Effect of Time Interval between Breast-Conserving Surgery and Radiation Therapy on Outcomes of Node-Positive Breast Cancer Patients Treated with Adjuvant Doxorubicin/Cyclophosphamide Followed by Taxane

Hyeon Kang Koh; Kyung Hwan Shin; Kyubo Kim; Eun Sook Lee; In Hae Park; Keun Seok Lee; Jungsil Ro; So-Youn Jung; Seeyoun Lee; Seok Won Kim; Han-Sung Kang; Eui Kyu Chie; Wonshik Han; Dong-Young Noh; Kyung-Hun Lee; Seock-Ah Im; Sung Whan Ha

doi:10.4143/crt.2015.111

Articles

Page Path: HOME > Cancer Res Treat > Volume 48(2); 2016 > Article

Original Article Effect of Time Interval between Breast-Conserving Surgery and Radiation Therapy on Outcomes of Node-Positive Breast Cancer Patients Treated with Adjuvant Doxorubicin/Cyclophosphamide Followed by Taxane: Hyeon Kang Koh, MD^1,2, Kyung Hwan Shin, MD^1,3,, Kyubo Kim, MD¹, Eun Sook Lee, MD³, In Hae Park, MD³, Keun Seok Lee, MD³, Jungsil Ro, MD³, So-Youn Jung, MD³, Seeyoun Lee, MD³, Seok Won Kim, MD³, Han-Sung Kang, MD³, Eui Kyu Chie, MD¹, Wonshik Han, MD⁴, Dong-Young Noh, MD⁴, Kyung-Hun Lee, MD⁵, Seock-Ah Im, MD⁵, Sung Whan Ha, MD¹; Cancer Research and Treatment : Official Journal of Korean Cancer Association 2016;48(2):483-490.
DOI: https://doi.org/10.4143/crt.2015.111
Published online: June 5, 2015

¹Department of Radiation Oncology, Seoul National University College of Medicine, Seoul, Korea

²Department of Radiation Oncology, Konkuk University Medical Center, Seoul, Korea

³Center for Breast Cancer, Research Institute and Hospital, National Cancer Center, Goyang, Korea

⁴Department of Surgery, Seoul National University College of Medicine, Seoul, Korea

⁵Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea

Correspondence: Kyung Hwan Shin, MD Department of Radiation Oncology, Seoul National University College of Medicine, 101 Daehak-ro, Jongno-gu, Seoul 03080, Korea
Tel: 82-2-2072-2524 Fax: 82-2-765-3317 E-mail: radiat@snu.ac.kr

• Received: March 19, 2015 • Accepted: April 22, 2015

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

11,448 Views
126 Download
10 Web of Science
9 Crossref
12 Scopus

prev next

Full Article

Download PDF

Abstract

Purpose
This study evaluated the effect of surgery-radiotherapy interval (SRI) on outcomes in patients treated with adjuvant radiotherapy (RT) after breast-conserving surgery (BCS) and adjuvant four cycles of doxorubicin/cyclophosphamide (AC) followed by four cycles of taxane.
Materials and Methods
From 1999 to 2007, 397 eligible patients were diagnosed. The effect of SRI on outcomes was analyzed using a Cox proportional hazards model, and a maximal chi-square method was used to identify optimal cut-off value of SRI for each outcome.
Results
The median SRI was 6.7 months (range, 5.6 to 10.3 months). A SRI of 7 months was the significant cut-off value for distant metastasis-free survival (DMFS) and disease-free survival (DFS) using a maximal chi-square method. For overall survival, a significant cut-off value was not found. The patients with SRI > 7 months had worse 6-year DMFS and DFS than those with SRI ≤ 7 months on univariate analysis (DMFS, 81% vs. 91%, p=0.003; DFS, 78% vs. 89%, p=0.002). On multivariate analysis, SRI > 7 months did not affect DMFS and DFS.
Conclusion
RT delayed for more than 7 months after BCS and adjuvant four cycles of AC followed by four cycles of taxane did not compromise clinical outcomes.
Key words: Breast neoplasms, Segmental mastectomy, Time-to-treatment, Radiotherapy, Adjuvant chemotherapy

Introduction

Since the Cancer and Leukemia Group B (CALGB) 9344 and the National Surgical Adjuvant Breast and Bowel Project (NSABP) B28 trials were reported, four cycles of doxorubicin/cyclophosphamide (AC) followed by four cycles of taxane has become a standard adjuvant chemotherapy regimen for patients with node-positive breast cancer [1,2]. The addition of taxane to AC improved disease-free survival (DFS), overall survival (OS), and local control (LC) despite a prolonged surgery-radiotherapy interval (SRI) [3].

However, delays between treatments can be harmful due to tumor doubling time, and delayed SRI can increase the development of radioresistance [4,5]. Several studies have identified a relationship between SRI and treatment outcomes in breast cancer. Most studies analyzed a heterogeneous population in terms of disease stage, nodal status, type of surgery, adjuvant chemotherapy, and adjuvant endocrine therapy. Hence, the results of these studies are contradictory, and the maximal safe SRI has not been established.

The aim of the present study is to examine the effect of SRI on treatment outcomes in breast cancer patients treated with breast-conserving surgery (BCS) and adjuvant chemotherapy with four cycles of AC plus four cycles of taxane.

