A Multi-Institutional Retrospective Analysis of Oncologic Outcomes for Patients With Locally Advanced Cervical Cancer Undergoing Platinum-Based Adjuvant Chemotherapy After Concurrent Chemoradiotherapy

Abstract

Objective:

To evaluated the oncologic outcomes associated with platinum-based adjuvant chemotherapy following concurrent chemoradiotherapy (CCRT) in the management of patients with locally advanced cervical cancer (LACC).

Methods:

A total of 695 patients with FIGO stage IB2, IIA2, IIB-IVA LACC treated at 6 medical facilities were enrolled and divided into 2 groups: 478 were assigned to CCRT alone (CCRT group) and 217 to adjuvant chemotherapy after CCRT (CCRT-ACT group). The treatment outcomes were retrospectively compared and reported after the propensity score matching (PSM) analysis.

Results:

With a median follow-up of 56.4 months, no statistically significant differences were found in overall survival (OS), disease-free survival (DFS), progression-free survival (PFS) and distance metastasis-free survival (DMFS) between 2 groups. In CCRT-ACT group, patients with lymph nodes involvement or squamous cell carcinoma (SCC) had significantly longer DMFS, but no significant benefit in survival outcomes were observed with more than 2 cycles of adjuvant chemotherapy. Moreover, patients with a high level of CA125 (>20.5U/mL) or SCC-Ag (>22.8μg/L) had a relatively better DFS or PFS, and grade 3-4 acute hematological toxicity, late urinary and lower gastrointestinal complications and diarrhea symptom were more frequent in CCRT-ACT group.

Conclusions:

Adjuvant chemotherapy after CCRT has a potential role in further improving disease control for LACC patients with lymph nodal-metastasis or SCC with a high level of CA125 or SCC-Ag. Due to increased treatment-related complications and diarrhea symptom affecting the quality of life, post-CCRT adjuvant chemotherapy with excessive cycles was not be considered as the most appropriate choice in general.

Keywords

uterine cervical cancer locally advanced stage concurrent chemoradiotherapy adjuvant chemotherapy prognosis

Introduction

Cervical cancer is a major health problem among a global female population. According to the World Health Organization, cervical cancer is the fourth most common cancer and the fourth leading cause of cancer-related mortality in women worldwide. Approximately 570,000 new patients were estimated to be diagnosed in 2018 representing 6.6% of all female cancers, with 311,000 deaths projected; more than 85% of these deaths occurring in low- and middle-income countries.¹ In developing countries like China, patients usually present with locally advanced stages.² Currently, concurrent chemoradiotherapy (CCRT) is recommended as the standard treatment strategy for locally advanced cervical cancer (LACC) due to its effectiveness in improving local control and reducing distant metastasis based on the encouraging results from several randomized trials.³ Although the use of combining chemotherapy with radiation has a therapeutic advantage over radiotherapy alone, about 30%-40% of patients with LACC failed to achieve a complete response to CCRT, and even experienced tumor relapse or distant metastasis after treatment.⁴ While several studies pertaining to adjuvant chemotherapy after CCRT in cases of LACC are available,^5
-7 survival benefit from the addition of adjuvant chemotherapy to CCRT in patients with LACC remains unclear. This retrospective clinical study was performed to report outcomes following platinum-based adjuvant chemotherapy after CCRT for LACC at multiple institutions.

Materials and Methods

Patients

We retrospectively analyzed 695 patients with 2009 International Federation of Gynecology and Obstetrics (FIGO) stage IB2, IIA2, IIB-IVA cervical cancer who were treated with definitive radiotherapy between 2007 and 2016 at 1 of 6 hospitals. Patient charts were reviewed for clinicopathological information from existing medical report and follow-up data.

None of the patients underwent prior treatment. Pre-treatment diagnostic evaluation consisted of a gynecological examination and a panel of laboratory and radiological tests (including computed tomographic/magnetic resonance imaging scan of the abdomen and pelvis, or positron emission tomography/computed tomography whenever possible). Eligibility criteria included: age < 75 years, Karnofsky performance status (KPS) scale ≥ 60, normal cardiovascular function, normal blood cell counts, and normal serum levels of blood urea nitrogen, creatinine, and bilirubin. The therapeutic regimen among these patients was CCRT alone (CCRT group), and CCRT plus adjuvant chemotherapy (CCRT-ACT group).

Treatment Schedule

All patients underwent definitive radiotherapy with a combination of pelvic external beam radiotherapy (EBRT) and high-dose-rate (HDR) intracavitary brachytherapy (ICBT). The pelvic EBRT at a total dose of 45 Gy-50.4 Gy was delivered using 3-dimensional conformal radiotherapy (3D CRT) technique or intensity-modulated radiotherapy (IMRT) technique. Four to 6 fractions of HDR ICBT (once a week) with a prescribed dose of 7-5 Gy were given at high-risk clinical target volume (CTVhr). The details of the radiotherapy were previously described.⁸

The concurrent chemotherapy was given weekly with intravenous cisplatin 30-40 mg/m² for 5 weeks during EBRT in all inclusion patients. In addition, a small number of patients having either pelvic/para-aortic lymph nodes involvement or local residual tumor were treated with the additional cycles of adjuvant chemotherapy after CCRT, depending on patient tolerance and response. The platinum-based adjuvant chemotherapy was administered every 3 weeks following CCRT. A combination regimen was paclitaxel (175 mg/m² on day 1) combined with either cisplatin (50 mg/m² on day 1) or carboplatin (AUC 5 on day 1).

Follow-Up Study

Before each cycle of treatment, a physical examination and routine hematologic analysis were conducted. After completing the whole protocol treatment, the disease status and the treatment-related toxic effects were evaluated by the routine work-up at the discretion of the attending physician every 3 months in the first year of follow-up, every 4-5 months in the second year, and every 6 months thereafter. In patients in whom regular follow-up information was not available, an effort was made to contact them by telephone or correspondence to obtain this information. Local recurrence and distant metastasis were calculated according to the follow-up examination results by imaging diagnosis and pathological biopsy. Late treatment-related complications were assessed according to the Radiation Therapy Oncology Group (RTOG) criteria. Quality of life (QoL) in patients was surveyed using the European Organization for Research and Treatment of Cancer quality of life questionnaire version 3 (EORTC QLQ-C30 V3.0).

