You are viewing the site in preview mode

Skip to main content


Escalated radiation and prophylactic extended field nodal irradiation are beneficial for FIGO IIIB cervical cancer patients’ prognosis



Currently, the standard treatment for locally advanced cervical cancer patients is concurrent chemoradiotherapy. Here we aim to evaluate therapeutic efficacy, treatment failure, toxicity and prognostic factors for FIGO IIIB cervical cancer patients.


A comprehensive retrospective analysis was performed to understand various factors which contribute to IIIB cervical cancer prognosis. In total 223 well defined patients were assigned according to their pathological subtype, age, pre-treatment HGB level, tumor size, pelvic lymph node (LN) metastasis, para-aortic LN metastasis as well as external irradiation technologies, treatment duration, point A EQD2 dose and concurrent chemotherapy cycles. We then performed correlation studies of these factors and OS, DFS, LCR, DMFS using univariate and multivariate analysis respectively.


We managed to achieve 207 (92.8%) complete response (CR) and 16 (7.2%) partial response (PR) with acceptable adverse effects. Notably, the 5 years OS, DFS, LCR, DMFS for these patients were 61.1, 55.2, 83.6 and 66.4% respectively. Importantly, our studies suggest that escalated point A EQD2 can significantly improve OS, DFS and LCR for FIGO IIIB cervical cancer patients, furthermore, patients without para-aortic LN metastasis who received prophylactic extended field irradiation have significant survival advantage for DFS and a tendency to improve OS and DMFS.


Our results suggest that FIGO IIIB cervical cancer patients should receive higher EQD2 (≥98Gy10) radiotherapy, moreover, patients without para-aortic LN metastasis should receive prophylactic extended field nodal irradiation to improve prognosis.


Cervical cancer is the fourth most common cancer in women worldwide, with approximately 528,000 newly reported cases and 266,000 death cases every year [1, 2]. Currently, the International Federation of Gynecology and Obstetrics (FIGO, clinical staging criteria is the standard for cervical cancer classification, according to which local advanced cervical cancer refers to the Ib2-IVa stages. Specifically, FIGO IIIB cervical cancer patients usually exhibit parametrial invasion which has extended to the pelvic wall. Moreover, patients usually display hydronephrosis and impaired renal function [3]. Nearly 25% of local advanced cervical cancers are defined as IIIB cervical cancer [4]. As the determination of IIIB cervical cancer is usually supported by pelvic and/or abdominal aortic lymph node metastasis [5], the prognosis for IIIB cervical cancer patients is generally unfavorable; previous studies have indicated that the local control failure can be varied from 10.63 to 41% [4,5,6,7], which could be as high as 50% for patients with bilateral uterine involvement.

The classical treatment strategy for FIGO IIIB cervical cancer patients is concurrent chemoradiotherapy (CCRT) [5, 6]. Notably, the intensity modulated radiotherapy (IMRT) is now the most widely used clinical radiotherapy technology which can deliver high dose internal irradiation while causing significantly less radiation-related tissue damage, with its unique dosimetric distribution feature, IMRT can reduce the radiation to organs at risks (OARs) without affecting the dose distributed to clinical target volume (CTV) [7]. A combination of radiotherapy with cisplatin-based chemotherapy is recommended by the National Cancer Institute (NCI), which has been used as the standard treatment strategy for cervical cancer for almost two decades. Several studies have been performed to evaluate the clinical efficacy and to define the prognostic factors for local advanced cervical cancer [8,9,10,11]. However, such studies focusing on IIIB cervical cancer patients in Chinese populations are still lacking. Here, we retrospectively analyzed therapeutic efficacy, treatment failure, toxicity and prognostic factors for 223 FIGO IIIB cervical cancer patients who were hospitalized in the Peking Union Medical College Hospital (PUMCH) from 2000 to 2014.


