Prognostic factors for relapse-free survival in stage IB-IIIA primary lung adenocarcinoma by epidermal growth factor receptor mutation status.

BACKGROUND: Pathological stage IB-IIIA lung adenocarcinoma with an epidermal growth factor receptor (EGFR) mutation (Mt) has a high recurrence rate even after complete resection. However, there have been few reports on the risk factors for Mt recurrence. This study aimed to analyze the clinicopathological factors related to the relapse-free survival (RFS) of patients with pathological stage IB-IIIA primary lung adenocarcinoma with and without an EGFR mutation.
METHODS: Patients who underwent curative surgery for Mt (n = 208) harboring the EGFR exon 21 L858R point mutation or EGFR exon 19 deletion mutation and EGFR mutation wild-type lung adenocarcinoma (Wt, n = 358) between January 2010 and December 2020 were included. Patients who received adjuvant EGFR-tyrosine kinase inhibitors were excluded. The prognostic factors for RFS were analyzed using a multivariable Cox regression analysis.
RESULTS: The 5-year RFS rates in the Mt and Wt groups were 43.5 and 52.3%, respectively (p = 0.907). Prognostic factors for RFS in the Mt group included smoking history (hazard ratio [HR], 1.49; p = 0.049), blood vessel invasion (HR, 1.84; p = 0.023), and lymph node metastasis (HR, 1.96; p = 0.005). However, adjuvant chemotherapy was not a prognostic factor (HR, 1.02; p = 0.906). In contrast, positron emission tomography (PET) max standardized uptake value (SUV) ≥ 6.0 (HR, 1.53; p = 0.042), lymphatic vessel invasion (HR, 1.54; p = 0.036), lymph node metastasis (HR, 1.79; p = 0.002), and adjuvant chemotherapy (HR, 0.60; p = 0.008) were prognostic factors for RFS in the Wt group.
CONCLUSIONS: Prognostic factors for RFS in stage IB-IIIA primary lung adenocarcinoma differ by epidermal growth factor receptor mutation status. The impact of adjuvant chemotherapy on RFS also differed by EGFR mutation status.

Background

Epidermal growth factor receptor (EGFR) mutations are found in 15–50% of non-small cell lung cancers (NSCLC), especially in women, non-smokers, Asians, and patients with adenocarcinoma [1, 2]. EGFR exon 19 deletion (Ex19) mutations and EGFR exon 21 L858R point mutation (Ex21) mutations are two major EGFR mutations and molecular targeted therapies, and EGFR-tyrosine kinase inhibitors (TKI) show antitumor effects against these cancers [3]. The overall survival (OS) of patients with unresectable EGFR mutation lung adenocarcinoma (Mt) has dramatically improved to 30–50 months with EGFR-TKI [4-6].

The postoperative recurrence rate of primary lung cancer has been reported to be 33% in pathological stage IB, 51% in stage II, and 61% in stage III [7]. Furthermore, the 5-year recurrence-free survival (RFS) rate for patients with Mt was poor (57.0% for stage IB, 46.6% for stage II, and 17.4% for stage IIIA) [8, 9]. To improve the postoperative prognosis of Mt, several clinical trials of adjuvant EGFR-TKI for pathological stage IB(II)-IIIA Mt have recently been conducted [10-14]. Adjuvant EGFR-TKI did not prolong RFS in the IMPACT trial [10]; however, the RADIENT, ADJUVANT, and ADAURA trials showed prolonged RFS with postoperative EGFR-TKI [11, 12, 14]. However, no clinical trials have shown that adjuvant EGFR-TKI prolongs overall survival (OS). The benefit of adjuvant EGFR-TKI is to improve RFS and reduce distant metastatic recurrence, especially brain and bone metastases, which leads to poor quality of life and poor prognosis [14-16]. Adjuvant EGFR-TKI in patients with favorable RFS would only increase drug toxicity [10, 12, 14] and would not be beneficial to the patient. Therefore, it is important to accurately assess the prognostic factors related to RFS.

The prognostic factors for RFS after complete resection of primary lung adenocarcinoma based on EGFR mutation status remain unclear. The aim of this study was to analyze clinicopathological prognostic factors for RFS after complete resection for pathologic stage IB-IIIA primary lung adenocarcinoma according to EGFR mutation status and to obtain basic knowledge on the selection of patients who should receive adjuvant therapy.

