To evaluate the efficacy of SOX combined with a programmed cell death protein-1 (PD-1) inhibitor compared with SOX alone in the perioperative management of locally advanced gastric cancer and to explore biomarkers that may predict response to anti-PD-1 therapy.
Methods
Data of patients with clinical stage T3–4aN0–3M0 (IIb–III) gastric cancer were reviewed to create a primary database. Patients treated with perioperative SOX combined with sintilimab were included in Group A, while those treated with SOX alone were included in Group B. After one-to-one propensity score matching, pathological response and short-term survival outcomes were compared between the two groups. In addition, potential efficacy-related biomarkers were analyzed.
Results
Between January 2018 and December 2022, a total of 150 patients were included in the analysis, with 75 patients in each group. The rates of pathological complete response (21.3% vs. 4.0%; P = 0.001) and major pathological response (45.3% vs. 22.7%; P = 0.003) in Group A were statistically higher than those in Group B. There was no significant difference in 1-year overall survival (92.8% vs. 92.0%; P = 0.392) and disease-free survival (88.9% vs. 88.0%; P = 0.357) between the two groups. Subgroup analysis of Group A showed that the pathological complete response (40.6% vs. 8.6%; P = 0.002) and major pathological response (65.6% vs. 28.6%; P = 0.002) rates were significantly higher in programmed death ligand-1-positive patients with a combined positive score of ≥ 5. A pathological complete response was achieved in 42.9% patients (3/7) with mismatch repair deficiency. For the two patients confirmed as Epstein-Barr virus-positive, one patient achieved a pathological complete response and the other achieved a major pathological response.
Conclusions
The adoption of SOX combined with a PD-1 inhibitor may improve the pathological response rate of patients with locally advanced gastric cancer, especially those with programmed death ligand-1 combined positive score ≥ 5, Epstein–Barr virus-positivity and mismatch repair deficiency. However, further prospective studies are still warranted to confirm the long-term survival benefit.
Xingmao Huang, Jingquan Fang and Ling Huang contributed equally to this work and should be considered as co-first authors.
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
BSA
Body surface area
CPS
Combined positive score
DFS
Disease-free survival
dMMR
MMR deficiency
EBV
Epstein–Barr virus
EBVaGC
EBV-associated gastric cancer
ICI
Immune checkpoint inhibitor
irAEs
Immune-related adverse events
LAGC
Locally advanced gastric cancer
MLH1
MutL homolog 1
MMR
Mismatch repair
MPR
Major pathological response
MSH2
MutS homolog 2
MSH6
MutS homolog 6
MSI
Microsatellite instability
OS
Overall survival
pCR
Pathological complete response
PD-1
Programmed cell death protein-1
PD-L1/2
Programmed death ligand-1/2
PMS2
PMS1 homolog 2
PSM
Propensity score matching
TRG
Tumor regression grading
Introduction
Gastric cancer ranks as the fifth most common malignancy and the fourth most common cause of cancer death around the world [1]. Most patients are diagnosed at an advanced stage. Radical gastrectomy is the main treatment strategy for locally advanced gastric cancer (LAGC) [2, 3]. However, postoperative tumor recurrence and distant metastasis are common and can lead to poor prognosis [4, 5].
Different management strategies have been proposed to improve the prognosis of patients with LAGC, and perioperative chemotherapy has increasingly become an important treatment modality [6]. Studies have shown that preoperative chemotherapy can eliminate occult micrometastases, achieve tumor downstaging, and improve the curative resection rate [7‐9]. Additional studies have shown that perioperative chemotherapy can improve the prognosis of patients with LAGC compared with adjuvant chemotherapy alone [8, 10]. However, the relatively low pathological complete response (pCR) rate was unsatisfactory, which may be caused by the high heterogeneity of gastric cancer.
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The introduction of immune checkpoint inhibitors (ICIs) has provided clinical benefits for patients with gastric cancer, especially those with late-stage disease [11‐13]. As ICIs, programmed cell death protein-1 (PD-1) inhibitors elicit a strong immune response by blocking the interaction of PD-1 with its ligands, programmed death ligand-1 [PD-L1] and PD-L2, which are highly expressed on cancer cells [14]. The CheckMate-649 trial reported that PD-1 inhibitors in combination with chemotherapy improved the overall survival (OS) and progression free survival (PFS) of patients with advanced gastric, gastroesophageal junction, or esophageal adenocarcinoma, especially for those with PD-L1 combined positive score (CPS) ≥ 5 [12]. Anti-PD-1 therapy also exerts a positive effect on patients with LAGC. The addition of PD-1 inhibitors to cytotoxic chemotherapy as neoadjuvant treatment for LAGC showed encouraging results in terms of pathological response [15‐18]. However, most studies were single-arm studies with small sample sizes, and there is a lack of effective biomarkers for predicting the efficacy of anti-PD-1 therapy.