Patient characteristics

In total 223 FIGO IIIB cervical cancer patients were retrospectively analyzed in this study. Patients’ age was from 29 to 79 years old, with a median age of 50 years old. The clinical stage was determined by clinical checkup combined with biopsy analysis before the first treatment and supported by CT or PET imaging in some cases. We then divided these patients not only based on their clinical characteristics, but also according to the treatment they received. All detailed information is summarized in Table 1.

Table 1 General patients’ information

Radiation therapy

All patients received both external beam radiation therapy (EBRT) and intracavitary brachytherapy (ICBT) when the patient’s health condition was allowed.

The radiation treatment was carried out as previously described [12]. The EBRT technologies included three-dimensional conformal radiotherapy (3D-CRT) and intensity modulated radiation therapy (IMRT). Forty-eight patients received 3D-CRT. Briefly, by using 15MV-X rays, we applied box irradiation technology with a total dose of 36-40Gy10 fractioned in 20 times followed by 5 fractions of a total 10Gy10 irradiation. The patients’ bladders and rectums were protected by a 4 cm central lead block. The other 175 patients received IMRT with a total dose of 45–50.4Gy10 fractioned for 25 to 28 times using 6MV-X rays which could cover 95% PTV (1.8Gy10/day, 5 days a week, 5 to 6 weeks). For patients with lymph nodes metastasis, the dosage was increased to 56-60Gy10 and an additional dose for proximal uterus area was administrated with a total 10Gy10 divided in 5 fractions.

The ICBT usually started 3 weeks after EBRT and was given once or twice a week. The standard protocol for ICBT was a cumulative dose of 36Gy10 prescribed to point A in 5 to 7 fractions according to the International Commission on Radiation Units and Measurements (ICRU) report 38. CT imaging was performed to support real-time treatment plans determination after the applicator implantation. The irradiation dose for rectum and bladder was strictly controlled as less than 70% of the point A. For the current study, the range for prescribed point A dose was from 22.5 to 130.4 Gy10 (EBRT from 10 to 70.2Gy10 and ICBT from 6 to 60Gy10).

Concurrent chemotherapy

One hundred fifty-five patients received more than 4 cycles of concurrent chemotherapy, 68 patients were treated with less than 4 cycles including 21 patients who didn’t receive any chemotherapy due to personal reasons. Patients diagnosed as squamous were treated with a weekly cisplatin-based regimen at a dose of 40 mg/m2/week for 4 to 6 weeks; for those adenocarcinoma patients, we applied PF regimen in addition which included cisplatin 70 mg/m2 on day 1 and fluorouracil 1000 mg/m2 from day 1 to day 4. The PF regimen was given every 3 weeks for a total of 1–2 cycles. When the treatment was finished, the outcome was evaluated according to guidelines proposed previously [13].

Toxicity and adverse effect assessment

All the patients were monitored for toxicities and adverse effects every week during the treatment. The severity of acute complications is classified according to the Common Terminology Criteria for Adverse Events (CTCAE v2.0) ( Late complications were graded according to the RTOG/EORTC 1987 toxicity scales [14].


All patients were required to have a review check every 3 months during the first 2 years after the final treatment, and twice a year during the third to fifth year after the treatment, and once a year starting from the 5th year after the last treatment. The review check includes blood biochemistry, SCC Ag, gynecological examination, pelvic MRI, chest and abdomen enhanced CT. The last follow up for the current study was carried out in May 2018.

Statistics analysis

Overall survival (OS) is defined as the time from the start of treatment to the date of death or to the date of censoring. Disease-free survival (DFS) is defined as the time interval between the start of treatment and the detection of recurrence, metastasis or death. Local control rate (LCR) is defined as the percentage of the arrest of cancer growth at the site of origin. Distant metastasis-free survival (DMFS) is defined as the beginning of radiotherapy to the detection of distant metastasis or distant metastasis -related death. OS, DFS, LCR and DMFS were calculated with the Kaplan-Meier method by using SPSS 17.0 statistical software and compared using the log-rank test. Log-rank method was also used to perform univariate analysis, when the factor was found significant (P < 0.05), the Cox regression model was used to execute multivariate analysis. P value < 0.05 was considered statistically significant.


