monitoring treatment, however, the
 markers have and will probably  always have a disadvantage in identifying an early
 tumor.  To date, only two, human gonadotropin (HCG) and alpha fetoprotein, are
 known to be sensitive and specific.  The problem with tumor markers as a means of
 making a diagnosis is that a tumor marker is developed from a certain volume of tumor. 
 By that time it is no longer an early but rather a biologically late tumor (Altchek, 292). 
 
         Many reports have described murine monoclonal antibodies (MAbs) as potential tools
 for diagnosing malignant ovarian tumors.  Yamada et al attempted to develop a MAb
 that can differentiate cells with early malignant change from adjacent benign tumor cells
 in cases of borderline malignancy.  They developed MAb 12C3 by immunizing mice with
 a cell line derived from a human ovarian tumor.  The antibody reacted with human
 ovarian carcinomas rather than with germ cell tumors.  MAb 12C3 stained 67.7% of
 ovarian epithelial malignancies, but exhibited an extremely low reactivity with other
 malignancies.  MAb 12C3 detected a novel antigen whose distribution in normal tissue is
 restricted.  According to Yamada et al, MAb 12C3 will serve as a powerful new tool for
 the histologic detection of early malignant changes in borderline epithelial neoplasms. 
 MAb 12C3 may also be useful as a targeting agent for cancer chemotherapy (Yamada,
 293-294).
 
         Currently there are several serum markers that are available to help make a diagnosis. 
 These include CA 125, CEA, DNB/70K, LASA-P, and serum inhibin.  Recently the
 urinary gonadotropin peptide (UCP) and the collagen-stimulating factor have been
 added.  Although the tumor markers have a low specificity and sensitivity, they are often
 used in screening for ovarian cancer.  A new tumor marker CA125-2 has greater
 specificity than CA125.  In general, tumor markers have a very limited role in screening
 for ovarian cancer.  
 
         The common epithelial cancer of the ovary is unique in killing the patient while being,
 in the vast majority of the cases, enclosed in the anatomical area where it initially
 developed: the peritoneal cavity.  Even with early localized cancer, lymph node
 metastases are not rare in the pelvic or aortic areas.  In most of the cases, death is due to
 intraperitoneal proliferation, ascites, protein loss and cachexia.  The concept of
 debulking or cytoreductive surgery is currently the dominant concept in treatment.
 
         The first goal in debulking surgery is inhibition of debulking surgery is inhibition of
 the vicious cycle of malnutrition, nausea, vomiting, and dyspepsia commonly found in
 patients with mid to advanced stage disease.  Cytoreductive surgery enhances the
 efficiency of chemotherapy as the survival curve of the patients whose largest residual
 mass size was, after surgery, below the 1.5 cm limit is the same as the curve of the
 patients whose largest metastatic lesions were below the 1.5 cm limit at the outset
 (Altchek, 422-424).
 
         The aggressiveness of the debulking surgery is a key question surgeons must face
 when treating ovarian cancers.  The debulking of very large metastatic masses makes no
 sense from the oncologic perspective.  As for extrapelvic masses the debulking, even if
 more acceptable, remains full of danger and exposes the patient to a heavy handicap. 
 For these reasons the extra-genital resections have to be limited to lymphadenectomy,
 omentectomy, pelvic abdominal peritoneal resections and rectosigmoid junction
 resection.  That means that stages IIB and IIC and stages IIIA and IIB are the only true
 indications for extrapelvic cytoreductive surgery.  Colectomy, ileectomy, splenectomy,
 segmental hepatectomy are only exceptionally indicated if they allow one to perform a
 real optimal resection. The standard cytoreductive surgery is the total hysterectomy with
 bilateral salpingoophorectomy.  This surgery may be done with aortic and pelvic lymph
 node sampling, omentectomy, and, if necessary, resection of the rectosigmoidal junction
 (Barber. 182-183).
 
         The concept of administering drugs directly into the peritoneal cavity as therapy of
 ovarian cancer was attempted more than three decades ago.  However, it has only been
 within the last ten years that a firm basis for this method of drug delivery has become
 established.  The essential goal is to expose the tumor to higher concentrations of drug
 for longer periods of time than is possible with systemic drug delivery.  Several agents
 have been examined for their efficacy, safety and pharmacokinetic advantage when
 administered via the peritoneal route. 
 
