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Clinical Trial
. 2015 Dec 15;21(24):5480-7.
doi: 10.1158/1078-0432.CCR-15-1346.

Prospective Validation of Pooled Prognostic Factors in Women with Advanced Cervical Cancer Treated with Chemotherapy with/without Bevacizumab: NRG Oncology/GOG Study

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Clinical Trial

Prospective Validation of Pooled Prognostic Factors in Women with Advanced Cervical Cancer Treated with Chemotherapy with/without Bevacizumab: NRG Oncology/GOG Study

Krishnansu S Tewari et al. Clin Cancer Res. .

Erratum in

Abstract

Purpose: In the randomized phase III trial, Gynecologic Oncology Group (GOG) protocol 240, the incorporation of bevacizumab with chemotherapy significantly increased overall survival (OS) in women with advanced cervical cancer. A major objective of GOG-240 was to prospectively analyze previously identified pooled clinical prognostic factors known as the Moore criteria.

Experimental design: Potential negative factors included black race, performance status 1, pelvic disease, prior cisplatin, and progression-free interval <365 days. Risk categories included low-risk (0-1 factor), mid-risk (2-3 factors), and high-risk (4-5 factors). Each test of association was conducted at the 5% level of significance. Logistic regression and survival analysis was used to determine whether factors were prognostic or could be used to guide therapy.

Results: For the entire population (n = 452), high-risk patients had significantly worse OS (P < 0.0001). The HRs of death for treating with topotecan in low-risk, mid-risk, and high-risk subsets are 1.18 [95% confidence interval (CI), 0.63-2.24], 1.11 (95% CI, 0.82-1.5), and 0.84 (95% CI, 0.50-1.42), respectively. The HRs of death for treating with bevacizumab in low-risk, mid-risk, and high-risk subsets are 0.96 (95% CI, 0.51-1.83; P = 0.9087), 0.673 (95% CI, 0.5-0.91; P = 0.0094), and 0.536 (95% CI, 0.32-0.905; P = 0.0196), respectively.

Conclusions: This is the first prospectively validated scoring system in cervical cancer. The Moore criteria have real-world clinical applicability. Toxicity concerns may justify omission of bevacizumab in some low-risk patients where survival benefit is small. The benefit to receiving bevacizumab appears to be greatest in the moderate- and high-risk subgroups (5.8-month increase in median OS). Clin Cancer Res; 21(24); 5480-7. ©2015 AACR.

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Figures

Figure 1
Figure 1
Prospective validation of the Moore criteria in the GOG 240 study population (n=452).
Figure 2
Figure 2
Kaplan Meier overall survival curves following risk stratification according to the Moore criteria among women with advanced cervical cancer treated with chemotherapy with and without bevacizumab. Panel A: Low-risk class (0-1 poor prognostic factor). Panel B: Mid-risk class (2-3 poor prognostic factors). Panel C: High-risk class (4-5 poor prognostic factors).
Figure 3
Figure 3
Successive improvement in median overall survival among women with advanced cervical cancer. The phase III experience of the Gynecologic Oncology Group (now, part of NRG Oncology).

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References

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