Treatment outcome evaluation

For the 223 FIGO IIIB cervical cancer patients included in this study, 207 of them showed complete response (CR) after the therapy (92.8%), and only 16 patients (7.2%) exhibited partial response (PR). Importantly, the 5-year OS, DFS, LCR and DMFS were 61.1, 55.2, 83.6 and 66.4% (Fig. 1a-d), suggesting the standard concurrent chemoradiotherapy was indeed very effective for FIGO IIIB cervical cancer patients.

Fig. 1

An overview of 5 years survival of FIGO IIIB cervical cancer patients treated with CCRT. The Kaplan-Meier survival curves for overall survival (OS) (a); disease progression-free survival (DFS); (b) local control rate (LCR); (c) and distant metastasis-free survival (DMFS); (d). The detail survival information is indicated separately in each figure, n = 223 patients for all survival analysis

Treatment failure patterns and toxicity

We observed 36 cases (16.1%) of local recurrence and 73 (32.7%) patients with distant metastasis, the details of which are summarized in Additional file 1: Table S1. Of note, there were 7 patients with both local recurrence and distant metastasis.

One major concern for CCRT treatment is the therapy-related toxicity. We have carefully evaluated both the acute toxicity and delayed toxicity. The most frequent grade 3 or 4 acute toxicity was hematological toxicity, followed by other symptoms such as frequent urination and diarrhea (Table 2). For the delayed toxicity, only few cases of complications in the urinary system and lower digestive tract were observed (Table 2). All these results indicated that CCRT was a safe therapeutic option for FIGO IIIB cervical cancer patients.

Table 2 Acute and delayed toxicity after treatment

Prognostic factors analysis

To comprehensively understand FIGO IIIB cervical cancer prognosis factors, the 223 patients were divided not only based on their clinical appearance but also according to the difference in their treatment (Additional file 1: Table S2). We then performed univariate analysis to determine prognostic factors for OS, DFS, LCR and DMFS respectively. Our data indicated that pre-treatment HGB level, tumor size, pelvic LNM, para-aortic LNM, EQD2 and concurrent chemotherapy significantly correlated with OS (Additional file 1: Figure S1 A-G); pre-treatment HGB level, tumor size, pelvic LNM, para-aortic LNM, treatment duration, EQD2 and concurrent chemotherapy cycles were significantly correlated with DFS (Additional file 1: Figure S2 A-G); moreover, tumor size, para-aortic LNM and EQD2 were highly associated with LCR (Additional file 1: Figure S3 A-C); finally, pelvic LNM, para-aortic LNM, treatment duration and concurrent chemotherapy cycles were prognostic factors for DMFS (Additional file 1: Figure S4 A-D).

Prognostic factors found to be significant (P < 0.05) by univariate analysis were then further analyzed using multivariate analysis. Our results suggested that pelvic LNM, para-aortic LNM, EQD2 and concurrent chemotherapy were independent prognostic factors for OS; pre-treatment HGB level, pelvic LNM, para-aortic LNM, EQD2 and concurrent chemotherapy cycles were independent prognostic factors for DFS; the independent prognostic factors for LCR included tumor size, para-aortic LNM and EQD2; and concurrent chemotherapy cycles was the only independent prognostic factor for DMFS (Table 3).