Statistical Analysis

In this retrospective study, the propensity score matching (PSM) was used to remove the effects of confounding due to measured baseline covariates when using observational data to estimate the effects of treatment. The matching covariates included Karnofsky performance status, lymph nodes status, histological subtypes, and FIGO stage were selected based on prior literature reports and known clinically prognostic factors. Categorical variables are presented as frequencies and percentages, and continuous variables are expressed as the median with range. The frequency distributions of clinicopathological parameters were compared between groups using Chi-square or Fisher’s exact tests. The probabilities of overall survival (OS), disease-free survival (DFS), progression-free survival (PFS) and distance metastasis-free survival (DMFS) were estimated by the Kaplan-Meier method and compared using log-rank test. Univariate and multivariate analyses were performed using the Cox proportional hazards regression model. The statistically significant variables in univariate analyses were included in the stepwise regression for multivariate analyses. Probit models were used for testing relationships for prognostic factors and the probability of survival. All statistical analyses were performed using SPSS for Windows version 18.0 (SPSS Inc., Chicago, IL, USA). All reported P-values were 2-sided, and P-values < 0.05 was considered to be statistically significant.

Ethical Statement

This retrospective study was registered with the Chinese Clinical Trial Registry (ChiCTR-PRC-16008822). All procedures performed in studies involving human participants were in accordance with the ethical standards of the independent Ethical Committee/Institutional Review Board of Jilin University (20160621) and conducted in accordance with the Declaration of Helsinki. Informed consent was waived due to the retrospective format of this study.

Results

Patient Characteristics

The baseline demographic and clinicopathological characteristics of these patients before and after PSM are shown in Table 1. Of the total patients before matching, the mean age at diagnosis was 52.0 years old (range 26-74), and 615 (88.5%) were histologically diagnosed with squamous cell carcinoma (SCC). Forty-two patients (6.1%) were staged as IB2, 88 patients (12.7%) as IIA2, 420 patients (60.4%) as IIB, 28 patients (4.0%) as IIIA, 105 patients (15.1%) as IIIB, and 12 patients (1.7%) as IVA. After completion of the treatment, CCRT group consisted of 478 patients who were treated with CCRT alone, whereas CCRT-ACT group was composed of 217 patients who received CCRT plus adjuvant chemotherapy. PSM analysis with 2: 1 matching was performed, 406 patients in CCRT group and 203 patients in CCRT-ACT group were included in the final analysis. The baseline characteristics of the 2 groups were well balanced and superimposable in all selected clinical characteristics.

Table 1.

Baseline Characteristics of the Patients Included in This Study.

Characteristics	Before PSM			After PSM
Characteristics	CCRT group	CCRT-ACT group	P-value	CCRT group	CCRT-ACT group	P-value
Number of patients	478	217		406	203
Age (years)			0.201			0.421
Median	52.0	53.5		53.0	53.5
Range	26-73	31-74		30-73	32-73
Karnofsky performance status			0.245			0.350
Median	80	80		80	80
Range	70-100	60-100		70-100	60-100
Lymph node metastasis			0.077			0.482
Negative	332	136		267	128
Positive	146	81		139	75
Histological subtypes			0.126			0.785
Squamous cell carcinoma	428	187		362	179
Adenocarcinoma	16	5		12	5
Others	34	25		32	19
FIGO stage			0.433			0.781
IB2	23	19		23	18
IIA2	64	24		45	23
IIB	289	131		249	122
IIIA	19	9		17	8
IIIB	75	30		64	28
IVA	8	4		8	4
HDR brachytherapy			0.126			0.220
7 Gy×4 f	198	92		183	87
6 Gy×5 f	215	84		175	77
5 Gy×6 f	65	41		58	39

Treatment Outcome and Survival Analysis

The median follow-up duration was 56.4 months (range 3.6-132.2). In the propensity matched cohort, Kaplan-Meier estimates comparing therapeutic regimens in total patients are illustrated in Figure 1. In patients of CCRT and CCRT-ACT groups, the 1/3/5-year OS rate was 95.8%/84.7%/80.0% and 99.0%/87.2%/80.8%; the 1/3/5-year DFS rate was 88.9%/79.8%/75.4% and 93.1%/80.3%/74.9%; the 1/3/5-year PFS rate was 88.7%/79.6%/74.1% and 92.6%/79.8%/73.4%; and the 1/3/5-year DMFS rate was 91.4%/87.7%/86.9% and 95.1%/88.2%/87.2%. The 2 groups of patients did not significantly differ in OS, DFS, PFS and DMFS (log-rank P = 0.438, 0.499, 0.438 and 0.231, respectively). For those patients with later stages, including tumor extending to the pelvic wall (IIIB) and invading adjacent organs (IVA), no statistically significant difference in outcomes was found between CCRT and CCRT-ACT groups (5-year OS: 73.6% and 87.5%, P = 0.117; DFS: 72.2% and 84.4%, P = 0.173; PFS: 62.5% and 71.9%, P = 0.267; DMFS: 91.7% and 90.6%, P = 0.118, respectively) (Supplementary Figure 1). As demonstrated in Supplementary Figure 2, adjuvant chemotherapy after CCRT played a role in DMFS compared with CCRT alone when evaluating patient outcomes for positive pelvic or para-aortic lymph nodes (5-year DMFS: 93.3% and 82.0%, P = 0.035).

Figure 1.

Kaplan-Meier survival estimates of (A) OS, (B) DFS, (C) PFS and (D) DMFS for LACC patients after PSM.

