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Perioperative treatment in resectable gastric cancer with spartalizumab in combination with fluorouracil, leucovorin, oxaliplatin and docetaxel (FLOT): a phase II study (GASPAR)



Perioperative chemotherapy and surgery are a standard of care for patients with resectable gastric or gastroesophageal junction (GEJ) adenocarcinoma. However, the prognosis remains poor for this population. The FLOT (fluorouracil, leucovorin, oxaliplatin, and docetaxel) regimen is considered as the new standard chemotherapy regimen for perioperative strategy, despite associated with a 5-year overall survival rate (OS) amounting 45% following radical surgery.

Immunotherapy with antibodies that inhibit PD-1/ PD-L1 interaction has recently emerged as a new treatment option with promising and encouraging early trial results for patients with advanced or metastatic gastric or GEJ adenocarcinoma. Currently, no trials have investigated the impact of perioperative immunotherapy in combination with chemotherapy for resectable gastric or GEJ adenocarcinoma.


GASPAR trial is a multicenter open-label, nonrandomized, phase II trial to evaluate the efficacy and safety of Spartalizumab in combination with the FLOT regimen as perioperative treatment for resectable gastric or GEJ adenocarcinoma. The main endpoint is the proportion of patients with pathological complete regression (pCR) in the primary tumour after preoperative treatment.

Systemic treatment will include a pre-operative neoadjuvant and a post-operative adjuvant treatment, during which FLOT regimen will be administered every two weeks for 4 cycles and Spartalizumab every four weeks for 2 cycles.

For patients with confirmed tumor resectability on imaging assessment, surgery will be realized within 4–6 weeks after the last dose of preoperative chemotherapy. Post-operative systemic treatment will then be initiated within 4–10 weeks after surgery.

Using a Simon’s two-stage design, up to 67 patients will be enrolled, including 23 in the first stage.


Currently, no trials have investigated the impact of immunotherapy in combination with FLOT chemotherapy as perioperative treatment for resectable gastric or GEJ adenocarcinoma. Some studies have suggested a change in the tumor immune micro-environment following neoadjuvant chemotherapy in this setting, reinforcing the relevance to propose a phase II trial evaluating efficacy and safety of Spartalizumab in combination with perioperative chemotherapy, with the aim of improving treatment efficacy and survival outcomes.

Trial registration

NCT04736485, registered February, 3, 2021.

Peer Review reports


Gastric cancer represents the fifth most common cancer and the third leading cause of cancer deaths in the world [1]. Perioperative chemotherapy and surgery are a standard of care for patients with resectable gastric or GastroEsophageal Junction (GEJ) adenocarcinoma. Despite this combination of treatment, the prognosis remains poor for this population.

Perioperative treatment was considered as the standard compared to surgery alone according to the randomized MAGIC trial, evaluating ECF (Epirubicin, Cisplatin and Fluorouracile), 3 pre- and 3 post-operative cycles in 503 patients with resectable locally advanced gastric or GEJ adenorcarcinoma [2]. Especially, an improved Overall Survival (OS) with a 5-year survival rate of 36% was observed, versus 23% for surgery alone. However, in a controlled open-label phase II/III trial conducted among 716 patients, the FLOT regimen (Fluorouracil, Leucovorin, Oxaliplatin, and doceTaxel), 4 pre- and 4 post-operative cycles, was associated with better OS compared to ECF as perioperative chemotherapy, with 50 months versus 35 months in median [3]. Moreover, there was a higher proportion of pathological Complete Response (pCR): 16% [95% CI: 10–23] versus 6% [95% CI: 3–11] [4]. Furthermore, a recent meta-analysis showed that pCR was clearly associated with lower risk of death and recurrence compared with patients with any residual disease, among 1 143 patients with resectable gastric or GEJ cancer, after neoadjuvant chemotherapy and radical surgery [5]. The FLOT regimen thus appears as the new standard chemotherapy regimen for perioperative strategy of resectable gastric or GEJ adenocarcinoma. However, the 5-year OS rate remains only at 45% following radical surgery [3]. New approaches are needed to improve these outcomes.