Table 3 Multivariate analysis for prognostic factors

Higher EQD2(point A) is correlated with better treatment outcome

As our data constantly suggested that EQD2 dosage was a detrimental factor for FIGO IIIB cervical cancer prognosis in various analysis, we further analyzed the correlation between EQD2 level and OS, DFS and LCR by distributing all the patients into high ((≥98Gy10), medium (90Gy10 ≤ EQD2 < 98Gy10) and low EQD2(22Gy10 < EQD2 < 90Gy10). As expected, high and medium EQD2 significantly improved patients’ OS and DFS compared to low EQD2 (Fig. 2a, b); surprisingly, we observed not only a markedly LCR improvement in patients treated with medium EQD2 compared to low EQD2, but also a significant advantage for LCR in high EQD2 treated patients compared to medium EQD2 treated patients (Fig. 2c). These data further strengthen our finding that higher EQD2 is associated with better prognosis.

Fig. 2

Higher EQD2 (point A) is correlated with better treatment outcome. All patients were further divided into 3 groups based on the EQD2 (point A), namely low EQD2(22Gy10<EQD2<90Gy10, blue line), medium EQD2 (90Gy10≤EQD2<98Gy10, green line) and high EQD2(≥98Gy10, grey line). The correlation between EQD2 (point A) and OS (a), DFS (b) and LCR (c) are presented. P values are indicated separately in the figures. n = 223 patients in total

Prophylactic extended field irradiation is an important treatment option for patients without para-aortic LN metastasis

Extended field irradiation is widely used for cervical cancer patients with para-aortic LN metastasis in clinical. In our department, for those patients (192 case) who exhibited no para-aortic LN metastasis suggested by CT or PET imaging, but with other aggressive tumor features such as common iliac LN metastasis [15], tumor size> 4 cm, pelvic wall involvement in both sides, we also applied prophylactic extended field irradiation as a supplementary treatment (107 cases). Surprisingly, when compared to those non-para-aortic LN metastases patients who didn’t receive such therapies (85 cases), we found a significant survival advantage in DFS and improved OS and DMFS (Fig. 3a-c) in patients with prophylactic extended field irradiation treatment, indicating that prophylactic extended field nodal irradiation is indeed an important supplement to improve prognosis of none para-aortic LN metastasis FIGO IIIB cervical cancer patients.

Fig. 3

Prophylactic extended field irradiation can improve prognosis in FIGO IIIB cervical cancer patients without para-aortic LN metastasis. The patients without para-aortic LN metastasis (n = 192) were divided into 2 groups according to whether they were treated with or without prophylactic extended field irradiation. The survival difference in OS (a), DFS (b) and DMFS (c) are presented and P values are indicated in each figure


Most cervical cancer cases can be prevented by routine screening, treatment of precancerous lesions or HPV vaccination, which dramatically decreases cervical cancer incidence and its related mortality [16]. Nevertheless, in many countries and regions which are lacking such procedures, cervical cancer is still a big threat to women as the survival ratio for advanced cervical cancer has not been significantly improved. Sangkittipaiboon et al analyzed 19 cases of stage III cervical cancer patients and revealed that both 5 years OS was 42.1% [17]. Gadducci et al reported a 5-year overall survival of 60% in 61 stage III cervical cancer patients [18], which was similar to our findings specifically in Chinese FIGO IIIB cervical cancer patients.

The treatment failure for cervical cancer therapy is usually defined as distant metastasis or local recurrence. Hong et al analyzed 1292 FIGO I-IV cervical cancer patients and observed that among 410 treatment failure cases, 82% of were reported within 2 years after therapy [19]. Of these patients, 213(52%) had distant metastasis, 162(40%) had local recurrence, and 35(8%) had both distant metastasis and local recurrence [19]. Waggoner reported that 90% of cervical cancer recurrence occurred within 3 years after the first treatment [2]. Katanyoo described that pelvic recurrence was one major treatment failure type for FIGO IIIB cervical cancer patients [20]. In our study, 36(16.1%) patients displayed local recurrence, which occurred between 6.5–25.9 months (median time was 13.3 months) after first therapy; while 73 (32.7%) patients had distant metastasis, which occurred within 30 months (median time was 12.2 months). In line with previous studies, lung was the most common metastatic target for FIGO IIIB cervical cancers. Of note, most patients who experienced treatment failure had tumors’ diameter > 4 cm, therefore, special or additional treatment are required for these patients.

