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Comparison of adjuvant and neoadjuvant chemotherapy in the management of advanced ovarian cancer: a retrospective study of 574 patients
- Arturas Inciura†1Email author,
- Andrius Simavicius†2,
- Elona Juozaityte†1,
- Juozas Kurtinaitis†3,
- Ruta Nadisauskiene†1,
- Eimantas Svedas†1 and
- Skirmantas Kajenas†1
© Inciura et al; licensee BioMed Central Ltd. 2006
Received: 12 December 2005
Accepted: 08 June 2006
Published: 08 June 2006
There is a lack of clinical data on the validity of neoadjuvant chemotherapy in the treatment of ovarian cancer. The aim of this study was to compare the impact of the adjuvant and neoadjuvant chemotherapy regimens on the clinical outcomes in patients with advanced ovarian cancer.
We performed a retrospective analysis of 574 patients with advanced ovarian cancer admitted to four Lithuanian oncogynaecology departments during 1993–2000. The conventional combined treatment of cytoreductive surgery and platinum-based chemotherapy was applied to both the group that underwent neoadjuvant chemotherapy (n = 213) and to the control group (n = 361). The selection criterion for neoadjuvant chemotherapy was large extent of the disease. Overall and progression-free survival rates and survival medians were calculated using life tables and the Kaplan-Meier method.
There was no difference in median overall survival between stage III patients treated with adjuvant chemotherapy and neoadjuvant chemotherapy (25.9 months vs. 29.3 months, p = 0.2508) and stage IV patients (15.4 months vs. 14.9 months, p = 0.6108). Similarly, there was no difference in median progression-free survival between stage III patients treated with adjuvant chemotherapy and neoadjuvant chemotherapy (15.7 months vs. 17.5 months, p = 0.1299) and stage IV patients (8.7 months vs. 8.2 months, p = 0.1817). There was no difference in the rate of the optimal cytoreductive surgery between patients who underwent the neoadjuvant chemotherapy and patients primarily treated with surgery (n = 134, 63% vs. n = 242, 67%, respectively).
There was no difference in progression-free or overall survival and in the rate of optimal cytoreductive surgery between the neoadjuvant and adjuvant chemotherapy groups despite the fact that patients receiving neoadjuvant chemotherapy had a more extensive disease. Multivariate analysis failed to prove that neoadjuvant chemotherapy could be considered as an independent prognostic factor for survival, and the findings need to be investigated in the future prospective randomised studies.
Ovarian cancer is the leading cause of death among all gynaecologic cancers in Europe and the United States. The incidence of ovarian cancer has been steadily increasing over the past 10 years in many countries, reaching the overall lifetime risk of 1.8% . Despite new medical and surgical advances and new chemotherapeutic regimens, the overall 5-year survival for patients with stage III and IV epithelial ovarian cancer has remained relatively unchanged over the last 40 years. After the application of cytoreductive surgery and adjuvant chemotherapy with cisplatin/cyclophosphamide, the 5-year survival among stage III cases is 10–20%, and among stage IV cases – even below 10%. The optimisation of the treatment is the only way to prolong the survival of such patients.
Frei in 1982 originally introduced the definition of neoadjuvant chemotherapy to describe chemotherapy treatment of primary solid tumours before surgical ablation. Tumour downstaging has been demonstrated for a variety of tumour types after neoadjuvant chemotherapy. Unlike most solid tumour types, resection of metastatic sites from ovarian cancer is an accepted practice. It was assumed that optimal cytoreductive surgery could be performed in only about 50% of patients with ovarian cancer stages III or IV. In this group of patients, neoadjuvant chemotherapy was applied as an alternative to conventional surgery. Neoadjuvant chemotherapy resulted in adequate tumour shrinkage and allowed for the surgical treatment of tumours previously considered to be unresectable. Neoadjuvant chemotherapy could lead to optimal conditions for cytoreductive surgery and further increase the survival rate. There is a number of assumed advantages and potential disadvantages of neoadjuvant chemotherapy. The proposed benefits include tumour downstaging, which allows for more conservative surgery or more optimal cytoreductive surgery for unresectable tumours. The potential disadvantages include the selection of resistant tumour cell clones, less complete tumour downstaging, and higher local relapse as a result of more conservative surgery and compromised wound healing. Retrospective data support a survival benefit to maximum tumour reduction in advanced stage ovarian cancer. Bristow RE et al. in a meta-analysis of 6885 patients demonstrated a significant positive correlation between the percentage of maximal cytoreduction and a log median survival time . However, 50 to 60% of patients with advanced disease are not optimally debulked . For this subset of patients, the overall prognosis is worse despite significant heterogeneity in tumour chemosensitivity.
