Journals / Turkish Journal of Obstetrics and Gynecology / 2020 / Cilt: 17 - Sayı: 2

Efficacy and safety of bevacizumab in Turkishpatients with metastatic and recurrent cervical cancer

Metastatik ve rekürren serviks kanser tanılı Türk hastalarda bevasizumabın etkinlik ve güvenliği

Pages
123–127
Publication Date
2022-11-06
DOI
—
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⚡ TL;DR(Too Long; Didn't Read)

Objective: To evaluate the efficacy of bevacizumab a monoclonal, antivascular endothelial growth factor antibody in combination with cytotoxic chemotherapy in Turkish patients with recurrent and metastatic cervical cancer.Materials and Methods: Data of 64 patients with metastatic or recurrent cervical cancer, receiving bevacizumab with first-line cisplatin or carboplatin and paclitaxel chemotherapy between 2013 and 2017 were retrospectively evaluated.Results: The mean age of the patients was 49 years (range, 28-68), the median follow-up time was 12 months (range, 2-53), the median progression-free survival (PFS) was eight months, and the median overall survival (OS) was 23 months.

📌 3 Key Takeaways

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Objective & Hypothesis:Objective: To evaluate the efficacy of bevacizumab a monoclonal, antivascular endothelial growth factor antibody in combination with cytotoxic chemotherapy in Turkish patients with recurrent and metastatic cervical cancer.Materials and Methods: Data of 64 patients with metastatic or recurrent cervical cancer, receiving bevacizumab with first-line cisplatin or carboplatin and paclitaxel chemotherapy between 2013 and 2017 were retrospectively evaluated.Results: The mean age of the patients was 49 years (range, 28-68), the median follow-up time was 12 months (range, 2-53), the median progression-free survival (PFS) was eight months, and the median overall survival (OS) was 23 months.
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Key Findings & Data:All 64 patients received a median of 6 (range, 1-12) bevacizumab and 6 (range, 2-12) chemotherapy cycles.
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Conclusion & Impact:While the most common all-grades adverse events were nausea, neutropenia, anemia, and peripheral sensory neuropathy, the most common grade ≥3 adverse events were neutropenia, anemia, and peripheral sensory neuropathy.Conclusion: Adding bevacizumab to platinum and paclitaxel chemotherapy in a case of metastatic or recurrent cervical cancer is an effective and tolerable treatment for Turkish patients.
🔬Design:Research Article
📍Scope:2013 Verileri
⚙️Variables:Domain Parameters

Abstract

Objective: To evaluate the efficacy of bevacizumab a monoclonal, antivascular endothelial growth factor antibody in combination with cytotoxic chemotherapy in Turkish patients with recurrent and metastatic cervical cancer.Materials and Methods: Data of 64 patients with metastatic or recurrent cervical cancer, receiving bevacizumab with first-line cisplatin or carboplatin and paclitaxel chemotherapy between 2013 and 2017 were retrospectively evaluated.Results: The mean age of the patients was 49 years (range, 28-68), the median follow-up time was 12 months (range, 2-53), the median progression-free survival (PFS) was eight months, and the median overall survival (OS) was 23 months. All 64 patients received a median of 6 (range, 1-12) bevacizumab and 6 (range, 2-12) chemotherapy cycles. The chemotherapy regimens used with bevacizumab were cisplatin and paclitaxel in 31 (48%) and carboplatin and paclitaxel in 33 (52%) patients. The survival in patients treated with bevacizumab and cisplatin plus paclitaxel was better-particularly in patients with no previous cisplatin-based radiosensitizer therapy-than those treated with carboplatin, paclitaxel, and bevacizumab (p=0.023). The bevacizumab dose was 7.5 mg/kg in 30 patients (47%) and 15 mg/kg in 34 patients (53%) every 21 days. No significant difference was reported in the OS and the PFS between the two groups. While the most common all-grades adverse events were nausea, neutropenia, anemia, and peripheral sensory neuropathy, the most common grade ≥3 adverse events were neutropenia, anemia, and peripheral sensory neuropathy.Conclusion: Adding bevacizumab to platinum and paclitaxel chemotherapy in a case of metastatic or recurrent cervical cancer is an effective and tolerable treatment for Turkish patients.