The major concern for FIGO IIIB cervical cancer patient’s treatment is the side effects. Many studies have already shown that IMRT can significantly reduce cervical cancer radiotherapy-related adverse effects compared to 3D-CRT. Chen et al reported that IMRT could induce 36 and 30% digestive and urinary tract acute adverse effects respectively compared to 80 and 60% of such effects induced by 3D-CRT [7]. Similarly, the incidence of IMRT-related digestive and urinary system chronic adverse effects were 6 and 9% compared to 34 and 23% which induced by 3D-CRT [21]. Importantly, we didn’t observe any survival difference between IMRT and 3D-CRT treated patients, indicating that IMRT was a safer radiotherapy technology compared to 3D-CRT without compromising any therapeutic efficacy. Importantly, we did notice extended-field irradiation or higher dose escalation were associated with more severe side effects, but the difference were not significant when compared to those patients with only pelvic irradiation or lower dose irradiation treatment.

The radiotherapy for FIGO IIIB cervical cancer patients includes both external beam radiation therapy (EBRT) and intracavitary brachytherapy (ICBT). ICBT, which uses point A as a reference [9] to modulate the equivalent total dose in 2-Gy fractions (EDQ2) in the targeting area, is an essential treatment to cervical cancer radiotherapy. Eifel et al reported that when point A EQD2 was less than 85Gy10, the five-year pelvic recurrence ratio was 33%, in contrast, this ratio was only 16% when point A EQD2 was greater than 85Gy10 [6]. Consistently, Schmid et al performed three-dimensional intracavitary radiation therapy and found that when EQD2 for the high-risk CTV (HRCTV) was greater than 87Gy10, the cervical cancer local control ratio was more than 95% [11]. In this study, most patients were treated with IMRT as external radiation therapy, in addition, intracavitary radiation therapy was designed and performed according to real-time CT or PET imaging to reduce radiation-related organ damage. When patients showed no obvious contraindications, 6 fractions of 6Gy10 intracavitary radiation was administrated. Thus, the point A EQD2 for intracavitary radiation was 48Gy10, and the total EQD2 for both IMRT and intracavitary radiation for point A could reach as high as 98 Gy10. This dose is higher than any other previous reports [22] and we believe this why we could achieve better prognosis. Indeed, the further investigation revealed escalated EQD2(point A) was associated with better survival. However, this strategy also introduced much more acute toxicity compared to a recent reported clinical trial result in India [23], we therefore tried to overcome these complications as previously described [24, 25], for example, we prescribed leucogen or rhG-CSF to control hematological toxicity; live Combined Bifidobacterium, Lactobacillus and Enterococcus Capsules were used to rescue intestinal flora as well as sulfasalazine or mesalazine to alleviate intestinal inflammation; when necessary, we applied levofloxacin to control kidney infection. With these measures, the delayed toxicity percentage in our patients was comparable to the Indian study [23].

Extended field nodal irradiation has been widely used to treat patients with para-aortic LN metastasis and has shown great benefit for such patients [26, 27]. In our study, for those patients without para-aortic LN metastasis but showing aggressive tumor features, we also prescribed them with prophylactic extended field nodal irradiation. Our data suggested that these patients showed marked survival advantage in DFS and improved OS as well as DMFS when compared to none para-aortic LN metastasis patients who didn’t receive such treatment. Although the advantage in OS and DMFS was not significant, which might be explained as the limited sample size, the other reason was the patients who received prophylactic extended field irradiation usually showed more aggressive carcinoma features before the treatment. Therefore, albeit further investigation with a larger patient’s sample is required, we propose that prophylactic extended field nodal irradiation is beneficial for cervical cancer patients with or without para-aortic LN metastasis.