Methods

Patients and word definitions

This study was approved by the Kanagawa Cancer Center IRB (2021 Eki-153). Of 1081 cases of pathological stage IB-IIIA (8th edition TNM classification) NSCLC who underwent segmentectomy or greater extent of lung resection at Kanagawa Cancer Center between January 2010 and December 2020, 703 patients had primary lung adenocarcinoma without adjuvant EGFR-TKI therapy. Of these, 566 patients were included in the study, excluding 57 patients (8.1%) who did not undergo EGFR mutation examination, 20 patients with uncommon EGFR mutations (2.8%), such as EGFR exon 18 G719X, and 60 patients (8.5%) who did not undergo positron emission tomography (PET)-computed tomography (CT). In this study, 208 patients with Mt (n = 208) harboring Ex21 and Ex19 and 358 patients with wild-type EGFR mutations (Wt) were included. TNM staging was based on the 8th edition of the TNM Classification for Lung and Pleural Tumors [17]. RFS was defined as the period from the date of surgery to the date of recurrence or any cause of death, wherein patients without recurrence were censored in the last observation period. Adjuvant chemotherapy included patients who completed at least three courses of platinum-based adjuvant chemotherapy or 2 years of oral tegafur-uracil after surgery.

Pathological examination and EGFR mutation analysis

Pathological diagnosis was made by a pathologist (Y.T.) based on hematoxylin and eosin staining of the tissue sections of formalin-fixed paraffin-embedded specimens. Tumor invasion size was evaluated by Elastica von Gieson (EVG) staining. Blood vessel invasion (BVI) and pleural invasion were also evaluated using EVG staining. Alcian blue-periodic acid Schiff and thyroid transcription factor-1 staining were performed for the supplemental diagnosis of adenocarcinoma, with additional D2–40 staining for lymphatic vessel invasion (LVI). BVI was defined as the destruction of blood vessel walls or invasion of tumor cells into the lumen of blood vessels in HE- or EVG-stained sections of the resected lung specimens. LVI was defined as tumor cell invasion into the lumen of lymphatic vessels in HE- or D2–40-stained sections. Tumor DNA was extracted from formalin-fixed paraffin-embedded surgically resected specimens, and EGFR mutations were analyzed using the Cobas® EGFR mutation test v2 [18, 19], the Cycleave/fragment method [20], and the loop-hybrid mobility shift assay method [21].

Adenocarcinoma subtypes were classified according to the International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society International Multidisciplinary Classification of Lung Adenocarcinoma (2011 IASLC/ATS/ERS classification) [22]. Based on the predominance of the components, lung adenocarcinoma specimens were categorized as invasive lepidic/acinar, papillary/mucinous/solid/micropapillary adenocarcinoma, and others. If lepidic, solid, or micropapillary components were observed in more than 1% of the lung cancer tissue sections, they were defined as lepidic, solid, or micropapillary components (+), respectively. Based on the classification by Yoshizawa et al. [23], adenocarcinoma in situ and minimally invasive adenocarcinoma were defined as low-grade adenocarcinoma, invasive lepidic adenocarcinoma, invasive acinar adenocarcinoma, invasive papillary adenocarcinoma, and invasive mucinous adenocarcinoma as intermediate-grade adenocarcinoma, and invasive solid adenocarcinoma and invasive micropapillary adenocarcinoma as high-grade adenocarcinoma.

Postoperative surveillance and definitions of recurrence

Patients were routinely examined on an outpatient basis every 3–6 months 1–3 years after resection of lung cancer and every 6–12 months after 4–5 years, with blood tumor markers, radiographs, and CT. If symptoms suggestive of recurrence appeared during follow-up, PET-CT or bone scintigraphy, head magnetic resonance imaging (MRI), or contrast-enhanced CT were added as appropriate. If any relapse was confirmed, we examined further recurrence sites using head MRI, CT, PET-CT, or bone scintigraphy. Based on the results of these examinations, the sites of recurrence and treatment after recurrence were determined at a joint conference consisting of thoracic surgeons, respiratory physicians, pathologists, and radiologists. Intrathoracic recurrence included cervicothoracic lymph node recurrence (mediastinal, hilar, cervical, and supraclavicular lymph node metastases), lung recurrence, and pleural dissemination. On the other hand, distant recurrence included central nerve system (CNS) recurrence (brain metastasis and meningeal dissemination), abdominal organ metastasis recurrence (liver, adrenal gland, intra-abdominal lymph node), and bone recurrence.

