Literature DB >> 33931498

Bevacizumab, carboplatin, and paclitaxel in the first line treatment of advanced ovarian cancer patients: the phase IV MITO-16A/MaNGO-OV2A study.

Gennaro Daniele1,2, Francesco Raspagliesi3, Giovanni Scambia4, Carmela Pisano5, Nicoletta Colombo6, Simona Frezzini7, Germana Tognon8, Grazia Artioli9,10, Angiolo Gadducci11, Rossella Lauria12, Annamaria Ferrero13, Saverio Cinieri14, Andrea De Censi15, Enrico Breda16, Paolo Scollo17, Ugo De Giorgi18, Andrea Alberto Lissoni19, Dionyssios Katsaros20, Domenica Lorusso3,4, Vanda Salutari4, Sabrina Chiara Cecere5, Eleonora Zaccarelli6, Margherita Nardin21, Giorgio Bogani3, Mariagrazia Distefano4, Stefano Greggi22, Maria Carmela Piccirillo1, Roldano Fossati23, Gaia Giannone24, Laura Arenare1, Ciro Gallo25, Francesco Perrone1, Sandro Pignata26.   

Abstract

OBJECTIVE: To explore the clinical and biological prognostic factors for advanced ovarian cancer patients receiving first-line treatment with carboplatin, paclitaxel, and bevacizumab.
METHODS: A multicenter, phase IV, single arm trial was performed. Patients with advanced (FIGO (International Federation of Gynecology and Obstetrics) stage IIIB-IV) or recurrent, previously untreated, ovarian cancer received carboplatin (AUC (area under the curve) 5), paclitaxel (175 mg/m2) plus bevacizumab (15 mg/kg) on day 1 for six 3-weekly cycles followed by bevacizumab single agent (15 mg/kg) until progression or unacceptable toxicity up to a maximum of 22 total cycles. Here we report the final analysis on the role of clinical prognostic factors. The study had 80% power with a two-tailed 0.01 α error to detect a 0.60 hazard ratio with a factor expressed in at least 20% of the population. Both progression-free and overall survival were used as endpoints.
RESULTS: From October 2012 to November 2014, 398 eligible patients were treated. After a median follow-up of 32.3 months (IQR 24.1-40.4), median progression-free survival was 20.8 months (95% CI 19.1 to 22.0) and median overall survival was 41.1 months (95% CI 39.1 to 43.5). Clinical factors significantly predicting progression-free and overall survival were performance status, stage, and residual disease after primary surgery. Neither baseline blood pressure/antihypertensive treatment nor the development of hypertension during bevacizumab were prognostic. There were two deaths possibly related to treatment, but no unexpected safety signal was reported.
CONCLUSIONS: Efficacy and safety of bevacizumab in combination with carboplatin and paclitaxel and as maintenance were comparable to previous data. Hypertension, either at baseline or developed during treatment, was not prognostic. Performance status, stage, and residual disease after primary surgery remain the most important clinical prognostic factors. TRIAL REGISTRATION NUMBER: EudraCT 2012-003043-29; NCT01706120. © IGCS and ESGO 2021. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  medical oncology; ovarian cancer; ovarian neoplasms

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Year:  2021        PMID: 33931498     DOI: 10.1136/ijgc-2021-002434

Source DB:  PubMed          Journal:  Int J Gynecol Cancer        ISSN: 1048-891X            Impact factor:   3.437


  2 in total

1.  Olaparib and paclitaxel in combination with carboplatin in treatment of ovarian cancer: influence on disease control.

Authors:  Heling Zhang; Ye Zhang
Journal:  Am J Transl Res       Date:  2022-01-15       Impact factor: 4.060

2.  Biological Role of Tumor/Stromal CXCR4-CXCL12-CXCR7 in MITO16A/MaNGO-OV2 Advanced Ovarian Cancer Patients.

Authors:  Crescenzo D'Alterio; Anna Spina; Laura Arenare; Paolo Chiodini; Maria Napolitano; Francesca Galdiero; Luigi Portella; Vittorio Simeon; Simona Signoriello; Francesco Raspagliesi; Domenica Lorusso; Carmela Pisano; Nicoletta Colombo; Gian Franco Zannoni; Nunzia Simona Losito; Rossella De Cecio; Giosuè Scognamiglio; Daniela Califano; Daniela Russo; Valentina Tuninetti; Maria Carmela Piccirillo; Piera Gargiulo; Francesco Perrone; Sandro Pignata; Stefania Scala
Journal:  Cancers (Basel)       Date:  2022-04-06       Impact factor: 6.639

  2 in total

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