PD-1 is a critical immune checkpoint receptor. It acts through its ligands, PD-L1 and PD-L2, while transducing a signal that inhibits T-cell proliferation, cytokine production, and cytolytic function, attenuating tumor immunity and facilitating tumor progression [6, 7]. PD-1 and its ligand PD-L1 are expressed on up to 50% of gastric or GEJ tumors, with a controversial impact on survival [8, 9]. Immunotherapy with antibodies that inhibit PD-1/PD-L1 interaction has recently emerged as a new treatment option with promising and encouraging early trial results for patients with advanced or metastatic gastric or GEJ adenocarcinoma [10]. Muro et al. conducted a phase Ib trial (KEYNOTE-012) in 39 patients with PD-L1-positive advanced gastric or GEJ adenocarcinoma to investigate the safety and activity of the anti-PD-1 antibody pembrolizumab [11]. Pembrolizumab demonstrated a 22% objective response rate with a manageable toxicity profile. Fuchs et al. conducted the KEYNOTE-059 phase II trial with pembrolizumab monotherapy in 259 patients with previously treated advanced gastric and GEJ cancer (at least 2 lines of treatment) and showed durable responses, with great response rate, especially for PD-L1 positive tumors [12]. Results from these studies allowed approval of pembrolizumab by the US FDA as third line treatment for patients with advanced or metastatic gastric or GEJ cancer PD-L1–positive. Moreover, an update of the KEYNOTE-059 trial demonstrated a manageable safety and promising efficacy of first-line immunotherapy combined with chemotherapy (cisplatin and fluorouracil) [13]. In a first-line study (KEYNOTE-062), Shitara et al. showed encouraging benefit with pembrolizumab versus chemotherapy among patients with untreated advanced gastric and GEJ cancer with higher levels of PD-L1 and microsatellite instability–high (MSI-H) tumours [14]. The CheckMate 649 trial recently showed that nivolumab and chemotherapy versus chemotherapy alone improved OS and progression-free survival (PFS) as first-line treatment in patients with non-HER-2-positive advanced gastric, GEJ or oesophageal cancer [15].

PDR001 (Spartalizumab) is a high-affinity, ligand-blocking, humanized Immunoglobulin G4 monoclonal antibody directed against PD-1 that blocks the binding of PD-L1 and PD-L2 [16]. Spartalizumab has demonstrated pharmacodynamic activity and a favorable toxicology profile in preclinical studies [17]. The available safety data from clinical studies indicate that PDR001 is generally well tolerated. As of the safety cut-off date of 26-Mar-2020, 1 702 patients across the 17 Novartis-sponsored clinical studies described have been treated with PDR001. In the open label multicenter phase I/II study of the safety and efficacy of PDR001 administered to patients with advanced malignancies, the results of phase I dose escalation among 58 patients have been published [17]. The maximum tolerated dose was not reached. The recommended phase II doses were determined as 400 mg Q4W or 300 mg Q3W. No dose-limiting toxicities were observed, and adverse events included those typical of other PD-1 antibodies. In the phase I step of this trial [17], the most common treatment-related adverse events of any grade were fatigue (22%), diarrhea (17%), pruritus (14%), hypothyroidism (10%), and nausea (10%).

In the GASPAR study herein presented, we aim to evaluate the efficacy and safety of Spartalizumab in combination with the FLOT regimen as perioperative treatment for resectable gastric or GEJ adenocarcinoma. Ancillary biological exploration is also planned to identify subgroups of responder patients. Indeed, cancer immunotherapies represent a major novel class of antitumor agents. However, the mechanism of action of these exciting new therapies is not completely understood and much remains to be learned regarding how best to leverage these new drugs in treating patients. Thus, to aid future patients, it is important to investigate the determinants of response or resistance to cancer immunotherapy and other treatments administered. These efforts may identify predictive biomarkers and generate information that could help in patient selection with personalized medicine programs (Fig. 1).