Statistical analysis

In comparison of clinicopathologic background of patients between Mt and Wt, continuous variables were compared using the Mann–Whitney U test, and categorical variables were compared between groups using Fisher’s exact tests. RFS of Mt and Wt patients was analyzed using the Kaplan–Meier method and compared using log-rank tests. Univariable and multivariable analyses were performed using the Cox proportional hazard regression model with the following variables: age (> 65 years), sex, smoking history, laterality, carcinoembryonic antigen (CEA) level (> 10 ng/ml), CT tumor size (> 4.0 cm), consolidation tumor size (> 4.0 cm), presence or absence of ground glass opacity (GGO), PET max standardized uptake value (SUV), surgical procedure, histological grade of adenocarcinoma, BVI, LVI, pleural invasion, lymph node metastasis (pN), predominant component of the adenocarcinoma, presence or absence of lepidic/solid/micropapillary components, adjuvant chemotherapy, and EGFR mutation subtype. Cut-off values for maxSUV was determined using receiver operating characteristic curve analysis. The cumulative incidence of intrathoracic/distant recurrence and recurrence to the CNS was analyzed using Gray’s test. Statistical significance was set at P < 0.05.

Results

The median follow-up period was 38.4 months. Among the 208 Mt, 96 (46.2%) were Ex21 and 112 (53.8%) were Ex19 (Table 1). A smaller CT tumor size and consolidation tumor size, lower frequency of GGO-absent tumors, lower PET maxSUV, higher frequency of invasive micropapillary adenocarcinoma, and lower frequency of invasive solid adenocarcinoma or high-grade adenocarcinoma were observed in Mt than in Wt (Table 1). However, LVI, pN (especially pN2), overall recurrence, and intrathoracic recurrence were observed more frequently in the Mt group than in the Wt group (Table 1).

Table 1

Comparison of clinicopathological features between epidermal growth factor receptor mutant and mutation-wild patients with pathological stage IB-IIIA lung cancer

Total n = 535	Mt (n = 208)	Wt (n = 358)	p valuesa)
Age	70 (35–90)	70 (36–90)	0.789b)
Male, (%)	86 (41.3)	260 (72.6)	< 0.001
Smoking history +, (%)	93 (44.7)	287 (80.2)	< 0.001
Left side, (%)	74 (35.6)	142 (39.7)	0.370
CEA (> 10 ng/ml)	34 (16.3)	61 (17.0)	0.907
CT tumor size, (cm)	3.1 (1.5–9.2)	3.4 (0.8–11.6)	0.033b)
Consolidation size, (cm)	2.7 (1.1–9.2)	3.2 (0.6–11.0)	0.001b)
GGO absent, (%)	128 (61.5)	306 (85.5)	< 0.001
PET maxSUV	4.9 (0.89–21.2)	7.4 (0–33.7)	< 0.001b)
Lobectomy	199 (95.7)	334 (93.3)	0.270
Invasive lepidic adenocarcinoma, (%)	24 (11.5)	24 (6.7)	0.060
Invasive acinar adenocarcinoma, (%)	78 (37.5)	76 (21.2)	< 0.001
Invasive papillary adenocarcinoma, (%)	77 (37.0)	85 (23.7)	0.001
Invasive mucinous adenocarcinoma, (%)	1 (0.5)	44 (12.3)	< 0.001
Invasive solid adenocarcinoma, (%)	14 (6.7)	104 (29.1)	< 0.001
Invasive micropapillary adenocarcinoma, (%)	11 (5.3)	4 (1.1)	0.004
High-grade adenocarcinoma	28 (13.5)	126 (45.2)	< 0.001
Lymphatic vessel invasion +, (%)	78 (37.5)	86 (24.0)	0.002
Blood vessel invasion +, (%)	122 (58.7)	198 (56.3)	0.482
Pleural invasion +, (%)	125 (60.1)	197 (55.3)	0.253
Nodal metastasis +, (%)	107 (51.4)	125 (34.9)	< 0.001
pN1	47 (22.6)	66 (18.4)	0.233
pN2	60 (28.8)	59 (16.5)	< 0.001
Lepidic component +, (%)	185 (88.9)	195 (54.5)	< 0.001
Solid component +, (%)	109 (52.4)	240 (67.0)	< 0.001
Micropapillary component +, (%)	121 (58.2)	128 (35.8)	< 0.001
Adjuvant chemotherapy, (%)	84 (40.4)	124 (34.6)	0.176
Pathological stage
Stage IB	82 (39.4)	142 (39.7)
Stage II	54 (26.0)	128 (35.8)
Stage IIIA	72 (34.6)	88 (24.6)	0.014
Recurrence +, (%)	92 (44.2)	121 (33.8)	0.015
Initial site of recurrence, (%)
Central nerve system	17 (8.2)	16 (4.5)	0.192
Bone	21 (10.1)	23 (6.4)	0.143
Abdominal organ	10 (4.8)	24 (6.7)	0.463
Lung	29 (13.9)	41 (11.5)	0.428
Cervico-thoracic lymph-node	38 (18.3)	43 (12.0)	0.047
Pleural dissemination	23 (11.1)	15 (4.2)	0.003
Distant or intrathoracic, (%)
Distant	37 (17.8)	57 (15.9)	0.639
Intrathoracic	76 (36.5)	84 (23.5)	0.001
EGFR mutation, (%)
Exon 21 L858R	96 (46.2)
Exon 19 deletion	112 (53.8)

