Dynamic alteration in SULmax predicts early pathological tumor response and short-term prognosis in non-small cell lung cancer treated with neoadjuvant immunochemotherapy

Introduction: Biomarkers predicting tumor response to neoadjuvant immunochemotherapy in non-small cell lung cancer (NSCLC) are still lacking despite great efforts. We aimed to assess the effectiveness of the immune PET Response Criteria in Solid Tumors via SULmax (iPERCIST-max) in predicting tumor response to neoadjuvant immunochemotherapy and short-term survival in locally advanced NSCLC.

Methods: In this prospective cohort study, we calculated SULmax, SULpeak, metabolic tumor volume (MTV), total lesion glycolysis (TLG) and their dynamic percentage changes in a training cohort. We then investigated the correlation between alterations in these parameters and pathological tumor responses. Subsequently, iPERCIST-max defined by the proportional changes in the SULmax response (△SULmax%) was constructed and internally validated using a time-dependent receiver operating characteristic (ROC) curve and the area under the curve (AUC) value. A prospective cohort from the Sun Yat-Sen University Cancer Center (SYSUCC) was also included for external validation. The relationship between the iPERCIST-max responsiveness and event-free survival in the training cohort was also investigated.

Results: Fifty-five patients with NSCLC were included in this study from May 2019 to December 2021. Significant alterations in post-treatment SULmax (p < 0.001), SULpeak (p < 0.001), SULmean (p < 0.001), MTV (p < 0.001), TLG (p < 0.001), and tumor size (p < 0.001) were observed compared to baseline values. Significant differences in SULpeak, SULmax, and SULmean between major pathological response (mPR) and non-mPR statuses were observed. The optimal cutoff values of the SULmax response rate were −70.0% and −88.0% using the X-tile software. The univariate and multivariate binary logistic regression showed that iPERCIST-max is the only significant key predictor for mPR status [OR = 84.0, 95% confidence interval (CI): 7.84–900.12, p < 0.001]. The AUC value for iPERCIST-max was 0.896 (95% CI: 0.776–1.000, p < 0.001). Further, external validation showed that the AUC value for iPERCIST-max in the SYSUCC cohort was 0.889 (95% CI: 0.698–1.000, p = 0.05). Significantly better event-free survival (EFS) in iPERCIST-max responsive disease (31.5 months, 95% CI 27.9–35.1) than that in iPERCIST-max unresponsive disease (22.2 months, 95% CI: 17.3–27.1 months, p = 0.024) was observed.

Conclusion: iPERCIST-max could better predict both early pathological tumor response and short-term prognosis of NSCLC treated with neoadjuvant immunochemotherapy than commonly used criteria. Furthermore, large-scale prospective studies are required to confirm the generalizability of our findings.

Introduction

Non-small cell lung cancer (NSCLC) is the most common cause of cancer-related death worldwide (Siegel et al., 2021), likely because most NSCLC patients (>70%) are diagnosed at advanced stages (Ramos-Esquivel et al., 2017). Immune checkpoint inhibitors (ICIs) have changed the landscape of advanced NSCLC treatment (Ramos-Esquivel et al., 2017; Uprety et al., 2020; Huang et al., 2021; Wang et al., 2021). It has been reported that a combination of ICIs and chemotherapy significantly improve the prognosis of NSCLC (Spicer et al., 2021; Wang et al., 2021; Zhao et al., 2021). Although previously published data showed that more than 40% of NSCLC patients achieved major pathological response after neoadjuvant immunochemotherapy (NAIC), a large proportion of patients still could not benefit from such treatment modality and developed disease progression rapidly (Jiang et al., 2022). As the clinical management strategies for responders significantly differ from nonresponders, a non-invasive method to early evaluate, or even predict the treatment response to NAIC is urgently needed.

