Comparison of concurrent chemoradiotherapy versus sequential radiochemotherapy in patients with completely resected non-small cell lung cancer.

PURPOSE: Our institution has implemented two different adjuvant protocols in treating patients with non-small cell lung cancer (NSCLC): chemotherapy followed by concurrent chemoradiotherapy (CT-CCRT) and sequential postoperative radiotherapy (PORT) followed by postoperative chemotherapy (POCT). We aimed to compare the clinical outcomes between the two adjuvant protocols.
MATERIALS AND METHODS: From March 1997 to October 2012, 68 patients were treated with CT-CCRT (n = 25) and sequential PORT followed by POCT (RT-CT; n = 43). The CT-CCRT protocol consisted of 2 cycles of cisplatin-based POCT followed by PORT concurrently with 2 cycles of POCT. The RT-CT protocol consisted of PORT followed by 4 cycles of cisplatin-based POCT. PORT was administered using conventional fractionation with a dose of 50.4-60 Gy. We compared the outcomes between the two adjuvant protocols and analyzed the clinical factors affecting survivals.
RESULTS: Median follow-up time was 43.9 months (range, 3.2 to 74.0 months), and the 5-year overall survival (OS), locoregional recurrence-free survival (LRFS), and distant metastasis-free survival (DMFS) were 53.9%, 68.2%, and 51.0%, respectively. There were no significant differences in OS (p = 0.074), LRFS (p = 0.094), and DMFS (p = 0.490) between the two protocols. In multivariable analyses, adjuvant protocol remained as a significant prognostic factor for LRFS, favouring CT-CCRT (hazard ratio [HR] = 3.506, p = 0.046) over RT-CT, not for OS (HR = 0.647, p = 0.229).
CONCLUSION: CT-CCRT protocol increased LRFS more than RT-CT protocol in patients with completely resected NSCLC, but not in OS. Further studies are warranted to evaluate the benefit of CCRT strategy compared with sequential strategy.

Introduction

Because surgery alone is not a satisfactory strategy for the treatment of non-small cell lung cancer (NSCLC), adjuvant treatment with postoperative chemotherapy (POCT) and postoperative radiotherapy (PORT) is usually recommended. Cisplatin-based POCT is the standard of care for stage II-III NSCLC patients who undergo complete resection [1,2]. However, the benefit of PORT has been an issue of debate. A meta-analysis showed that while PORT significantly lowered local recurrence, it had a detrimental effect on survival [3]. However, such harmful effect on survival can be attributed to old-fashioned radiotherapy techniques with increased cardiopulmonary toxicity. Modern radiotherapy using linear accelerator can improve local control and survival [4]. A large-scaled retrospective study using data set of Surveillance, Epidemiology, and End Results (SEER) reported a survival benefit of PORT for N2 disease [5]. The Adjuvant Navelbine International Trialist Association (ANITA) trial also showed a potential benefit of PORT for N2 disease in the setting of POCT [6]. Recently, a review of the data from the National Cancer Data Base (NCDB) showed additional survival benefit of PORT in patients with N2 disease who received adjuvant chemotherapy [7-9]. Therefore, PORT can be considered as an adjuvant therapy after POCT in patients with N2 disease as well as those with a close or positive resection margin status.

In October 1996, before POCT became a standard of care for stage II-III NSCLC, adjuvant chemotherapy followed by concurrent chemoradiotherapy (CT-CCRT) was established as an institutional protocol for patients showing pathologic N1-2 disease (mainly N2) or a close/positive resection margin. After POCT became a standard of care, sequential PORT followed by POCT (RT-CT) has been a routine protocol in our institution with a consensus of a multidisciplinary team [10].

In cases where both POCT and PORT are administered after surgery, the optimal way of combining these two therapies has not yet been discovered. In this study, we aimed to compare the clinical outcomes between our two historical protocols (CT-CCRT vs. RT-CT).

