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).
References
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Table 1.
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) |
Table 2.
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) |