We admitted that our study also had some limitations, first, this is a single-center retrospective analysis, a multi-centers study included many more patients will be more informative; secondly, the intracavitary brachytherapy used in our study was 2 dimensional, thus we could only evaluate the dosage using EQD2, which might not be so accurate when compared to 3 dimensional intracavitary brachytherapy; thirdly, only 30 patients received less than 90Gy10 irradiation, this limited numbers might impair the accuracy when interpreting the correlations between higher dosage irradiation and prognosis.


Our retrospective study confirms that concurrent chemoradiotherapy (CCRT) is an efficient and safe treatment for FIGO IIIB cervical cancer patients. We provide systematic understanding of various prognostic factors which contribute to IIIB cervical cancer patients’ prognosis in China. Moreover, we propose that FIGO IIIB cervical cancer patients should be treated with higher EQD2 (≥98Gy10) radiotherapy plus at least 4 rounds of chemotherapy when possible, and patients without para-aortic LN metastasis should be also treated with prophylactic extended field irradiation to improve prognosis.



Three-dimensional conformal radiotherapy


Concurrent chemoradiotherapy


Complete response


Computed tomography


Clinical target volume


Disease-free survival


Distant metastasis-free survival


External beam radiation therapy


Equivalent dose in 2 Gy fractions


Federation of Gynecology and Obstetrics




Intracavitary brachytherapy


International Commission on Radiation Units


Intensity modulated radiotherapy


Local control rate


Lymph node


National Cancer Institute


Organs at risks


Overall Survival


Positron emission tomography


Partial response


  1. 1.

    Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, et al. Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 2015;136:E359–86.

  2. 2.

    Waggoner S. Cervical cancer. Lancet. 2003;361:2217–25.

  3. 3.

    Patel K, Foster NR, Kumar A, Grudem M, Longenbach S, Bakkum-Gamez J, et al. Hydronephrosis in patients with cervical cancer: an assessment of morbidity and survival. Support Care Cancer. 2015;23:1303–9.

  4. 4.

    Zuliani AC, Cunha Mde O, Esteves SC, Teixeira JC. Brachytherapy for stage IIIB squamous cell carcinoma of the uterine cervix: survival and toxicity. Rev Assoc Med Bras. 2010;56:37–40.

  5. 5.

    Ahmed RS, Kim RY, Duan J, Meleth S, De Los Santos JF, Fiveash JB. IMRT dose escalation for positive para-aortic lymph nodes in patients with locally advanced cervical cancer while reducing dose to bone marrow and other organs at risk. Int J Radiat Oncol Biol Phys. 2004;60:505–12.

  6. 6.

    Eifel PJ, Winter K, Morris M, Levenback C, Grigsby PW, Cooper J, et al. 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 Clin Oncol. 2004;22:872–80.

  7. 7.

    Chen MF, Tseng CJ, Tseng CC, Kuo YC, Yu CY, Chen WC. Clinical outcome in posthysterectomy cervical cancer patients treated with concurrent cisplatin and intensity-modulated pelvic radiotherapy: comparison with conventional radiotherapy. Int J Radiat Oncol Biol Phys. 2007;67:1438–44.

  8. 8.

    Parker K, Gallop-Evans E, Hanna L, Adams M. Five years’ experience treating locally advanced cervical cancer with concurrent chemoradiotherapy and high-dose-rate brachytherapy: results from a single institution. Int J Radiat Oncol Biol Phys. 2009;74:140–6.

  9. 9.

    Grigsby PW, Williamson JF, Chao KSC, Perez CA. Cervical tumor control evaluated with ICRU 38 reference volumes and integrated reference air kerma. Radiother Oncol. 2001;58:19–23.

  10. 10.

    Morris M, Eifel PJ, Lu J, Grigsby PW, Levenback C, Stevens RE, et al. Pelvic radiation with concurrent chemotherapy compared with pelvic and para-aortic radiation for high-risk cervical cancer. N Engl J Med. 1999;340:1137–43.