We conducted a retrospective study to evaluate the efficacy of SOX combined with sintilimab compared with SOX alone in the perioperative management of patients with stage IIb–III LAGC using propensity score matching (PSM) and to explore biomarkers that may predict response to anti-PD-1 therapy.
Methods
Study design
This was a single-center, retrospective study conducted using PSM. The study aimed to compare the short-term effects of perioperative chemotherapy plus a PD-1 inhibitor versus chemotherapy alone in patients with stage IIb–III gastric cancer.
The data of 897 patients with LAGC who received perioperative treatment at the Department of Gastric Surgery, Zhejiang Cancer Hospital, China, between January 2018 and December 2022 were collected and reviewed to create an analytical database. The main selection criteria were: aged 18 to 75 years, histological diagnosis of gastric cancer, clinical stage T3–4aN0–3M0 (IIb–III) disease, received perioperative treatment (SOX plus sintilimab/SOX alone) and radical gastrectomy, Eastern Cooperative Oncology Group performance status 0–1, with adequate organ function to tolerate chemoimmunotherapy or surgery. Patients were excluded if they had remnant gastric cancer, concomitant malignancies or refractory autoimmune diseases, a long-term history of steroid or immunosuppressant use, or missing clinicopathological data. A total of 658 patients were excluded due to the adoption of other treatment modalities (n = 419), loss to follow-up (n = 97), palliative-intent gastrectomy (n = 49), insufficient data (n = 81), and incomplete treatment (n=12). The remaining 239 patients who met the selection criteria were enrolled. Patients treated with perioperative SOX plus sintilimab were included in Group A (n = 79), while those treated with SOX alone were included in Group B (n = 160).
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In order to reduce selection bias and ensure comparability between the two groups, PSM without replacement was performed in a 1:1 ratio with a 0.05 caliper width. The resulting propensity score-matched pairs were used in subsequent analyses. Covariates included age, sex, and clinical stage, which were considered to have an effect on the study endpoints. Balance was checked by computing absolute standardized mean differences (SMD) between the two groups for each covariate in the PSM sample. A SMD threshold of 0.2 was considered to detect substantial imbalance. After PSM, the propensity score-matched cohort comprised 75 patients in each group and the baseline variables between the groups were comparable (P > 0.05, SMD < 0.200, Table 1). The process of patient selection is presented in Fig. 1.
Table 1
Baseline characteristics before and after propensity score matching (PSM)
Variable
Before PSM
After PSM
Group A (n = 79)
Group B (n = 160)
P-value
SMD
Group A (n = 75)
Group B (n = 75)
P-value
SMD
Age (years)
0.088
0.235
0.866
0.029
≤ 60
33 (41.8)
49 (30.6)
29 (38.7)
28 (37.3)
> 60
46 (58.2)
111 (69.4)
46 (61.3)
47 (62.7)
Gender
0.790
0.037
0.707
0.062
Male
59 (74.7)
122 (76.3)
55 (73.3)
57 (76.0)
Female
20 (25.3)
38 (23.8)
20 (26.7)
18 (24.0)
Clinical stage (cTNM)
0.570
0.078
0.754
0.050
IIb
7 (8.9)
18 (11.3)
5 (6.7)
6 (8.0)
III
72 (91.1)
142 (88.8)
70 (93.3)
69 (92.0)
Preoperative CEA
0.787
0.039
0.402
0.136
≤ 5
61 (77.2)
126 (78.8)
59 (78.7)
63 (84.0)
> 5
18 (22.8)
34 (21.3)
16 (21.3)
12 (16.0)
Preoperative CA125
0.167
0.185
0.239
0.191
≤ 35
65 (82.3)
142 (88.8)
62 (82.7)
67 (89.3)
> 35
14 (17.7)
18 (11.3)
13 (17.3)
8 (10.7)
Preoperative CA199
0.371
0.123
0.577
0.091
≤ 37
56 (70.9)
122 (76.3)
54 (72.0)
57 (76.0)
> 37
23 (29.1)
38 (23.8)
21 (28.0)
18 (24.0)
CEA carcinoembryonic antigen, CA125 carbohydrate antigen 125, CA199 carbohydrate antigen199
Fig. 1
Flow diagram of the patient selection process. *Including 3 patients treated with SOX plus sintilimab and 9 patients treated with SOX alone
×
This study was approved by the Ethics Committee of Zhejiang Cancer Hospital (approval number: IRB-2022-592) and was conducted in accordance with the Declaration of Helsinki. Informed consent was obtained from each patient enrolled in the study.