Materials and Methods

1. Patient population

From October 1999 to June 2007, 397 patients with node-positive breast cancer underwent BCS, adjuvant four cycles of AC followed by four cycles of taxane, and adjuvant radiotherapy (RT) in sequence at the National Cancer Center and Seoul National University Hospital, Korea.

2. Treatment

All patients had BCS with axillary lymph node dissection or sentinel lymph node biopsy. The original pathologic report was reviewed to collect histologic data. All patients received four cycles of doxorubicin 60 mg/m² by slow intravenous push and then cyclophosphamide 600 mg/m² intravenous infusion over 30 minutes every 21 days followed by four additional 21-day cycles of taxane (paclitaxel 175 mg/m² intravenous or docetaxel 75 mg/m² intravenous as a 3-hour infusion on day 1 of each cycle).

Adjuvant RT was delivered after chemotherapy was completed. All patients underwent whole breast RT using 6-15 MV photons. Seven patients were treated with hypofractionated RT of 39 Gy using 3 Gy per fraction and the rest of the patients received conventional RT of 50-50.4 Gy at 1.8-2.0 Gy per fraction. An additional 9-16.2 Gy electron-boost using 1.8-3.0 Gy/fraction was delivered to the tumor bed. The addition of regional RT was decided at the discretion of the treating radiation oncologist’s assessment of regional failure risk. Two hundred and seventeen patients (54.7%) received 45-50.4 Gy at 1.8-2.0 Gy/fraction to the axillary and supraclavicular (SCL) regions. Among these patients, only one patient received additional RT to the internal mammary node (IMN) region.

Adjuvant hormonal therapy (HT) was given to most patients with estrogen receptor (ER)–positive or progesterone receptor (PR)–positive tumors. Three hundred and eight patients (77.6%) had ER-positive or PR-positive tumors. Among these patients, 251 received tamoxifen, 46 received aromatase inhibitors, 10 did not receive HT, and one patient had unavailable data. One patient received tamoxifen without hormonal receptor expression. If adjuvant HT was indicated, it was given with RT in most cases.

There were 71 patients (17.9%) with HER2-positive (immunohistochemistry 3+ or fluorescence in situ hybridization positive) tumors. Fifteen of these patients were treated with adjuvant trastuzumab and four patients received adjuvant lapatinib. Adjuvant trastuzumab or lapatinib were given on a 21-day cycle for one year and could be used with RT.

3. Statistical analysis

The interval between surgery and RT was defined as the time from the date of the first oncologic surgery to the first day of RT. The definition of ipsilateral breast tumor recurrence (IBTR) was recurrence of invasive breast cancer or ductal carcinoma in situ in the same breast treated with RT. Loco-regional recurrence (LRR) included IBTR, ipsilateral axillary lymph node recurrence, IMN recurrence, and SCL recurrence. Failure at any other site was considered a distant metastasis (DM). Each failure was scored as an event regardless of recurrence at other sites. Contralateral breast tumor recurrence was not counted as a failure but as a secondary malignancy. An event for DFS included IBTR, LRR and DM. The Kaplan-Meier method was used to calculate the actuarial rates of ipsilateral breast tumor recurrence-free survival (IBTRFS), loco-regional recurrence-free survival (LRRFS), distant metastasis-free survival (DMFS), DFS, and OS. Comparison between groups was performed by two-sided log-rank tests. Cox proportional hazards model was used for multivariate analysis and analysis of the effect of SRI on clinical outcomes. Maxstat, a maximal chi-square method in R 2.13.0 (R Development Core Team, Vienna, Austria, http://www.R-project.org) was used to identify optimal cut-off value of SRI for each outcome. Two-tailed null hypotheses of no difference were rejected if p-values were less than 0.05, or, equivalently, if the 95% confidence intervals (CIs) of hazard ratio estimates excluded 1. All statistical analyses, except Maxstat, were carried out using SPSS ver. 16.0 (SPSS Inc., Chicago, IL).

Results

1. Patient characteristics

Table 1 summarizes the patient and tumor characteristics. The median age of patients at diagnosis was 45 years old (range, 22 to 73 years). Most patients had invasive ductal carcinoma (94.5%) according to the World Health Organization’s classification system. Positive or close resection margin was reported in 13.6% of all cases following the last surgery. There were 192 patients (48.9%) with histologic grade III tumor, 114 patients (31.6%) with extensive intraductal component (EIC), 314 patients (79.1%) with lymphovascular space invasion (LVI) and 137 patients (36.0%) with Ki-67 greater than 15%. The pathologic stage by American Joint Committee on Cancer (AJCC) seventh edition was IIA in 115 patients (29.0%), IIB in 131 patients (33.0%), IIIA in 98 patients (24.7%), IIIB in one patient (0.3%), and IIIC in 52 patients (13.0%).

2. Outcomes

The median follow-up duration of all patients was 65 months (range, 9 to 137 months). During follow-up, there were 12 cases of IBTR, 20 cases of LRR, 45 cases of DM, and 24 deaths. The actuarial 6-year IBTRFS was 96.9%, LRRFS 93.8%, DMFS 87.6%, DFS 85.5%, and OS 93.9%.