We also carried out a subgroup analysis and investigated the survival in LACC patients only with SCC. The CCRT-ACT group had a similar 1/3/5-year OS rate (98.9%/88.9%/83.2% for CCRT-ACT, and 97.2%/87.6%/82.3% for CCRT, P = 0.443), DFS rate (93.3%/81.6%/76.5% for CCRT-ACT, and 91.7%/82.0%/77.1% for CCRT, P = 0.867) and PFS rate (92.7%/81.0%/75.4% for CCRT-ACT, and 91.7%/82.0%/76.0% for CCRT, P = 0.727) compared to CCRT group. As illustrated in Figure 2, SCC patients treated with adjuvant chemotherapy after CCRT displayed significant improvements in 1/3/5-year DMFS rate (95.0%/92.2%/91.1% for CCRT-ACT, and 90.9%/87.8%/87.0% for CCRT, P = 0.032). Notably, it is the subgroup of patients with non-SCC did not differ significantly in OS, DFS, PFS and DMFS between CCRT and CCRT-ACT groups (log-rank P = 0.134, 0.103, 0.078 and 0.074 for OS, DFS, PFS and DMFS, respectively) (Supplementary Figure 3).

Figure 2.

Kaplan-Meier survival estimates of (A) OS, (B) DFS, (C) PFS and (D) DMFS for LACC patients with SCC after PSM.

A total of 179 SCC patients were treated with post-CCRT adjuvant chemotherapy in which less than or equal to 2 cycles adjuvant chemotherapy regimen was used for 95 patients and more than 2 cycles for 84 patients. For the SCC patients receiving adjuvant chemotherapy after CCRT, no significant differences were observed in the respective 5-year OS, DFS, PFS or DMFS rate between patients treated within 2 cycles and more than 2 cycles of adjuvant chemotherapy (OS rate: P = 0.181; DFS rate: P = 0.428; PFS rate: P = 0.604; DMFS rate: P = 0.497). The survival curves for the 2 subgroups are shown in Figure 3.

Figure 3.

Kaplan-Meier survival estimates of (A) OS, (B) DFS, (C) PFS and (D) DMFS for SCC patients in CCRT-ACT group with ≤2 vs >2 cycles adjuvant chemotherapy after PSM.

Prognostic Factors Analysis

To identify independent prognostic factors, univariate and multivariate analyses using the Cox proportional hazards regression model were performed. As shown in Table 2, the univariate analysis demonstrated that baseline hemoglobin level, tumor markers (SCC antigen, SCC-Ag; cancer antigen 125, CA125) and histological subtypes were significantly associated with 5-year OS, DFS and PFS (P = 0.025, 0.017, 0.002 and 0.000 for OS; 0.040, 0.011, 0.020 and 0.009 for DFS; 0.007, 0.018, 0.004 and 0.002 for PFS, respectively). Furthermore, univariate analysis of age, histological subtypes, FIGO stage and lymph node metastasis with 5-year DMFS showed a trend toward significance (P = 0.029, 0.002, 0.004 and 0.032, respectively). In the multivariate analysis, it was found that SCC-Ag was an independent predictor of 5-year OS, DFS and PFS (P = 0.020, 1.08 [1.02, 1.14 for OS; P = 0.018, 1.04 [1.01, 1.08] for DFS; P = 0.035, 1.04 [1.00, 1.08] for PFS, respectively), and CA125 was another independent predictor of 5-year OS and PFS (P = 0.003, 1.01 [1.01, 1.02] for OS; P = 0.001, 1.01 [1.00, 1.01] for PFS, respectively). Age and histological subtypes remained as independent prognostic factors for 5-year DMFS (P = 0.011, 1.03 [1.00, 1.04] with age; P = 0.001, 4.05 [1.80, 8.21] with adenocarcinoma; P = 0.000, 6.88 [3.22, 14.26] with other types of carcinoma, respectively) (Table 3).

Table 2.

Univariate Analyses of Factors Affecting 5-Year OS, DFS, PFS and DMFS After PSM.

Variables	OS		DFS		PFS		DMFS
Variables	Wals χ²	P-value	Wals χ²	P-value	Wals χ²	P-value	Wals χ²	P-value
Age	3.02	0.091	0.70	0.402	1.74	0.190	4.86	0.029
Gravidity	0.03	0.873	0.76	0.383	0.26	0.604	1.23	0.268
Number of children	0.01	0.963	0.58	0.440	0.25	0.612	0.02	0.892
Menarcheal age	0.18	0.670	2.45	0.123	1.58	0.210	1.31	0.252
BMI	1.02	0.342	2.10	0.140	0.86	0.352	1.77	0.183
WBC	1.10	0.287	0.56	0.450	1.92	0.165	0.40	0.482
NEUT %	0.04	0.840	0.10	0.742	0.44	0.513	0.01	0.965
NEUT	0.04	0.845	0.01	0.986	0.12	0.730	0.01	0.955
LYM %	0.05	0.816	0.14	0.715	0.24	0.625	0.01	0.972
LYM	0.05	0.820	0.01	0.964	0.70	0.418	0.01	0.944
RBC	0.82	0.388	0.20	0.654	0.50	0.482	0.05	0.820
HGB	4.95	0.025	4.25	0.040	7.21	0.007	0.34	0.470
PLT	0.33	0.530	0.06	0.745	0.43	0.519	0.13	0.721
ALT	1.03	0.320	2.05	0.150	1.14	0.285	1.00	0.319
AST	1.40	0.186	0.01	0.942	1.59	0.192	0.45	0.501
GGT	0.30	0.595	0.02	0.886	0.19	0.660	0.01	0.971
ALP	1.20	0.262	0.78	0.392	0.64	0.425	0.69	0.402
GLU	1.23	0.251	0.07	0.780	1.33	0.249	0.01	0.954
BUN	0.60	0.440	1.20	0.274	0.66	0.412	0.73	0.392
CRE	0.01	0.970	1.07	0.308	0.06	0.800	0.48	0.473
TP	1.50	0.210	0.01	0.975	1.61	0.206	0.01	0.979
ALB	0.07	0.790	0.20	0.657	1.01	0.307	0.35	0.552
SCC-Ag	5.60	0.017	6.40	0.011	5.11	0.018	0.84	0.346
CA125	11.34	0.002	4.64	0.020	8.52	0.004	0.91	0.337
Histological subtypes	34.01	0.000	9.95	0.009	12.74	0.002	13.24	0.002
FIGO stage	5.72	0.392	1.12	0.895	4.42	0.516	14.82	0.004
Past medical history	1.44	0.194	1.56	0.215	1.73	0.194	1.55	0.215
Lymph node metastasis	2.19	0.135	0.53	0.462	3.10	0.071	4.53	0.032

BMI: body mass index; NEUT: neutrophilic granulocyte; LYM: lymphocyte; HGB: hemoglobin; PLT: blood platelet; ALT: alanine aminotransferase; AST: aspartate aminotransferase; GGT: glutamyltranspeptidase; ALP: alkaline phosphatase; GLU: glucose; BUN: blood urea nitrogen; CRE: creatinine; TP: treponema pallidum; ALB: albumin; SCC-Ag: squamous cell carcinoma antigen; CA125: cancer antigen 125.