Methods / design

The GASPAR study is a multicenter, open-label, non-randomized phase II trial conducted to evaluate the efficacy and safety of Spartalizumab in combination with the FLOT regimen as perioperative treatment for resectable gastric or GEJ adenocarcinoma in patients (Fig. 1). The GASPAR protocol and this manuscript have been written in accordance with standard protocol items, namely recommendations for interventional trials (SPIRIT).

Fig. 1
figure 1

Flow chart of GASPAR study

Primary outcome

The primary objective of the study is to assess the pathologic response after pre-operative treatment by Spartalizumab in combination with the FLOT regimen for resectable gastric or GEJ adenocarcinoma.

Secondary outcomes

The secondary objectives are:

  • To evaluate the impact of perioperative treatment on survival outcomes (disease-free and overall survivals)

  • To evaluate the histological R0 resection margin

  • To establish the association between pCR and survival outcomes (disease-free and overall survivals)

  • To determine the safety profile of the combination of Spartalizumab and FLOT regimen

  • To evaluate the post-operative morbidity and mortality

Study population

Eligibility criteria are precised in Table 1. The GASPAR study addresses patients with untreated localized gastric or GEJ adenocarcinoma considered resectable.

Table 1 Eligibility criteria

Study sites

The list of study sites is indicated on The participation of 13 French centres is planned (Table 2).

Table 2 Participating centers

Study treatments

Eligible patients who have completed screening and have signed the written informed consent to participate to this phase II trial will receive a treatment by Spartalizumab plus FLOT regimen, initiated within 15 days after inclusion. Systemic treatment will include a pre-operative neoadjuvant 8-week phase of treatment and a post-operative 8-week phase of treatment.

The administered treatment will be FLOT associated to Spartalizumab as follows:

Standard FLOT regimen:

  1. o

    Docetaxel 50 mg/m2 IV infusion on D1

  2. p

    Oxaliplatine 85 mg/m2 IV infusion on D1

  3. q

    Leucovorin 200 mg/m2 IV infusion on D1

  4. r

    Fluorouracile 2600 mg/m2 24 h IV infusion on D1

Chemotherapy will be administered every two weeks for 4 pre-operative cycles (8 weeks) and 4 post-operative cycles (8 weeks).

Spartalizumab (PDR001): patients will receive the fixed dose of 400 mg per IV infusion over 30 minutes on D1 every four weeks for 2 pre-operative cycles (8 weeks) and 2 post-operative cycles (8 weeks).

For patients with confirmed resectability of the tumor by an imaging assessment (TAP CT-scan and optional MRI and endoscopy), surgery will be realized within 4–6 weeks after the last dose of preoperative chemotherapy and will depend on tumoral localization:

for gastric tumors, surgery will consist on a total or subtotal distal (for antropyloric tumors) gastrectomy with D2 lymphadenectomy,

for type 1 GEJ tumors, transthoracic esophagectomy (Ivor-Lewis procedure) with resection of the proximal stomach and 2-field (mediastinal and abdominal) lymphadenectomy,

for type 2 or 3 GEJ tumors, gastrectomy with transhiatal distal oesophagectomy and D2 lymphadenectomy.

Local pathologists from selected expert centers will perform standardized evaluation of pathological response in surgically resected specimens. Tumour regression grade will be assessed according to the Becker regression criteria [18].

Post-operative systemic treatment will be initiated within 4–10 weeks after surgery.

Premedication is not recommended for Spartalizumab. Also, it is recommended to use antiemetic treatment according to the ASCO/MASCC recommendation guideline with aprepitant and setron before FLOT regimen.