CT Computed tomography, GGO Ground glass opacity, PET Positron emission tomography, SUV Standardized uptake value, EGFR Epidermal growth factor receptor, Mt EGFR mutant lung cancer, Wt EGFR mutation-wild lung cancer

a Fisher’s exact test

b Mann-Whitney U test

The 5-year RFS rates for the Mt and Wt groups were 43.5 and 52.3%, respectively (p = 0.907, Fig. 1a). In patients with Mt, smoking history (hazard ratio [HR], 1.49; 95% confidence interval [CI], 1.00–2.22; p = 0.049), BVI (HR, 1.84; 95% CI, 1.09–3.12; p = 0.023), and pN (HR, 1.96; 95% CI, 1.23–3.12; p = 0.005) were poor prognostic factors for RFS (Table 2). Defining Mt patients with smoking history, BVI, or pN as Mt high-risk patients (n = 174) and Mt patients with none of the above as Mt low-risk patients (n = 34), the RFS of Mt high-risk patients was significantly lower than that of Mt low-risk patients (36.5% vs. 81.8%, p < 0.001, Fig. 1b).

Fig. 1

Relapse-free survival (RFS) of Mt and Wt patients did not differ (p = 0.907, (a)). The RFS of Mt high-risk patient was significantly worse than Mt low-risk patients (36.5% vs. 81.8%, p < 0.001, (b)). The RFS of Wt high-risk patients was significantly worse than Wt low-risk patients (44.6% vs. 73.3%, p < 0.001, (c))

Table 2

Univariable and multivariable analyses of recurrence-free survival of patients with EGFR-Mt lung cancer