Materials and Methods

Using our institutional tumor registry database, we identified 68 patients who underwent both PORT and POCT after complete surgical resection for NSCLC between 1997 and 2012. For staging work-up, chest computed tomography (CT), bronchoscopy, enhanced brain CT or magnetic resonance imaging (MRI), and bone scan or positron emission tomography (PET) were routinely performed. Lobectomy or pneumonectomy with mediastinal lymph node dissection were performed in patients with clinical N0-1 or single-station minimal N2 disease. Pathologic stages were described according to the 7th edition of American Joint Committee on Cancer (AJCC) TNM classification.

PORT was administered in patients with pathologic N1-2 disease (mainly N2) and positive or close resection margins. Before 2002, PORT was performed using the conventional two-dimensional technique (2D-RT) with megavoltage beams (≥6 MV). Initial anterior/posterior–posterior/anterior fields included an ipsilateral hilum and involved lymph nodal stations plus its next draining stations, and a dose of 30.6–41.4 Gy using conventional fractionation (1.8–2.0 Gy/day) was irradiated. Two off-cord oblique fields were implemented to boost the ipsilateral hilum and involved nodal stations with a dose up to 50.4–60.0 Gy. After 2002, three-dimensional conformal radiation therapy (3D-CRT) was adopted using megavoltage photon beam. For 3D-CRT, CT simulation was scanned under the free-breathing condition. The initial clinical target volume (CTV) included a bronchial stump, involved mediastinal lymph nodal stations, and its next draining stations. The boost CTV only included a bronchial stump and involved nodal stations. The planning target volume (PTV) was expanded in all directions from the CTV with a margin of 1.0–1.5 cm. Conventional fractionation was used with a dose of 44–45 Gy for initial volume, and the boost volume was irradiated up to 50.4–60.0 Gy. In case of a close resection margin (less than 5 mm), the region of the close margin was boosted up to doses of 66 Gy.

POCT was administered in patients with pathologic stage II/III according to our institutional protocols; 1) CT-CCRT protocol (adjuvant chemotherapy followed by concurrent chemoradiotherapy): two cycles of cisplatin-basted chemotherapy were administered, followed by PORT concurrently with two cycles of chemotherapy [11] and 2) RT-CT protocol (sequential PORT followed by POCT): PORT was administered within 4–6 weeks after surgery, followed by 4 cycles of cisplatin-based adjuvant chemotherapy [10].

To assess comorbidity, we calculated an age-adjusted Charlson comorbidity score by using of previous established International Classification of Disease—10 diagnosis codes from inpatient and outpatient records—from the time of first visit of each patient to the date of surgical resection [12].

We then analyzed the pattern of first failures and clinical parameters influencing locoregional recurrence-free survival (LRFS), distant metastasis-free survival (DMFS) and overall survival (OS). We compared the pattern of first failures and survivals between CT-CCRT and RT-CT protocols. Comparison between the two protocols was analyzed using a chi-square test or Fisher exact test for categorical variables and the Student t-test or the Mann-Whitney U test for continuous variables. Survival time was calculated by the interval between the date of the surgery and the date of the last follow-up or events (death event for OS, first loco-regional failure for LRFS, and first distant metastasis for DMFS). Survivals were calculated using the Kaplan-Meier method. The log-rank test and Cox proportional hazards regression model were used for univariable and multivariable analyses, respectively. Factors with a p-value of less than 0.2 by a univariable analysis were used for a multivariable analysis. Two sided p-values less than 0.05 were regarded as statistically significant. All statistical analyses were performed using R statistical packages [13]. This study was reviewed and approved by the Ajou University School of Medicine Institutional Review Board (AJIRB-MED-MDB-13-036).