Optimal surgery after neoadjuvant chemotherapy is feasible for 60–94% of patients with advanced ovarian cancer [4–8]. The responses of ovarian cancer to neoadjuvant chemotherapy vary from 60% to 80%. This allows for predicting chemosensitive tumours after neoadjuvant chemotherapy. Patients with tumours sensitive to chemotherapy can be treated with optimal cytoreductive surgery, and increased overall and progression-free survival can be expected. In contrast, the feasibility of optimal surgery and the prognosis of patients with chemoresistant tumours are lesser.
Retrospective studies in which patients with advanced ovarian cancer were treated with neoadjuvant chemotherapy followed by cytoreductive surgery.
No. of patients treated with neoadjuvant chemotherapy
Kuhn W et al. (8)
Better median survival in the group treated with neoadjuvant chemotherapy compared with the group treated with primary cytoreductive surgery
Onnis A et al. (9)
In 46% of operated patients, the residual tumour was < 2 cm. An improvement in the quality of surgery and disease-free period was observed, while survival rate did not improve when comparing the neoadjuvant chemotherapy group to the group that received adjuvant chemotherapy
Shimizu Y et al. (10)
In 46% of operated patients, the residual tumour was < 2 cm. Survival for the optimally debulked neoadjuvant chemotherapy group was significantly higher than that for the optimally debulked adjuvant chemotherapy group
Vergote I et al. (11)
Crude survival was higher when selecting about one-half of patients for neoadjuvant chemotherapy
Surwit E. et al. (12)
Median survival was 22 months
Schwartz PE et al. (13)
No statistical difference was observed in overall and progression-free survival between the group treated with neoadjuvant chemotherapy and the conventionally treated group
Jacob JH et al. (14)
The same survival as in 18 matched controls
Lim JT et al. (15)
Neoadjuvant chemotherapy can make patients operable
Lawton FG et al. (16)
78% of patients were treated with neoadjuvant chemotherapy, of whom in 89% the residual tumour was < 2 cm
Ansquer Y et al. (17)
Better survival of patients treated with neoadjuvant chemotherapy compared to patients with non-debulked tumours
Recchia F et al. (18)
Median survival was 28 months for stage IV patients
Loizzi V et al. (19)
Survival in the neoadjuvant and adjuvant chemotherapy groups was similar
Kayikcioglu F et al. (20)
Primary neoadjuvant chemotherapy followed by cytoreductive surgery did not appear to worsen the prognosis
Morice P et al. (21)
Survival rates were similar in patients who underwent interval debulking surgery or primary debulking surgery
Ivanov S et al. (22)
The five-year survival rate following the neoadjuvant chemotherapy was the same as in case of conventional chemotherapy
Recently, the efficiency of neoadjuvant chemotherapy in ovarian cancer treatment has been widely discussed, but data for the legitimation of this treatment technique are not sufficient. We found that it is important to analyse and share experience in clinical practice due to the favourable situation in Lithuania where there is already a formed tradition to apply neoadjuvant chemotherapy.
The aim of this study was to evaluate the role of neoadjuvant chemotherapy in the management of advanced ovarian cancer compared to adjuvant chemotherapy, and to determine the impact of the neoadjuvant chemotherapy on the optimisation of cytoreductive surgery.