Recurrent-fee survivalVariable	Univariable analysis			Multivariable analysis
	HR	95% CI	p value	HR	95% CI	p value
Age (≥65)	0.95	0.64–1.44	0.829
Gender (Male)	1.21	0.82–1.81	0.333
Smoking history (+)	1.43	0.96–2.12	0.079	1.49	1.00–2.22	0.049
Side (left)	1.48	0.99–2.23	0.058	1.36	0.90–2.06	0.139
CEA (> 10 ng/ml)	1.85	1.14–3.00	0.013	1.29	0.77–2.14	0.334
CT tumor size (> 4.0 cm)	1.31	0.85–2.02	0.224
Consolidation size (> 4.0 cm)	1.43	0.90–2.27	0.127
GGO (−)	1.48	0.98–2.24	0.066	1.24	0.80–1.92	0.337
PET maxSUV (≥6.0)	2.21	1.48–3.28	< 0.001	1.37	0.88–2.12	0.161
Surgical procedure (segmentectomy)	0.46	0.11–1.88	0.282
Invasive lepidic adenocarcinoma	0.61	0.30–1.26	0.182
Invasive acinar adenocarcinoma	0.78	0.52–1.17	0.225
Invasive papillary adenocarcinoma	1.29	0.85–1.95	0.225
Invasive solid adenocarcinoma	1.64	0.83–3.27	0.156
Invasive micropapillary adenocarcinoma	1.18	0.52–2.71	0.690
High grade adenocarcinoma	1.54	0.91–2.61	0.104
Lymphatic vessel invasion (+)	2.02	1.36–3.00	< 0.001	1.25	0.81–1.93	0.308
Blood vessel invasion (+)	2.96	1.86–4.73	< 0.001	1.84	1.09–3.12	0.023
Pleural invasion (+)	1.10	0.73–1.66	0.645
Nodal metastasis (+)	2.71	1.77–4.14	< 0.001	1.96	1.23–3.12	0.005
Lepidic component (+)	1.05	0.56–1.97	0.877
Solid component (+)	1.02	0.69–1.52	0.916
Micropapillary component (+)	1.34	0.89–2.03	0.161
Adjuvant chemotherapy (%)	1.02	0.69–1.53	0.906
EGFR exon 21L858R	1.01	0.68–1.50	0.962

CT Computed tomography, GGO Ground glass opacity, PET Positron emission tomography, SUV Standardized uptake value, EGFR Epidermal growth factor receptor, HR Hazards ratio, CI Confidence interval

In Wt patients, PET maxSUV ≥6.0 (HR, 1.53; 95% CI, 1.02–2.31; p = 0.042), LVI (HR, 1.54; 95% CI, 1.03–2.30; p = 0.036), pN (HR, 1.79; 95% CI, 1.23–2.60; p = 0.002) and adjuvant chemotherapy (HR, 0.60; 95% CI, 0.42–0.88; p = 0.008) were independent prognostic factors for RFS (Table 3). Defining Wt patients with PET maxSUV ≥6.0, LVI, or pN as Wt high-risk patients (n = 264) and Wt patients with none of the above as low-risk patients (n = 94), the RFS of Wt high-risk patients was significantly lower than that of Wt low-risk patients (44.6% vs. 73.3%, p < 0.001, Fig. 1c).

Table 3

Univariable and multivariable analyses of recurrence-free survival of patients with EGFR-Wt lung cancer

Recurrent-fee survivalVariable	Univariable analysis			Multivariable analysis
	HR	95% CI	p value	HR	95% CI	p value
Age (≥65)	1.28	0.88–1.87	0.189
Gender (Male)	1.66	1.13–2.47	0.013	1.71	0.97–3.00	0.062
Smoking history (+)	1.46	0.93–2.28	0.097	0.97	0.51–1.83	0.915
Side (left)	0.81	0.58–1.14	0.228
CEA (> 10 ng/ml)	1.33	0.88–2.00	0.172
CT tumor size (> 4.0 cm)	1.46	1.05–2.03	0.025	2.07	0.87–4.94	0.102
Consolidation size (> 4.0 cm)	1.47	1.05–2.05	0.025	0.84	0.34–2.07	0.707
GGO (−)	0.90	0.58–1.42	0.665
PET maxSUV (≥6.0)	1.98	1.38–2.83	< 0.001	1.53	1.02–2.31	0.042
Surgical procedure (segmentectomy)	1.19	0.64–2.21	0.575
Invasive lepidic adenocarcinoma	0.49	0.22–1.12	0.093	0.71	0.31–1.67	0.438
Invasive acinar adenocarcinoma	1.12	0.76–1.63	0.576
Invasive papillary adenocarcinoma	1.24	0.86–1.80	0.244
Invasive mucinous adenocarcinoma	0.58	0.32–1.05	0.072	0.74	0.36–1.49	0.393
Invasive solid adenocarcinoma	1.01	0.70–1.45	0.963
Invasive micropapillary adenocarcinoma	1.29	0.32–5.21	0.720
High-grade adenocarcinoma	1.17	0.83–1.64	0.378
Lymphatic vessel invasion (+)	1.84	1.30–2.61	0.001	1.54	1.03–2.30	0.036
Blood vessel invasion (+)	1.55	1.10–2.17	0.011	1.18	0.79–1.77	0.424
Pleural invasion (+)	1.09	0.78–1.51	0.625
Nodal metastasis (+)	2.90	1.94–4.34	< 0.001	1.79	1.23–2.60	0.002
Lepidic component (+)	1.30	0.94–1.80	0.118
Solid component (+)	1.49	1.03–2.16	0.035	1.00	0.63–1.56	0.987
Micropapillary component (+)	1.35	0.97–1.87	0.078	1.21	0.85–1.73	0.298
Adjuvant chemotherapy (+)	0.73	0.51–1.04	0.081	0.60	0.42–0.88	0.008