Results

Among a total of 68 patients, 45 patients (66.2%) were males and the median age was 58 years (range, 30 to 69 years). The CT-CCRT and RT-CT protocols were administered in 25 (36.8%) and 43 patients (63.2%), respectively. The types of surgery included lobectomy in 53 patients (77.9%) and pneumonectomy in 15 (22.1%). Squamous cell carcinoma and adenocarcinoma were observed in 36 patients (52.9%) and 24 patients (35.3%), respectively. Pathologic nodal stages were N1 in 15 patients (22.1%) and N2 in 51 patients (75.0%), while 2 patients with pN0 disease showed a close resection margin of less than 5 mm. The median dose of PORT was 54.0 Gy (range, 39.6 to 64.4 Gy) and the median cycle of POCT was 4 (range, 2 to 6).

Patient characteristics for CT-CCRT and RT-CT protocols are summarized in Table 1. There were no significant differences in proportions of gender, history of smoking, comorbidity index, tumor histology, type of surgery, T-stage and N-stage between the two protocols. The age of the patients in the CT-CCRT protocol was significantly older than that of patients in the RT-CT protocol (mean age, 58.7 vs. 52.9 years; p = 0.025). The proportion of patients showing ECOG PS 2 in the RT-CT protocol was significantly higher than that of patients in the CT-CCRT protocol (0% vs. 14.0 %; p = 0.050). The absolute value of preoperative forced expiratory volume in 1 second (FEV1) in the RT-CT protocol was significantly higher than that of the CT-CCRT protocol (mean FEV1, 2.2 L vs. 2.7 L; p = 0.002). The postoperative FEV1 was available in 35 patients (51.5%) and there was no significant difference between the two protocols. Twenty-one patients (84.0%) who underwent the CT-CCRT protocol were treated by 2D-RT, while 42 patients (97.7%) who received the RT-CT protocol were treated with 3D-CRT. Radiation was delivered with a significantly higher dose in the RT-CT protocol compared to that in the CT-CCRT protocol (mean dose, 52.8 Gy vs. 55.8 Gy, p = 0.013). The median POCT cycle was 4 in both protocols. Mild to moderate radiation esophagitis was found in 2 patients (8.0%) for the CT-CCRT protocol, and in 11 patients (25.6%) for the RT-CT protocol (p = 0.145). The rate of symptomatic radiation pneumonitis treated with steroid was not significantly different between the two protocols (24.0% vs. 9.3%, p = 0.195). There was also no significant difference in hematologic toxicities of grade 3–4 (20.0% vs. 46.5%, p = 0.054). Comparing the pattern of first failures, there were no significant differences in locoregional recurrence (LR), distant metastasis (DM), and both LR and DM between the two protocols (Table 2).

Table 1.

Patient characteristics according to treatment protocols

Characteristic	CT-CCRT (n = 25)	RT-CT (n = 43)	p-value
Age (yr)	58.7 ± 8.4	52.9 ± 10.7	0.025
Gender			0.106
Male	13	32
Female	12	11
Smoking history			0.579
Yes	10	13
No	15	30
ECOG PS			0.050
0–1	25	37
2	0	6
Comorbidity index			0.206
<3	13	29
≥3	12	14
Preoperative FEV1 (L)	2.2 ± 0.5	2.7 ± 0.7	0.002
Postoperative FEV1 (L)[a)]	2.2 ± 0.9	2.0 ± 0.6	0.718
Tumor histology			0.694
Squamous cell	13	23
Adenocarcinoma	10	14
Others	2	6
Type of surgery			0.550
Lobectomy	18	35
Pneumonectomy	7	8
Pathologic T stage			0.347
T1	5	4
T2	13	29
T3	7	10
Pathologic N stage			0.095
N0	2	0
N1	7	8
N2	16	35
Radiotherapy technique			<0.001
Two-dimensional	21	1
Three-dimensional	4	42
Radiotherapy dose (Gy)	52.8 ± 5.5	55.8 ± 4.3	0.013

Values are presented as mean ± standard deviation or number.