Treatment
Perioperative chemotherapy and immunotherapy
SOX plus sintilimab was administered to patients in Group A, while those in Group B were treated with SOX alone. Patients received 2–4 cycles of preoperative treatment and 4–6 cycles of postoperative treatment, with each cycle lasting 3 weeks. The dose of SOX regimen was calculated according to body surface area (BSA): oxaliplatin (130 mg/m2) was administered intravenously on Day 1 and S-1 (BSA < 1.25 m2, 80 mg/day; 1.25 ≤ BSA < 1.50 m2, 100 mg/day; BSA ≥ 1.50m2, 120 mg/day) was administered orally on Days 1–14, followed by a 1-week rest. Sintilimab (200 mg every 3 weeks) was administered intravenously on Day 1 after the beginning of each cycle in Group A.
Surgery
All patients underwent D2 radical gastrectomy according to the Japanese Gastric Cancer Treatment Guidelines [19, 20]. Distal or total gastrectomy was performed according to tumor location. Different reconstruction methods, including Roux-en-Y esophagojejunostomy, Billroth II gastrojejunostomy, and Billroth I gastroduodenostomy, were performed according to the extent of gastrectomy. Resected specimens were assessed by two experienced pathologists to determine the overall response and pathological staging after neoadjuvant treatment. The residual tumor (R) classification was used to categorize tumor status after treatment. Surgical margins with no residual tumor, microscopic residual tumor, and macroscopic residual tumor were defined as R0, R1, and R2 resection, respectively [21]. Postoperative complications were graded according to the Clavien–Dindo classification [22].
Endpoints and assessment
The pCR rate was the primary endpoint, and the major pathological response (MPR), R0 resection, disease-free survival (DFS) and OS rates were analyzed as the secondary endpoints.
Adverse events were graded according to the latest version of the National Cancer Institute’s Common Terminology Criteria for Adverse Events (CTCAE, V.3.0) [23]. Tumor response was assessed in accordance with the Response Evaluation Criteria in Solid Tumors (RECIST) guidelines (version 1.1) [24]. The responses were categorized as follows: complete response (CR), partial response (PR), stable disease (SD), and progressive disease (PD). Tumor regression grading (TRG) was adopted to evaluate the tumor regression of resected specimens. TRG was defined as follows: TRG1a, no residual tumor cells; TRG1b, < 10% residual tumor cells; TRG2, 10–50% residual tumor cells; TRG3, > 50% residual tumor cells [25]. Resected specimens without viable tumor cells were considered as pCR (TRG1a). Less than 10% residual tumor cells after preoperative treatment were considered as MPR (TRG1a/b). Downstaging was assessed by comparing the differences between clinical and pathological staging.
PD-L1 expression, mismatch repair (MMR) status, and Epstein-Barr virus (EBV)-positivity were retrospectively assessed in formalin-fixed, paraffin-embedded biopsy samples from Group A patients. PD-L1 expression was determined using immunohistochemistry (PD-L1, Clone 22C3; Dako) and described using CPS. CPS was defined as the total number of PD-L1-positive cells, including tumor cells, lymphocytes, and macrophages, divided by the total number of living tumor cells multiplied by 100. Patients with a CPS ≥ 1 were considered PD-L1-positive. MMR proteins, including MLH1 (clone ES05; Dako), MSH2 (clone FE11; Dako), MSH6 (clone EP49; Dako), and PMS2 (clone EP51; Dako), were stained by immunohistochemistry to determine MMR status. Loss of any of the four MMR proteins was defined as MMR deficiency (dMMR). Additionally, in situ hybridization was performed to evaluate the EBV status (EBV-0050; EBER ISH Kit, MXB).
Follow-up
After treatment, follow-up was performed every 3 months for the first 2 years and then every 6 months from years 3 to 5. Follow-up was mainly conducted by telephone and outpatient review. Physical examination, imaging studies, and blood tests (including tumor markers) were performed regularly in the outpatient clinic. DFS was calculated from the date of gastrectomy until the date of recurrence. OS was calculated from the date of diagnosis until the date of death or last follow-up. The last follow-up was performed on February 28, 2023.