CT Computed tomography, GGO Ground glass opacity, PET Positron emission tomography, SUV Standardized uptake value, EGFR Epidermal growth factor receptor, HR Hazards ratio, CI Confidence interval

The cumulative incidence of intrathoracic metastasis (p < 0.001, Fig. 2a), distant metastasis (p = 0.002, Fig. 2c), and CNS metastasis (p = 0.045, Fig. 2e) was significantly higher in Mt high-risk patients relative to Mt low-risk patients. The cumulative incidence of intrathoracic metastasis (p < 0.001, Fig. 2b) and distant metastasis (p < 0.001, Fig. 2d) was significantly higher in Wt high-risk patients than in Wt low-risk patients, and the cumulative incidence of CNS metastasis tended to be higher in Wt-high-risk patients than in Wt-low-risk patients (p = 0.096, Fig. 2f).

Fig. 2

The cumulative incidence of intrathoracic metastasis, distant metastasis, and metastasis to the central nervous system (CNS) was significantly higher in Mt high-risk patients than in Mt low-risk patients (a, c, e). The cumulative incidence of intrathoracic and distant metastases was higher in Wt high-risk patients than in Wt low-risk patients (b, d). The cumulative incidence of CNS metastasis tended to be higher in Wt high-risk patients than in Wt low-risk patients (f)

Figure 3 shows the difference in RFS between patients treated with and without adjuvant chemotherapy in the Mt and Wt high-risk groups. There was no difference in RFS between patients treated with or without adjuvant chemotherapy in Mt high-risk patients (p = 0.201, Fig. 3a). In Wt high-risk patients, RFS was significantly better in patients who received adjuvant chemotherapy than in those who did not receive adjuvant chemotherapy (p < 0.001, Fig. 3b).

Fig. 3

There was no difference in RFS between patients treated with or without adjuvant chemotherapy in Mt high-risk patients (p = 0.201, (a)). In Wt high-risk patients, RFS was significantly better in patients who received adjuvant chemotherapy than in those who did not receive adjuvant chemotherapy (p < 0.001, (b))

Discussion

This is the first study to examine prognostic factors for RFS after complete resection of stage IB-IIIA (8th edition TNM classification) pulmonary adenocarcinoma according to EGFR mutation status. Smoking history, BVI, and pN were prognostic factors for RFS of Mt patients; however, adjuvant chemotherapy did not contribute to RFS in Mt patients. In contrast, PET maxSUV≥6.0, LVI, pN, and adjuvant chemotherapy were prognostic factors for RFS in Wt patients. Mt and Wt high-risk patients had a higher cumulative incidence of recurrence than Mt and Wt low-risk patients, respectively.

In this study, the RFS of patients with stage IB-IIIA Mt was 43.5%. This reflects a poor outcome, and there is room for prognostic improvement. In the present study, there was no statistically significant difference in the RFS between Mt and Wt. This was due to the crossover of RFS curves at approximately 40 months after surgery. In our previous study, we showed that Wt recurrence occurred early postoperatively, whereas Mt recurrence tended to be slower than that of Wt [24]. The reason for the crossover may be related to Mt recurrence later in the postoperative period, although recurrence occurred more frequently than in Wt. Conversely, recurrence and smoking-related non-lung cancer deaths in Wt occurred earlier in the postoperative period. There is an urgent need for evidence on adjuvant therapy to reduce recurrence and improve the prognosis of patients with stage IB-IIIA Mt.