Characteristics of patients, disease, and treatment
Number of patients
Age by years:
Other types (clear cell, undifferentiated and mixed)
Number of chemotherapy cycles
The last date of follow-up was December 31st 2003. The dates of death and the cause of death were obtained from the records of the Lithuanian Cancer Registry. No patients were found alive by December 31st 2003, and no other causes of death rather than ovarian cancer were certified in the death certificates. Two endpoints have been used in the study – the date of death (overall survival) and the date of disease progression (progression-free survival). Overall and progression-free survival rates and survival medians were calculated using life tables and the Kaplan-Meier method. The univariate and multivariate Cox proportional hazards modelling was applied in order to evaluate the significance of prognostic factors (age, morphology, treatment (adjuvant or neoadjuvant chemotherapy), the optimality of surgery, and the duration of first-line chemotherapy) on the overall survival and disease-free survival. The survival estimates and the Cox proportional hazard modelling were performed using procedures of the STATA (version 7). The hazard ratio was calculated in order to establish the difference in the degree of survival between the groups, and to account for differences that might have been the effects of tumour stage, treatment, age, and other patient characteristics. The ratio of less than one indicated fewer deaths compared to the reference group, whereas the ratio greater than one indicated the opposite. The log-rank test was used to investigate the difference in overall and disease-free survival rates between the studied groups. Mantel-Haenszel estimate was used to estimate the odds ratio of cytoreductive surgery followed by neoadjuvant treatment. Estimates were also controlled by age and stage. All the statistical tests were two-tailed, and p-values of less than 0.05 were considered to be significant. The study was approved by the local ethical committee (approval number – BE-2-53-A).
The median overall survival in stage III patients treated with neoadjuvant chemotherapy was 778 days (25.9 months) [95% CI 723–850], and in those treated conventionally – 879 days (29.3 months) [95% CI 780–951] (p = 0.2508). The median progression-free survival in stage III patients treated with neoadjuvant chemotherapy was 471 days (15.7 months) [95% CI 388–515], and in those treated with adjuvant chemotherapy – 524 days (17.5 months) [95% CI 478–567] (p = 0.1299). The median survival in stage IV patients treated with neoadjuvant chemotherapy was 463 days (15.4 months) [95% CI 403–503], and in those treated conventionally – 446 days (14.9 months) [95% CI 411–502] (p = 0.6108). The median progression-free survival in stage IV patients treated with neoadjuvant chemotherapy was 261 days (8.7 months) [95% CI 237–291], and in those treated with adjuvant chemotherapy – 245 days (8.2 months) [95% CI 213–287] (p = 0.1817).
There were no significant differences in overall survival between both treatment groups in case of serous (p = 0.396), endometrioid (p = 0.197), and mucinous tumours (p = 0.256). No significant differences in progression-free survival between neoadjuvant and standard treatment groups were found in case of serous (p = 0.299), endometrioid (p = 0.098), and mucinous tumours (p = 0.509) either.
No statistical difference was observed in the overall survival (p = 0.065) or in the progression-free survival (p = 0.094) between the group treated with neoadjuvant chemotherapy and the conventionally treated group for those patients who underwent optimal cytoreduction. No statistical difference was observed in the overall survival (p = 0.117) or in the progression-free survival (p = 0.791) between the group treated with neoadjuvant chemotherapy and the conventionally treated group for those patients who underwent not optimal cytoreduction. The analysis of subgroups of patients with different histological subtypes of tumours showed no significant difference in overall and progression-free survival for optimally and suboptimally debulked patients between neoadjuvant chemotherapy and standard treatment.