3. Surgery-radiotherapy interval

The median interval between surgery and RT was 6.7 months (range, 5.6 to 10.3 months). Because the association between SRI as a continuous variable and clinical outcomes should be confirmed before finding an optimal cut-off value using maximal chi-square method, a Cox proportional hazard model was performed to estimate the association of SRI with each clinical outcome (Table 2). An increase of SRI was related to worse DMFS (p=0.002), DFS (p=0.003), and OS (p=0.008). The optimal cut-off value of SRI for DMFS and DFS was 7 months by maximal chi-square method (p=0.024 and p=0.016, respectively) (Figs. 1 and 2). Even though the optimal cut-off value of SRI for OS was 7.5 months, it was not statistically significant (p=0.255). When a SRI of 7 months was applied, there were 275 patients in the group with a SRI ≤ 7 months and 122 patients in the group with SRI > 7 months. The 6-year actuarial DMFS for patients with SRI > 7 months was 81% versus 91% for patients with SRI ≤ 7 months (p=0.003), and DFS was 78% versus 89% (p=0.002), respectively (Table 3).

4. Univariate analysis and multivariate analysis

Table 3 provides univariate and multivariate analyses of prognostic factors for 6-year outcomes. Patients younger than 40 years old, ER-negative, and PR-negative tumors showed poor prognosis in IBTRFS and LRRFS. The 6-year IBTRFS for patients age < 40 years versus ≥ 40 years was 93% versus 98% (p=0.001) and the 6-year LRRFS was 91% versus 95% (p=0.037), respectively. The 6-year IBTRFS for patients with ER-negative tumors versus ER-positive tumors was 93% versus 99% (p=0.001) and the 6-year LRRFS was 87% versus 97% (p < 0.001), respectively. PR-negative tumors showed worse 6-year IBTRFS than PR-positive tumors (93% for PR-negative vs. 99% for PR-positive, p < 0.001) and worse 6-year LRRFS (89% for PR-negative vs. 97% for PR-positive, p < 0.001). Histology, tumor size, tumor grade, resection margin, EIC, LVI, HER-2, menopause status, Ki-67, nodal stage and stage group did not have an impact on IBTRFS and LRRFS.

Tumor size, tumor grade, ER status, PR status, nodal stage, and stage group were analyzed as prognosticators for the 6-year DMFS and DFS. Larger tumors were a poor prognostic factor for DMFS (95% for tumor size ≤ 2 cm vs. 82% for tumor size > 2 cm, p < 0.001) and for DFS (93% for tumor size ≤ 2 cm vs. 81% for tumor size > 2 cm, p=0.001). Higher tumor grade negatively affected DMFS (100% for grade I vs. 92% for grade II vs. 82% for grade III, p=0.003) and DFS (100% for grade I vs. 91% for grade II vs. 79% for grade III, p=0.006). ER-negative tumors showed worse 6-year DMFS than ER-positive tumors (79% for ER-negative vs. 91% for ER-positive, p < 0.001) and 6-year DFS (75% for ER-negative vs. 90% for ER-positive, p < 0.001). The 6-year DMFS for patients with PR-negative tumors versus PR-positive tumors was 83% versus 90% (p=0.029) and the 6-year DFS was 78% versus 89% (p=0.001), respectively. Higher nodal stage was a negative prognosticator for DMFS (94% for N1 vs. 80% for N2 vs. 72% for N3, p < 0.001) and DFS (91% for N1 vs. 77% for N2 vs. 72% for N3, p < 0.001). Higher stage group presented poorer prognosis for DMFS (94% for stage II vs. 77% for stage III, p < 0.001) and DFS (99% for stage II vs. 86% for stage III, p < 0.001).

Larger tumor (97% for tumor size ≤ 2 cm vs. 91% for tumor size > 2 cm, p=0.012), ER-negative tumor (96% for ER-positive vs. 88% for ER-negative, p < 0.001), higher nodal stage (99% for N1 vs. 87% for N2 vs. 85% for N3, p < 0.001), and higher stage group (99% for stage II vs. 86% for stage III, p < 0.001) negatively affected OS.

A multivariate analysis was performed to exclude confounding factors for outcomes. In multivariate analysis, patients younger than 40 years old had a worse prognosis for IBTRFS; tumor size more than 2 cm had worse prognosis for DMFS; nodal stage was an independent prognostic factor for OS. A SRI of greater than 7 months, however, lost its prognostic significance on multivariate analysis.

Discussion

In the present study, the actuarial 6-year IBTRFS, LRRFS, DMFS, DFS, and OS rates for patients treated with BCS, adjuvant AC plus taxane, and adjuvant RT in sequence were 96.9%, 93.8%, 87.6%, 85.5%, and 93.9%, respectively. RT delayed for more than 7 months did not affect clinical outcomes in this population.

Since the introduction of adjuvant chemotherapy in breast cancer, many clinicians have studied the optimal SRI for patients treated with adjuvant chemotherapy. In 1993, Buchholz et al. [6] arbitrarily divided patients who received various types of chemotherapy regimens into two groups: SRI ≤ 6 months and > 6 months. They showed that SRI > 6 months negatively affected LC, DFS, and OS. Review articles have been published on the optimal timing of adjuvant RT in breast cancer [7-10]. These researchers concluded that SRI should not exceed 20-24 weeks after surgery when adjuvant chemotherapy was given [7-9]. A recent Cochrane review concluded that breast cancer outcomes were not compromised regardless of the sequence of adjuvant treatments within 7 months after surgery [10]. Among the patients treated with adjuvant chemotherapy in these review articles, most received cyclophosphamide, methotrexate, and 5-fluorouracil (CMF) regimen.