Statistical analysis
Categorical variables were presented as frequencies and percentages, and analyzed using either the Chi-square test or Fisher's exact test depending on the situation. Continuous variables were compared using the Mann–Whitney U test. Survival curves were plotted using the Kaplan–Meier method and compared using the log-rank test. A two-tailed P-value < 0.05 was considered statistically significant. All statistical analyses were conducted using SPSS (version 26.0; SPSS Inc., Chicago, IL, USA).
Results
Clinicopathological characteristics
In the entire cohort, 112 patients (74.7%) were men. The median age was 64 (range: 31–75) years. One hundred and thirty-nine patients (92.7%) had stage III disease. Most patients (96.0%) had gastric adenocarcinoma. Furthermore, 88.7% of tumors were poorly differentiated. Regarding tumor location, 83.3% of tumors were located in the stomach, while the remaining 16.7% were located at the gastroesophageal junction. Detailed information is provided in Table 1 and 2.
Table 2
Clinicopathological characteristics before and after propensity score matching (PSM)
Variable
Before PSM
After PSM
Group A (n = 79)
Group B (n = 160)
P-value
Group A (n = 75)
Group B (n = 75)
P-value
Radical resection
0.174*
1.000*
R0 resection
79 (100.0)
155 (96.9)
75 (100)
74 (98.7)
Non-R0 resection
0 (0.0)
5 (3.1)
0 (0.0)
1 (1.3)
Surgical procedures
0.910
1.000
Distal gastrectomy
31 (39.2)
64 (40.0)
29 (38.7)
29 (38.7)
Total gastrectomy
48 (60.8)
96 (60.0)
46 (61.3)
46 (61.3)
Reconstruction method
0.111*
0.153*
Billroth I
0 (0.0)
10 (6.3)
0 (0.0)
4 (5.3)
Billroth II
31 (39.2)
54 (33.8)
29 (38.7)
25 (33.3)
Roux-en-Y esophagojejunostomy
48 (60.8)
96 (60.0)
46 (61.3)
46 (61.3)
Tumor location
0.703*
0.421
Upper
21 (26.6)
51 (31.9)
20 (26.7)
26 (34.7)
Middle
22 (27.8)
39 (24.4)
22 (29.3)
16 (21.3)
Lower
36 (45.6)
68 (42.5)
33 (44.0)
33 (44.0)
Total stomach
0 (0.0)
2 (1.3)
0 (0.0)
0 (0.0)
Pathologic stage (ypTNM)
< 0.001
0.006
ypT0N0M0
16 (20.3)
4 (2.5)
16 (21.3)
3 (4.0)
I
19 (24.1)
34 (21.3)
18 (24.0)
14 (18.7)
II
17 (21.5)
42 (26.3)
17 (22.7)
23 (30.7)
III
27 (34.2)
80 (50.0)
24 (32.0)
35 (46.7)
Differentiation degree
0.610
0.440
Poorly
70 (88.6)
138 (86.3)
68 (90.7)
65 (86.7)
Moderately-highly
9 (11.4)
22 (13.8)
7 (9.3)
10 (13.3)
Pathological type
0.290*
0.557*
Adenocarcinoma
74 (93.7)
156 (97.5)
71 (94.7)
73 (97.3)
Signet-ring cell carcinoma
2 (2.5)
2 (1.3)
2 (2.7)
0 (0.0)
Other※
3 (3.8)
2 (1.3)
2 (2.7)
2 (2.7)
Nerve infiltration
0.722
0.479
No
51 (64.6)
107 (66.9)
50 (66.7)
54 (72.0)
Yes
28 (35.4)
53 (33.1)
25 (33.3)
21 (28.0)
Vascular tumor embolus
0.795
0.484
No
51 (64.6)
106 (66.3)
49 (65.3)
53 (70.7)
Yes
28 (35.4)
54 (33.8)
26 (34.7)
22 (29.3)
Postoperative CEA
0.309
0.290
≤ 5
67 (84.8)
143 (89.4)
65 (86.7)
69 (92.0)
> 5
12 (15.2)
17 (10.6)
10 (13.3)
6 (8.0)
Postoperative CA125
0.542
0.723
≤ 35
54 (68.4)
103 (64.4)
51 (68.0)
53 (70.7)
> 35
25 (31.6)
57 (35.6)
24 (32.0)
22 (29.3)
Postoperative CA199
0.688
0.575
≤ 37
71 (89.9)
141 (88.1)
67 (89.3)
69 (92.0)
> 37
8 (10.1)
19 (11.9)
8 (10.7)
6 (8.0)
CEA carcinoembryonic antigen, CA125 carbohydrate antigen 125, CA199 carbohydrate antigen199
*Fisher’s test
※Including adenosquamous carcinoma and squamous cell carcinoma
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Treatment outcomes
Perioperative treatment
In both groups, the median number of preoperative treatment cycles was three, and the median number of postoperative treatment cycles was four. After neoadjuvant treatment, all patients underwent D2 radical gastrectomy. R0 resection was performed in 75 patients (100%) in Group A and 74 patients (98.7%) in Group B, with no significant difference between the groups (P = 1.000, Table 2). Four patients in Group B underwent multivisceral resection due to tumor invasion or lymph node metastasis (splenectomy in three patients, pancreatectomy in two patients, and colectomy in one patient).