To anticipate some potential interactions with Spartalizumab and/or FLOT regimen, the use of concomitant medications is defined in the protocol. Thus, some treatments and/or procedures are permitted, namely G-CSF (in secondary prophylaxis of severe or febrile neutropenia, or in primary prophylaxis from first cycle of treatment), erythropoietin and/or transfusions, anti-diarrheal medications in case of diarrhea, pain medication, and/or nutritional support, at the discretion of the investigator. Conversely, other systemic anticancer agents (chemotherapy, hormonal therapy other than megestrol acetate, immunotherapy) or other treatments not part of protocol-specified anticancer therapy, live vaccines, systemic glucocorticoids for any purpose other than to modulate symptoms from an adverse event that is suspected to have an immunologic etiology (the use of physiologic doses of corticosteroids may be approved after consultation with the Sponsor) are not authorized. In addition, drugs known to prolong the QTc interval should be used with caution.

Study assessments

The overview of study assessments and procedures is detailed in Table 3. Tumoral evaluation will be performed with CT-scan (thoracic and abdomino-pelvic) at baseline, before surgery, at the end of treatment, thereafter every 3 months for the first 2 years and every 6 months for the next 3 years in the absence of tumoral progression. Disease assessment evaluation will be determined locally according to RECIST v1.1 (Response Evaluation Criteria in solid Tumors) criteria.

Table 3 Overview of study assessments of the GASPAR trial

For further ancillary biological studies, we plan to constitute a blood and tumor collection with the aim to evaluate the impact of biomarkers (ctDNA and tissue) in terms of oncological outcomes and response to treatment. These biomarkers may include ctDNA levels over time, PD-L1 expression, MSI status, EBV (Epstein-Barr Virus) status and TMB (Tumor Mutational Burden). Exploration of tumor organoid culture is also planned only for patients enrolled in Centre François Baclesse with additional specific written consent form.

Statistical design overview

Sample size determination

We used an optimal Simon’s two stage phase II design to estimate the sample size. According to Al-Batran S-E et al. outcomes [4], patients rate achieving pathological complete regression with FLOT regimen was 16% [95%CI: 10–23] (observed in 128 patients). To assess efficacy of FLOT regimen combined with Spartalizumab, we assume a histological complete response rate p < 10% as unacceptable (corresponding to the lower CI limit of response rate in Al-Batran), and a response rate p > 23% as demonstrating efficacy of the treatment combination (corresponding to the upper CI limit). With an alpha level of 5% and statistical power of 80%, 58 assessable patients are required, including 20 in the first stage.

Taking into account that 15% of patients will be lost or non-assessable, we plan to include a total of 67 patients in the trial (23 in the first stage and 44 in the second).

Statistical analyses

All enrolled patients who will receive at least one dose of study medication will be evaluable for the efficacy analysis, as well as included in the safety analysis. A safety analysis will be planned after a follow-up of one month following surgery of the tenth enrolled patient, during which enrolment will be halted. It will aim to precisely describe safety data up to one month post-surgery, the potential delays in performing surgery and the reasons for postponing it, as well as the perioperative complications that will have occurred.

After the 23th inclusion, the planned interim analysis on efficacy will be performed, during which enrolment will not be halted. According to Simon’s two-stage design, a minimum of 3 complete responses out of 20 assessable patients in the first stage will allow pursuing the study in the second stage. Otherwise, the study will stop for insufficient efficacy.

On the 58 assessable patients considered for the final analysis, the study will conclude to efficacy if at least 10 complete responses are observed. Additionally, the response rate will be estimated with a 95%CI confidence interval.

Then, Chi-squared test and T-Student test will be used to measure association of, respectively, qualitative and quantitative variables with pCR response. Time-to-event variables will be summarized by the Kaplan–Meier estimator. Association of time-to-event variables with factors of interest will be measured by a Cox model and the log-rank test. Adverse events of the treatment combing Spartalizumab and FLOT regimen will be described according to NCI CTCAE criteria v5.0 and tabulated by grade and frequencies, based on time of occurrence and relationship to treatment. The tolerance profile of the association will be summarized by duration of treatment, reasons of discontinuation, dose reduction rates and reasons for dose reductions.