CT-CCRT, adjuvant chemotherapy followed by concomitant chemoradiotherapy; RT-CT, sequential postoperative radiotherapy followed by adjuvant chemotherapy; ECOG PS, Eastern Cooperative Oncology Group performance status; FEV1, forced expiratory volume in 1 second.

Postoperative FEV1 was available in 35 patients (51.5%).

Table 2.

Pattern of first failures according to treatment protocols

First failure site	CT-CCRT (n = 25)	RT-CT (n = 43)	p-value
Locoregional	0 (0)	2 (4.7)	0.528
Distant metastasis	6 (24.0)	7 (16.3)	0.527
Both locoregional and distant metastasis	4 (16.0)	13 (30.2)	0.251

Values are presented as number (%).

CT-CCRT, adjuvant chemotherapy followed by concomitant chemoradiotherapy; RT-CT, sequential postoperative radiotherapy followed by adjuvant chemotherapy.

The median follow-up time of 68 patients was 43.9 months (range, 3.2 to 74.0 months), and the OS was 53.9% at 5 years. The 5-year LRFS and DMFS were 68.2% and 51.0%, respectively. Patients with CT-CCRT protocol showed favourable LRFS, but unfavourable OS compared to the RT-CT protocol (5-year LRFS, 82.8% vs. 60.3%, p = 0.094; 5-year OS, 44.0% vs. 61.3%, p = 0.074). There was no significant difference in DMFS between the two protocols (5-year DMFS, 53.3% vs. 46.4%, p = 0.490) (Table 3).

Table 3.

Univariable analyses for clinical variables affecting survivals

Variable	5-yr LRFS (%)	p-value (log-rank)	5-yr DMFS (%)	p-value (log-rank)	5-yr OS (%)	p-value (log-rank)
Age (<58 vs. ≥58 yr)	68.6 vs. 67.2	0.632	50.0 vs. 52.0	0.793	65.3 vs. 43.3	0.072
Gender (male vs. female)	73.0 vs. 59.4	0.071	55.3 vs. 42.7	0.084	53.6 vs. 54.6	0.855
Smoking history (no vs. yes)	65.3 vs. 69.5	0.223	48.0 vs. 52.0	0.233	60.8 vs. 50.7	0.472
ECOG PS (0–1 vs. 2)	69.3 vs. 53.3	0.188	54.7 vs. 0.0	0.174	53.4 vs. 62.5	0.955
Comorbidity index (<2 vs. ≥2)	62.8 vs. 70.4	0.873	51.5 vs. 50.6	0.861	66.2 vs. 49.4	0.081
Preoperative FEV1 (<2.5 L vs. ≥2.5 L)	64.3 vs. 73.8	0.189	47.5 vs. 57.5	0.407	46.7 vs. 61.9	0.378
Surgery (lobectomy vs. pneumonectomy)	65.3 vs. 82.5	0.375	49.5 vs. 54.5	0.961	56.0 vs. 45.7	0.242
Tumor histology (squamous vs. others)	63.7 vs. 74.1	0.297	42.7 vs. 61.5	0.165	55.3 vs. 51.6	0.786
Pathologic T stage (1–2 vs. 3)	69.4 vs. 63.5	0.747	54.8 vs. 41.7	0.612	55.9 vs. 49.3	0.573
Pathologic N stage (0–1 vs. 2)	67.0 vs. 68.7	0.424	44.7 vs. 52.8	0.835	50.4 vs. 55.2	0.999
Radiation dose (<54 Gy vs. ≥54 Gy)	72.2 vs. 64.4	0.548	59.0 vs. 44.9	0.675	51.2 vs. 56.1	0.885
Protocol (CT-CCRT vs. RT-CT)	82.8 vs. 60.3	0.094	59.9 vs. 46.4	0.490	44.0 vs. 61.3	0.074

LRFS, locoregional recurrence-free survival; DMFS, distant metastasis-free survival; OS, overall survival; ECOG PS, Eastern Cooperative Oncology Group performance status; FEV1, forced expiratory volume in 1 second; CT-CCRT, adjuvant chemotherapy followed by concomitant chemoradiotherapy; RT-CT, sequential postoperative radiotherapy followed by adjuvant chemotherapy.