Table 3.

Multivariate Analyses for Outcomes According to Prognostic Factors After PSM.

Variables	OS			DFS			PFS			DMFS
Variables	Wals χ²	HR [95% CI]	P-value	Wals χ²	HR [95% CI]	P-value	Wals χ²	HR [95% CI]	P-value	Wals χ²	HR [95% CI]	P-value
Age			—			—			—	5.39	1.03 [1.00, 1.04]	0.011
SCC-Ag	5.12	1.08[1.02, 1.14]	0.020	5.21	1.04 [1.01, 1.08]	0.018	4.65	1.04 [1.00, 1.08]	0.035			—
CA125	8.24	1.01[1.01, 1.02]	0.003			—	10.52	1.01 [1.00, 1.01]	0.001			—
Histological subtypes			—			—			—	23.20		0.000
SCC											1.00
Adenocarcinoma										12.62	4.05 [1.80, 8.21]	0.001
Others										20.45	6.88 [3.22, 14.26]	0.000

HR: hazards ratio; CI: confidence interval.

Probit Regression Models With a Probability of Survival Related to Tumor Markers

Probit regression was used to model the probability of survival results as a function of the tumor marker level. We found that in both CCRT-ACT and CCRT groups, the probability of survival declined with an increase in the levels of CA125 or SCC-Ag (Table 4). Patients with CA125 above the cut-off value (19.8U/mL for DFS; 20.5U/mL for PFS) receiving adjuvant chemotherapy after CCRT differed significantly in DFS and PFS than CCRT alone. Also, the CCRT-ACT group had significantly higher DFS than the CCRT group with the lowest possible cut-off value of SCC-Ag (22.8μg/L) (Figure 4).

Table 4.

Probit Regression Analysis for Relationship Between Tumor Markers and Survival After PSM.

Survival results		CA125				SCC-Ag
Survival results		β [95% CI]	S.E.	Z	P-value	β [95% CI]	S.E.	Z	P-value
OS	CCRT group	0.01 [0.00, 0.01]	0.01	2.81	0.005	0.03 [0.02, 0.05]	0.01	3.78	0.000
	CCRT-ACT group	0.05 [−0.10, 0.16]	0.10	1.21	0.226	0.01 [−0.02, 0.03]	0.09	0.26	0.795
DFS	CCRT group	0.01 [0.00, 0.01]	0.01	3.37	0.001	0.02 [0.01, 0.04]	0.01	2.50	0.012
	CCRT-ACT group	0.12 [0.08, 0.16]	0.02	5.53	0.000	0.09 [0.05, 0.14]	0.02	3.92	0.000
PFS	CCRT group	0.01 [0.01, 0.02]	0.01	4.65	0.000	0.01 [0.01, 0.12]	0.01	2.31	0.021
	CCRT-ACT group	0.42 [0.13, 0.44]	0.07	6.30	0.000	0.02 [−0.05, 0.07]	0.06	0.17	0.865
DMFS	CCRT group	0.01 [−0.01, 0.02]	0.01	0.52	0.603	0.02 [0.01, 0.05]	0.01	2.14	0.032
	CCRT-ACT group	−0.01 [−0.08, 0.09]	0.15	−0.45	0.651	−0.02 [−0.10, 0.09]	0.03	−0.33	0.641

Figure 4.

Probit regression models of data sets with probability of survival (y axis) related to tumor marker levels (x axis). A, Probability of DFS with CA125. B, Probability of PFS with CA125. (C) Probability of DFS with SCC-Ag.

Treatment-Related Complications

The acute and late adverse events for treatment were summarized in Table 5. The most common acute toxicity found in both groups was hematologic toxicity. Twenty-five patients (6.2%) had grade 3-4 acute hematological toxicity in CCRT group, while 27 (13.3%) in CCRT-ACT group (P = 0.003). The other acute toxicities about vagina mucosa, upper/lower gastrointestinal and urinary tract had no significant difference between the 2 groups.

Table 5.

Treatment-Related Toxicities of CCRT and CCRT-ACT Groups After PSM.

Toxicities	CCRT group		CCRT-ACT group		χ²	P-value
Toxicities	Grade 0-2	Grade 3-4	Grade 0-2	Grade 3-4	χ²	P-value
Acute toxicities
Hematology	381	25	176	27	8.84	0.003
Vagina mucosa	379	27	188	15	0.12	0.734
Upper gastrointestinal tract	393	13	197	6	0.03	0.869
Lower gastrointestinal tract	387	19	195	8	0.17	0.676
Urinary tract	380	26	191	12	0.06	0.813
Late toxicities
Upper gastrointestinal tract	404	2	201	2	0.03	0.859^#
Lower gastrointestinal tract	391	15	187	16	4.91	0.027
Urinary tract	405	1	196	7	8.38	0.004^#

^# Continuity correction chi-square test.

With regard to late complications of treatment, the most common adverse events were upper/lower gastrointestinal and urinary toxicities. In CCRT group, grade 2 or below, and 3-4 upper gastrointestinal complications occurred in 404 (99.5%) and 2 (0.5%) patients, and 201 (99.0%) and 2 (1.0%) patients in CCRT-ACT group, respectively (P = 0.859). However, grade 3-4 lower gastrointestinal complications were more common in patients from CCRT-ACT group than in those of CCRT group (16 [7.9%] vs 15 [3.7%], P = 0.027). Concerning urinary toxicities, grade 3-4 was observed in 7 patients from CCRT-ACT group, which was more than CCRT group (7 [3.4%] vs 1 [0.2%], P = 0.004).