After the neoadjuvant chemotherapy, optimal cytoreductive surgery was performed in 134 patients (63%). Optimal cytoreductive surgery was also performed in 242 conventionally treated patients (67%). Similar rates of optimal cytoreductive surgery were established in the neoadjuvant chemotherapy and conventional therapy groups for stage III patients younger than 65 years of age (79% vs. 78%). The possibility to perform optimal cytoreduction for stage III patients up to 65 years of age did not differ when choosing either adjuvant or neoadjuvant treatment (OR = 1.06 [0.58–2.00], p = 0.839). Similar rates of optimal cytoreductive surgery were established in the neoadjuvant chemotherapy and conventional therapy groups for stage III patients older than 65 years of age (66% vs. 62%). Possibilities to perform optimal surgery for stage III patients aged over 65 years in comparison with the younger ones decreased – only two thirds of all patients aged over 65 years were debulked optimally. The possibility of optimal surgery was a bit greater after neoadjuvant chemotherapy, comparing to adjuvant chemotherapy, but no statistically significant difference between these treatment methods was found (OR = 1.18 [0.58–2.42], p = 0.626). Similar rates of optimal cytoreductive surgery were established in the neoadjuvant chemotherapy and conventional therapy groups for stage IV patients younger than 65 years of age (36% vs. 54%). The possibility to undergo optimal surgery did not significantly differ for stage IV patients younger than 65 years of age irrespectively of whether the treatment was started with surgery or with adjuvant chemotherapy (OR = 0.48 [0.12–1.83], p = 0.226). Similar rates of optimal cytoreductive surgery were established in the neoadjuvant chemotherapy and conventional therapy groups for stage IV patients older than 65 years of age (12% vs. 15%). The possibility of optimal surgery for the patients aged over 65 years remained the same in both groups irrespectively of whether the treatment was started with surgery or with neoadjuvant chemotherapy (OR = 0.77 [0.11–4.52], p = 0.741).
The possibility to perform optimal surgery after neoadjuvant chemotherapy did not significantly increase for patients with serous (OR = 0.37 [0.44–1.54], p = 0.543), endometrioid (OR = 0.22 [0.39–1.78], p = 0.639), and mucinous tumours (OR = 0.24 [0.42–1.68], p = 0.622).
In multivariate analysis, the independent prognostic factors for better overall survival of patients with stage III and IV ovarian cancer were optimal cytoreductive surgery (p = 0.0001), age (<65 years) (p = 0.002) and serous carcinomas (p = 0.015). Univariate Cox analysis showed that neoadjuvant chemotherapy did not influence the overall (HR = 0.89, CI [0.74–1.08], p = 0.252) and progression-free survival (HR = 0.86, CI [0.71–1.04], p = 0.131) for patients with stage III ovarian cancer. According to the estimates of the multivariate Cox analysis, age, stage, tumour morphology, optimal surgery, and the number of the first-line chemotherapy cycles were similar predictors of overall (HR = 0.91, CI [0.75–1.11], p = 0.401) and progression-free survival (HR = 0.90, CI [0.74–1.09], p = 0.299) for the adjuvant and neoadjuvant chemotherapy groups of patients with stage III ovarian cancer.
The results of univariate and multivariate Cox analyses for patients with stage IV ovarian cancer were similar to those in patients with stage III ovarian cancer. Univariate Cox analysis showed that the application of neoadjuvant chemotherapy, comparing to adjuvant chemotherapy, did not influence the overall (HR = 1.10, CI [0.74–1.64], p = 0.614) and progression-free survival (HR = 1.30, CI [0.87–1.94], p = 0.186). According to the estimates of the multivariate Cox analysis, age, stage, tumour morphology, optimal surgery, and the number of the first-line chemotherapy cycles were similar predictors of overall (HR = 1,15, CI [0.76–1.75], p = 0.494) and progression-free survival (HR = 1.36, CI [0.90–2.08], p = 0.140) for the adjuvant and neoadjuvant chemotherapy groups of patients with stage IV ovarian cancer.