18F-FDG PET/CT, with its ability to depict both anatomical and functional changes, has been widely applied in oncological routines. The glucometabolism within a tumor, as revealed by PET imaging, was found to correlate with the expression of immune checkpoint programmed death 1 (PD-1), and the quantitative measurement of metabolic changes was found to associate with pathological response to NAIC (Lopci et al., 2016; Tao et al., 2020). Hence, 18F-FDG PET/CT might be utilized for early response evaluation. Prior studies have proposed several response-evaluation criteria for novel immunotherapies, of which the PET Response Criteria in Solid Tumors (PERCIST) (Joo Hyun et al., 2016) and the immune PERCIST (iPERCIST) standards were the most well-known (Goldfarb et al., 2019). Despite the reasonable diagnostic and predictive performance, their clinical implementation was hindered by several drawbacks (Tao et al., 2020). Both criteria require SULpeak, a value that reveals the average SUV within a small sphere (usually 1.2 cm in diameter) around the most hypermetabolic voxel, rendering small lesions with a metabolic diameter of less than 1 cm unmeasurable. Moreover, the partial volume effect might incur considerable measuring bias (Soret et al., 2007). Compared with SULpeak, a SULmax value, which reflects the most metabolically active portion of a potentially heterogeneous mass, was applicable in most lesions, thus is routinely reported and more clinically feasible (Wahl et al., 2009; Lodge et al., 2012). Moreover, prior studies found SULmax highly reproducible and comparable with proper standardization of the scanning protocol, despite the theoretical reproducibility issues. Hence, we hypothesize that a SULmax-based protocol might be clinically practical yet robust for the response evaluation and prediction of NAIC.

In light of the above, we proposed a SULmax-based protocol, named iPERCIST-max, to evaluate and predict treatment response to NAIC and tested our model’s diagnostic and prognostic performance in a training and an independent external validation cohort.

Materials and methods

Patients and study design

This prospective study was proved by the institutional review board (The Ethics Committee of the Guangdong Provincial People’s Hospital, No. GDREC2019687H). All procedures involved in this study were performed in accordance with the Declaration of Helsinki (as revised in 2013). Written informed consent was obtained from each participant in the study.

Data were collected from two prospectively maintained cohorts starting from May 2019 to December 2021: 1) A training cohort from our local institute and 2) an external validation cohort from an independent institute from Sun Yat-sen University Cancer Center.

The included patients met the following criteria: 1) Pathologically confirmed as NSCLC (Stage IB-IIIC AJCC 8th edition) that was potentially resectable after neoadjuvant therapy; 2) treatment-naïve and adequate organ function. Exclusion criteria were as follows: 1) Epidermal growth factor receptor (EGFR)-sensitive mutation; 2) previous autoimmune disease; 3) prior treatment with drugs that target T-cell co-stimulation pathways (such as checkpoint inhibitors).

A flowchart describing the study design is presented in Figure 1. All patients underwent baseline ¹⁸F-FDG PET/CT (B-PET) examination within 14 days before neoadjuvant therapy incorporating PD-1 inhibitors (200 mg) plus platinum-doublet chemotherapy every 3 weeks. After 2-4 cycles of neoadjuvant therapy, a follow-up ¹⁸F-FDG PET/CT (F-PET) was performed. When F-PET showed progressive disease, a second F-PET was performed after 4–8 weeks (Goldfarb et al., 2019).

FIGURE 1

FIGURE 1. Flowchart of the study design. Fifty-eight patients were assessed for eligibility; eventually, fifty-five cases were included for subsequent analysis.

Image acquisition and analysis

All patients in our training cohort were scanned using the same scanner (Biograph HI-REZ 16; Siemens Healthcare, Henkestr, Germany), following the criteria of the uniform protocols for imaging in clinical trials (UPICT) (Graham et al., 2015). Supplementary File S1 describing the details of the imaging protocol was provided. All images were evaluated using a commercial medical image-processing workstation (uWS-MI, United Imaging Healthcare, Shanghai, China). Two experienced nuclear medicine physicians (TT S & YL J) who were blinded to the patients’ clinical information independently analyzed the PET/CT images, resolving disagreements through consensus. Metabolic parameters including SULmax, SULpeak, SULmean, MTV in mL, and TLG were recorded on a lesion basis. Additionally, thoracic CECT images were reviewed by two board-certified radiologists (H Y & XC Z) who were blinded to the PET/CT study.

Response evaluation

We proposed the iPERCIST-max criteria based on the proportional changes in the SULmax response (△SULmax%) using the following formula:

$\frac{SubsequentSULmax-baselineSULmax}{baselineSULmax}\times 100\%.(1)$

The patients were divided into the following three groups based on tumor responses assessed by △SULmax%: iPERCIST-max complete metabolic responsive disease (imCMRD), responsive metabolic disease (imRMD), and unresponsive metabolic disease (imUMD). The optimal cutoff values for grouping were determined using a X-tile software (Camp et al., 2004).