Although there is some evidence on SRI for patients who received adjuvant chemotherapy as mentioned above, there are no analyses of SRI in patients treated exclusively with four cycles of AC plus four cycles of taxane. In general, the AC plus taxane regimen takes longer to complete than a CMF regimen. However, CALGB 9344 demonstrated that the addition of a taxane to AC for node-positive breast cancer improved LC as well as DFS and OS [3]. Therefore, an acceptable SRI for AC plus taxane regimen needs to be established.

There have been studies of the relationship between SRI and LC for breast cancer patients treated with adjuvant chemotherapy regimens including anthracycline. Livi et al. [11] performed a subgroup analysis on patients treated with adjuvant chemotherapy (65% with 6 cycles of CMF regimen, 20% with anthracycline-based regimen and 15% with other regimens), adjuvant RT and no HT. Multivariate analysis showed RT timing was an independent prognostic factor for local relapse especially in the group of SRI > 180 days (p=0.045). However, other studies have shown that SRI was not associated with LC. Yock et al. [12] suggested that more than 7 months of SRI did not compromise LC in patients who received four or six cycles of CMF or AC regimen. Cefaro et al. [13] also concluded that SRI ≥ 6 months did not affect LC in patients who underwent an unspecified number of cycles of CMF or an anthracycline-based regimen. Corradini et al. [14] showed delayed RT did not compromise LRRFS in the chemotherapy group in a cohort study of 1,393 patients. In the present study, we found that SRI was not associated with IBTRFS and LRRFS in Cox proportional hazards model for node-positive breast cancer patients treated with BCS and four cycles of AC followed by four cycles of taxane.

As for other outcomes, there was no association between SRI and DMFS, DFS, and/or OS. Two studies indicated that SRI was not associated with DFS and OS in breast cancer patients treated with adjuvant chemotherapy before RT [5,12]. Yock et al. [12] showed that SRI had no effect on distant failure. Corradini et al. [14] suggested SRI ≥ 24 weeks did not compromise OS. Downing et al. [15] used path analysis to investigate the relationship among survival, SRI and receipt of adjuvant chemotherapy before RT or after RT. They also concluded that SRI was not related to survival in the path model (hazard ratio, 1.00; 95% CI, 0.99 to 1.01 per week increase). In the current study, the optimal cut-off value of SRI for DMFS and DFS was 7 months, and there was no significant optimal cut-off value of SRI for OS. More than 7 months of SRI resulted in poor prognosis for DMFS and DFS on univariate analysis, but the significance was lost on multivariate analysis. Therefore, 7 months of SRI seemed to have no significant effect on clinical outcomes in our study population.

Our study has both limitations and strengths. Given the retrospective nature of the study, the potential for selection bias cannot be excluded. Our study has a smaller sample size and shorter follow up period than previous studies of SRI or outcomes in breast cancer [5,11,14]. However, the study population is homogeneous in respect to the treatment.

Conclusion

More than 7 months of SRI did not compromise clinical outcomes of node-positive breast cancer patients treated with BCS, adjuvant AC followed by taxane, and RT in sequence. Because it is clearly unethical to randomize SRI among patients who receive the same treatment regimen, future research is needed on a larger data set to confirm the effect of SRI on the treatment outcomes in breast cancer.

NOTES

Conflict of interest relevant to this article was not reported.

Fig. 1.

Maximal chi-square method for distant metastasis-free survival (DMFS) (p=0.024). The cut-off value of surgery-radiotherapy interval (SRI) was set to what provided the best separation of DMFS into two groups, where the standardized log-rank statistics take their maximum.

Fig. 2.

Maximal chi-square method for disease-free survival (DFS) (p=0.016). The cut-off value of surgery-radiotherapy interval (SRI) was set to what provided the best separation of DFS into two groups, where the standardized log-rank statistics take their maximum.

Table 1.

Patient and tumor characteristics

Variable	No. of patients (%)
Age (yr)
< 40	87 (21.9)
≥ 40	310 (78.1)
Histology
IDCa	375 (94.5)
ILCa	6 (1.5)
Others	16 (4.0)
Tumor location
Right breast	183 (46.1)
Left breast	214 (53.9)
Tumor size (cm)
≤ 2	166 (41.8)
> 2	231 (58.2)
Tumor grade^a)
I	13 (3.3)
II	188 (47.8)
III	192 (48.9)
Resection margin
Negative	343 (86.4)
Close (≤ 2 mm)	48 (12.1)
Positive	6 (1.5)
EIC^a)
No	247 (68.4)
Yes	114 (31.6)
LVI^a)
No	53 (14.4)
Yes	314 (79.1)
Ki-67 (%)^a)
≤ 15	244 (64.0)
> 15	137 (36.0)
Estrogen receptor
Negative	114 (28.7)
Positive	283 (71.3)
Progesterone receptor
Negative	122 (30.7)
Positive	275 (69.3)
HER-2 receptor^a)
Negative	325 (82.1)
Positive^b)	71 (17.9)
Menopause status^a)
Premenopausal	228 (59.4)
Postmenopausal	125 (32.6)
Perimenopausal	31 (8.1)
Stage by AJCC 7th edition
IIA (T1N1)	115 (29.0)
IIB (T2N1)	131 (33.0)
IIIA (T1-2N2,T3N1-2)	98 (24.7)
IIIB (T4N1-2)	1 (0.3)
IIIC (N3)	52 (13.0)
Nodal stage (pathological)
N1mi	13 (3.3)
N1	237 (59.7)
N2	95 (23.9)
N3	52 (13.1)
Radiation field
Breast only	180 (45.3)
Breast and regional lymphatics	217 (54.7)