         Cisplatin has undergone the most extensive evaluation for regional delivery.  Cisplatin
 reaches the systemic compartment in significant concentrations when it is administered
 intraperitoneally.  The dose limiting toxicity of intraperitoneally administered cisplatin is
 nephrotoxicity, neurotoxicity and emesis.  The depth of penetration of cisplatin into the
 peritoneal lining and tumor following regional delivery is only 1 to 2 mm from the
 surface which limits its efficacy.  Thus, the only patients with ovarian cancer who would
 likely benefit would be those with very small residual tumor volumes.  Overall,
 approximately 30 to 40% of patients with small volume residual ovarian cancer have
 been shown to demonstrate an objective clinical response to cisplatin-based locally
 administered therapy with 20 to 30% of patients achieving a surgically documented
 complete response.  As a general rule, patients whose tumors have demonstrated an
 inherent resistance to cisplatin following systemic therapy are not considered for
 treatment with platinum-based intraperitoneal therapy (Altchek, 444-446).
 
         In patients with small volume residual disease at the time of second look laparotomy,
 who have demonstrated inherent resistance to platinum-based regimens, alternative
 intraperitoneal treatment programs can be considered.  Other agents include
 mitoxantrone, and recombinant alpha-interpheron.  Intraperitoneal mitoxanthone has
 been shown to have definite activity in small volume residual platinum-refractory ovarian
 cancer.  Unfortunately, the dose limiting toxicity of the agent is abdominal pain and
 adhesion formation, possibly leading to bowel obstruction.  Recent data suggests the
 local toxicity of  mitoxanthone can be decreased considerably by delivering the agent in
 microdoses.  
 
         Ovarian tumors may have either intrinsic or acquired drug resistance.  Many
 mechanisms of drug resistance have been described.  Expression of the MDR1 gene that
 encodes the drug efflux protein known as p-glycoprotein, has been shown to confer the
 characteristic multi-drug resistance to clones of some cancers.  The most widely
 considered definition of platinum response is response to first-line platinum treatment
 and disease free interval.  Primary platinum resistance may be defined as any progression
 on treatment.  Secondary platinum resistance is the absence of progression on primary
 platinum-based therapy but progression at the time of platinum retreatment for relapse
 (Sharp, 205-207).
 
         Second-line chemotherapy for recurrent ovarian cancer is dependent on preferences of
 both the patient and physician.  Retreatment with platinum therapy appears to offer
 significant opportunity for clinical response and palliation but relatively little hope for
 long-term cure.  Paclitaxel (trade name: Taxol), a prototype of the taxanes, is cytotoxic
 to ovarian cancer.  Approximately 20% of platinum failures respond to standard doses of
 paclitaxel.  Studies are in progress of dose intensification and intraperitoneal
 administration (Barber, 227-228).  This class of drugs is now thought to represent an
 active addition to the platinum analogs, either as primary therapy, in combination with
 platinum, or as salvage therapy after failure of platinum. 
 
         In advanced stages, there is suggestive evidence of partial responsiveness of OCCA to
 radiation as well as cchemotherapy, adriamycin, cytoxan, and cisPlatinum-containing
 combinations (Yoonessi, 295).  Radiation techniques include intraperitoneal radioactive
 gold or chromium phosphate and external beam therapy to the abdomen and pelvis.  The
 role of radiation therapy in treatment of ovarian canver has diminished in prominence as
 the spread pattern of ovarian cancer and the normal tissue bed involved in the treatment
 of this neoplasm make effective radiation therapy difficult.  When the residual disease
 after laparotomy is bulky, radiation therapy is particularly ineffective.  If  postoperative
 radiation is prescribed for a patient, it is important that theentire abdomen and pelvis are
 optimally treated to elicit a response from the tumor (Sharp, 278-280).
 
         In the last few decades, the aggressive attempt to optimize the treatment of
 ovarian clear cell adenocarcinoma and ovarian cancer in general has seen remarkable
 improvements in the response rates of patients with advanced stage cancer without
 dramatically improving long-term survival.  The promises of new drugs with activity
 when platinum agents fail is encouraging and fosters hope that, in the decades to come,
 the endeavors of surgical and pharmacoogical research will make ovarian cancer an
 easily treatable disease.
 
 
 
 
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 Current Clinical Trials Oncology.  (1996).  Green Brook, NJ:  Pyros Education.
 
 De La Cuesta, R., & Eichorn, J.  (1996). Histologic transformation of benign
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 Kennedy, A., & Biscotti, C.  (1993). Histologic correlates of progression-free interval and
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 O'Brien, M., Schofield, J., & Tan, S.  (1993). Clear cell epithelial ovarian cancer: Bad
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 Piver, S. (Ed.).  (1987). Ovarian Malignancies.  New York:  Churchill Livingstone.
 
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 Yamada, K., & Kiyoshi, O.  (1995). Monoclonal antibody, Mab 12C3, is a sensitive                       
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