The median time between preoperative treatment and surgery was 29 (range 22–54) days in Group A and 30 (range: 21–49) days in Group B (P = 0.265). The median time between surgery and postoperative treatment was 27 (range 21–32) and 26 (range 21–29) days, respectively (P = 0.307).
In the entire cohort, surgical complications were observed in 16 patients (10.7%), including nine patients in Group A (pneumonia in five patients, intraperitoneal infection in two patients, and abdominal hemorrhage and anastomotic leakage in one patient each) and seven patients in Group B (pneumonia in three patients, anastomotic leakage in two patients, and intraperitoneal and wound infection in one patient each). There was no significant difference between the two groups (P = 0.597). The postoperative condition of these patients improved after symptomatic treatment. No surgery-related deaths occurred in either group.
Tumor regression and survival
Tumor responses were assessed in all patients. CR, PR, and SD were achieved in 5 (6.7%), 48 (64.0%), and 22 (29.3%) patients in group A, and 2 (2.7%), 46 (61.3%), and 27 (36.0%) patients in group B, respectively, without a significant difference (P = 0.434, Supplementary Table S1). After surgery, the pathological regression of resected specimens was evaluated according to the Becker criteria. In the entire cohort, 19 patients (12.7%) achieved pCR (TRG1a), including 16 patients (21.3%) in Group A and three patients (4.0%) in Group B, with a significant difference between the groups (P = 0.001). The MPR rate was significantly higher in Group A than in Group B (45.3% vs. 22.7%, respectively; P = 0.003). Significant downstaging of TNM stage and the T and N categories were observed in Group A. Detailed information is provided in Tables 3 and Supplementary Tables S2, S3.
Table 3
Pathological evaluation of response to neoadjuvant treatment in GC patients
Variable
Group A (No., %)
Group B (No.,%)
P-value
TRG
0.006
1a
16 (21.3)
3 (4.0)
1b
18 (24.0)
14 (18.7)
2
32 (42.7)
43 (57.3)
3
9 (12.0)
15 (20.0)
pCR
16 (21.3)
3 (4.0)
0.001
MPR
34 (45.3)
17 (22.7)
0.003
All discharged patients were followed-up, with a median duration of 26 (range: 6–52) months. Median OS and DFS data are not yet mature. The 1-year OS rate was 92.8% for Group A and 92.0% for Group B, with no statistical difference between the groups (P = 0.392). The 1-year DFS rate for Group A and Group B was 88.9% and 88.0%, respectively (P = 0.357; Fig. 2).
Fig. 2
Kaplan–Meier estimates of overall survival (A) and disease free survival (B) of patients in group A and group B
×
Safety profile
As shown in Table 4, grade 3 or 4 adverse events were identified in 17 (22.7%) patients in Group A and 13 (17.3%) patients in Group B during the neoadjuvant treatment period, with no significant difference (P = 0.414). Meanwhile, during the adjuvant treatment period, grade 3 or 4 adverse events were observed in 11 (14.7%) patients in Group A and 5 (6.7%) patients in Group B (P = 0.113). In the entire cohort, the most common hematological toxicities were leucopenia, neutropenia, and anemia, while the most common non-hematological toxicities were transaminase elevation, vomiting, and pneumonia. In Group A, two patients suffered from grade 3 hypothyroidism and were treated with thyroid hormone and steroid hormone. The condition of all patients with adverse events was well-controlled after conversion treatment. No treatment-related deaths occurred in either group.