IDCa, invasive ductal carcinoma; ILCa, invasive lobular carcinoma; EIC, extensive intraductal component; LVI, lymphovascular space invasion; AJCC, American Joint Committee on Cancer.

^a) Analysis with available data,

^b) Immunohistochemistry 3+ or fluorescence in situ hybridization positive.

Table 2.

The effect of SRI on clinical outcomes and optimal cut-off value of SRI

	p-value of cox proportional hazards model	Optimal cut-off value (mo)	p-value of maximal chi-square test
IBTRFS	0.239	-	-
LRRFS	0.110	-	-
DMFS	0.002	7	0.024
DFS	0.003	7	0.016
OS	0.008	7.5	0.255

SRI, surgery-radiotherapy interval; IBTRFS, ipsilateral breast tumor recurrence-free survival; LRRFS, locoregional recurrence-free survival; DMFS, distant metastasis-free survival; DFS, disease-free survival; OS, overall survival.

Table 3.

Prognostic factors for 6-year outcomes

	No.	IBTRFS (%)	Uni^a)	Multi^b)	LRRFS (%)	Uni^a)	Multi^b)	DMFS (%)	Uni^a)	Multi^b)	DFS (%)	Uni^a)	Multi^b)	OS (%)	Uni^a)	Multi^b)
Age (yr)
< 40	87	93	0.001	0.011	91	0.037	0.096	86	0.639	-	83	0.262	-	94	0.900	-
≥ 40	310	98			95			88			86			94
Histology
IDCa	375	97	0.768	-	94	0.630	-	88	0.659	-	86	0.566	-	93	0.831	-
ILCa	6	100			100			100			100			100
Others	16	100			100			93			93			93
Tumor size (cm)
≤ 2	166	98	0.279	-	96	0.055	-	95	< 0.001	0.022	93	0.001	0.060	97	0.012	0.193
> 2	231	96			92			82			81			91
Tumor grade^c)
I	13	100	0.752	-	100	0.690	-	100	0.003	0.322	100	0.006	0.654	100	0.091	-
II	188	98			93			92			91			97
III	192	96			94			82			79			90
Resection margin
(-)	343	97	0.168	-	94	0.673	-	88	0.642	-	85	0.990	-	94	0.607	-
Close or (+)	54	100			95			89			89			90
EIC^c)
(-)	247	97	0.818	-	93	0.340	-	86	0.264	-	84	0.246	-	93	0.927	-
(+)	114	96			94			90			87			94
LVI^c)
(-)	53	98	0.764	-	91	0.800	-	91	0.077	-	90	0.193	-	93	0.925	-
(+)	314	96			94			87			84			94
ER
(-)	114	93	0.001	0.340	87	< 0.001	0.174	79	< 0.001	0.073	75	< 0.001	0.105	88	0.006	0.131
(+)	283	99			97			91			90			96
PR
(-)	122	93	< 0.001	0.131	89	< 0.001	0.211	83	0.029	0.374	78	0.001	0.864	90	0.071	0.752
(+)	275	99			97			90			89			96
HER-2^c)
(-)	325	97	0.761	-	94	0.559	-	88	0.171	-	87	0.168		94	0.504	-
(+)	71	96			94			84			80			90
Menopause status^c)
Premenopausal	228	96	0.219	-	95	0.643	-	89	0.755	-	87	0.505		95	0.372	-
Postmenopausal	125	99			94			86			85			92
Perimenopausal	31	96			85			82			76			91
N stage
N1	250	98	0.817	-	96	0.251	-	94	< 0.001	0.922	91	< 0.001	0.980	99	< 0.001	0.045
N2	95	95			89			80			77			87
N3	52	98			93			72			72			85
Ki-67 (%)^c)
≤ 15	244	97	0.514	-	94	0.887	-	86	0.612	-	85	0.710	-	94	0.725	-
> 15	137	96			94			89			86			93
Stage
II	246	98	0.871	-	96	0.128	-	94	< 0.001	0.920	91	< 0.001	0.898	99	< 0.001	0.950
III	151	96			91			77			76			86
SRI (mo)
≤ 7	275	98	0.263	-	95	0.101	-	91	0.003	0.146	89	0.002	0.134	96	0.022	0.415
> 7	122	96			91			81			78			90

IBTRFS, ipsilateral breast tumor recurrence-free survival; LRRFS, locoregional recurrence-free survival; DMFS, distant metastasis-free survival; DFS, disease-free survival; OS, overall survival; IDCa, invasive ductal carcinoma; ILCa, invasive lobular carcinoma; EIC, extensive intraductal component; LVI, lymphovascular space invasion; ER, estrogen receptor; PR, progesterone receptor; SRI, surgery-radiotherapy interval.

