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Home » Gynecologic Cancers

ONCOLOGY. Vol. 22 No. 10
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Areas of Confusion in Oncology 

What Is the Role of Neoadjuvant Chemotherapy in the Management of Ovarian Cancer?

By Peter E. Schwartz, MD
John Slade Ely Professor of
Obstetrics, Gynecology and
Reproductive Sciences
Yale University School of Medicine
New Haven, Connecticut

| September 1, 2008
This article is part of a CME activity described in Oncology Vol. 22 No. 10


Prospective Randomized Trials

No prospective randomized trials in the United States have evaluated neoadjuvant chemotherapy against conventional treatment for advanced ovarian cancer. One international prospective randomized trial conducted by the European Organisation for Research and Treatment of Cancer (EORTC) has completed accrual of patients. The EORTC 55791 trial randomized over 700 women to receive either neoadjuvant chemotherapy for three cycles, followed by cytoreductive surgery and then three additional cycles of chemotherapy, or surgery followed by six cycles of chemotherapy.[35] For the latter arm, there was an option to perform interval cytoreduction following three cycles of chemotherapy if the surgeon declared that it was his or her intent to do so prior to performing the initial surgery.

(MORE: The Many Challenges of Neoadjuvant Chemotherapy for Ovarian Cancer)

A very similar trial, Chemotherapy or Upfront Surgery (CHORUS), is now accruing patients in a UK study.[35] Over 300 patients have joined this trial, which has a total goal of accruing 550 patients. Finally, the Japanese Clinical Oncology Group is inviting patients to participate in a prospective randomized trial wherein 350 women will be randomized to receive either four cycles of carboplatin(Drug information on carboplatin) and paclitaxel(Drug information on paclitaxel) followed by surgery and four additional cycles of treatment, or initial cytoreductive surgery followed by eight cycles of carboplatin and paclitaxel.[36]

Future of Neoadjuvant Chemotherapy for Advanced Ovarian Cancer

Preliminary results from the EORTC 55791 study are expected to be available in the fall of 2008 (personal communication). The initially released results will focus on morbidity. Survival data should be available in the spring of 2009. If there is no difference in survival between conventional therapy and neoadjuvant chemotherapy in the EORTC data and the morbidity is improved among women receiving neoadjuvant chemotherapy, neoadjuvant chemotherapy may become an accepted standard technique for the management of patients with advanced-stage ovarian cancer. Indeed, the latter is already true in Ottawa, Canada.[37]

Aletti et al have proposed a treatment strategy for patients with stage IV disease.[38] Neoadjuvant chemotherapy would be offered to patients with multiple hepatic metastases or extensive pleural disease. Patients with a good performance status (American Society of Anesthesiologists [ASA] 1 or 2) would undergo attempted debulking. Those with poor performance status (ASA 3 or 4) would undergo laparoscopy. For the latter, those found to have extensive peritoneal or unresectable disease would receive neoadjuvant chemotherapy, while those who did not would undergo an attempt at primary debulking.

The Southwest Oncology Group recently provided preliminary data on survival for patients believed to be not optimally cytoreducible. These advanced-stage disease patients received neoadjuvant chemotherapy for three cycles and then underwent cytoreductive surgery.[39] Those who were optimally cytoreduced received intraperitoneal chemotherapy to complete their treatment. The survival data were similar to results seen in patients who underwent surgery followed by chemotherapy in a conventional manner.[39]

Laparoscopic surgery has become a routine part of the management of patients with gynecologic cancers. It is often used by European gynecologic oncologists to determine whether a patient can initially be optimally cytoreduced. Should neoadjuvant chemotherapy become an accepted standard of care, it is possible that among those who achieve a clinical complete response or who have limited and isolated tumor nodules noted on posttreatment CT scans, selected patients will then undergo laparoscopic surgery to remove residual disease as well as reproductive organs that are still in place.

