Tumor regression grade and overall survival following gastrectomy with neoadjuvant therapy for gastric cancer.

Authors

null

Michelle A Savoldy

USF Morsani College of Medicine, Tampa, FL

Michelle A Savoldy , Andrew J Sinnamon , Rutika Mehta , Luis Pena , Sean P. Dineen , Gregory Y Lauwers , Jose Mario Pimiento

Organizations

USF Morsani College of Medicine, Tampa, FL, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL

Research Funding

No funding received

Background: Perioperative chemotherapy is the standard of care for locoregional gastric cancers in western populations. However, the impact of response to therapy as a biomarker of cancer survival has not been fully defined. This study focuses on the pathological response to neoadjuvant chemotherapy, as measured by tumor regression grade (TRG), for gastric cancer and its impact on patient outcomes, primarily overall survival. Methods: Patients undergoing gastrectomy for nonmetastatic invasive gastric adenocarcinoma following perioperative chemotherapy (clinical T2+/N+cM0) were identified from an institutional database (2000-2021). Demographics, clinical staging including histologic grade, surgical factors and survival outcomes were included. The association between TRG and overall survival from time of surgery was assessed. OS was estimated using the Kaplan Meier method with adjustment for covariates using Cox regression. Results: One hundred seventeen patients were identified. Median age was 65 years (IQR 57–73). The majority of the patients were male (n = 64, 55%). Seventy-six patients underwent total gastrectomy, 22 subtotal gastrectomy, and 19 distal gastrectomy. Six patients (5.1%) had a TRG of 0, 18 patients (15.4%) had a TRG of 1, 25 patients (21.4%) had a TRG of 2, and 68 patients (58.1%) had a TRG of 3. Median survival overall was 40.9 months (95% CI 28.7–66.4). TRG status was not significantly different between chemotherapy regimens (doublet vs triplet, p = 0.96). Median survival was longest in the TRG 0 group (86.9 months), followed sequentially by TRG 1 (74.5 months), TRG 2 (51.5 months), and lastly, TRG 3 group with 27.0 months. Increased tumor regression (lower TRG) was significantly associated with prolonged survival (p < 0.01 by log-rank for trend). After adjustment for clinical patient factors and tumor factors, TRG remained significantly associated with overall survival (Table; TRG hazard ratio 1.62, p = 0.007). In addition to TRG status, clinical T4 tumors and diffuse histology were associated with poor survival (cT4 hazard ratio 2.09, p = 0.039, diffuse histology hazard ratio 1.82 (p = 0.071). Conclusions: In patients receiving perioperative chemotherapy for treatment of gastric cancer, response to therapy as defined by TRG is independently prognostic of survival.

Variable
Hazard Ratio (95% CI)
P
TRG*
1.62 (1.14-2.29)
0.007
Histology


Intestinal
Ref
--
Diffuse
1.82 (0.95-3.50)
0.071
Signet ring cell
1.53 (0.80-2.95)
0.199
NOS
3.57 (0.96-13.1)
0.054
Other
2.13 (0.48-9.50)
0.321
Clinical T4
2.09 (1.04-4.21)
0.039

*TRG treated as ordinal

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Abstract Details

Meeting

2022 ASCO Gastrointestinal Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session A: Cancers of the Esophagus and Stomach and Other GI Cancers

Track

Esophageal and Gastric Cancer,Other GI Cancer

Sub Track

Tumor Biology, Biomarkers, and Pathology

DOI

10.1200/JCO.2022.40.4_suppl.355

Abstract #

355

Poster Bd #

Online Only

Abstract Disclosures