^a) Log-rank test,

^b) Cox regression analysis,

^c) Analysis with available data.

REFERENCES

1. Henderson IC, Berry DA, Demetri GD, Cirrincione CT, Goldstein LJ, Martino S, et al. Improved outcomes from adding sequential paclitaxel but not from escalating doxorubicin dose in an adjuvant chemotherapy regimen for patients with node-positive primary breast cancer. J Clin Oncol. 2003;21:976–83. Article PubMed
2. Mamounas EP, Bryant J, Lembersky B, Fehrenbacher L, Sedlacek SM, Fisher B, et al. Paclitaxel after doxorubicin plus cyclophosphamide as adjuvant chemotherapy for node-positive breast cancer: results from NSABP B-28. J Clin Oncol. 2005;23:3686–96. Article PubMed
3. Sartor CI, Peterson BL, Woolf S, Fitzgerald TJ, Laurie F, Turrisi AJ, et al. Effect of addition of adjuvant paclitaxel on radiotherapy delivery and locoregional control of node-positive breast cancer: cancer and leukemia group B 9344. J Clin Oncol. 2005;23:30–40. Article PubMed
4. Johnson A. The timing of treatment in breast cancer: gaps and delays in treatment can be harmful. Breast Cancer Res Treat. 2000;60:201–9. Article PubMed
5. Karlsson P, Cole BF, Colleoni M, Roncadin M, Chua BH, Murray E, et al. Timing of radiotherapy and outcome in patients receiving adjuvant endocrine therapy. Int J Radiat Oncol Biol Phys. 2011;80:398–402. Article PubMed PMC
6. Buchholz TA, Austin-Seymour MM, Moe RE, Ellis GK, Livingston RB, Pelton JG, et al. Effect of delay in radiation in the combined modality treatment of breast cancer. Int J Radiat Oncol Biol Phys. 1993;26:23–35. Article PubMed
7. Tsoutsou PG, Koukourakis MI, Azria D, Belkacemi Y. Optimal timing for adjuvant radiation therapy in breast cancer: a comprehensive review and perspectives. Crit Rev Oncol Hematol. 2009;71:102–16. Article PubMed
8. Ruo Redda MG, Verna R, Guarneri A, Sannazzari GL. Timing of radiotherapy in breast cancer conserving treatment. Cancer Treat Rev. 2002;28:5–10. Article PubMed
9. Huang J, Barbera L, Brouwers M, Browman G, Mackillop WJ. Does delay in starting treatment affect the outcomes of radiotherapy? A systematic review. J Clin Oncol. 2003;21:555–63. Article PubMed
10. Hickey BE, Francis DP, Lehman M. Sequencing of chemotherapy and radiotherapy for early breast cancer. Cochrane Database Syst Rev. 2013;4:CD005212Article
11. Livi L, Borghesi S, Saieva C, Meattini I, Rampini A, Petrucci A, et al. Radiotherapy timing in 4,820 patients with breast cancer: university of florence experience. Int J Radiat Oncol Biol Phys. 2009;73:365–9. Article PubMed
12. Yock TI, Taghian AG, Kachnic LA, Coen JJ, Assaad SI, Powell SN. The effect of delaying radiation therapy for systemic chemotherapy on local-regional control in breast cancer. Breast Cancer Res Treat. 2004;84:161–71. Article PubMed
13. Cefaro GA, Genovesi D, Marchese R, Di Tommaso M, Di Febo F, Ballone E, et al. The effect of delaying adjuvant radiation treatment after conservative surgery for early breast cancer. Breast J. 2007;13:575–80. Article PubMed
14. Corradini S, Niemoeller OM, Niyazi M, Manapov F, Haerting M, Harbeck N, et al. Timing of radiotherapy following breast-conserving surgery: outcome of 1393 patients at a single institution. Strahlenther Onkol. 2014;190:352–7. Article PubMed
15. Downing A, Gilthorpe MS, Dodwell D, Lawrence G, Forman D. Waiting times for radiotherapy after breast-conserving surgery and the association with survival: a path analysis. Clin Oncol (R Coll Radiol). 2011;23:442–8. Article PubMed