Univariable analyses for clinical variables influencing survival are presented in Table 3. There was no significant factor affecting OS, LRFS, and DMFS. The age at diagnosis (<58 vs. ≥58) and comorbidity index (<2 vs. ≥2) were found to be marginally significant factors affecting OS (age, p = 0.072; comorbidity index, p = 0.081). Male patients showed favourable trend compared to female patients in LRFS (p = 0.071) and DMFS (p = 0.084).

The results of multivariable analysis are summarized in Table 4. There were no significant variables affecting on DMFS and OS (Fig. 1A and 1C). The adjuvant protocol (CT-CCRT vs. RT-CT) remained as a statistically significant prognostic factor for LRFS (HR = 3.506, p = 0.046) (Fig. 1B).

Table 4.

Multivariable analyses for clinical variables affecting survivals

Variable	LRFS			DMFS			OS
	HR	95% Cl	p-value	HR	95% Cl	p-value	HR	95% Cl	p-value
Age (<58 vs. ≥58 yr)	-	-	-	-	-	-	1.284	0.535-3.082	0.575
Gender (male vs. female)	2.525	0.827-7.712	0.104	1.525	0.647-3.592	0.334	-	-	-
ECOG PS (0-1 vs. 2)	0.754	0.183-3.100	0.696	1.567	0.504-4.867	0.430	-	-	-
Comorbidity index (<2 vs. ≥2)	-	-	-	-	-	-	1.594	0.532-4.772	0.405
Preoperative FEV1 (<2.5 L vs. ≥2.5 L)	0.581	0.195-1.720	0.326	-	-	-	-	-	-
Tumor histology (squamous vs. others)	-	-	-	0.775	0.315-1.909	0.580	-	-	-
Protocol (CT-CCRT vs. RT-CT)	3.506	1.020-12.053	0.046	-	-	-	0.647	0.318-1.315	0.229

LRFS, locoregional recurrence-free survival; DMFS, distant metastasis-free survival; OS, overall survival; HR, hazard ratio; CI, confidence interval; ECOG PS, Eastern Cooperative Oncology Group performance status; FEV1, forced expiratory volume in 1 second; CT-CCRT, adjuvant chemotherapy followed by concomitant chemoradiotherapy; RT-CT, sequential postoperative radiotherapy followed by adjuvant chemotherapy.

Fig. 1.

Kaplan-Meier survival curves. (A) Overall survival. (B) Locoregional recurrence-free survival. (C) Distant metastasis-free survival between adjuvant chemotherapy followed by concomitant chemoradiotherapy (CT-CCRT) and sequential postoperative radiotherapy followed by adjuvant chemotherapy (RT-CT) protocols.

Discussion and Conclusion

In this study, we compared the outcomes of two institutionally historical protocols (CT-CCRT vs. RT-CT) in patients with completely resected NSCLC, and our results showed that the CT-CCRT protocol had statistically significant favourable prognostic value in LRFS compared with the RT-CT protocol, while there were no differences in OS or DMFS. Patient characteristics were not different between two protocols except age, ECOG PS, preoperative FEV1, radiotherapy technique and radiation dose (Table 1). Although preoperative FEV1 was significantly different (mean, 2.2 L vs. 2.7 L, p = 0.002), postoperative FEV1, which could have a significant effect on OS [14], was not different between the two protocols. The higher proportion of ECOG PS 2 may have influenced the poorer outcome of the RT-CT protocol, but it did not have prognostic values in both univariable and multivariable analyses. The age of patients in the CT-CCRT protocol was older than that of RT-CT protocol (mean, 58.7 vs. 52.9; p = 0.025) and this may have negatively affected the outcomes in patients treated with the CT-CCRT protocol. However, age also was not a prognostic factor for survivals (Tables 3 and 4). Radiation was more irradiated in RT-CT protocol than CT-CCRT protocol, due to the different proportion of RT-techniques used in the protocols. In the clinical setting, the dose difference of 3 Gy did not seem to be significant (mean, 52.8 Gy vs. 55.8 Gy; p = 0.013).