Additionally, as references, metabolic and morphological responses were also evaluated using iPERCIST and iRECIST criteria (Goldfarb et al., 2019). Specifically, iPERCIST categorized patients into: Immune complete metabolic response (iCMR), partial metabolic response (iPMR), stable disease (iSMD), unconfirmed progressive metabolic disease PMD (iUPMD), and confirmed PMD (iCPMD); whereas iRECIST (Ayati et al., 2021) classified patients into: immune-complete response (iCR), immune-partial response (iPR), immune-stable disease (iSD), immune-confirmed progressive disease (iCPD), and unconfirmed PD (iUPD). Responsive diseases were defined as either metabolically (iCMR & iPMR per iPERCIST or imCMRD & imRMD per IPERCIST-max as mRD) or morphologically (iCR & iPR, as RD) alterations. Likewise, metabolic and morphological unresponsive disease were diagnosed as mUD (iSMD & iCPMD per iPERCIST or imUMD per iPERCIST-max) and UD (iSD & iCPD), respectively. Notably, upon the diagnosis of iUPMD or iUPD, a second F-PET/CECT study was performed 4–8 weeks later to verify the diagnosis (Eisenhauer et al., 2009; Seymour et al., 2017). (Supplementary Table S1 for a comparison of the iPERCIST, iRECIST, and iPERCIST-max criteria).

Outcome evaluation

Two experienced pathologists independently performed pathological assessments according to the current standard protocol. Pathological complete response (pCR) was defined as no evidence of residual viable tumor after neoadjuvant treatment. The major pathological response (mPR) was defined as less than 10% residual viable tumor following neoadjuvant treatment. Event-free survival (EFS) was calculated from the date of treatment initiation to the date of the first progression (local recurrence of tumor or distant metastasis) or death from any cause (Zheng et al., 2021). Censored data included those who were lost to follow-up or at the time of the final analysis.

Statistical analysis

Comparisons of intergroup continuous variables were performed using the Student’s t-test or the Mann-Whitney method whenever suitable. Categorical variables were compared using the chi-squared test or Fisher’s exact test, where suitable. The intraclass correlation coefficient (ICC) was calculated for quantification of the agreement between proportion changes in SULmax (△SULmax%) and in SULpeak (△SULpeak%). Notably, an ICC value between 0.81 and 1.00 suggests an excellent agreement (Zhao et al., 2015). Univariate followed by multivariate binary logistic regressions were used to identify independent predictors of mPR, following a three-step approach (Zhou et al., 2022). The power of prediction models was assessed by the area under the curve (AUC) value acquired from the Time-dependent receiver operating characteristic (ROC) curves. All tests were two-tailed, and p < 0.05 denotes statistical significance. All statistical analyses were performed using SPSS v26 software (IBM Corporation, Armonk, NY, United States) and R 4.0.0 (R Core Team 2020).

Results

Patient characteristics

Fifty-five patients (males: n = 50; females: n = 5) with a median age of 66 [Interquartile range (IQR) 58–69] years were enrolled in the training cohort, while 13 patients were enrolled in the external validation cohort. Detailed patient characteristics were tabulated in Table 1.

TABLE 1

TABLE 1. Patient characteristics. Values are presented as n (%) or median (interquartile range).

Treatment responses to NAIC

In the training cohort, 36 patients were deemed surgical candidates after the treatment, and the post-surgical histological studies confirmed that 13 (36.1%) patients achieved pCR while 23 (63.9%) achieved mPR. Likewise, in the independent validation cohort, 12 patients underwent surgery and 9 (75%) patients achieved mPR status.

PET imaging parameters in mPR and pCR patients

Significant alterations in post-treatment SULmax (p < 0.001), SULpeak (p < 0.001), SULmean (p < 0.001), MTV (p < 0.001), TLG (p < 0.001), and tumor size (p < 0.001) were observed compared with baseline values (Supplementary Figure S1) for all patients. Specifically, mPR patients presented with significantly lower SULpeak, SULmax, and SULmean than non-mPR (p < 0.05, as shown in Figures 2A–C). The median response rates of SULmax, SULpeak, and SULmean were significantly higher in the pCR cohort than in the non-pCR cohort (Figures 2D–F).

FIGURE 2

FIGURE 2. Association between PET-related parameters and pathological responses. (A) SULmax between mPR and non-mPR cohorts; (B) SULpeak between mPR and non-mPR cohorts; (C) SULmean between mPR and non-mPR cohorts; (D) SULmax between pCR and non-pCR cohorts; (E) SULpeak between pCR and non-pCR cohorts; (F) SULmean between pCR and non-pCR cohorts.