Surgery influences the survival of patients with advanced ovarian cancer . Vergote I. et al. showed that the median survival of patients is increased only after a complete removal of a tumour (tumour mass after cytoreductive surgery is <1 g) . Optimal cytoreductive surgery is possible in only to 40–50% of patients with advanced stage ovarian cancer . Five-year survival after not optimal cytoreductive surgery does not exceed 10% . Instead of standard treatment by cytoreductive surgery and adjuvant chemotherapy, patients with advanced ovarian cancer are also treated with neoadjuvant chemotherapy (drug-induced preoperative cytoreduction), which in the opinion of some investigators can create better conditions for optimal cytoreductive surgery. It is believed that such treatment with neoadjuvant chemotherapy improves the survival of patients. Neoadjuvant chemotherapy makes more conservative surgery feasible and, for patients with poor performance status, decreases the risk of postoperative complications. Unfortunately, up to now no randomized studies evaluating the efficacy of neoadjuvant chemotherapy in patients with advanced ovarian cancer have been conducted. Some published studies are mainly retrospective and numbers of patients treated with neoadjuvant chemotherapy and analysed in these studies are small.
The survival of patients treated with neoadjuvant chemotherapy following cytoreductive surgery is similar to those in whom treatment was started with cytoreductive surgery [13, 14, 19, 20, 26, 27]. Some studies showed that neoadjuvant chemotherapy increases the overall or progression-free survival [8–11]. In contrast to those data, the results of our study showed that the rate of optimal surgery and survival of patients with ovarian cancer did not increase after neoadjuvant chemotherapy. Nevertheless, more advanced tumours in the group of patients who underwent neoadjuvant chemotherapy, and similar overall and disease-free survival results in both treatment groups allow for the assumption that neoadjuvant chemotherapy might have a positive impact in patients with advanced ovarian carcinomas. Prospective randomized clinical trials are needed to clarify the validity of neoadjuvant chemotherapy.
Usually, neoadjuvant chemotherapy is administered expecting that inoperable tumours will decrease in size, and it will be possible to perform optimal surgery leading to better survival results. Only a few studies showed significantly better tumour resection rates after neoadjuvant chemotherapy comparing to conventional treatment [8, 17]. We established that independently of patients' age, the possibility to perform optimal surgery after neoadjuvant chemotherapy did not increase in patients with stage III and IV ovarian cancer. A similar number of optimal cytoreductive procedures in both groups shows that neoadjuvant chemotherapy administered in the presence of more extensive ovarian cancer might increase the possibility to perform optimal surgery. It was assumed that neoadjuvant chemotherapy could improve the chance of optimal surgery and survival for selected patients who cannot be debulked optimally using primary cytoreductive surgery . Currently, there are no established criteria that would help to determine which treatment – neoadjuvant or adjuvant chemotherapy – should be administered to patients with advanced ovarian cancer. Future investigations are needed in order to identify patients who will benefit from neoadjuvant chemotherapy.
There was no difference in progression-free or overall survival, although patients receiving neoadjuvant chemotherapy had a more extensive disease. The rate of optimal cytoreductive surgery was not statistically different between the neoadjuvant and adjuvant chemotherapy groups; however, neoadjuvant chemotherapy was administered in cases of more extensive ovarian cancer. Multivariate analysis did not prove that neoadjuvant chemotherapy could be an independent prognostic factor for survival, and the findings need to be investigated in future prospective randomised studies.
The Authors are grateful to the Lithuanian Cancer Registry for supplying the data. They also thank the oncologists of Klaipeda hospital and Kaunas Oncology hospital for contributing clinical material.
