Advantage of complex treatment of IIA–IIIB cervical cancer with extended lymphodissection
Abstract
The aim of the
study was to evaluate the overall and recurrence–free survival of patients with
cervical cancer of stages IIA–IIIB stages treated with neoadjuvant chemotherapy
(NAChT) and radical extended surgery.
Material and
methods. The long-term results of treatment of 154 patients
with morphologically verified cervical cancer of IIA and IIIB stages were
studied in the clinical. Histologically, the tumor is predominantly represented
by squamous cell carcinoma 87% (n=134), in other cases adenocarcinoma.
Patients underwent combined treatment as part of NAChT with platinum
preparations and taxane derivatives and extended uterine extirpation with
appendages (n=154). Depending on the morphological characteristics of
the tumor in the adjuvant mode, 46.7% (n=72) (group 1) remained under
observation; 35.1% (n=54) received non-adjuvant chemotherapy (group 2)
and 18.2% (n=28) chemoradiotherapy (group 3). The median follow-up time
was 43.5 [16.7;58.9] months (from 3.3 to 80.7 months).
Results. Radical operations (R0) after chemotherapy were performed in 93.5% (n=144)
cases, and R1 resections were significantly higher in group 2 patients, 18% (n=5),
p=0.018 with glandular tumor differentiation of 21.4% (n=6);
42.9% (n=66) of deaths were registered during the follow-up. The 3-year
disease-free survival rate was 60.5%, the overall survival rate (S) was 61.3%,
where the lowest value was recorded in the group with AChT of 53.6%.
Conclusion. NAChT for cervical cancer of stages IIA–IIIB stages allows in some
cases to achieve conditions for performing radical operations. The use of
complex treatment, including neoadjuvant chemotherapy followed by radical
surgery, can improve relapse-free survival rates. Carrying out the developed
modification of the operation of extended uterine extirpation of type III with
extended lymphodissection after NAChT makes it possible to achieve high
survival rates in patients with cervical cancer of stages IIA–IIIB, regardless
of the volume and type of adjuvant therapy.
Keywords: cervical cancer; neoadjuvant chemotherapy; radical hysterectomy; recurrence-free survival; chemoradiotherapy; overall survival
Funding. The study had no sponsor support.
Conflict of
interest. The authors declare no conflict of interest.
For citation: Hakimova G.G., Hakimov G.A., Sabirova S.A., Mamazhonov H.I., Tashmetov
M.N., Hakimova S.G., Rakhmonov A.N. Advantage of complex treatment of IIA-IIIB
cervical cancer with extended lymphodissection. Clinical and Experimental
Surgery. Petrovsky Journal. 2025; 13 (1): 58–64. DOI: https://doi.org/10.33029/2308-1198-2025-13-1-58-64 (in Russian)
References
- Bray F., Laversanne M., Sung H., Ferlay J., Siegel R.L., Soerjomataram I., et al. Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2024; 74 (3): 229–63. DOI: https://doi.org/10.3322/caac.21834 Epub 2024 Apr 4. PMID: 38572751.
- World Health Organisation. 17 November 2023 Cervical cancer. URL: https://www.who.int/ru/news-room/fact-sheets/detail/cervical-cancer (in Russian)
- Kietpeerakool C., Aue-Aungkul A., Galaal K., Ngamjarus C., Lumbiganon P. Nerve sparing radical hysterectomy compared to standard radical hysterectomy for women with early stage cervical cancer (stage Ia2 to IIa). Cochrane Database Syst Rev. 2019; 2: CD012828.
- van Bommel P.F., van Lindert A.C., Kock H.C., et al. A review of prognostic factors in early-stage carcinoma of the cervix (FIGO IB and IIA) and implications for treatment strategy. Eur J Obstet Gynecol Reprod Biol. 1987; 26 (1): 69–84.
- Peters W.A., Liu P.Y., Barrett R.J., et al. Concurrent chemotherapy and pelvic radiation therapy compared with pelvic radiation therapy alone as adjuvant therapy after radical surgery in high-risk early-stage cancer of the cervix. J Clin Oncol. 2000; 18 (8): 1606–13.
- Rotman M., Sedlis A., Piedmonte M.R., et al. A phase III randomized trial of postoperative pelvic irradiation in Stage IB cervical carcinoma with poor prognostic features: follow-up of a gynecologic oncology group study. Int J Radiat Oncol Biol Phys. 2006; 65 (1): 169–76.
- Sedlis A., Bundy B.N., Rotman M.Z., et al. A randomized trial of pelvic radiation therapy versus no further therapy in selected patients with stage IB carcinoma of the cervix after radical hysterectomy and pelvic lymphadenectomy: a Gynecologic Oncology Group Study. Gynecol Oncol. 1999; 73 (2): 177–83.