Comparison of iRECIST and iPERCIST evaluation

At the first radiological evaluation, 4 of 55 (7.3%) patients were evaluated as iUPD, 20 (36.4%) as iSD, and 31 (56.4%) as iPR. All the iUPD patients were identified as iCPD after the second evaluation. Based on the iRECIST criteria, none of the patients achieved iCR despite 13 pCR cases. Meanwhile, 5 of the 55 (9.1%) patients were classified as iUPMD, seven (12.7%) as iSMD, 38 (69.1%) as iPMR, and five (9.1%) as iCMR based on the iPERCIST criteria. Subsequent PET-scan verified that four out of the five iUPMD cases were iCPMD, and one patient presented with pseudoprogressive disease. Three of the five iCMR patients underwent surgery, and all achieved pCR status. Despite the above stated differences, a significant association was observed in mPR status vs. iRECIST responsiveness (Figure 3A, p = 0.019) and iPERCIST responsiveness (Figure 3B, p = 0.025). Comparisons in diagnostic indicators among different criteria were shown in Supplementary Table S2.

FIGURE 3

FIGURE 3. Differences in radiological disease responsiveness between mPR and non-mPR status based on iRECIST/iPERCIST/iPERCIST-max. (A) iRECIST; (B) iPERCIST; (C) iPERCIST-max. Green color represents responsive disease, while red color represents unresponsive disease.

Diagnostic performance of the proposed iPERCIST-max method

The ICC used to establish the agreement between the SULmax and SULpeak response rates was 0.994 (95% CI 0.990-0.997). The optimal cutoff values of the SULmax response rate were -70.0% and -88.0% using the X-tile software. Subsequently, tumor response represented by △SULmax% higher than -70% was defined as imUMD, those whose SULmax response rate was lower than -70.0% as imRMD, and those whose SULmax response rate was lower than -88.0% as imCMRD. All imCMRD patients who underwent surgery achieved pCR status. Moreover, a significantly higher proportion of imRMD was observed in the mPR cohort than in the non-mPR cohort (χ2 = 12.17, p < 0.001) (Figure 3C). Figure 4 showed a typical case who achieved imRMD after two cycles of NAIC and had mPR status after surgery. Furthermore, the univariate and multivariate binary logistic regression showed that iPERCIST-max was the only significant key predictor for mPR status [OR = 84.0, 95% confidence interval (CI): 7.84–900.12, p < 0.001] (Table 2).

FIGURE 4

FIGURE 4. A 53-year-old man with squamous cell carcinoma, who had marked metabolic changes on PET scanning after two cycles of neoadjuvant immunochemotherapy and was classified as responder per iPERCIST-max. (A) Baseline PET-CT fusion image of the primary tumor and lymph nodes; (B) Follow-up PET-CT fusion image showed markedly reduced metabolic activity of the tumor. (C) pathological examination revealed this patient had mPR disease. mPR, major pathological response.

TABLE 2

TABLE 2. Univariate and multivariate binary logistic regression analyses. RD: responsive disease; UD: unresponsive disease; MRD: metabolic responsive disease; MUD: metabolic unresponsive disease; cT: clinical T stage; cN: clinical N stage; cTNM: clinical Tumor-nodal-metastasis stage.

We utilized ROC and AUC values to better quantify the overall discriminatory power of various prediction models in predicting the mPR status. ROC analyses for comparisons in mPR status among iRECIST, iPERCIST, and iPERCIST-max were shown in Supplementary Figure S2. The AUC values for iRECIST responsiveness, iPERCIST responsiveness, and iPERCIST-max were 0.688 (95% CI: 0.498–0.877, p = 0.070), 0.625 (95% CI: 0.419–0.831, p = 0.227), and 0.896 (95% CI: 0.776–1.000, p < 0.001), respectively.

Furthermore, the Sun Yat-Sen University Cancer Center (SYSUCC) cohort was used to externally validate the robustness of iPERCIST-max. AUC value for iPERCIST-max predicting mPR status was 0.889 (95% CI: 0.698–1.000, p = 0.05).