Figure & Data

REFERENCES

Citations

Citations to this article as recorded by

MiR-210 regulates lung adenocarcinoma by targeting HIF-1α
Guolei Cao, Peiwen Fan, Ronghui Ma, Qinghe Wang, Lili He, Haiwen Niu, Qin Luo
Heliyon.2023; 9(5): e16079. CrossRef
Timing of postmastectomy radiotherapy following adjuvant chemotherapy for high-risk breast cancer: A post hoc analysis of a randomised controlled clinical trial
Si-Ye Chen, Guang-Yi Sun, Yu Tang, Hao Jing, Yong-Wen Song, Jing Jin, Yue-Ping Liu, Xu-Ran Zhao, Yu-Chun Song, Bo Chen, Shu-Nan Qi, Yuan Tang, Ning-Ning Lu, Ning Li, Hui Fang, Ye-Xiong Li, Shu-Lian Wang
European Journal of Cancer.2022; 174: 153. CrossRef
Timing of Postmastectomy Radiotherapy Following Adjuvant Chemotherapy for High-Risk Breast Cancer: A Post-Hoc Analysis of a Randomised Controlled Clinical Trial
Si-Ye Chen, Guang-Yi Sun, Yu Tang, Hao Jing, Yong-Wen Song, Jing Jin, Yue-Ping Liu, Xu-Ran Zhao, Yu-Chun Song, Bo Chen, Shu-Nan Qi, Yuan Tang, Ning-Ning Lu, Ning Li, Hui Fang, Ye-Xiong Li, Shu-Lian Wang
SSRN Electronic Journal .2022;[Epub] CrossRef
Social Determinants of Racial Disparities in Breast Cancer Mortality Among Black and White Women
Oluwole Adeyemi Babatunde, Jan M. Eberth, Tisha Felder, Robert Moran, Samantha Truman, James R. Hebert, Jiajia Zhang, Swann Arp Adams
Journal of Racial and Ethnic Health Disparities.2021; 8(1): 147. CrossRef
How Does the Interval Between Completion of Adjuvant Chemotherapy and Initiation of Radiotherapy Impact Clinical Outcomes in Operable Breast Cancer Patients?
Lu Cao, Cheng Xu, Gang Cai, Wei-Xiang Qi, Rong Cai, Shu-Bei Wang, Dan Ou, Min Li, Kun-Wei Shen, Jia-Yi Chen
Annals of Surgical Oncology.2021; 28(4): 2155. CrossRef
Saving the Breast Saves the Lives of Breast Cancer Patients
Mohammad Esmaeil Akbari, Maryam Khayamzadeh, Hamid Reza Mirzaei, Afshin Moradi, Atieh Akbari, Farid Moradian, Neda Khalili
International Journal of Surgical Oncology.2020; 2020: 1. CrossRef
Timing of Chemotherapy and Radiotherapy Following Breast-Conserving Surgery for Early-Stage Breast Cancer: A Retrospective Analysis
Si-Ye Chen, Yu Tang, Shu-Lian Wang, Yong-Wen Song, Hui Fang, Jian-Yang Wang, Hao Jing, Jiang-Hu Zhang, Guang-Yi Sun, Xu-Ran Zhao, Jing Jin, Yue-Ping Liu, Bo Chen, Shu-Nan Qi, Ning Li, Yuan Tang, Ning-Ning Lu, Hua Ren, Zi-Hao Yu, Ye-Xiong Li
Frontiers in Oncology.2020;[Epub] CrossRef
Evaluation of tissue computed tomography number changes and dosimetric shifts after conventional whole-breast irradiation in patients undergoing breast-conserving surgery
Joo Hwan Lee, Dong Soo Lee, So Hyun Park, Young Kyu Lee, Jeong Soo Kim, Yong Seok Kim
Tumor Biology.2018; 40(8): 101042831879188. CrossRef
The influence of timing of radiation therapy following breast-conserving surgery on 10-year disease-free survival
Marissa C van Maaren, Reini W Bretveld, Jan J Jobsen, Renske K Veenstra, Catharina GM Groothuis-Oudshoorn, Hendrik Struikmans, John H Maduro, Luc JA Strobbe, Philip MP Poortmans, Sabine Siesling
British Journal of Cancer.2017; 117(2): 179. CrossRef

PubReader
ePub Link

Cite

CITE: export Copy Download Format; Close

Download Citation

Download a citation file in RIS format that can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Reference Manager.

Format:

RIS — For EndNote, ProCite, RefWorks, and most other reference management software
BibTeX — For JabRef, BibDesk, and other BibTeX-specific software

Include:

Citation for the content below
Citation and abstract for the content below

Effect of Time Interval between Breast-Conserving Surgery and Radiation Therapy on Outcomes of Node-Positive Breast Cancer Patients Treated with Adjuvant Doxorubicin/Cyclophosphamide Followed by Taxane

Cancer Res Treat. 2016;48(2):483-490. Published online June 5, 2015

DOI: https://doi.org/10.4143/crt.2015.111

XML Download

Abstract
Introduction
Materials and Methods
Results
Discussion
Conclusion
NOTES
REFERENCES

Fig. 1. Maximal chi-square method for distant metastasis-free survival (DMFS) (p=0.024). The cut-off value of surgery-radiotherapy interval (SRI) was set to what provided the best separation of DMFS into two groups, where the standardized log-rank statistics take their maximum.

Fig. 2. Maximal chi-square method for disease-free survival (DFS) (p=0.016). The cut-off value of surgery-radiotherapy interval (SRI) was set to what provided the best separation of DFS into two groups, where the standardized log-rank statistics take their maximum.

Fig. 1.

Fig. 2.