- Koh W.J., Abu-Rustum N.R., Bean S., Bradley K., Campos S.M., Cho K.R., et al. Cervical cancer, version 3.2019, NCCN Clinical Practice Guidelines in oncology. J Natl Compr Canc Netw. 2019; 17 (1): 64–84. DOI: https://doi.org/10.6004/jnccn.2019.0001
- Marth C., Landoni F., Mahner S., McCormack M., Gonzalez-Martin A., Colombo N.; ESMO Guidelines Committee. Cervical cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2017; 28 (suppl 4): iv72–83. DOI: https://doi.org/10.1093/annonc/mdx220
- Maksimov S.Ya. Primarily multiple tumors of the organs of the reproductive system. Prakticheskaya onkologiya [Practical Oncology]. 2009; 10 (2): 117–23. (in Russian)
- Dueñas-González A., Zarbá J.J., Patel F., et al. Phase III, open-label, randomized study comparing concurrent gemcitabine plus cisplatin and radiation followed by adjuvant gemcitabine and cisplatin versus concurrent cisplatin and radiation in patients with stage IIB to IVA carcinoma of the cervix. J Clin Oncol. 2011; 29 (13): 1678–85.
- Khokhlova S.V., Kolomiets L.A., Kravets O.A., Krikunova L.I., Morkhov K.Y., Nechushkina V.M., et al. Practical recommendations on the treatment of malignant tumours of the Russian Society of Clinical Oncology. RUSSCO. 2019; 9 (3s2): 203–17. (in Russian)
- Kravets O.A., Kuznetsov V.V., Morkhov K.Y., Nechushkina V.M., Khokhlova S.V. Clinical recommendations on the diagnosis and treatment of cervical cancer. Moscow, 2018: 17 p. (in Russian)
- Khakimov G.A., Tashmetov M.N., Khakimova G.G., Musurmonov H.U., Khakimova Sh.G. Possibilities of aggressive oncosurgery in the treatment of IIA–IIIB stages of cervical cancer. Meditsinskiy alfavit [Medical Alphabet]. 2022; (31): 50–4. DOI: https://doi.org/10.3 3667/2078-5631-2022-31-50-54 (in Russian)
- Clinical recommendations. Cervical cancer: standards for the management of patients for physicians. Developers Association of oncologists of Russia, Russian Society of Clinical Oncology, Russian Society of specialists in the prevention and treatment of tumours of the reproductive system. Date of approval 20 December 2019. (in Russian)
- Wassie M., Argaw Z., Tsige Y., et al. Survival status and associated factors of death among cervical cancer patients attending at Tikur Anbesa Specialized Hospital, Addis Ababa, Ethiopia: a retrospective cohort study. BMC Cancer. 2019; 19: 1221. DOI: https://doi.org/10.1186/s12885-019-6447-x
- Carneiro S.R., Fagundes M.A., do Rosário P.J.O., Neves L.M.T., Souza G.D.S., Pinheiro M.D.C.N. Five-year survival and associated factors in women treated for cervical cancer at a reference hospital in the Brazilian Amazon. PLoS One. 2017; 12 (11): e0187579. DOI: https://doi.org/10.1371/journal.pone.0187579 PMID: 29145414; PMCID: PMC5690614.
- Chopra S., Gupta M., Mathew A., Mahantshetty U., Engineer R., Lavanya G., et al. Locally advanced cervical cancer: a study of 5-year outcomes. Indian J Cancer. 2018; 55 (1): 45–9. DOI: https://doi.org/10.4103/ijc.IJC_428_17
- Saevec V.V., Vajenin A.V., Jarov A.V., Chernova L.F., Shimotkina I.G., Gybaidyllina T.N., et al. Features multicomponent treatment of locally advanced cervical cancer account histological structure of the tumor. Malignant Tumours. 2015; 2: 40–5. DOI: https://doi.org/10.18027/2224-5057-2015-2-40-45
- Ovodenko D.L., Khabas G.N., Kreynina Yu.M., Seregin А.A., Aleshikova O.I., Ashrafyan L.A. Stage IB2–IIIB cervical cancer: neoadjuvant chemotherapy, radical surgery and patient survival. Sibirskiy onkologicheskiy zhurnal [Siberian Journal of Oncology]. 2021; 20 (3): 82–9. DOI: https://doi.org/10.21294/1814-4861-2021-20-3-82-89 (in Russian)
- Wang S., Zhang D.S., Pan T., Liu S., Wang M.K. Efficacy of concurrent chemoradiotherapy plus adjuvant chemotherapy on advanced cervical cancer. Chin J Cancer. 2010; 29 (11): 959–63. DOI: https://doi.org/10.5732/cjc.010.10186 PMID: 20979696.
- Ashing-Giwa K. T., Lim J., Tang J. Surviving cervical cancer: does health-related quality of life influence survival? Gynecol Oncol. 2010; 118 (1): 35–42.
- Chen J.G., Chen H.Z., Zhu J., Yang Y.L., Zhang Y.H., Huang P.X., et al. Cancer survival in patients from a hospital-based cancer registry, China. J Cancer. 2018; 9 (5): 851–60.