The relationship between the iPERCIST-max responsiveness and event-free survival

The longest and median follow-up time was 35.5 and 21.0 months, respectively. iRECIST, iPERCIST, and iPERCIST-max can stratify patients into distinctive survival groups. Interestingly, no events (recurrence, metastasis, death, etc.) occurred in the imCMRD group at the last follow-up. The imCMRD group exhibited superior EFS compared to the other groups classified by iPERCIST-max (p < 0.001). Significantly better EFS in iPERCIST-max mRD (31.5 months, 95% CI: 27.9–35.1) than that in iPERCIST-max mUD (22.2 months, 95% CI: 17.3–27.1 months, p = 0.024) was observed (Figure 5A). Moreover, the 1-year survival AUC was 0.776 (95% CI: 0.575–0.976; p < 0.001) (Figure 5B). Significant differences in EFS were also seen between the UD and RD cohorts when classified using the iRECIST responsiveness (p = 0.033) and iPERCIST responsiveness (p = 0.004).

FIGURE 5

FIGURE 5. Survival difference in iPERCIST-max groups and internal validation of the robustness of iPERCSIT-max. (A) Kaplan-Meier estimated event-free survival between the responsive disease group and unresponsive disease group stratified by iPERCIST-max. (B) Time-dependent receiver-operating-characteristics (ROC) analysis for assessment of iPERCIST-max.

Discussion

Although the NSCLC treatment is profoundly shifting in the treatment paradigm due to recent advances in immunotherapy (Spicer et al., 2021; Zhao et al., 2021), it is clinically challenged by the lack of a robust and easy-to-use method to distinguish responders from non-responders. Hence, we proposed an iPERCIST-max model to predict the treatment response to NAIC. We found this method non-inferior to iPERCIST and iRECIST criteria in terms of robustness (Figure 3) but outperformed the latter in feasibility due to more straightforward clinical applications. Thus, the iPERCIST-max model might better suit the response evaluation to NAIC in NSCLC patients than iPERCIST and iRECIST criteria.

iPERCIST has been validated in multiple studies for its performance in assessing treatment responses to immunotherapies, using proportional changes in SULpeak values (Tao et al., 2020). However, as shown in our research, its clinical application was significantly challenged by its inability to index small lesions, mainly nodal and pulmonary metastasis [21 of 132 (15.6%) at baseline and 56 of 132 (42.2%) at follow-up]. Interestingly, SULmax, which was believed to be affected by multiple factors such as quanton noises, thus lacks the reproducibility for a quantitative study, was found effective in the treatment evaluation in this study. We hypothesize that with the modern advancement of novel PET hardware and proper standardization of the imaging acquisition protocol, the variation of SULmax has been minimized, evidenced by a high agreement between the SULpeak and SULmax measurement in this study [ICC = 0.994 (95% CI 0.990-0.997)] and in others (Kumar et al., 2013).

Owing to the broader clinical applicability of SULmax, we decided to develop iPERCIST-max based on △SULmax%. Using −70.0% as the cutoff value calculated from the X-tile, the iPERCIST-max divided patients into imCMRD, imRMD and imUMD.

Subsequent binary logistic regression and ROC curve analysis demonstrated the ability of iPERCIST-max to predict the mPR status. Furthermore, external validation using an independent SYSUCC cohort further enhanced the applicability of iPERCIST-max.

The difference in the mPR prediction power between iPERCIST-max and iPERCIST is mainly due to the choice of the optimal cutoff value. The cutoff value for the iPERCIST responsiveness-based model was 30%, the selection of which could falsely include patients with non-mPR status. Tao et al. reported that an increase in △SULmax% and △SULpeak% was positively associated with the degree of pathological regression, which indicated that pathological responses that achieved mPR were significantly associated with a −90% proportional change in metabolism. From this aspect, it is reasonable to locate a cut-off value higher than 30%.

Beer et al. and Ayati et al. reported better overall survival (OS) and progression-free survival in the RD cohort than in the UD cohort classified by the PERCIST and RECIST cohorts (Beer et al., 2019; Ayati et al., 2021). Similarly, our study revealed that both CT-based and PET-based criteria could stratify the survival difference between radiological/metabolic responders and nonresponders. In contrast to these findings, Rossi et al. showed no significant difference in OS prediction ability between morphological- and metabolic-based criteria (Rossi et al., 2020), indicating that PERCIST or iPERCIST may have limited clinical applicability in certain cohorts. In the present study, further survival analysis showed that the iPERCIST-max model could not only predict mPR status but could also stratify patients into ordinal survival groups (Figure 5A). The AUC value at 1 year and 2 years reached 0.776 (95% CI, 0.575–0.976; p < 0.001) and 0.751 (95% CI, 0.637–0.957) respectively, suggesting the robustness of the iPERCIST-max model.