Table 4
Perioperative treatment-related adverse events
Neoadjuvant treatment
Adjuvant treatment
Group A (n.%)
Group B (n.%)
Group A (n.%)
Group B (n.%)
Any grade
Grade 3–4
Any grade
Grade 3–4
Any grade
Grade 3–4
Any grade
Grade 3–4
Total
70 (93.3)
17 (22.6)
67 (89.3)
13 (17.3)
68 (90.7)
11 (14.7)
64 (85.3)
5 (6.7)
Hematological
Leucopenia
39 (52.0)
4 (5.3)
37 (49.3)
3 (4.0)
32 (42.7)
2 (2.7)
28 (37.3)
2 (2.7)
Neutropenia
33 (44.0)
4 (5.3)
34 (45.3)
3 (4.0)
36 (48.0)
3 (4.0)
23 (30.7)
1 (1.3)
Anemia
32 (42.7)
2 (2.7)
34 (45.3)
2 (2.7)
25 (33.3)
1 (1.3)
30 (40.0)
2 (2.7)
Thrombocytopenia
21 (28.0)
3 (4.0)
25 (33.3)
4 (5.3)
13 (17.3)
2 (2.7)
9 (12.0)
2 (2.7)
Non-hematological
Elevated ALT/AST
18 (24.0)
4 (5.3)
19 (25.3)
3 (4.0)
21 (28.0)
3 (4.0)
13 (17.3)
1 (1.3)
Nausea/vomiting
15 (20.0)
2 (2.7)
13 (17.3)
1 (1.3)
8 (10.7)
1 (1.3)
10 (13.3)
1 (1.3)
Pneumonia
5 (6.7)
0 (0.0)
4 (5.3)
0 (0.0)
1 (1.3)
0 (0.0)
0 (0.0)
0 (0.0)
Diarrhea
5 (6.7)
0 (0.0)
3 (4.0)
0 (0.0)
1 (1.3)
0 (0.0)
2 (2.7)
0 (0.0)
Elevated creatinine
4 (5.3)
0 (0.0)
2 (2.7)
0 (0.0)
4 (5.3)
0 (0.0)
6 (8.0)
0 (0.0)
Dermatitis
2 (2.7)
0 (0.0)
0 (0.0)
0 (0.0)
1 (1.3)
0 (0.0)
0 (0.0)
0 (0.0)
Hypothyroidism
4 (5.3)
2 (2.7)
0 (0.0)
0 (0.0)
1 (1.3)
0 (0.0)
0 (0.0)
0 (0.0)
Hyperthyroidism
1 (1.3)
0 (0.0)
0 (0.0)
0 (0.0)
0 (0.0)
0 (0.0)
0 (0.0)
0 (0.0)
ALT alanine aminotransferase, AST aspartate aminotransferase
Potential biomarkers
PD-L1 expression, MMR status, and EBV-positivity were analyzed in Group A patients. Detailed information is provided in Table 5 and Supplementary Tables S4–S6. PD-L1 data were available for 67 patients. The number of patients with a CPS < 1, 1 ≤ CPS < 5, 5 ≤ CPS < 10, and CPS ≥ 10 was 20 (29.9%), 15 (22.4%), 14 (20.9%), and 18 (26.9%), respectively. Forty-seven patients (70.1%) were PD-L1-positive (CPS ≥ 1). The pCR rate of PD-L1-positive and -negative patients was 27.7% and 15.0% (P = 0.215), and the MPR rate was 48.9% and 40.0% (P = 0.502), respectively. Further analysis showed that the pCR (40.6% vs. 8.6%; P = 0.002) and MPR (65.6% vs. 28.6%; P = 0.002) rates were higher in patients with a CPS ≥ 5 compared to those with a CPS < 5, with significant differences between the groups. MMR data were available for 71 patients, of whom seven (9.9%) had dMMR. Three patients (42.9%) with dMMR achieved pCR. EBV data were available for 65 patients. Only two patients (3.1%) were EBV-positive (one achieved pCR; the other achieved MPR). Both EBV-positive patients had a CPS of 5 and pMMR.