Unresolved Questions

The critical question regarding neoadjuvant chemotherapy for the management of advanced-stage ovarian cancer concerns the estimation of surgical cytoreducibility. The survival data, which have been available since 1974, strongly suggest that the best approach to the initial treatment of advanced-stage ovarian cancer is to resect all gross cancer.[40] Estimating cytoreducibility by diagnostic imaging, serum biomarkers, laparoscopic, and molecular biologic techniques has proven to be less than completely reliable. Efforts must be made to identify patients with advanced disease who can be cytoreduced to no gross residual disease, as they benefit the most from this approach.

A second question is: How many cycles of chemotherapy should be given prior to performing the surgery? The excellent findings obtained by the Yale group were the result of giving six cycles of chemotherapy (carboplatin and paclitaxel) prior to patients undergoing cytoreductive surgery.[21] The EORTC and CHORUS trials selected three cycles of chemotherapy prior to surgery. The Japanese Clinical Oncology Group trial uses four cycles of chemotherapy prior to surgery.[36]

Finally, and perhaps most significantly, the management of residual disease—which may represent chemoresistant clones of cancer cells—identified at the time of surgery following neoadjuvant chemotherapy will remain an issue. The possibility exists that the cancer that persists after neoadjuvant chemotherapy for advanced-stage ovarian cancer represents ovarian cancer stem cells, which are known to be inherently chemotherapy-resistant.[41] Strategies for treating ovarian cancer stem cells are currently being developed.

Recommendations

Medically compromised patients who are physically unable to tolerate aggressive cytoreductive surgery should undergo neoadjuvant chemotherapy first, followed by aggressive cytoreductive surgery if their medical condition improves. Likewise, patients with stage IV ovarian cancer do poorly with conventional therapy, and thus, neoadjuvant chemotherapy should become a standard alternative approach to treating this particular group of women.

All women with stage IIIC disease should be evaluated by a gynecologic oncologist. If the gynecologic oncologist feels the patient can be optimally cytoreduced to no macroscopic residual disease, surgery should be the first step in treatment. If it is expected that macroscopic disease will be left behind, the patient should be offered the choice of either neoadjuvant chemotherapy or conventional therapy.

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This article reviewed

Neoadjuvant Chemotherapy for Ovarian Cancer: The Debate Reconsidered

The Many Challenges of Neoadjuvant Chemotherapy for Ovarian Cancer





Case Report: Successful Neoadjuvant Chemotherapy in a Woman With ‘Untreatable’ Ovarian Cancer

An 84-year-old G7, P7 Latin American woman developed progressive weight loss, abdominal bloating, and nonspecifi c abdominal discomfort 2 months before presenting to her community hospital in April 2000. On evaluation at that hospital she was found to have massive ascites, an omental cake, and bilateral malignant pleural effusions. A computed tomography–guided biopsy of the omental cake was consistent with a poorly differentiated adenocarcinoma of ovarian origin.

The patient’s serum CA-125 level was 2,833 U/mL. Her past medical history was signifi cant for her having undergone a total abdominal hysterectomy for benign indications 40 years ago and stable angina responsive to nitroglycerin. She had a history of shingles (April 1999) involving her left chest wall. She also had glaucoma and arthritis. Her past surgical history was signifi cant for the total abdominal hysterectomy, an appendectomy, a cholecystectomy, and removal of a benign schwannoma from her spinal cord. Physical examination was signifi cant for diminished breath sounds at both lung bases and egophony at the right base posteriorly. Her abdomen was distended. A palpable mass was present in the upper midabdomen, as was a fluid wave.

An omental biopsy and the pleural effusion cytology were consistent with a poorly differentiated adenocarcinoma of gynecologic origin. The patient’s daughter was advised at the community hospital to take her mother home and avoid any active intervention, as the disease was far too advanced to be treated in this elderly woman.

The daughter elected to bring the patient to Yale-New Haven Hospital to see if any treatment was possible. The patient was admitted to the Gynecologic Oncology Service, where neoadjuvant chemotherapy consisting of carboplatin and paclitaxel was recommended. The patient received six cycles of intravenous carboplatin using a dose based on an area under the curve (AUC) of 5 and intravenous paclitaxel at a dose of 175 mg/m2. The patient and her family noted that 3 weeks after the first cycle of chemotherapy she was feeling better and her abdominal girth was declining.