  11. 11.

    Schmid MP, Kirisits C, Nesvacil N, Dimopoulos JC, Berger D, Pötter R. Local recurrences in cervical cancer patients in the setting of image-guided brachytherapy: a comparison of spatial dose distribution within a matched-pair analysis. Radiother Oncol. 2011;100:468–72.

  12. 12.

    Wang W, Meng Q, Hou X, Lian X, Yan J, Sun S, et al. Efficacy and toxicity of image-guided intensity-modulated radiation therapy combined with dose-escalated brachytherapy for stage IIB cervical cancer. Oncotarget. 2017;8:102965–73.

  13. 13.

    Therasse P, Arbuck SG, Eisenhauer EA, Wanders J, Kaplan RS, Rubinstein L, et al. New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada. J Natl Cancer Inst. 2000;92:205–16.

  14. 14.

    Herrmann T, Knorr A, Dörner K. The RTOG/EORTC classification criteria for early and late radiation reactions. Radiobiol Radiother (Berl). 1987;28:519–28.

  15. 15.

    Huang L, Zheng M, Liu JH, Xiong Y, Ding H, Tang L, et al. Risk factors and prognosis of IB-IIB cervical carcinoma with common iliac lymph node metastasis. Chin J Cancer. 2010;29:431–5.

  16. 16.

    Tota JE, Ramana-Kumar AV, El-Khatib Z, Franco EL. The road ahead for cervical cancer prevention and control. Curr Oncol. 2014;211:255–64.

  17. 17.

    Sangkittipaiboon S. Long-term outcomes of concurrent chemoradiotherapy with weekly carboplatin in locally-advanced carcinoma of the uterine cervix patients. J Med Assoc Thail. 2014;97:12–9.

  18. 18.

    Gadducci A, Fabrini MG, Perrone F, Manfredi B, Fanucchi A, Laliscia C, et al. Pattern of failures and clinical outcome of patients with locally advanced cervical cancer treated with a tailored integrated therapeutic approach. Anticancer Res. 2010;30:3731–6.

  19. 19.

    Hong JH, Tsai CS, Lai CH, Chang TC, Wang CC, Chou HH, et al. Recurrent squamous cell carcinoma of cervix after definitive radiotherapy. Int J Radiat Oncol Biol Phys. 2004;60:249–57.

  20. 20.

    Katanyoo K. Comparing treatment outcomes of stage IIIB cervical cancer patients between those with and without lower third of vaginal invasion. J Gynecol Oncol. 2017;28:e79.

  21. 21.

    Novetsky AP, Einstein MH, Goldberg GL, Hailpern SM, Landau E, Fields AL, et al. Efficacy and toxicity of concomitant cisplatin with external beam pelvic radiotherapy and two high-dose-rate brachytherapy insertions for the treatment of locally advanced cervical cancer. Gynecol Oncol. 2007;105:635–40.

  22. 22.

    Pötter R, Tanderup K, Kirisits C, de Leeuw A, Kirchheiner K, Nout R, et al. The EMBRACE II study: the outcome and prospect of two decades of evolution within the GEC-ESTRO GYN working group and the EMBRACE studies. Clin Transl Radiat Oncol. 2018;9:48–60.

  23. 23.

    Shrivastava S, Mahantshetty U, Engineer R, Chopra S, Hawaldar R, Hande V, et al. Cisplatin chemoradiotherapy vs radiotherapy in FIGO stage IIIB squamous cell carcinoma of the uterine cervix: a randomized clinical trial. JAMA Oncol. 2018;4:506–13.

  24. 24.

    Sturdza A, Potter R, Fokdal LU, Haie-Meder C, Tanj LT, Mazeron R, et al. Image guided brachytherapy in locally advanced cervical cancer: improved pelvic control and survival in RetroEMBRACE, a multicenter cohort study. Radiother Oncol. 2016;120:428–33.