QoL Status of Patients

EORTC QLQ-C30 V3.0 was used to evaluate the QoL status of patients. The scores range of each subscale or item ranged from 0-100. The higher score indicates better functioning or QoL, as well as a higher rate of symptoms or problems. The comparisons suggested that the majority of QoL aspects were similar in the 2 groups at long-term follow-up. However, the symptom scale in diarrhea was significantly different, and patients who underwent adjuvant chemotherapy after CCRT more frequently suffered from diarrhea than those treated with CCRT only (P = 0.000) (Table 6).

Table 6.

Mean Scores of Subscale/Item of EORTC QLQ-C30 V3.0 in CCRT and CCRT-ACT Groups After PSM.

Subscale/Item	Mean score (SD)
Subscale/Item	CCRT group	CCRT-ACT group	t	P-value
Global health quality of life	67.59 (35.67)	68.86 (16.53)	0.48	0.630
Functional scale
Physical	83.54 (19.21)	84.21 (13.45)	0.45	0.656
Role	85.12 (11.21)	85.62 (13.54)	0.48	0.629
Emotional	83.45 (17.64)	83.67 (13.49)	0.16	0.876
Cognitive	80.95 (19.73)	81.47 (16.46)	0.32	0.747
Social	85.21 (13.93)	84.99 (10.46)	−0.20	0.843
Symptom scale and/or items
Fatigue	20.43 (8.11)	19.56 (9.46)	−1.18	0.139
Nausea and vomiting	9.24 (3.15)	8.93(4.24)	−1.02	0.310
Pain	19.01 (7.74)	18.22 (8.87)	−1.13	0.259
Dyspnea	14.23 (3.58)	13.92 (4.56)	−0.92	0.360
Insomnia	30.25 (7.23)	30.86 (12.01)	0.78	0.436
Appetite loss	17.12 (5.12)	16.85 (4.65)	−0.63	0.528
Constipation	9.15 (2.63)	9.07 (4.73)	−0.27	0.789
Diarrhea	11.16 (4.21)	16.82 (6.43)	13.02	0.000
Financial difficulties	25.10 (7.52)	24.92 (5.30)	−0.31	0.760

Discussion

Cervical cancer is one of the most common malignancies and recognized as a major public health problem in China with an increasing incidence and younger age at diagnosis.⁹ The incidence of cervical cancer in Chinese married women is highly ranked among female malignant tumors. It is also the common cause of death among women in China presenting in a locally advanced stage. As CCRT is the main aspect of curative treatment of LACC, much of the treatment consists of providing adequate facilities for good-quality EBRT, ICBT, and delivery of adequate concurrent chemotherapy.¹⁰

Adjuvant chemotherapy is the absolute gold standard in the therapy of many tumor types. In contrast, the role of adjuvant chemotherapy for cervical cancer is not fully understood. Furthermore, detailed information on the effects of adjuvant chemotherapy, when added to CCRT, is still not available.¹¹ In China, adjuvant chemotherapy is generally performed in some patients with cervical cancer at a locally advanced stage, who are at high risk for recurrence and able to tolerate further treatment after CCRT.¹² Yet, the clinical feasibility of treatment with CCRT, followed by adjuvant chemotherapy in a larger group of LACC patients still remains unclear.

In this retrospective multicenter study, data from patients with LACC in stage IB2, IIA2, IIB-IVA, of which mainly IIA2, IIB and IIIB, were collected to make a clinical efficacy comparison between CCRT-ACT and CCRT group. In opposition to the benefits of the additional use of adjuvant chemotherapy after CCRT that has been reported by numerous previous studies,^13
-15 we did not find significant differences related to longer OS, DFS, PFS and DMFS between CCRT-ACT and CCRT group after a median follow-up of 56.4 months. When patients were divided into subgroups based upon whether or not with more advanced stages, OS, DFS, PFS of patients with stage IIIB and IVA in CCRT-ACT group was higher than that of those in CCRT group. However, the difference was not statistically significant. Kim YB et al.¹⁶ assessed the cervical cancer patients with stage IB and IIB who underwent CCRT followed by adjuvant chemotherapy in another retrospective analysis. According to the results of 5-year OS and DFS rates for patients in CCRT and CCRT-ACT groups (85% vs 80%, and 83% vs 78%, respectively), the data failed to show the discernable therapeutic advantage of adjuvant chemotherapy administered after CCRT. This was partly supported by findings from the randomized controlled trial of Tangjitgamol S et al.¹⁷ which found no significant benefit in response rate and survival of adjuvant chemotherapy with paclitaxel plus carboplatin after CCRT for LACC of stage IIB-IVA compared to standard treatment of CCRT alone. Nonetheless, it may be of some therapeutic advantage over CCRT alone in cervical cancer patients with positive pelvic or para-aortic lymph nodes who received post-CCRT adjuvant chemotherapy in the present study. Abe A et al.¹⁸ and Yuan Y et al.¹⁹ also reported encouraging results of adjuvant chemotherapy after completion of CCRT in an attempt to improve outcomes in the management of lymph nodal-metastatic cervical cancer. Future clinical trials are required for confirmation of the clinical efficacy of adjuvant chemotherapy, especially for the patients with poor prognostic factors.