- Jemal A, Thomas A, Murray T, Thun M: Cancer statistics, 2002. CA Cancer J Clin. 2002, 52: 23-47.View ArticlePubMedGoogle Scholar
- Bristow RE, Tomacruz RS, Armstrong DK, Trimble EL, Montz FJ: Survival effect of maximal cytoreductive surgery for advanced ovarian carcinoma during the platinum era: a meta-analysis. J Clin Oncol. 2002, 20: 1248-1259. 10.1200/JCO.20.5.1248.View ArticlePubMedGoogle Scholar
- Inciura A, Juozaityte E, Nadisauskiene R, Cigriejiene VM, Kajenas S, Vaitkiene D, Vaidotiene L, Simavicius A: Surgical treatment of advanced epithelial ovarian cancer. Medicina. 2004, 40: 205-215.PubMedGoogle Scholar
- Rose PG, Nerenstone S, Brady M, Clarke-Pearson D, Olt G, Rubin SC, Moore DH: A phase III randomized study of interval secondary cytoreduction in patients with advanced stage ovarian carcinoma with suboptimal residual disease: a Gynecologic Oncology Group study [abstract]. Proc Am Soc Clin Oncol. 2002, 21: 201a-Google Scholar
- Chambers JT, Chambers SK, Voynick IM, Schwartz PE: Neoadjuvant chemotherapy in stage X ovarian carcinoma. Gynecol Oncol. 1990, 37: 327-331. 10.1016/0090-8258(90)90361-N.View ArticlePubMedGoogle Scholar
- Morice P, Brehier-Ollive D, Rey A, Atallah D, Lhomme C, Pautier P, Pomel C, Camatte S, Duvillard P, Castaigne D: Results of interval debulking surgery in advanced stage ovarian cancer: an exposed-non-exposed study. Ann Oncol. 2003, 14: 74-77. 10.1093/annonc/mdg003.View ArticlePubMedGoogle Scholar
- Mazzeo F, Berliere M, Kerger J, Squifflet J, Duck L, D'Hondt V, Humblet Y, Donnez J, Machiels JP: Neoadjuvant chemotherapy followed by surgery and adjuvant chemotherapy in patients with primarily unresectable, advanced-stage ovarian cancer. Gynecol Oncol. 2003, 90: 163-169. 10.1016/S0090-8258(03)00249-X.View ArticlePubMedGoogle Scholar
- Kuhn W, Rutke S, Spathe K, Schmalfeldt B, Florack G, von Hundelshausen B, Pachyn D, Ulm K, Graeff H: Neoadjuvant chemotherapy followed by tumor debulking prolongs survival for patients with poor prognosis in International Federation of Gynecology and Obstetrics stage IIIC ovarian carcinoma. Cancer. 2001, 92: 2585-2591. 10.1002/1097-0142(20011115)92:10<2585::AID-CNCR1611>3.0.CO;2-#.View ArticlePubMedGoogle Scholar
- Onnis A, Marchetti M, Padovan P, Castellan L: Neoadjuvant chemoterapy in advanced ovarian cancer. Eur J Gynaecol Oncol. 1996, 17: 393-396.PubMedGoogle Scholar
- Shimizu Y, Hasumi K: Treatment of stage III and IV ovarian cancer: is neoadjuvant chemotherapy effective?. Nippon Sanka Fujinka Gakkai Zasshi. 1993, 45: 1007-1014.PubMedGoogle Scholar
- Vergote IB, De Wever I, Decloedt J, Tjalma W, Van Gramberen M, van Dam P: Neoadjuvant chemotherapy versus primary debulking surgery in advanced ovarian cancer. Sem Oncol. 2000, 27: 31-36.Google Scholar
- Surwit E, Childers J, Atlas I: Neoadjuvant chemotherapy for advanced ovarian cancer. Int J Gynecol Cancer. 1996, 6: 356-361. 10.1046/j.1525-1438.1996.06050356.x.View ArticleGoogle Scholar
- Schwartz PE, Rutherford TJ, Chambers JT, Kohorn EI, Thiel RP: Neoadjuvant chemoterapy for advanced ovarian cancer: long term survival. Gynecol Oncol. 1999, 72: 93-99. 10.1006/gyno.1998.5236.View ArticlePubMedGoogle Scholar
- Jacob JH, Gershenson DM, Morris M, Copeland LJ, Burke TW, Wharton JT: Neoadjuvant chemoterapy and interval debulking for advanced epithelial ovarian cancer. Gynecol Oncol. 1991, 42: 146-150. 10.1016/0090-8258(91)90335-3.View ArticlePubMedGoogle Scholar