The patient had a serum CA-125 level of 10 U/mL following her fourth cycle of chemotherapy. Following the sixth cycle, she underwent an exploratory laparotomy, omentectomy, bilateral salpingo-oophorectomy, and multiple intraperitoneal and retroperitoneal biopsies. The final pathology report revealed no evidence of cancer in any surgical specimens. Occasional psammoma bodies were seen microscopically in the omentum.

The patient has received no additional therapy but has been followed closely ever since. She has been able to visit her home in Argentina annually for vacations. At 92 years old, she is disease-free 8 years after the original diagnosis of ovarian cancer.


THE ISSUES
• Does neoadjuvant chemotherapy improve outcome in advanced-stage ovarian cancer patients?
• If so, which patients benefit most from this strategy?

THE OPTIONS
• Neoadjuvant chemotherapy, in a variety of regimens still being investigated, followed by aggressive cytoreductive surgery
• Conventional therapy—aggressive cytoreductive surgery followed by aggressive chemotherapy

RECOMMENDATIONS
• Patients unable to tolerate aggressive cytoreductive surgery should undergo neoadjuvant chemotherapy first.
• Neoadjuvant chemotherapy should become a standard alternative approach to treating patients with stage IV ovarian cancer.
• Women with stage IIIC disease should be evaluated by a gynecologic oncologist to determine the likelihood of optimal cytoreducibility. If residual macroscopic disease would be expected with surgery alone, the patient should be offered the option of neoadjuvant chemotherapy.


References

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3. Chambers JT, Chambers SK, Voynick IM, et al: Neoadjuvant chemotherapy in stage X ovarian carcinoma. Gynecol Oncol 37:327-331, 1990.

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5. Schwartz PE: Neoadjuvant chemotherapy for the management of ovarian cancer. Best Pract Res Clin Obstet Gynaecol 16:585-596, 2002.

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8. Qayyum A, Coakley FV, Westphalen AC, et al: Role of CT and MR imaging in predicting optimal cytoreduction of newly diagnosed primary epithelial ovarian cancer. Gynecol Oncol 96:301-306, 2005.

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10. Bristow RE, Duska L, Lambrou N, et al: A model for predicting surgical outcomes in patients with advanced ovarian carcinoma using computed tomography. Cancer 89:1532-1540, 2000.

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19. Angioli R, Palaia I, Zullo MA, et al: Diagnostic open laparoscopy in the management of advanced ovarian cancer. Gynecol Oncol 100:455-461, 2006.

20. Deffieux C, Castaigne D, Pomel C: Role of laparoscopy to evaluated candidates for complete cytoreduction in advanced stages of epithelial ovarian cancer. Int J Gynecol Cancer 16:35-40, 2006.

21. Fagotti A, Ferrandina G, Fanfani F, et al: A laparoscopy-based score to predict surgical outcome in patients with advanced ovarian carcinoma: A pilot study. Ann Surg Oncol 13:1156-1161, 2006.

22. Berchuck A, Iversen ES, Lancaster JM, et al: Prediction of optimal versus suboptimal cytoreduction of advanced-stage serous ovarian cancer with the use of microarrays. Am J Obstet Gynecol 190:910-925, 2004.

23. Bristow RE, Eisenhauer EL, Santillan A, et al: Delaying the primary surgical effort for advanced ovarian cancer: A systematic review of neoadjuvant chemotherapy and interval cytoreduction. Gynecol Oncol 104:480-490, 2007.

24. Bristow RE, Chi DS: Platinum-based neoadjuvant chemotherapy and interval surgical cytoreduction for advanced ovarian cancer: A meta-analysis. Gynecol Oncol 103:1070-1076, 2006.