Currently, adjuvant EGFR-TKIs may prolong RFS in patients with Mt, but not OS. In RADIENT trial, adjuvant erlotinib therapy prolonged RFS with compared with placebo after complete resection of stage IB-IIIA Mt (46.4 months vs. 28.5 months, p = 0.039) but not OS [11]. In ADJUVANT trial, adjuvant gefitinib therapy pathologic stage II-IIIA Mt prolonged RFS compare with platinum-based combination therapy (28.7 months vs. 18.0 months, HR 0.60, p = 0.005) [12], however, no difference was observed in OS between the two therapies [13]. In the IMPACT study, adjuvant gefitinib therapy for stage II-IIIA Mt did not prolong RFS (Median RFS 35.9 months vs. 25.1 months, p = 0.63) and OS (5 years OS 78.0% vs. 74.6%, p = 0.89) compared with platinum-based adjuvant chemotherapy [10]. The most recent ADAURA trial showed significantly better RFS with adjuvant osimertinib therapy compared with placebo for pathologic stage IB-IIIA Mt (not reached vs 27.5 months, HR 0.20, p < 0.001) [14]. In the ADAURA trial, the incidence of central nervous system (CNS) events was 2% in the osimertinib group and 11% in the placebo group, and CNS-RFS was prolonged with adjuvant osimertinib therapy [14]. However, OS results have not yet been reported.

Various adverse events were reported in these trials. Grade ≥ 3 and grade ≥ 4 adverse events of adjuvant EGFR-TKIs were reported to be 12–41.7% and 1–4%, respectively [10, 12, 14]. Therefore, adjuvant EGFR-TKIs should be administered only to patients with poor RFS after curative surgery. However, few studies have examined the prognostic factors for RFS by EGFR mutation status in stage IB-IIIA adenocarcinoma patients whose stages are usually indicated for adjuvant therapy. Ni et al. reported that among stage I-III Mt patients (n = 531), tumor size, N stage, Ki67, and CK20 were risk factors for overall recurrence [25]. Saw et al. reported that higher stage, nonacinar and nonlepidic adenocarcinoma subtype, sublobar resection, positive resection margins, and lymphovascular invasion (LI) were independent risk factors for recurrence in stage IA-IIIA Mt (n = 389), while higher stage and LI were independent risk factors for recurrence in stage IA-IIIA Wt (n = 334) [26]. The present study revealed that smoking history, BVI, and pN were poor prognostic factors for RFS among patients with stage IB-IIIA Mt. Although pN was a common poor prognostic factor for RFS in Wt and Mt patients, other risk factors differed. This study suggests that it is important to recognize that clinicopathological poor prognostic factors of RFS for stage IB-IIIA adenocarcinoma vary according to EGFR mutation status.

LI combining BVI and LVI has been reported to be associated with distant recurrence and early recurrence after complete resection of NSCLC [27-29], and is a poor prognostic factor for RFS [30, 31] and OS [32]. LVI alone increases the risk of recurrence. Harada et al. reported that LVI was a poor prognostic factor for OS after complete resection of stage I NSCLC, whereas BVI was not [30]. In contrast, a meta-analysis reported that BVI was a poor prognostic factor for RFS after resection of stage I NSCLC [31]. Kato et al. reported that LVI and BVI were risk factors for recurrence [33]. Mimae et al. reported that LVI and BVI were independent poor prognostic factors for RFS among pN (−) lung adenocarcinoma patients, whereas only BVI was a risk factor for recurrence in patients with pN (+) lung adenocarcinoma [34]. None of these studies have examined the association between EGFR mutations. The present study revealed that BVI is a poor prognostic factor for RFS in patients with Mt, and LVI is a poor prognostic factor for RFS in patients with Wt. It is suggested that LI should be analyzed separately for each EGFR mutation status in LVI and BVI.