  25. 25.

    Rijkmans EC, Nout RA, Rutten IHHM, Ketelaars M, Neelis KJ, Laman MS, et al. Improved survival of patients with cervical cancer treated with image-guided brachytherapy compared with conventional brachytherapy. Gynecol Oncol. 2014;135:231–8.

  26. 26.

    Rotman M, Pajak TF, Choi K, Clery M, Marcial V, Grigsby PW, et al. Prophylactic extended-field irradiation of para-aortic lymph nodes in stage IIB and bulky IB and IIA cervical carcinomas. JAMA. 1995;274:387–93.

  27. 27.

    Kim JH, Kim JY, Yoon MS, Kim YS, Lee JH, Kim HJ, et al. Prophylactic irradiation of para-aortic lymph nodes for patients with locally advanced cervical cancer with and without CA9 expression (KROG 07-01):a randomized, open-label, multicenter, phase 2 trial. Radiother Oncol. 2016;120:383–9.

Download references


We would like to thank all the patients involved in this study for sharing their information during the follow-up period. We are also very grateful to all the members of our department for helpful discussions.


This project was supported by the Ministry of Science and Technology of the People’s Republic of China (grant number 2016YFC0105207).

Availability of data and materials

The datasets used and/or analyzed during the current study are available upon reasonable request.

Author information

The study was conceived and designed by KH and FZ, QM and WW performed data collection, data analysis and data interpretation; XL, XH, XL, SS, JY, ZL and ZM helped with patient’s follow-up and data collection; KH and FZ coordinated the whole study; QM and KH wrote the manuscript and prepared the figures together with help of WW and FZ. All authors read and approved the final manuscript.

Correspondence to Ke Hu or Fuquan Zhang.

Ethics declarations

Ethics approval and consent to participate

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. This study was approved by the ethic community of Peking Union Medical College.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Additional file

Additional file 1:

Figure S1. Univariate analysis of different prognostic factors for overall survival (OS). (A) Pathology type and OS. P = 0.062; (B) pre-treatment HGB level and OS. P = 0.018; (C) Tumor size and. P = 0.019; (D Pelvic LNM and. P = 0.001; (E) Para-aortic LNM and OS. P < 0.001; (F) EQD2 (Point A) and OS. P < 0.001; (G) Concurrent chemotherapy cycles and OS. P = 0.004. Figure S2. Univariate analysis of different prognostic factors for disease free survival (DFS). (A) pre-treatment HGB level and DFS. P = 0.022; (B) Tumor size and DFS. P = 0.044; (C) Pelvic LNM and DFS. P < 0.001; (D) Para-aortic LNM and DFS. P < 0.001; (E) Treatment duration and DFS. P = 0.04; (F) EQD2 (Point A) and DFS. P < 0.001; (G) Concurrent chemotherapy cycles and DFS. P = 0.005. Figure S3. Univariate analysis of different prognostic factors for local control rate (LCR). (A) Tumor size and LCR. P = 0.039; (B) Para-aortic LNM and LCR. P < 0.001; (C) EQD2 (Point A) and LCR. P < 0.001; Figure S4. Univariate analysis of different prognostic factors for distant metastasis free survival (DMFS). (A) Pelvic LNM and DMFS. P < 0.001; (B) Para-aortic LNM and DMFS. P < 0.001; (C) Treatment duration and DMFS. P = 0.018; (D) Concurrent chemotherapy cycles and DMFS. P = 0.024. Table S1. Details for treatment failure patterns. Table S2. Univariate analysis for prognostic factors. (DOCX 474 kb)

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark


  • Cervical cancer
  • EQD2
  • IMRT
  • Prophylactic extended field irradiation


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate. Please note that comments may be removed without notice if they are flagged by another user or do not comply with our community guidelines.