Pseudo-progression might challenge the treatment evaluation, leading to premature termination of a potentially effective treatment; however, our data showed a low incidence of pseudo-progression (1 in 55,1.8%), which is in accordance with published data (Chiou and Burotto, 2015; Katz et al., 2018; Lee et al., 2018).

Despite these promising results, this study has several limitations. The sample size is small, and we excluded patients with EGFR-mutant adenocarcinoma, resulting in a biased disease population, which might prohibit the direct generalization of our conclusion into other cohorts. Further large-scale prospective studies with an unbiased disease population (without exclusion of adenocarcinoma) are needed to validate our proposal.

Conclusion

iPERCSIT-max based on temporal changes in PET metabolic parameters, particularly △SULmax% could better predict both early pathological tumor response and prognosis of NSCLC treated with NAIC than commonly used criteria.

Data availability statement

The raw data supporting the conclusion of this article will be made available by the authors, without undue reservation.

Ethics statement

This prospective study was proved by the institutional review board (The Ethics Committee of the Guangdong Provincial People’s Hospital, No. GDREC2019687H). All procedures involved in this study were performed in accordance with the Declaration of Helsinki (as revised in 2013). Written informed consent was obtained from each participant in the study.

Author contributions

TS, SH, and YJ: Conceptualization; Data curation; Formal analysis; Project administration; Resources; Software; Validation; Visualization; Roles/Writing—original draft; Writing—review and editing. HY, JW, CL, XZ, YT, XB, JT, HZ, DZ, LX, GC, YZ, and SW: Methodology; Project administration; Resources; Roles/Writing—original draft; Writing—review and editing. HX and GQ: Conceptualization; Funding acquisition; Investigation; Supervision; Roles/Writing—original draft; Writing—review and editing.

Funding

This work was supported by a grant from the 2020–2021 Popularization of Science and Technology Innovation Special Project of Guangdong Province of China (2020A1414070007); the Science and Technology Program of Guangzhou, China (202206010103); and Natural Science Foundation of Guangdong Province (2022A1515012469), and the Foundation of Medical Science and Technology Research of Guangdong Province (B2022075).

Acknowledgments

We would like to thank Editage (www.editage.com/) for English language editing.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fbioe.2022.1010672/full#supplementary-material

Supplementary Figure S1 | Paired sample test for PET-associated metabolic characteristics. (A) SULmax. (B) SULpeak; (C) SULmean; (D) MTV; (E) TLG; (F) size. Blue dots represent patients at baseline PET-CT evaluation, while red dots represents patients at the final time of tumor response evaluation. *, p < 0.05; **, p < 0.01, ***, p < 0.001. MTV, metabolic tumor volume; TLG, total lesion glycolysis; PreT: pretreatment; PostT: posttreatment.

Supplementary Figure S2 | Receiver-operating-characteristics (ROC) analysis for assessment of iRECIST, iPERCIST and iPERCIST-max in predicting major pathological response status. (A) iRECIST; (B) iPERCIST; (C) iPERCIST-max.

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Glossary

AUC area under the curve

B-PET baseline 18F-FDG PET/CT

EFS event-free survival

EGFR epidermal growth factor receptor

F-PET follow-up PET/CT

ICC intraclass correlation coefficient

ICIs Immune checkpoint inhibitors

iPERCIST-max the immune PET Response Criteria in Solid Tumors via SULmax

iPERCIST the immune PERCIST

imCMRD iPERCIST-max complete metabolic responsive disease

imRMD iPERCIST-max responsive metabolic disease

imUMD iPERCIST-max unresponsive metabolic disease

iCMR immune complete metabolic response

iPMR immune partial metabolic response

iSMD immune stable disease

iUPMD immune unconfirmed progressive metabolic disease

iCR immune-complete response

iPR immune-partial response

iSD immune-stable disease

i(C/U)PD immune (confirmed/unconfirmed) progressive disease

mPR major pathological response

NSCLC non-small cell lung cancer

MTV metabolic tumor volume

NAIC neoadjuvant immunochemotherapy

PD-1 programmed death 1

pCR pathological complete response

PERCIST PET Response Criteria in Solid Tumors

SYSUCC Sun Yat-Sen University Cancer Center

△SULmax% proportional changes in the SULmax response

TLG total lesion glycolysis

UPICT uniform protocols for imaging in clinical trials