The reason why BVI is a prognostic factor for RFS is unclear. In tumor cells with high EGFR expression, tumor cells produce vascular endothelial growth factor (VEGF) and interleukin-8, which regulate and promote intratumoral vascular invasion [35]. Moreover, EGFR signaling induces angiogenic factors from mesenchymal stem cells in tumors and regulates tumor cell migration [36]. C-type lectin 11A, which promotes vascular endothelial cell differentiation, is highly expressed in EGFR-mutant lung cancer cells and promotes angiogenesis triggered by VEGF [37]. These basic research findings showed the possibility that Mt may metastasize more frequently by efficient angiogenesis than Wt. Three angiogenesis inhibitors are currently used for advanced primary lung cancer: bevacizumab, ramucirumab, and nintedanib. Because Mt patients with BVI are at a high risk of recurrence, future clinical trials of adjuvant therapy with these angiogenesis inhibitors in addition to EGFR-TKIs may be considered.

In both Mt and Wt, pN was an important prognostic factor, and this result was consistent with a previous report [27, 28, 34]. In the present study, smoking history was also a prognostic factor in Mt smoking and has been reported to have a shorter OS than non-smokers in unresectable stage IIIB-IV Mt, and the prognosis is worsened by the increased amount of smoking [38]. Progression-free survival after EGFR-TKI treatment for unresectable advanced Mt has been reported to be shorter in smokers than in non-smokers [39]. Because lung cancer in smoking patients had a 10-fold higher mutation burden than those in non-smokers [40, 41], it is possible that Mt in patients with a smoking history had higher cell proliferative activity than those without a smoking history. Further molecular pathological analysis may be needed for Mt patients with a history of smoking.

It has been reported that solid predominant adenocarcinoma has a higher maxSUV than other histologic types of lung adenocarcinoma [42]. In this study, a lower solid component rate, higher lepidic component rate, and lower frequency of high-grade adenocarcinoma in Mt than in Wt resulted in a lower maxSUV in Mt than in Wt. This result was consistent with previous studies showing lower PET maxSUVs in Mt than in Wt [2, 26]. In the present study, PET maxSUV≥6.0 was a poor prognostic factor for RFS in Wt, but not in Mt. Because of the low potential of 18F-fluorodeoxyglucose (FDG) accumulation in Mt, maxSUV may not accurately predict the prognosis of patients with Mt. In contrast, Wt has a high potential for FDG accumulation and is useful in predicting prognosis after resection of stage IB-IIIA Wt.

The efficacy of adjuvant chemotherapy for Mt has been reported to be lower than that for Wt in stage I [43] and stage II/III [44] lung adenocarcinoma in a propensity-matched analysis. Consistent with previous reports, the present study showed that adjuvant chemotherapy did not affect RFS in stage IB-IIIA Mt and Mt high-risk patients; therefore, adjuvant chemotherapy may not be necessary for Mt. Mt patients who had a smoking history, BVI, and pN were more likely to relapse. These high-risk Mt patients are candidates for adjuvant therapy other than chemotherapy, such as EGFR-TKI, and further clinical trials are warranted. Surprisingly, Mt patients with none of these factors, that is, Mt low-risk patients, did not develop distant metastasis (Fig. 2a, c, e), suggesting that adjuvant therapy may not be necessary for Mt low-risk patients. In contrast, adjuvant chemotherapy was a favor prognostic factor for RFS in patients with Wt. Because adjuvant chemotherapy may improve the prognosis of Wt patients with PET SUVmax ≥6.0, LVI, or pN, that is, Wt high-risk patients, should receive aggressive adjuvant chemotherapy.

Our study has several limitations. First, this was a single-center, retrospective study. Second, among the 703 patients with pathological stage IB-IIIA primary lung adenocarcinoma during the analysis period, 8.3% and 8.5% of the patients did not undergo EGFR mutation analysis and PET-CT, respectively. These patients were excluded from this study, which may have caused a selection bias. Third, Wt patients are a heterogeneous population that includes patients with KRAS, ALK, and ROS-1 mutation lung cancer. It is necessary to examine the poor prognostic factors for RFS for each gene mutation in lung cancer in the future.

Conclusions

In conclusion, we found that poor prognostic factors for RFS in stage IB-IIIA differ according to EGFR mutation status. Smoking history, BVI, and pN were unfavorable factors for RFS in Mt patients. In contrast, PET maxSUV≥6.0, LVI, pN, and adjuvant chemotherapy were prognostic factors for RFS in Wt patient.