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Randomized Controlled Trial
. 2010 Dec;119(3):531-7.
doi: 10.1016/j.ygyno.2010.08.020. Epub 2010 Sep 15.

Health-related quality of life outcomes associated with four cisplatin-based doublet chemotherapy regimens for stage IVB recurrent or persistent cervical cancer: a Gynecologic Oncology Group study

Affiliations
Randomized Controlled Trial

Health-related quality of life outcomes associated with four cisplatin-based doublet chemotherapy regimens for stage IVB recurrent or persistent cervical cancer: a Gynecologic Oncology Group study

David Cella et al. Gynecol Oncol. 2010 Dec.

Abstract

Purpose: To assess the differences in health-related quality of life (HRQL) of 4 cisplatin containing doublet chemotherapy combinations in women with advanced/recurrent cervical carcinoma.

Methods: Patients were randomized to three-week cycles of paclitaxel + cisplatin (PC); vinorelbine + C (VC); gemcitabine + C (GC); or topotecan + C (TC). We report HRQL results from data available on 434 eligible patients enrolled into this 513 patient trial. HRQL was assessed with the Functional Assessment of Cancer Therapy-Cervix (FACT-Cx) the FACT/Gynecologic Oncology Group (FACT/GOG) four-item neurotoxicity scale, and the 0-10 "worst pain" item from the Brief Pain Inventory, at baseline (pre-treatment), prior to beginning cycle 2, prior to beginning cycle 5, and at 9 months after enrollment. As reported by Monk et al. (2009) [13] VC, GC and TC were found not to be superior to PC with regard to progression-free survival or overall survival.

Results: The trial was terminated early due to planned interim futility analysis, reducing power for HRQL analysis from 85% to 55%. Patients receiving VC, GC and TC doublets did not report significantly different HRQL, neuropathy, or pain from those who received the PC (control) doublet. Patients receiving PC tended to report worse neuropathy during treatment than patients who received other doublets (especially GC and TC), but the differences were not statistically significant.

Conclusion: None of the 3 experimental doublets was different from PC in terms of HRQL during treatment. Long-term toxicity data are inconclusive. Except where patients may wish to reduce their risk of worsening pre-treatment neuropathy, PC remains the standard of care for this disease.

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Conflict of interest statement

Conflict of interest statement

Dr. Cecelia H. Boardman is on the Speaker’s Bureau at Glaxo-Smith-Kline, Merck and Eli Lillly. She is also a surgical proctor at Intuitive.

All other co-authors have no conflict of interest to declare.

Figures

Fig. 1
Fig. 1
a: Mean FACT-Cx TOI scores (FACT-Cx TOI = Functional Assessment of Cancer Therapy-Cervix Trial Outcome Index), PC = paclitaxel plus cisplatin; VC = vinorelbine plus cisplatin; GC = gemcitabine plus cisplatin; TC = topotecan plus cisplatin. b: Mean FACT/GOG-Ntx Subscale Scores (FACT/GOG-Ntx = Functional Assessment of Cancer Therapy/Gynecologic Oncology Group Neurotoxicity Scale), PC = paclitaxel plus cisplatin; VC = vinorelbine plus cisplatin; GC = gemcitabine plus cisplatin; TC = topotecan plus cisplatin. c: Mean BPI scores (BPI = Brief Pain Inventory), PC = paclitaxel plus cisplatin; VC = vinorelbine plus cisplatin; GC = gemcitabine plus cisplatin; TC = topotecan plus cisplatin.
Fig. 2
Fig. 2
Mean FACT/GOG-Ntx scores of patients reporting any neurotoxicity (FACT/GOG-Ntx = Functional Assessment of Cancer Therapy/Gynecologic Oncology Group Neurotoxicity Scale), PC = paclitaxel plus cisplatin; VC = vinorelbine plus cisplatin; GC = gemcitabine plus cisplatin; TC = topotecan plus cisplatin.

References

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    1. Monk BJ, Huang HQ, Cella D, Long HJ. Quality of life outcomes from a randomized phase III trial of cisplatin with or without topotecan in advanced carcinoma of the cervix: a Gynecologic Oncology Group study. J Clin Oncol. 2005;23:4617–25. - PubMed
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