Özet

Amaç: Monoklonal, antivasküler endotelyal büyüme faktörü antikoru olan bevasizumabın sitotoksik kemoterepilerle birlikte kullanımının metastatik,tekrarlayan serviks kanserli Türk hasta popülasyonunda etkinliğini değerlendirmeyi amaçladık. Gereç ve Yöntemler: Metastatik, tekrarlayan serviks kanseri tanısıyla 2013 ve 2017 yılları arasında ilk seri tedavide sisplatin veya carboplatin ve paklitakselkemoterapisi ile bevasizumab kullanan hastaların dosyalarını geriye dönük olarak inceledik. Bulgular: Altmış dört hastanın verisini değerlendirdik. Ortalama yaş 49 (aralık, 28-68), ortanca takip süresi 12 aydı (aralık, 2-53), ortanca progresyonsuzsağkalım süresi 8 ay ve ortanca genel sağkalım süresi 23 aydı. Ortanca bevasizumab ve kemoterapi kür sayısı altı idi. Bevasizumab ile birlikte kullanılankemoterapi rejimleri 31 hastada (4%8) sisplatin ve paklitaksel, 33 hastada (%52) karboplatin, ve paklitakseldi. Daha önce radyoterapi duyarlılaştırıcı olaraksisplatin almayan hastalarda sağkalım süresi sisplatinli tedavi alan hastalarda karboplatinli tedaviden daha iyiydi (p=0,023). Bevasizumab dozu 30 hastada(%47) 7,5 mg/kg ve 34 hastada (%53) 15 mg/kg 21 günde bir idi. İki grup arasında genel sağkalım ve progresyonsuz sağkalım farkı yoktu. Tüm gradlardaen sık görülen yan etkiler bulantı, nötropeni, anemi ve periferal duysal nöropati, en sık görülen grad ≥3 yan etkiler ise nötropeni, anemi ve periferal duysalnöropatiydi. Sonuç: Metastatik ve tekrarlayan serviks kanserli Türk hasta popülasyonunda platin ve bevasizumab tedavisi etkin ve güvenli bir tedavidir.

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Cite This Article

ERCELEP, Ö., ÖZÇELİK, M., ALİUSTAOĞLU, M., TATAROĞLU, D., SÜRMELİ, H., DEĞİRMENCİ, M., İNANÇ, M., GÜMÜŞ, M. (2022). Efficacy and safety of bevacizumab in Turkishpatients with metastatic and recurrent cervical cancer. Turkish Journal of Obstetrics and Gynecology, Cilt: 17 - Sayı: 2, 123–127. https://ajindex.com/articles/612968

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References (13)

  1. Siegel R, Ward E, Brawley O, Jemal A. Cancer statistics, 2011: The impact of eliminating socioeconomic and racial disparities on premature cancer deaths. CA Cancer J Clin 2011;61:212
  2. Cervical cancer. Estimated incidence, mortality and prevalence worldwide in 2012. http://globocan.iarc.fr/Pages/fact_sheets_ cancer.aspx (Accessed on March 18, 2015)
  3. Monk BJ, Herzog TJ. The evolution of cost-effective screening and prevention of cervical carcinoma: Implications of the 2006 consensus guidelines and human papillomavirus vaccination. Am J Obstetric Gynecology 2007;197:337-9
  4. Monk BJ, Tewari KSL. Chapter 3: Invasive cervical cancer, in DiSaia PJ, Creasman WT (eds): Clinical Gynecologic Oncology (ed 7). New York, NY, Mosby, Inc, 2007, pp 55-124 5. Monk BJ, Tewari KS, Koh WJ. Multimodality therapy for locally advanced cervical carcinoma: State of the art and future directions. J Clin Oncol 2007;25:2952-65
  5. Tewari KS, Monk BJ. Gynecologic oncology group trials of chemotherapy for metastatic and recurrent cervical cancer. Curr Oncol Rep 2005;7:419-44
  6. Long HJ III, Bundy BN, Grendys EC, Benda JA, McMeekin DS, Sorosky J, et al. Randomized phase III trial of cisplatin with or without topotecan in carcinoma of the uterine cervix: A Gynecologic Oncology Group study. J Clin Oncol 2005;23:4626-33
  7. Folkman J, D’Amore PA. Blood vessel formation: What is its molecular basis? Cell 1996;87:1153e-5
  8. Hlatky L, Hahnfeldt P, Tsionou C, Coleman CN. Environmental controls and effects in angiogenesis. Br J Cancer 1996;74:S151e-S6
  9. Tewari KS, Sill MW, Long HJ, Penson RT, Huang H, Ramondetta LM, et al. Improved survival with bevacizumab in advanced cervical cancer. N Engl J Med 2014;370:734-43
  10. Greer BE, Koh WJ, Abu-Rustum NR, Apte SM, Campos SM, Chan J, et al. Cervical cancer. J Natl Compr Canc Netw 2010;8:1388-416
  11. Monk BJ, Sill MW, McMeekin DS, Cohn DE, Ramondetta LM, Boardman CH, et al. Phase III trial of four cisplatin-containing doublet combinations in stage ıvb, recurrent, or persistent cervical carcinoma: A Gynecologic Oncology Group Study. J Clin Oncol 2009;27:4649-55
  12. Saito I, Kitagawa R, Fukuda H, Shibata T, Katsumata N, Konishi I, et al. A randomized, phase III trial of paclitaxel plus carboplatin (TC) versus paclitaxel plus cisplatin (TP) in stage IVb, persistent or recurrent cervical cancer: Japan Clinical Oncology Group study (JCOG0505). J Clin Oncol 2010;40:90-3
  13. Leung DW, Cachianes G, Kuang WJ, Goeddel DV, Ferrara N. Vascular