Our CT-CCRT protocol had been adopted during a time before POCT became a standard of care (from October 1996 to mid-2005). But, the RT-CT protocol, which was established in mid-2005, has been implemented as a current active protocol in our institution. Considering the variety of developments in chemotherapy and radiotherapy over time, the recent RT-CT protocol should have showed superior outcomes compared to that of the old CT-CCRT protocol. However, the two protocols did not show significant differences in OS and DMFS. Rather, the CT-CCRT protocol showed superior outcomes compared to the RT-CT protocol in controlling locoregional disease, despite CCRT protocol having mainly adopted 2D-RT (Fig. 1B) (Table 4). These results suggest that the CT-CCRT protocol can be effective in controlling locoregional disease, which may lead to a potential OS benefit.

Although its use has been an issue of debate, PORT can be administered in patients with N2 disease based on several large-scale population-based studies which favored the use of PORT even in the era of POCT [5,8,9]. When PORT is determined to be implemented in the clinical setting, the way of combining PORT with POCT can become an important issue in order to maximize the effect of adjuvant therapies. Currently, POCT followed by PORT is generally accepted when combining two adjuvant therapies due to the concrete evidence supporting the survival benefit of POCT. However, the POCT-first strategy may delay the start of PORT delayed by more than 4–5 months after surgery. Considering the relatively high locoregional tumor burden compared to that of systemic metastasis and the better response rate of radiation therapy than chemotherapy, delaying PORT may lead to the loss of opportune timing in controlling locoregional residual tumors. In the case of PORT-first, POCT can be started within 3 months after surgery due to the shorter treatment time of PORT (5–6 weeks) compared to that of POCT (12–16 weeks). Our RT-CT protocol reflected such rationales, and we reported that the outcomes of PORT-first strategy were comparable to those of the POCT-first strategy, while also preserving the survival benefit of POCT [10]. In this context, concurrent administration of PORT and POCT (CCRT) can be an ideal way to combine two adjuvant therapies. It can minimize the delay time of both PORT and POCT. Locoregional control can be achieved more effectively by radio-sensitization. This benefit, however, can be offset by increases in treatment-related complications. The results of this study show the improved LRFS of the CT-CCRT protocol compared to the RT-CT protocol without any apparent increases in complications. Although these results may not represent all complications, several other studies adopting the CCRT protocol report its comparable outcomes and acceptable complication profiles [15-19]. Shen et al. [20] reported an early closed randomized trial comparing POCT vs. postoperative concurrent chemoradiotherapy (POCRT). This trial showed that POCRT increased both locoregional and distant disease free survival rate compared with POCT alone in patients with IIIA-N2 NSCLC. However, there was no increase of OS rate in PORCT. Although there have been no definite studies supporting the benefit of adjuvant CCRT, the tendency of increased LRFS or DFS suggests the need of a large-scaled randomized trial evaluating the OS benefit comparing CCRT with POCT alone or sequential RT-CT/CT-RT strategies in patients with IIIA-N2 disease.

The result of this study are limited because of the comparison between two protocols were performed consecutively in our institution. This study is also limited by a small sample size, heterogeneous study population (including pN1 disease), and single-institutional retrospective study design. However, despite these limitations, the results of this study suggest again the potential role of adjuvant CCRT in locoregional tumor control.

In conclusion, CT-CCRT protocol increased LRFS compared to RT-CT protocol in patients with completely resected NSCLC, but not in OS and DMFS. Further large-scaled randomized studies are warranted to evaluate the benefit of CCRT strategy compared with sequential CT-RT or RT-CT strategy.