Clinical relevance of addition of conventional treatment to concurrent chemoradiotherapy in patients with FIGO stage III-IV cervical cancer: a retrospective analysis of a Japanese cohort

被引:0
作者
Kurosu, Hiroyuki [1 ]
Todo, Yukiharu [1 ]
Yamada, Ryutaro [1 ]
Minowa, Kaoru [1 ]
Tsuruta, Tomohiko [1 ]
Minobe, Shinichiro [1 ]
Nishiyama, Noriaki [2 ]
Kato, Hidenori [1 ]
机构
[1] Natl Hosp Org, Hokkaido Canc Ctr, Div Gynecol Oncol, Sapporo, Hokkaido, Japan
[2] Natl Hosp Org, Hokkaido Canc Ctr, Div Radiat Oncol, Sapporo, Hokkaido, Japan
关键词
uterine cervical neoplasms; chemoradiotherapy; drug therapy; lymph node enlargement; RADIATION-THERAPY; PLUS CISPLATIN; ONCOLOGY-GROUP; PHASE-III; CHEMOTHERAPY; RADIOTHERAPY; CARCINOMA; OUTCOMES;
D O I
10.1093/jjco/hyab191
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Concurrent chemoradiotherapy has limited therapeutic efficacy for stage III-IV cervical cancer. Even if systematic chemotherapy or extended-field radiation added to concurrent chemoradiotherapy might not improve survival in patients with advanced cervical cancer. Background Concurrent chemoradiotherapy has limited therapeutic efficacy for stage III-IV cervical cancer. We aimed to identify a subgroup of patients with stage III-IV cervical cancer who benefit from concurrent chemoradiotherapy with additional treatment. Methods We retrospectively reviewed 120 patients with stage III-IV cervical cancer who were treated with concurrent chemoradiotherapy from 2002 to 2018. We compared overall survival between patients treated with concurrent chemoradiotherapy alone and those who received concurrent chemoradiotherapy with additional conventional treatments (systemic chemotherapy before and/or after concurrent chemoradiotherapy and/or extended-field radiation). Prognostic factors were statistically analysed. Results Overall, 44 (36.7%) and 21 (17.5%) patients were radiologically diagnosed with pelvic and para-aortic lymph node enlargement, respectively. The median tumour diameter was 5.7 cm. A total of 69 (57.5%) patients received no additional treatment, and 51 (42.5%) received additional treatment. Cox regression analysis identified the following prognostic factors: histological non-squamous cell carcinoma (hazard ratio, 3.9; 95% confidence interval, 1.8-8.2), tumour diameter of >= 6 cm (hazard ratio, 2.1; 95% confidence interval, 1.2-3.7), radiological pelvic lymph node enlargement (hazard ratio, 2.1; 95% confidence interval, 1.1-4.0) and radiological para-aortic lymph node enlargement (hazard ratio, 2.1; 95% confidence interval, 1.1-4.1). Even in the lowest risk group (no risk factors), the 5-year overall survival rate was lower in the additional treatment group than in the concurrent chemoradiotherapy alone group (78.7% vs. 80.9%, respectively; log-rank test, P = 0.79). Conclusions Addition of conventional treatments to concurrent chemoradiotherapy might not improve survival in patients with advanced cervical cancer. Novel treatment strategies including immune checkpoint inhibitors should be considered for such patients.
引用
收藏
页码:244 / 250
页数:7
相关论文
共 29 条
[1]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21492, 10.3322/caac.21609]
[2]   Cervical cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up [J].
Colombo, N. ;
Carinelli, S. ;
Colombo, A. ;
Marini, C. ;
Rollo, D. ;
Sessa, C. .
ANNALS OF ONCOLOGY, 2012, 23 :27-32
[3]   Concurrent chemoradiotherapy vs. radiotherapy alone in locally advanced cervix cancer: A systematic review and meta-analysis [J].
Datta, Niloy Ranjan ;
Stutz, Emanuel ;
Liu, Michael ;
Rogers, Susanne ;
Klingbiel, Dirk ;
Siebenhuner, Alexander ;
Singh, Shalini ;
Bodis, Stephan .
GYNECOLOGIC ONCOLOGY, 2017, 145 (02) :374-385
[4]   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].
Duenas-Gonzalez, Alfonso ;
Zarba, Juan J. ;
Patel, Firuza ;
Alcedo, Juan C. ;
Beslija, Semir ;
Casanova, Luis ;
Pattaranutaporn, Pittayapoom ;
Hameed, Shahid ;
Blair, Julie M. ;
Barraclough, Helen ;
Orlando, Mauro .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (13) :1678-1685
[5]  
Duska LR., 2015, PEMBROLIZUMAB CHEMOR
[6]   Japan Society of Gynecologic Oncology guidelines 2017 for the treatment of uterine cervical cancer [J].
Ebina, Yasuhiko ;
Mikami, Mikio ;
Nagase, Satoru ;
Tabata, Tsutomu ;
Kaneuchi, Masanori ;
Tashiro, Hironori ;
Mandai, Masaki ;
Enomoto, Takayuki ;
Kobayashi, Yoichi ;
Katabuchi, Hidetaka ;
Yaegashi, Nobuo ;
Udagawa, Yasuhiro ;
Aoki, Daisuke .
INTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY, 2019, 24 (01) :1-19
[7]   Pelvic irradiation with concurrent chemotherapy versus pelvic and para-aortic irradiation for high-risk cervical cancer: An update of radiation therapy oncology group trial (RTOG) 90-01 [J].
Eifel, PJ ;
Winter, K ;
Morris, M ;
Levenback, C ;
Grigsby, PW ;
Cooper, J ;
Rotman, M ;
Gershenson, D ;
Mutch, DG .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (05) :872-880
[8]   Survival and recurrence after concomitant chemotherapy and radiotherapy for cancer of the uterine cervix: a systematic review and meta-analysis [J].
Green, JA ;
Kirwan, JM ;
Tierney, JF ;
Symonds, P ;
Fresco, L ;
Collingwood, M ;
Williams, CJ .
LANCET, 2001, 358 (9284) :781-786
[9]   Investigation of the freely available easy-to-use software 'EZR' for medical statistics [J].
Kanda, Y. .
BONE MARROW TRANSPLANTATION, 2013, 48 (03) :452-458
[10]   UTERINE CERVICAL-CARCINOMA - EVALUATION OF PELVIC LYMPH-NODE METASTASIS WITH MR-IMAGING [J].
KIM, SH ;
KIM, SC ;
CHOI, BI ;
HAN, MC .
RADIOLOGY, 1994, 190 (03) :807-811