Journal List > J Gynecol Oncol > v.29(3) > 1093912

Bogani, Tagliabue, Signorelli, Ditto, Martinelli, Chiappa, Mosca, Sabatucci, Leone, Maggiore, Lorusso, and Raspagliesi: A score system for complete cytoreduction in selected recurrent ovarian cancer patients undergoing secondary cytoreductive surgery: predictors- and nomogram-based analyses

Abstract

Objective

To test the applicability of the Arbeitsgemeinschaft Gynäkologische Onkologie (AGO) and Memorial Sloan Kettering (MSK) criteria in predicting complete cytoreduction (CC) in patients undergoing secondary cytoreductive surgery (SCS) for recurrent ovarian cancer (ROC).

Methods

Data of consecutive patients undergoing SCS were reviewed. The Arbeitsgemeinschaft Gynäkologische Onkologie OVARian cancer study group (AGO-OVAR) and MSK criteria were retrospectively applied. Nomograms, based on AGO criteria, MSK criteria and both AGO and MSK criteria were built in order to assess the probability to achieve CC at SCS.

Results

Overall, 194 patients met the inclusion criteria. CC was achieved in 161 (82.9%) patients. According to the AGO-OVAR criteria, we observed that CC was achieved in 87.0% of patients with positive AGO score. However, 45 out of 71 (63.4%) patients who did not fulfilled the AGO score had CC. Similarly, CC was achieved in 87.1%, 61.9% and 66.7% of patients for whom SCS was recommended, had to be considered and was not recommended, respectively. In order to evaluate the predictive value of the AGO-OVAR and MSK criteria we built 2 separate nomograms (c-index: 0.5900 and 0.5989, respectively) to test the probability to achieve CC at SCS. Additionally, we built a nomogram using both the aforementioned criteria (c-index: 0.5857).

Conclusion

The AGO and MSK criteria help identifying patients deserving SCS. However, these criteria might be strict, thus prohibiting a beneficial treatment in patients who do not met these criteria. Further studies are needed to clarify factors predicting CC at SCS.