Due to tumor heterogeneity, it is unlikely that the additional use of adjuvant chemotherapy after CCRT could show some improvement in clinical outcomes in patients with cervical cancer with different histological subtypes.²⁰ Zhang MQ et al.²¹ evaluated their experience with chemoradiotherapy for LACC patients only with SCC. They treated patients (stage IIB-IIIB) with CCRT followed by consolidation chemotherapy with paclitaxel and nedaplatin and demonstrated that this treatment regimen was well tolerated and effective. Although the analogical finding in our study was that the addition of adjuvant chemotherapy had no substantial impact on survival in LACC patients receiving CCRT, our protocols employing CCRT followed by adjuvant chemotherapy resulted in longer DMFS in LACC patients with SCC. Adjuvant chemotherapy that follows CCRT can potentially improve distant control of LACC with SCC, as argued by Jelavić TB et al.²² The improvement in distance metastasis control seems to be caused by a higher response rate to post-CCRT adjuvant chemotherapy in SCC patients. It is worth noting that in our study, only 46.9% of LACC patients with SCC received more than 2 cycles of adjuvant chemotherapy, and 53.1% received within 2 cycles, which was probably due to increased treatment-related morbidity or other causes. Furthermore, our data also showed that adjuvant chemotherapy with more than 2 cycles did not result in significantly improved survival compared to that within 2 cycles of adjuvant chemotherapy. Some clinical studies have confirmed that the addition of adjuvant chemotherapy after CCRT does leads to an increase in the risks of treatment-related adverse effects, requiring coordinated supportive care so as to avoid treatment delays and hospitalizations during the treatment course, as well as relatively poor compliance of patients.¹⁶ These observations related to the untoward effects of more cycles of adjuvant chemotherapy seems to preclude definitive conclusions regarding the true superiority of this modality. Although we failed to observe the potential beneficial effects in the small number of patients with non-SCC receiving adjuvant chemotherapy after CCRT, it is worthwhile to further expand the number of samples to study the treatment effect of patients who are more prone to suffer disease failure.²³

Chemotherapy comprising a platinum agent has been reported to be highly effective in advanced and recurrent cervical cancer.^24,25 Studies have shown that chemotherapy improves survival and decreases local and distant recurrence, yet at the expense of a varying degree of toxicity and morbidity.²⁶ In the present study, platinum-based chemotherapy after CCRT was administered as adjuvant chemotherapy and comprised paclitaxel combined with either cisplatin or carboplatin. Adjuvant chemotherapy following CCRT increased the severity of the grade 3 or higher acute hematological toxicity and late urinary and lower gastrointestinal complications. In contrast, the frequency of other toxicities did not differ between CCRT-ACT and CCRT group. Some researchers have focused on the radiation toxicity after completing treatment with chemoradiotherapy.^5,16,17 It was reported that hematological adverse event was the more prominent in acute toxicities during the treatment of CCRT followed by adjuvant chemotherapy compared with CCRT alone, however, the incidence of late radiation bladder and gastrointestinal complications did not significantly differ between CCRT-ACT and CCRT groups. The results might be related to differences in sensitivity to chemoradiotherapy in patients from different research groups.

Cervical cancer has long-term effects on health-related QoL of cancer survivors after treatment.²⁷ Few research studies have focused on the QoL of LACC survivors.²⁸ In this study, no differences in the global health QoL and functional scale were found between 2 groups; nevertheless, bowel morbidity was prevalent after treatment with definitive chemoradiotherapy in the symptom scale analysis. The LACC patients in CCRT-ACT groups more frequently experienced severe diarrhea symptoms than those who underwent CCRT only. Many patients treated for cervical cancer have long-term complaints regarding bowel function.²⁹ Digestive system interventions should be valued in improving QoL of cervical cancer chemoradiotherapy patients.³⁰

The tumor markers, including SCC-Ag and CA125, were identified as significant risk factors for survival (OS, DFS and PFS) in the multivariate analysis. These observations as well as the roles these risk factors have in predicting prognoses in LACC patients, have been reported by several previous studies.^31,32 Likewise, older patients and non-SCC patients were at higher risk for distant metastasis. Atahan IL et al.³³ evaluated possible prognostic factors in patients with LACC (88% with IIB-IIIB), reporting adenocarcinoma as one of the independent predictors for DMFS. In another study by Yokoi E et al.³⁴ compared the survival outcomes in patients with SCC and adenocarcinoma/adenosquamous carcinoma among patients with LACC. Patients with non-SCC histology experienced significantly worse survival outcomes than those with SCC. Additionally, the reason for the worse outcome in elderly patients may be somewhat aggressive tumor factors.³⁵

Based on analyses of tumor markers in patients treated with chemoradiotherapy, adjuvant chemotherapy after CCRT might presented a probability of greater DFS and PFS in patients with high level of CA125 (the lowest possible cut-off values were 19.8 and 20.5U/mL, respectively). The level of SCC-Ag was also significantly linked to DFS; more specifically, a greater DFS in CCRT-ACT patients was probably amplified a profit from high SCC-Ag level (above 22.8μg/L) compared with patients receiving CCRT alone. Our study supported the hypothesis that patients who could have been screened for high levels of tumor markers, especially CA125 and SCC-Ag, might have a greater survival benefit from adjuvant chemotherapy after CCRT.

In conclusion, this study was undertaken in a developing country where the majority of the global burden of cervical cancer resides. Our data failed to show the discernable therapeutic advantage of adjuvant chemotherapy given after CCRT in OS, DFS, PFS and DMFS for patients with LACC. However, adjuvant chemotherapy after CCRT had a more favorable distant metastasis control in managing LACC patients, particularly with pelvic/para-aortic lymph nodes involvement or SCC, than those treated with CCRT alone. It is a remarkable fact that the post-CCRT adjuvant chemotherapy with excessive cycle numbers should not be considered as the more appropriate choice, in order to avoid the probability of unnecessary cumulative toxicity, especially severe acute hematological toxicity, late urinary and lower gastrointestinal complications. Diarrhea might be one of the main symptoms affecting the QoL in LACC patients undergoing adjuvant chemotherapy after CCRT. Moreover, compared with standard CCRT treatment, patients with tumor markers above the threshold levels (CA125 > 20.5 U/mL, SCC-Ag > 22.8 μg/L) might have greater DFS and PFS from adjuvant chemotherapy after CCRT. The limitations of the present study is its retrospective nature. Well-designed prospective, randomized clinical trials are required to confirm further the clinical efficacy of CCRT plus adjuvant chemotherapy in patients with LACC.

