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CASE/ DIAGNOSIS:43-year old female with recently diagnosed stage IIIB endometrioid adenocarcinoma of the right ovary


MDExpert - Assessment and Recommendations

Disclaimer: This opinion is based solely on my review of those medical records provided to MDExpert by the treating physician. I have not examined the patient nor is it my present intent to do so in the future. Those opinions to be rendered herein are intended for advisory purposes only. It is within the sole discretion of the treating physician to determine the course, scope, and extent of treatment. It is expressly agreed and understood that my review of those records provided and the rendering of any opinion based upon my review of those records provided do not create a physician/patient relationship.

MDEXPERT TREATMENT RECOMMENDATION AND RATIONALE

This young woman with stage IIIB ovarian cancer has attained a clinically defined complete response following standard platinum/paclitaxel based chemotherapy.  While this is gratifying, it is by no means uncommon in the subgroup of patients with minimal disease following completion of initial surgery.  Her chance of future recurrence is not small, and probably exceeds 70%.  Unfortunately, at the present time, additional therapy for patients in remission has not been proven to substantially influence survival.  The proposed clinical trial of 3 vs. 12 months of Taxol is an ongoing GOG/SWOG study and has been accruing patients since November 1999.  No survival data is available for the over 200 patients who have been enrolled to date.  I believe the rationale behind this study is sound, and would strongly encourage the patient to participate in this study. 

ADDITIONAL INFORMATION OR TESTING THAT WILL FACILITATE OR IMPROVE TREATMENT DECISION-MAKING:

Does the patient have any significant neuropathy?  Taxol, in the doses used in the study being contemplated, could exacerbate preexisting neuropathy.  If the patient has neuropathy greater than grade 1, I would defer further Taxol.

TREATMENT ALTERNATIVES AND THE ADVANTAGES OR DISADVANTAGES OF EACH:

The patient could consider a second look laparotomy, with further treatment being based on the status of disease noted at surgery.  While this remains a popular option with some gynecologic oncologists, second look surgeries have yet to be shown to influence survival.  The potential benefit of a second look is that if minimal or microscopic disease is found further therapy can be given with the knowledge that cancer is indeed still present.   Based upon my experience, in patients with Stage IIIB tumors who have undergone optimal cytoreductive surgery, and who have rapid normalization of CA-125 following institution of chemotherapy, the likelihood of detecting residual disease at second look is probably only about 25%.  I believe a small proportion of these patients can be cured by additional chemotherapy.  Intraperitoneal based treatment as well as high dose chemotherapy with stem cell support are reasonable options to explore in this subgroup.  Nevertheless, I do not believe that second look surgery is standard of care anymore, and the efficacy of high dose chemotherapy or intraperitoneal chemotherapy in patients with a positive second look have not been proven to influence cure rates.

Aside from GOG study 178, I am unaware of any other clinical trials for patients felt to be in remission following initial chemotherapy for epithelial ovarian cancer.  In the absence of an NIH approved clinical trial, I would not favor further cytotoxic chemotherapy in this patient (unless a second look surgery documents the persistence of disease).

Finally, this patient should be aware that PET scanning has been touted as being a more sensitive test that CT scan as a means of detecting residual ovarian cancer.  This opinion is not universally endorsed, and both false positive and false negative results have been reported.  For this reason, if she should contemplate having a PET scan, I would favor confirming a positive result surgically, which can often be done laparoscopically.

ARE THERE ANY CLINICAL TRIALS THAT YOU ARE AWARE OF, AND WOULD SPECIFICALLY RECOMMEND FOR THIS PATIENT:

Other than GOG 178, no.

ADDITIONAL SPECIFIC QUESTIONS FROM THE PATIENT/PATIENT’S FAMILY:

Please assess the value for this patient in participating in a study of maintenance Taxol after having completed 6 cycles of carboplatin-taxol.

This is a very reasonable study.  While toxicity will not be minimal, I would expect most patients should be able to tolerate Taxol, in the doses prescribed, with manageable side effects.  Quality of life is important, and it should be emphasized to the patient that, if she begins maintenance Taxol, she can withdraw from the study at any point if she feels the risks outweigh the benefits.

SHOULD THE PATIENT’S SIBLINGS OR CHILDREN BE CONCERNED ABOUT GENETIC RISK FACTORS:

I do not believe so.  First, the patient has no children.  Even though the patient was diagnosed at an age younger than most women with ovarian cancer, the family history presented does not suggest to me that the likelihood of her carrying a BRCA1 or 2 mutation is much greater than 10%.  Accordingly, the risk that her brother would carry a BRCA mutation would probably be less than 5%, and his children (if any) would have a similarly small risk.

PROGNOSIS:

Guarded, but cure is clearly possible in this case.  If the disease recurs, chance of cure diminishes drastically.  Odds favor her being alive 5 years from now, though many patients with stage IIIB ovarian cancer alive at 5 years will unfortunately have or develop recurrent disease.

By: Steven Waggoner, M.D.

University of Chicago Cancer Research Center

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