References

1. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2017. CA Cancer J Clin. 2017; 67:7–30.
crossref
2. Cowan RA, Eriksson AG, Jaber SM, Zhou Q, Iasonos A, Zivanovic O, et al. A comparative analysis of prediction models for complete gross resection in secondary cytoreductive surgery for ovarian cancer. Gynecol Oncol. 2017; 145:230–5.
crossref
3. van de Laar R, Massuger LF, Van Gorp T, IntHout J, Zusterzeel PL, Kruitwagen RF. External validation of two prediction models of complete secondary cytoreductive surgery in patients with recurrent epithelial ovarian cancer. Gynecol Oncol. 2015; 137:210–5.
crossref
4. Minaguchi T, Satoh T, Matsumoto K, Sakurai M, Ochi H, Onuki M, et al. Proposal for selection criteria of secondary cytoreductive surgery in recurrent epithelial ovarian, tubal, and peritoneal cancers. Int J Clin Oncol. 2016; 21:573–9.
crossref
5. Janco JM, Kumar A, Weaver AL, McGree ME, Cliby WA. Performance of AGO score for secondary cytoreduction in a high-volume U.S. center. Gynecol Oncol. 2016; 141:140–7.
crossref
6. da Costa AA, Valadares CV, Mantoan H, Saito A, Salvadori MM, Guimarães AP, et al. The value of secondary cytoreductive surgery in recurrent ovarian cancer and application of a prognostic score. Int J Gynecol Cancer. 2016; 26:449–55.
7. Eriksson AG, Graul A, Yu MC, Halko A, Chi DS, Zivanovic O, et al. Minimal access surgery compared to laparotomy for secondary surgical cytoreduction in patients with recurrent ovarian carcinoma: perioperative and oncologic outcomes. Gynecol Oncol. 2017; 146:263–7.
crossref
8. Berek JS, Hacker NF, Lagasse LD, Nieberg RK, Elashoff RM. Survival of patients following secondary cytoreductive surgery in ovarian cancer. Obstet Gynecol. 1983; 61:189–93.
9. Harter P, du Bois A, Hahmann M, Hasenburg A, Burges A, Loibl S, et al. Surgery in recurrent ovarian cancer: the Arbeitsgemeinschaft Gynaekologische Onkologie (AGO) DESKTOP OVAR trial. Ann Surg Oncol. 2006; 13:1702–10.
crossref
10. Pfisterer J, Harter P, Canzler U, Richter B, Jackisch C, Hahmann M, et al. The role of surgery in recurrent ovarian cancer. Int J Gynecol Cancer. 2005; 15(Suppl 3):195–8.
crossref
11. Angioli R, Capriglione S, Aloisi A, Ricciardi R, Scaletta G, Lopez S, et al. A Predictive score for secondary cytoreductive surgery in recurrent ovarian cancer (SeC-score): a single-centre, controlled study for preoperative patient selection. Ann Surg Oncol. 2015; 22:4217–23.
crossref
12. Harter P, Sehouli J, Reuss A, Hasenburg A, Scambia G, Cibula D, et al. Prospective validation study of a predictive score for operability of recurrent ovarian cancer: the Multicenter Intergroup Study DESKTOP II. A project of the AGO Kommission OVAR, AGO Study Group, NOGGO, AGO-Austria, and MITO. Int J Gynecol Cancer. 2011; 21:289–95.
crossref
13. Chi DS, McCaughty K, Diaz JP, Huh J, Schwabenbauer S, Hummer AJ, et al. Guidelines and selection criteria for secondary cytoreductive surgery in patients with recurrent, platinum-sensitive epithelial ovarian carcinoma. Cancer. 2006; 106:1933–9.
crossref
14. Tian WJ, Chi DS, Sehouli J, Tropé CG, Jiang R, Ayhan A, et al. A risk model for secondary cytoreductive surgery in recurrent ovarian cancer: an evidence-based proposal for patient selection. Ann Surg Oncol. 2012; 19:597–604.
crossref
15. Raspagliesi F, Bogani G, Ditto A, Martinelli F, Chiappa V, Borghi C, et al. Implementation of extensive cytoreduction resulted in improved survival outcomes for patients with newly diagnosed advanced-stage ovarian, tubal, and peritoneal cancers. Ann Surg Oncol. 2017; 24:3396–405.
crossref
16. AGO Study Group. Study comparing tumor debulking surgery versus chemotherapy alone in recurrent platinum-sensitive ovarian cancer (DESKTOP III). ClinicalTrials.gov Identifier: NCT01166737 [Internet]. Bethesda, MD: National Institutes of Health;2010. [updated 2017 Feb 14; cited 2017 Sep 11]. Available from:. www.clinicaltrials.gov.
17. Coleman RL. Making of a phase III study in recurrent ovarian cancer: the odyssey of GOG 213. Clin Ovarian Cancer. 2008; 1:78–80.
crossref
18. van de Laar R, Zusterzeel PL, Van Gorp T, Buist MR, van Driel WJ, Gaarenstroom KN, et al. Cytoreductive surgery followed by chemotherapy versus chemotherapy alone for recurrent platinum-sensitive epithelial ovarian cancer (SOCceR trial): a multicenter randomised controlled study. BMC Cancer. 2014; 14:22.
crossref
19. van de Laar R, Kruitwagen RF, IntHout J, Zusterzeel PL, Van Gorp T, Massuger LF. Surgery for recurrent epithelial ovarian cancer in the Netherlands: a population-based cohort study. Int J Gynecol Cancer. 2016; 26:268–75.
20. Tian WJ, Jiang R, Cheng X, Tang J, Xing Y, Zang RY. Surgery in recurrent epithelial ovarian cancer: benefits on Survival for patients with residual disease of 0.1–1 cm after secondary cytoreduction. J Surg Oncol. 2010; 101:244–50.
21. Laas E, Luyckx M, De Cuypere M, Selle F, Daraï E, Querleu D, et al. Secondary complete cytoreduction in recurrent ovarian cancer: benefit of optimal patient selection using scoring system. Int J Gynecol Cancer. 2014; 24:238–46.
crossref
22. Salani R, Santillan A, Zahurak ML, Giuntoli RL 2nd, Gardner GJ, Armstrong DK, et al. Secondary cytoreductive surgery for localized, recurrent epithelial ovarian cancer: analysis of prognostic factors and survival outcome. Cancer. 2007; 109:685–91.
crossref