Supplemental Material

Supplemental Material, sj-jpg-1-ccx-10.1177_1073274821989307 - A Multi-Institutional Retrospective Analysis of Oncologic Outcomes for Patients With Locally Advanced Cervical Cancer Undergoing Platinum-Based Adjuvant Chemotherapy After Concurrent Chemoradiotherapy

Supplemental Material, sj-jpg-1-ccx-10.1177_1073274821989307 for A Multi-Institutional Retrospective Analysis of Oncologic Outcomes for Patients With Locally Advanced Cervical Cancer Undergoing Platinum-Based Adjuvant Chemotherapy After Concurrent Chemoradiotherapy by Ning Wu, Xing Su, Honglin Song, Ying Li, Fei Gu, Xiaoge Sun, Xiaofan Li and Guanghui Cheng in Cancer Control

Supplemental Material

Supplemental Material, sj-jpg-2-ccx-10.1177_1073274821989307 - A Multi-Institutional Retrospective Analysis of Oncologic Outcomes for Patients With Locally Advanced Cervical Cancer Undergoing Platinum-Based Adjuvant Chemotherapy After Concurrent Chemoradiotherapy

Supplemental Material, sj-jpg-2-ccx-10.1177_1073274821989307 for A Multi-Institutional Retrospective Analysis of Oncologic Outcomes for Patients With Locally Advanced Cervical Cancer Undergoing Platinum-Based Adjuvant Chemotherapy After Concurrent Chemoradiotherapy by Ning Wu, Xing Su, Honglin Song, Ying Li, Fei Gu, Xiaoge Sun, Xiaofan Li and Guanghui Cheng in Cancer Control

Supplemental Material

Supplemental Material, sj-jpg-3-ccx-10.1177_1073274821989307 - A Multi-Institutional Retrospective Analysis of Oncologic Outcomes for Patients With Locally Advanced Cervical Cancer Undergoing Platinum-Based Adjuvant Chemotherapy After Concurrent Chemoradiotherapy

Supplemental Material, sj-jpg-3-ccx-10.1177_1073274821989307 for A Multi-Institutional Retrospective Analysis of Oncologic Outcomes for Patients With Locally Advanced Cervical Cancer Undergoing Platinum-Based Adjuvant Chemotherapy After Concurrent Chemoradiotherapy by Ning Wu, Xing Su, Honglin Song, Ying Li, Fei Gu, Xiaoge Sun, Xiaofan Li and Guanghui Cheng in Cancer Control

Footnotes

Authors’ Note

This retrospective study was registered with the Chinese Clinical Trial Registry (ChiCTR-PRC-16008822). All procedures performed in studies involving human participants were in accordance with the ethical standards of the independent Ethical Committee/Institutional Review Board of Jilin University (20160621) and conducted in accordance with the Declaration of Helsinki. Informed consent was exempted due to the retrospective format of this study.

Acknowledgments

The authors thank the patients and their colleagues Drs. Dan Shi, Xin Guo, Mingyuan He, Baocai Liu, Yiping Zhang, and Zhuang Mao for participating in this study.

Declaration of Conflicting Interests

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding

The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was partially supported by grants from the National Natural Science Foundation of China (grant number: 82073331, 81201737); Project of Science and Technology Development Plan of Jilin Province (grant number: 20200201524JC); Jilin University Undergraduate Education Reform Research Project (grant number: 2017XYB080); Medical Education Research Project of Chinese Medical Association Medical Education Branch, China Higher Education Society Medical Education Committee (grant number: 2018B-N15054); Youth Science and Technology Training Program in Health Commission of Jilin Province (grant number: 2018Q014) and Jilin Province Higher Education Research Project of Jilin Association for Higher Education (grant number: JGJX2020D30). The funding source had no role in the design of this study and will not have any role during its execution, analyses, interpretation of the data, writing assistance, or decision to submit results.

ORCID iD

Guanghui Cheng, MD, PhD

Supplemental Material

Supplemental material for this article is available online.

References

Bray

Ferlay

Soerjomataram

Siegel

Torre

Jemal

Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68(6):394–424.

Goss

Strasser-Weippl

Lee-Bychkovsky

, et al. Challenges to effective cancer control in China, India, and Russia. Lancet Oncol. 2014;15(5):489–538.

Rose

Bundy

Watkins

, et al. Concurrent cisplatin-based radiotherapy and chemotherapy for locally advanced cervical cancer. N Engl J Med. 1999;340(15):1144–1153.

Kumar

Gupta

Integrating chemotherapy in the management of cervical cancer: a critical appraisal. Oncology. 2016;91(1):8–17.

Kim

Han

Kim

. Phase II study of consolidation chemotherapy after adjuvant or primary concurrent chemoradiation using paclitaxel and carboplatin to treat high-risk early-stage or locally advanced cervical cancer. Cancer Res Treat. 2012;44(2):97–103.

Yavas

Sen

Oner

Celik

Ata

. Adjuvant carboplatin and paclitaxel after concurrent cisplatin and radiotherapy in patients with locally advanced cervical cancer. Int J Gynecol Cancer. 2019;29(1):42–47.

Todo

Watari

. Concurrent chemoradiotherapy for cervical cancer: background including evidence-based data, pitfalls of the data, limitation of treatment in certain groups. Chin J Cancer Res. 2016;28(2):221–227.

Zhao

Han

Cheng

Zhao

. Dosimetric research into target regions and organs at risk in three-dimensional intracavitary brachytherapy techniques for Chinese patients with cervical carcinoma. J Radiat Res. 2019;60(1):124–133.

Liu

Shi

Cai

, et al. Disparities in cancer incidence among Chinese population versus migrants to developed regions: a population-based comparative study. Cancer Epidemiol Biomarkers Prev. 2019;28(5):890–899.

10.

Umayahara

Takekuma

Hirashima

, et al. Phase II study of concurrent chemoradiotherapy with weekly cisplatin and paclitaxel in patients with locally advanced uterine cervical cancer: The JACCRO GY-01 trial. Gynecol Oncol. 2016;140(2):253–258.

11.