Table 5
Associations between the expression of PD-L1 and pathological response
Variable
CPS < 1 (n = 20)
CPS ≥ 1 (n = 47)
P-value
CPS < 5 (n = 35)
CPS ≥ 5 (n = 32)
P-value
TRG
0.738
0.008
1a
3 (15.0)
13 (27.7)
3 (8.6)
13 (40.6)
1b
5 (25.0)
10 (21.3)
7 (20.0)
8 (25.0)
2
9 (45.0)
18 (38.3)
19 (54.3)
8 (25.0)
3
3 (15.0)
6 (12.8)
6 (17.1)
3 (9.4)
pCR
3 (15.0)
13 (27.7)
0.215
3 (8.6)
13 (40.6)
0.002
MPR
8 (40.0)
23 (48.9)
0.502
10 (28.6)
21 (65.6)
0.002
Discussion
In this study, we compared the efficacy of SOX plus a PD-1 inhibitor and SOX alone for the perioperative management of patients with stage IIb–III LAGC, focusing on pathological response and potential biomarkers. The pCR and downstaging rates of patients treated with perioperative SOX plus sintilimab were significantly higher than those of patients treated with SOX alone, which met the endpoints of this study as expected. Further analysis revealed that PD-L1 CPS ≥ 5, dMMR, or EBV-positivity were associated with improved efficacy.
The clinical benefit of neoadjuvant chemotherapy in patients with gastric cancer has been widely studied. Randomized trials reported that the addition of chemotherapy before gastrectomy improves the radical resection rate and prognosis compared to surgery alone [9, 10, 26, 27]. However, the pathological response rate of patients receiving neoadjuvant chemotherapy was relatively low, and the long-term survival was still unsatisfactory. Therefore, more effective strategies are needed to improve the efficacy and prognosis of LAGC.
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Previous studies have demonstrated that immunotherapy may enhance the antitumor activity of chemotherapeutic drugs by exerting a synergistic effect [28, 29]. Furthermore, several studies have shown that the combination of chemotherapy and ICIs can improve the efficacy and prognosis of patients with advanced gastric cancer [11, 12, 30]. Encouraged by these results, studies focusing on the efficacy and safety of preoperative chemotherapy in combination with a PD-1 inhibitor were performed in patients with LAGC. Jiang et al. [16] evaluated the benefit of preoperative oxaliplatin/capecitabine plus sintilimab for patients with resectable gastric and gastroesophageal junction cancer in a single-arm phase II trial. Improved pCR (19.4%, 7/36) and MPR (47.2%, 17/36) rates were achieved compared to traditional neoadjuvant chemotherapy. In our study, the pCR and MPR rates of patients treated with perioperative SOX plus sintilimab were significantly higher than those of patients treated with SOX alone, showing superiority in the pathological response to this combination strategy directly based on the PD-1 inhibitor. However, for patients treated with neoadjuvant nivolumab monotherapy followed by gastrectomy, Hasegawa et al. [31] reported that the pCR (3.2%, 1/31) and MPR (16.1%, 5/31) rates were lower than those of patients treated with combination therapy, indicating that the effect of immunotherapy based on a single agent may be limited and the synergistic effect of immunotherapy and chemotherapy may yield better results. However, it remains unclear whether the superiority in pathological regression could translate into a survival benefit for patients with LAGC treated with chemotherapy and PD-1 inhibitors. Jiang et al. [16] showed that the 1-year OS and DFS rates in patients treated with preoperative chemotherapy plus sintilimab were 94.1% and 90.3%, respectively. In our study, the survival curves gradually separated during the follow-up period, however, there was no significant difference in the 1-year OS and DFS rates between the two groups. Long-term follow-up is needed to determine the survival benefit of perioperative chemotherapy plus immunotherapy in these patients. Moreover, the ongoing phase III KEYNOTE-585 trial of the perioperative XP/FP/FLOT regimen combined with pembrolizumab, with the primary endpoint of OS, will provide additional data in the future [32].
Regarding the safety of preoperative treatment, a meta-analysis reported that the incidence of grade 3–4 adverse events in patients treated with neoadjuvant chemoimmunotherapy and chemotherapy was 20.6% and 25.7%, respectively, with no significant difference (P = 0.380) [33]. Similarly, our results indicated that the addition of a PD-1 inhibitor to chemotherapy did not significantly increase the incidence of adverse events compared to chemotherapy alone. Therefore, the toxicity of PD-1 inhibitors in combination with chemotherapy may be tolerable. However, the potential immune-related adverse events (irAEs) should not be ignored. Previous studies indicate that organ-specific irAEs occur most frequently in the endocrine organs and skin, followed by the gastrointestinal and pulmonary tracts, most of which are grade 1–2 [16, 17]. In our study, a total of five patients (6.7%) in Group A experienced irAEs, including two cases of grade 3 hypothyroidism that required hormone replacement therapy. With the increased use of ICIs in the treatment of LAGC, it is important to be aware of potential adverse events and to become better at recognizing and managing these specific toxicities.