Fig. 1.
OS according to CC at SCS. CC, complete cytoreduction; OS, overall survival; SCS, secondary cytoreductive surgery.
jgo-29-e40f1.tif
Fig. 2.
Nomogram displaying the probability of CC according to the variables included in the AGO-OVAR score.
AGO-OVAR, Arbeitsgemeinschaft Gynäkologische Onkologie OVARian cancer study group; CC, complete cytoreduction; ECOG, Eastern Cooperative Oncology Group; RD, residual disease.
jgo-29-e40f2.tif
Fig. 3.
Nomogram displaying the probability of CC according to the variables included in the modified MSK criteria. CC, complete cytoreduction; DFI, disease-free interval; MSK, Memorial Sloan Kettering.
jgo-29-e40f3.tif
Fig. 4.
Nomogram displaying the probability of CC according to the variables included in the AGO-OVAR score and MSK modified criteria. AGO-OVAR, Arbeitsgemeinschaft Gynäkologische Onkologie OVARian cancer study group; CC, complete cytoreduction; DFI, disease-free interval; ECOG, Eastern Cooperative Oncology Group; MSK, Memorial Sloan Kettering; RD, residual disease.
jgo-29-e40f4.tif
Table 1.
Main characteristics of the study population
Characteristics Value
Age (yr)
Mean (SD) 61.6 (±12.5)
Median (quartiles*) 63.0 (53, 71)
BMI (kg/m2)
Mean (SD) 24.7 (±4.2)
Median (quartiles*) 25.4 (20, 36)
ECOG performance status
0 151 (77.8)
1 43 (22.2)
CA125 at first diagnosis (UI/L)
Mean (SD) 328.5 (±682.2)
Median (quartiles*) 103 (42, 234.3)
Type of ovarian cancer
High-grade serous 140 (72.5)
Low-grade serous 4 (2.0)
Endometrioid 19 (9.8)
Clear cells 9 (4.6)
Undifferentiated 20 (10.3)
Mucinous 2 (1.0)
FIGO stage
I 5 (2.6)
II 9 (4.6)
III 139 (72.7)
IV 21 (10.8)
Unknown 20 (10.3)
RD
No macroscopic tumor at the end of 146 (75.2)
surgery (RD=0)  
Macroscopic tumor at the end of surgery 42 (21.6)
(RD>0)  
Unknown 6 (3.1)
Site of recurrent disease
Retroperitoneal 39 (20.1)
Single peritoneal 62 (31.9)
Multiple peritoneal 77 (39.7)
Carcinomatosis 16 (8.3)
Ascites
Yes 23 (11.9)
No 124 (63.9)
Unknown 47 (24.2)
DFI, (mo)
Mean (SD) 43.9 (±38.5)
Median (quartiles*) 32.5 (18, 59.5)
Follow-up (mo)
Mean (SD) 32.2 (±20.9)
Median (quartiles*) 26 (17, 43.7)

Values are presented as number (%). BMI, body mass index; CA125, cancer antigen 125; DFI, disease-free interval; ECOG, Eastern Cooperative Oncology Group; FIGO, International Federation of Gynecology and Obstetrics; RD, residual disease; SD, standard deviation.

* Quartiles indicates the 25 and 75 percentiles.

Table 2.
Factors predicting complete cytoreduction at the time of secondary cytoreductive surgery
Characteristic Univariate analysis Multivariate analysis
OR (95% CI) p-value OR (95% CI) p-value
Age (years)* 1.01 (0.80–1.46) 0.616
BMI (kg/m2)* 0.93 (0.84–1.17) 0.544
ECOG   0.22  
ECOG 0 Reference    
ECOG 1 0.59 (0.25–1.36)    
Histotype   0.019   0.14
High-grade serous Reference Reference
Low grade serous & mucinous 0.31 (0.05–1.83) 0.198 0.45 (0.04–4.85) 0.508
Endometrioid 2.83 (0.36–22.42) 0.325 2.02 (0.23–17.77) 0.525
Clear cells 0.31 (0.07–1.36) 0.122 0.20 (0.03–1.23) 0.083
Undifferentiated 0.24 (0.09–0.65) 0.005 0.29 (0.09–1.00) 0.05
CA125 levels 0.99 (0.99–1.001) 0.266
Stage at presentation   N.E.  
I–II Reference    
III–IV N.E.    
RD at primary cytoreductive surgery   0.037   0.239
RD0 Reference   Reference  
RD>0 0.42 (0.19–0.95)   0.55 (0.20–1.49)  
Site of recurrent disease   0.137    
Peritoneal multiple site Reference  
Retroperitoneal 1.78 (0.54–5.87) 0.345
Peritoneal single site 1.06 (0.43–2.60) 0.905
Carcinomatosis 0.34 (0.11–1.10) 0.071    
Ascites   0.086   0.138
No Reference   Reference  
Yes 0.43 (0.16–1.13)   0.44 (0.15–1.31)  
Disease-free interval   0.019   0.43
<12 months Reference   Reference  
≥12 months 3.16 (1.21–8.26)   1.62 (0.49–5.36)  

BMI, body mass index; CA125, cancer antigen 125; CI, confidence interval; ECOG, Eastern Cooperative Oncology Group; N.E., no estimate; OR, odds ratio; RD, residual disease.

* OR per 10-year increase in age and one-unit increase in BMI.

TOOLS
Similar articles