Wang

Chou

Yang

, et al. A randomized trial comparing concurrent chemoradiotherapy with single-agent cisplatin versus cisplatin plus gemcitabine in patients with advanced cervical cancer: An Asian Gynecologic Oncology Group study. Gynecol Oncol. 2015;137:462–467.

12.

Chung

Jian

Cheng

, et al. Extended-field radiotherapy and high-dose-rate brachytherapy with concurrent and adjuvant cisplatin-based chemotherapy for locally advanced cervical cancer: a phase I/II study. Gynecol Oncol. 2005;97(1):126–135.

13.

Ali

Valimohammad

Abbasi

Mansha

Hafiz

Qureshi

. Chemoradiation and the role of adjuvant chemotherapy in lymph nodal-metastatic cervical cancer. J Glob Oncol. 2018;4:1–4.

14.

Dueñas-González

Zarbá

Patel

, 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):1678–1685.

15.

Choi

Lee

Kim

, et al. Phase II study of consolidation chemotherapy after concurrent chemoradiation in cervical cancer: preliminary results. Int J Radiat Oncol Biol Phys. 2007;68(3):817–822.

16.

Kim

Cho

Keum

, et al. Concurrent chemoradiotherapy followed by adjuvant chemotherapy in uterine cervical cancer patients with high-risk factors. Gynecol Oncol. 2007;104(1):58–63.

17.

Tangjitgamol

Tharavichitkul

Tovanabutra

, et al. A randomized controlled trial comparing concurrent chemoradiation versus concurrent chemoradiation followed by adjuvant chemotherapy in locally advanced cervical cancer patients: ACTLACC trial. J Gynecol Oncol. 2019;30(4):e82.

18.

Abe

Furumoto

Nishimura

Irahara

Ikushima

. Adjuvant chemotherapy following concurrent chemoradiotherapy for uterine cervical cancer with lymphadenopathy. Oncol Lett. 2012;3(3):571–576.

19.

Yuan

You

Wang

. Adjuvant chemotherapy after radiotherapy or concurrent chemoradiotherapy for pelvic lymph node-positive patients with locally advanced cervical cancer: a propensity score matching analysis [published May 30, 2020]. Int J Gynecol Cancer. 2020;ijgc–2020-001230.

20.

Wang

Liu

Meng

Zhang

. Comparison of treatment outcomes between squamous cell carcinoma and adenocarcinoma of cervix after definitive radiotherapy or concurrent chemoradiotherapy. Radiat Oncol. 2018;13(1):249.

21.

Zhang

Liu

Wang

. Concurrent chemoradiotherapy with paclitaxel and nedaplatin followed by consolidation chemotherapy in locally advanced squamous cell carcinoma of the uterine cervix: preliminary results of a phase II study. Int J Radiat Oncol Biol Phys. 2010;78(3):821–827.

22.

Jelavić

Miše

Strikic

Ban

Vrdoljak

. Adjuvant chemotherapy in locally advanced cervical cancer after treatment with concomitant chemoradiotherapy—room for improvement? Anticancer Res. 2015;35(7):4161–4165.

23.

Pan

Yang

Wen

Tong

Tang

. Does adenocarcinoma have a worse prognosis than squamous cell carcinoma in patients with cervical cancer? A real-world study with a propensity score matching analysis. J Gynecol Oncol. 2020;31(6):e80.

24.

Boussios

Seraj

Zarkavelis

, et al. Management of patients with recurrent/advanced cervical cancer beyond first line platinum regimens: where do we stand? A literature review. Crit Rev Oncol Hematol. 2016;108:164–174.

25.

Zhang

Nie

Long

Zhang

. Comparison of nedaplatin- and cisplatin-based concurrent chemoradiotherapy in locally advanced cervical cancer patients: a propensity score analysis. Int J Gynecol Cancer. 2018;28(5):1029–1037.

26.

Song

Kong

Zhang

, et al. A retrospective analysis of cisplatin/carboplatin plus paclitaxel in advanced or recurrent cervical cancer. J Obstet Gynaecol. 2019;39(3):389–394.

27.

Greenwald

McCorkle

Baumgartner

Gotay

Neale

. Quality of life and disparities among long-term cervical cancer survivors. J Cancer Surviv. 2014;8(3):419–426.

28.

Zhao

Pan

, et al. Quality of life in women with cervical precursor lesions and cancer: a prospective, 6-month, hospital-based study in China. Chin J Cancer. 2014;33(7):339–345.

29.

Gargiulo

Arenare

Pisano

, et al. Long-term toxicity and quality of life in patients treated for locally advanced cervical cancer. Oncology. 2016;90(1):29–35.

30.

Jensen

NBK

Pötter

Kirchheiner

, et al. Bowel morbidity following radiochemotherapy and image-guided adaptive brachytherapy for cervical cancer: physician- and patient reported outcome from the EMBRACE study. Radiother Oncol. 2018;127(3):431–439.

31.

Lee

Kim

, et al. Tumour size, volume, and marker expression during radiation therapy can predict survival of cervical cancer patients: a multi-institutional retrospective analysis of KROG 16-01. Gynecol Oncol. 2017;147(3):577–584.

32.

Takeda

Sakuragi

Okamoto

, et al. Preoperative serum SCC, CA125, and CA19-9 levels and lymph node status in squamous cell carcinoma of the uterine cervix. Acta Obstet Gynecol Scand. 2002;81(5):451–457.

33.

Atahan

Onal

Ozyar

Yiliz

Selek

Kose

. Long-term outcome and prognostic factors in patients with cervical carcinoma: a retrospective study. Int J Gynecol Cancer. 2007;17(4):833–842.

34.

Yokoi

Mabuchi

Takahashi

, et al. Impact of histological subtype on survival in patients with locally advanced cervical cancer that were treated with definitive radiotherapy: adenocarcinoma/ adenosquamous carcinoma versus squamous cell carcinoma. J Gynecol Oncol. 2017;28(2):e19.

35.

Wang

Fang

, et al. Differences in the outcomes and complications between elderly and younger uterine cervical cancer patients treated by definitive radiotherapy—a propensity score-matched study. Gynecol Oncol. 2017;145(2):277–283.

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