25. McGuire WP, Hoskins WJ, Brady MF, et al: Cyclophosphamide and cisplatin compared with paclitaxel and cisplatin in patients with stage III and stage IV ovarian cancer. N Engl J Med 334:1-6, 1996.

26. Armstrong DK, Bundy B, Wenzel L, et al: Intraperitoneal cisplatin and paclitaxel in ovarian cancer. N Engl J Med 354:34-43, 2006.

27. Eisenkop SM, Spirtos NM, Friedman RL, et al: Relative influence of tumor volume before surgery and the cytoreductive outcome on survival for patients with advanced ovarian cancer. A prospective study. Gynecol Oncol 90:390-396, 2003.

28. Vergote I, deWever I, Tjalma W, et al: Neoadjuvant chemotherapy or primary surgery in advanced ovarian carcinoma: A retrospective analysis of 285 patients. Gynecol Oncol 71:431-436, 1998.

29. Rafii A, Deval B, Geay J-F, et al: Treatment of FIGO stage IV ovarian carcinoma: Results of primary surgery or interval surgery after neoadjuvant chemotherapy: A retrospective study. Int J Gynecol Cancer 17:777-783, 2007.

30. Eitan R, Levine DA, Abu-Rustum N, et al: The clinical significance of malignant pleural effusions in patients with optimally debulked ovarian carcinoma. Cancer 103:1397-1401, 2005.

31. Juretzka MM, Abu-Rustum N, Sonoda Y, et al: The impact of video-assisted thoracic surgery (VATS) in patients with suspected advanced ovarian malignancies and pleural effusions. Gynecol Oncol 104:670-674, 2007.

32. Schmeler KM, Sun CC, Bodurka DC, et al: Neoadjuvant chemotherapy for low-grade serous carcinoma of the ovary or peritoneum. Gynecol Oncol 108:510-514, 2008.

33. Gershenson DM, Sun CC, Lu KH, et al: Clinical behavior of stage II-IV low-grade serous carcinoma of the ovary. Obstet Gynecol 108:361-368, 2006.

34. Chan YM, Ng TY, Ngan H, et al: Quality of life in women treated with neoadjuvant chemotherapy for advanced ovarian cancer: A prospective longitudinal study. Gynecol Oncol 88:9-16, 2003.

35. Crawford SC, Vasey PA, Paul J, et al: Does aggressive surgery only benefit patients with less advanced ovarian cancer? Results from and international comparison within the SCOTROC-1 trial. J Clin Oncol 23:8802-8811, 2005.

36. Onda T, Matsumoto K, Shibata T, et al: Phase III trial of upfront debulking surgery versus neoadjuvant chemotherapy for stage III/IV ovarian, tubal and peritoneal cancers: Japan Clinical Oncology Group study. JCO 0602. Jpn J Clin Oncol 38:74-77, 2008.

37. Le T, Faught W, Hopkins L, et al: Primary chemotherapy and adjuvant tumor debulking in the management of advanced-stage epithelial ovarian cancer. Int J Gynecol Cancer 15:770-775, 2005.

38. Aletti GD, Dowdy SC, Podratz KC, et al: Analysis of factors impacting operability in stage IV ovarian cancer. Rationale use of a triage system. Gynecol Oncol 105:84-89, 2007.

39. Tiersten A, Liu P, Smith H, et al: Phase II evaluation of neoadjuvant chemotherapy and interval debulking followed by intraperitoneal chemotherapy in women with stage III and IV epithelial ovarian, fallopian tube, or primary peritoneal cancer: A Southwest Oncology Group study (abstract 3). Presented at the 39th Annual Meeting of the Society of Gynecologic Oncologists, Tampa, Fla, March 9, 2008. Gynecol Oncol 108:S3, 2008.

40. Griffiths CT: Surgical resection of tumor bulk in the primary treatment of ovarian carcinoma. Natl Cancer Inst Mongr 421:101-104, 1975.

41. Rossi DJ, Jamieson CHM, Weissman IL: Stem cells and the pathways to aging and cancer. Cell 132:681-696, 2008.


 
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