Biomarkers are increasingly driving systemic therapy. PD-L1 expression, MMR status, and EBV-positivity have been identified as potential biomarkers for immunotherapy benefit, however, evidence in the perioperative setting is still unclear [6]. Therefore, further exploratory analyses were performed in patients treated with PD-1 inhibitors in this study.
PD-L1 is a widely accepted biomarker for immunotherapy in gastric cancer. The CPS, which indicates PD-L1 expression levels on tumor cells and tumor-related immune cells, may be useful in predicting the efficacy of anti-PD-1 therapy [34]. However, the optimal cutoff value has not been established. Tang et al. [15] and Guo et al. [17] reported a higher pathological response rate in patients with a CPS ≥ 1 who were treated with preoperative chemoimmunotherapy. However, superior pCR and MPR rates were only observed in patients with a CPS ≥ 5 in the present study. Therefore, further research is needed to determine the appropriate cutoff value of PD-L1 CPS, which could improve patient selection for perioperative treatment.
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Patients with microsatellite instability (MSI)/dMMR are characterized by increased PD-L1-positive T-cell infiltration and are more likely to respond to PD-1 inhibitors [35]. In this study, the pathological regression rate in patients with dMMR was higher than that in those with proficient MMR, indicating that the combination of chemotherapy and immunotherapy may be beneficial in these patients. However, whether patients with dMMR gastric cancer treated with perioperative chemoimmunotherapy have a superior prognosis compared to patients treated with chemotherapy alone is not clear, and there is still a lack of consensus on the treatment of these patients. An exploratory analysis of the MAGIC trial [36] revealed that preoperative chemotherapy may exert a negative effect on the prognosis of patients with MSI/dMMR LAGC. Meanwhile, the GERCOR NEONIPIGA phase II trial [37] reported a promising pCR rate (58.6%, 17/29) in patients with resectable MSI/dMMR gastric/gastroesophageal junction adenocarcinoma (T2–4NxM0) who were treated with neoadjuvant nivolumab plus ipilimumab. However, the most effective perioperative strategies for the management of patients with MSI/dMMR gastric cancer remain controversial, and further clinical studies are warranted.
As a distinct molecular subtype of gastric cancer, EBV-positivity has also been reported as a biomarker for anti-PD-1 therapy. Previous studies have indicated that EBV-associated gastric cancer (EBVaGC) exhibits higher expression of PD-L1 and lymphocytic infiltration [38, 39]. Patients with EBVaGC may be more susceptible to PD-1 blockade and may have a better prognosis [40‐42]. Tang et al. [15] reported an exceptional pCR rate of 33.3% (2/6) in patients with EBVaGC who were treated with neoadjuvant PD-1 blockade plus chemotherapy. In this study, both patients with EBV-positive gastric cancer had encouraging outcomes: one achieved MPR and the other achieved pCR. Therefore, patients with EBVaGC may be an additional population with high potential for clinical benefit to chemoimmunotherapy.
Although the baseline characteristics were balanced and comparable between the two groups after PSM, there are several limitations in the present study. First, this was a single-center study, and selection bias was unavoidable given the retrospective design of the study. Second, the safety results of perioperative chemotherapy plus PD-1 inhibitor may be compromised due to the exclusion of some patients with incomplete treatment. Third, long-term survival and recurrence could not be fully analyzed due to the relatively short follow-up period. Finally, we did not explore the efficacy of perioperative chemotherapy plus PD-1 inhibitors in patients with different genomic backgrounds (tumor mutation burden, high microsatellite instability, etc.). Despite these limitations, our results are valuable for future research on the perioperative management of patients with LAGC.
In conclusion, perioperative SOX plus sintilimab may improve tumor downstaging and pathological regression rate of LAGC. Patients with PD-L1 CPS ≥ 5, EBV-positivity, or dMMR responded better to chemoimmunotherapy. However, long-term survival requires further follow-up, and more prospective clinical studies with larger sample sizes are needed to validate the findings of our study.
Acknowledgements
We thank all the study participants and research staff who participated in this work.
Declarations
Conflict of interest
The authors declare no competing interests.
Ethical approval and informed consent
This study was approved by the Ethics Committee of Zhejiang Cancer Hospital (approval number: IRB-2022-592) and was conducted according to the Declaration of Helsinki. Informed consent was obtained from each patient enrolled in the study.
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