- Lim JT, Green JA: Neoadjuvant carboplatin and ifosfamide chemoterapy for inoperable FIGO stage III and IV ovarian carcinoma. Clin Oncol. 1993, 5: 198-202. 10.1016/S0936-6555(05)80227-4.View ArticleGoogle Scholar
- Lawton FG, Redman CW, Luesley DM, Chan KK, Blackledge G: Neoadjuvant (cytoreductive) chemotherapy combined with intervention debulking surgery in advanced, unresected epithelial ovarian cancer. Obstetr Gynecol. 1989, 73: 61-65.Google Scholar
- Ansquer Y, Leblanc E, Clough K, Morice P, Dauplat J, Mathevet P, Lhomme C, Scherer C, Tigaud JD, Benchaib M, Fourme E, Castaigne D, Querleu D, Dargent D: Neoadjuvant chemotherapy for unresectable ovarian carcinoma: a French multicenter study. Cancer. 2001, 91: 2329-2334. 10.1002/1097-0142(20010615)91:12<2329::AID-CNCR1265>3.0.CO;2-U.View ArticlePubMedGoogle Scholar
- Recchia F, De Filipps S, Rosselli M, Saggio G, Carta G, Rea S: Primary chemotherapy in stage IV ovarian cancer. A prospective phase II study. Eur J Gynaecol Oncol. 2001, 22: 287-291.PubMedGoogle Scholar
- Loizzi V, Cormio G, resta L, Rossi CA, Di Gilio AR, Cuccovillo A, Selvaggi L: Neoadjuvant chemotherapy in advanced ovarian cancer: a case-control study. Int J Gynecol Cancer. 2005, 15: 217-223. 10.1111/j.1525-1438.2005.15206.x.View ArticlePubMedGoogle Scholar
- Kayikcioglu F, Kose MF, Boran N, Caliskan E, Tulunay G: Neoadjuvant chemotherapy of primary surgery in advanced epithelial ovarian carcinoma. Int J Gynecol Cancer. 2001, 11: 466-470. 10.1046/j.1525-1438.2001.01064.x.View ArticlePubMedGoogle Scholar
- Morice P, Dubernard G, Rey A, Atallah D, Pautier P, Pomel C, Lhomme C, Duvillard P, Castaigne D: Results of interval debulking surgery compared with primary debulking surgery in advanced stage ovarian cancer. J Am Coll Surg. 2003, 197: 955-963. 10.1016/j.jamcollsurg.2003.06.004.View ArticlePubMedGoogle Scholar
- Ivanov S, Ivanov S, Khadzhiolov N: Prognostic factors and better survival rate after the treatment of advanced ovarian cancer with neoadjuvant chemotherapy. Akush Ginekol. 2004, 43: 17-9.Google Scholar
- Hoskins WJ: Surgical staging and cytoreductive surgery of epithelial ovarian cancer. Cancer. 1993, 71: 1534-1540.View ArticlePubMedGoogle Scholar
- Vergote IB, De Wever I, Tjalma W, Van Gramberen M, Decloedt J, van Dam P: Neoadjuvant chemoterapy or primary debulking surgery in advanced ovarian carcinoma: a retrospective analysis of 258 patients. Gynecol Oncol. 1998, 71: 431-436. 10.1006/gyno.1998.5213.View ArticlePubMedGoogle Scholar
- Huober J, Meyer A, Wagner U, Wallwiener D: The role of neoadjuvant chemoterapy and interval laparatomy in advanced ovarian cancer. J Cancer Res Clin Oncol. 2002, 128: 153-160. 10.1007/s00432-001-0312-3.View ArticlePubMedGoogle Scholar
- Neijt JP, ten Bokkel Huinink WW, van der Burg ME, van Oosterom AT, Willemse PH, Heintz AP, van Lent M, Trimbos JB, Bouma J, Vermorken JB: Randomized trial comparing two combination chemotherapy regimens (CHAP-5 v CP) in advanced ovarian carcinoma. J Clin Oncol. 1987, 5: 1157-1168.PubMedGoogle Scholar
- Hegazy M, Hegazi R, Elshafei M, Elshamy M, Eltatoongy M, Halim A: Neoadjuvant chemotherapy versus primary surgery in advanced ovarian carcinoma. World J Surg Oncol. 2005, 3: 57-10.1186/1477-7819-3-57.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2407/6/153/prepub
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