Variable	No. of patients (%)
Age (yr)
< 40	87 (21.9)
≥ 40	310 (78.1)
Histology
IDCa	375 (94.5)
ILCa	6 (1.5)
Others	16 (4.0)
Tumor location
Right breast	183 (46.1)
Left breast	214 (53.9)
Tumor size (cm)
≤ 2	166 (41.8)
> 2	231 (58.2)
Tumor grade^a)
I	13 (3.3)
II	188 (47.8)
III	192 (48.9)
Resection margin
Negative	343 (86.4)
Close (≤ 2 mm)	48 (12.1)
Positive	6 (1.5)
EIC^a)
No	247 (68.4)
Yes	114 (31.6)
LVI^a)
No	53 (14.4)
Yes	314 (79.1)
Ki-67 (%)^a)
≤ 15	244 (64.0)
> 15	137 (36.0)
Estrogen receptor
Negative	114 (28.7)
Positive	283 (71.3)
Progesterone receptor
Negative	122 (30.7)
Positive	275 (69.3)
HER-2 receptor^a)
Negative	325 (82.1)
Positive^b)	71 (17.9)
Menopause status^a)
Premenopausal	228 (59.4)
Postmenopausal	125 (32.6)
Perimenopausal	31 (8.1)
Stage by AJCC 7th edition
IIA (T1N1)	115 (29.0)
IIB (T2N1)	131 (33.0)
IIIA (T1-2N2,T3N1-2)	98 (24.7)
IIIB (T4N1-2)	1 (0.3)
IIIC (N3)	52 (13.0)
Nodal stage (pathological)
N1mi	13 (3.3)
N1	237 (59.7)
N2	95 (23.9)
N3	52 (13.1)
Radiation field
Breast only	180 (45.3)
Breast and regional lymphatics	217 (54.7)

	p-value of cox proportional hazards model	Optimal cut-off value (mo)	p-value of maximal chi-square test
IBTRFS	0.239	-	-
LRRFS	0.110	-	-
DMFS	0.002	7	0.024
DFS	0.003	7	0.016
OS	0.008	7.5	0.255

	No.	IBTRFS (%)	Uni^a)	Multi^b)	LRRFS (%)	Uni^a)	Multi^b)	DMFS (%)	Uni^a)	Multi^b)	DFS (%)	Uni^a)	Multi^b)	OS (%)	Uni^a)	Multi^b)
Age (yr)
< 40	87	93	0.001	0.011	91	0.037	0.096	86	0.639	-	83	0.262	-	94	0.900	-
≥ 40	310	98			95			88			86			94
Histology
IDCa	375	97	0.768	-	94	0.630	-	88	0.659	-	86	0.566	-	93	0.831	-
ILCa	6	100			100			100			100			100
Others	16	100			100			93			93			93
Tumor size (cm)
≤ 2	166	98	0.279	-	96	0.055	-	95	< 0.001	0.022	93	0.001	0.060	97	0.012	0.193
> 2	231	96			92			82			81			91
Tumor grade^c)
I	13	100	0.752	-	100	0.690	-	100	0.003	0.322	100	0.006	0.654	100	0.091	-
II	188	98			93			92			91			97
III	192	96			94			82			79			90
Resection margin
(-)	343	97	0.168	-	94	0.673	-	88	0.642	-	85	0.990	-	94	0.607	-
Close or (+)	54	100			95			89			89			90
EIC^c)
(-)	247	97	0.818	-	93	0.340	-	86	0.264	-	84	0.246	-	93	0.927	-
(+)	114	96			94			90			87			94
LVI^c)
(-)	53	98	0.764	-	91	0.800	-	91	0.077	-	90	0.193	-	93	0.925	-
(+)	314	96			94			87			84			94
ER
(-)	114	93	0.001	0.340	87	< 0.001	0.174	79	< 0.001	0.073	75	< 0.001	0.105	88	0.006	0.131
(+)	283	99			97			91			90			96
PR
(-)	122	93	< 0.001	0.131	89	< 0.001	0.211	83	0.029	0.374	78	0.001	0.864	90	0.071	0.752
(+)	275	99			97			90			89			96
HER-2^c)
(-)	325	97	0.761	-	94	0.559	-	88	0.171	-	87	0.168		94	0.504	-
(+)	71	96			94			84			80			90
Menopause status^c)
Premenopausal	228	96	0.219	-	95	0.643	-	89	0.755	-	87	0.505		95	0.372	-
Postmenopausal	125	99			94			86			85			92
Perimenopausal	31	96			85			82			76			91
N stage
N1	250	98	0.817	-	96	0.251	-	94	< 0.001	0.922	91	< 0.001	0.980	99	< 0.001	0.045
N2	95	95			89			80			77			87
N3	52	98			93			72			72			85
Ki-67 (%)^c)
≤ 15	244	97	0.514	-	94	0.887	-	86	0.612	-	85	0.710	-	94	0.725	-
> 15	137	96			94			89			86			93
Stage
II	246	98	0.871	-	96	0.128	-	94	< 0.001	0.920	91	< 0.001	0.898	99	< 0.001	0.950
III	151	96			91			77			76			86
SRI (mo)
≤ 7	275	98	0.263	-	95	0.101	-	91	0.003	0.146	89	0.002	0.134	96	0.022	0.415
> 7	122	96			91			81			78			90

Table 1. Patient and tumor characteristics

IDCa, invasive ductal carcinoma; ILCa, invasive lobular carcinoma; EIC, extensive intraductal component; LVI, lymphovascular space invasion; AJCC, American Joint Committee on Cancer.

Analysis with available data,

Immunohistochemistry 3+ or fluorescence in situ hybridization positive.

Table 2. The effect of SRI on clinical outcomes and optimal cut-off value of SRI

Table 3. Prognostic factors for 6-year outcomes

Log-rank test,

Cox regression analysis,

Analysis with available data.