Data monitoring committee

An Independent Data Monitoring Committee (IDMC) will be set-up to ensure the protection of patients, to ensure the ethical conduct of the study, to evaluate the benefit/risk ratio of the study and to ensure an independent review of the scientific outcomes during and at completion of the study.

The committee will include a biostatistician, a pharmacologist and a medical oncologist.

The members of the IDMC will be consulted before the trial initiation, at safety analysis one month after surgery of the 10th enrolled patients, thereafter, at the interim and final analyses.

Data management

A Web Based Data Capture (WBDC) system will be used for data collection and query handling. The investigator will ensure that data are recorded on the eCRFs as specified in the study protocol and in accordance with the instructions provided.

The investigator ensures the accuracy, completeness, and timeliness of the data recorded and of the provision of answers to data queries according to the Clinical Study Agreement. The investigator will sign the completed eCRFs. A copy of the completed eCRFs will be archived at the study site.

Withdrawal from study

The reasons for why a patient may discontinue to participate to the study or interrupt the treatment include the following circumstances:

  • Disease progression

  • Need to initiate another anti-tumor treatment, including radiotherapy

  • Unacceptable toxicity, not compatible with study treatment

  • Patient's decision (the data already collected during the search can be kept and exploited unless the patient opposes it)

  • Intercurrent illness or other reason that requires stopping treatment of the study

  • Patient lost to view

  • Investigator's decision.

Any patient who prematurely withdraws from the study treatment only will continue to be followed, unless he/she withdraws from the study.


Currently, no trials have investigated the impact of neoadjuvant immunotherapy in combination with chemotherapy for resectable gastric or GEJ adenocarcinoma. Nevertheless, some studies suggest a change in the tumor immune micro-environment following neoadjuvant chemotherapy in locally advanced gastric cancer, with an increased expression of immune markers. Thus; tumor samples, before and after neoadjuvant chemotherapy, of 60 patients with locally advanced gastric cancer were retrospectively identified and analyzed by multiplex immunohistochemistry, with a panel including PD-1 and PD-L1 [19]: following neoadjuvant chemotherapy, the overall median expression levels of PD1 and PD-L1 were significantly increased; moreover, high upregulation levels of these checkpoint molecules were correlated with survival benefits.

All these data are encouraging in the use of immunotherapy in combination with perioperative chemotherapy, with the aim of improving treatment efficacy and survival outcomes. In this context, we propose a non-randomized phase 2 study to assess the efficacy and safety of Spartalizumab in combination with the FLOT regimen as perioperative treatment for resectable gastric or GEJ adenocarcinoma.

Availability of data and materials

Not applicable.



Adverse event


Alanine aminotransferase


American Society of Clinical Oncology


Aspartate aminotransferase

CA 19.9:

Carbohydrate antigen 19.9


Complete blood cells count


Carcinoembryonic antigen


Confidence intervals


Computed tomography


Common Terminology Criteria for Adverse Events


Circulating tumor DNA


Epstein–barr virus




Eastern Cooperative Oncology Group


Electronic case report form


Food and Drug Administration


Formalin-fixed paraffin-embedded


Gastroesophageal junction


Gamma glutamyltransferase


Hepatitis B virus


Hepatitis C virus


Human immunodeficiency virus


Independent data monitoring committee


Multinational Association of Supportive Care in Cancer


Magnetic resonance imaging


Microsatellits instability


New York Heart Association


National cancer institute


Overall survival


Peripheral blood mononuclear cells


Pathological complete regression


Programmed death-1


Programmed death-ligand 1


Programmed death-ligand 2


Corrected QT interval


Response evaluation criteria in solid tumors


Standard Protocol Items, Recommendations for Interventional Trials


Serum thyroxine


Thorax, abdomen and pelvis


Tumor mutational burden


Thyroid stimulating hormone


White blood cell count


Web Based Data Capture


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We are grateful to the members of the Independent Data Monitoring Committee for their involvement in the conduction of this trial. We thank the Data Processing Centre (DPC) of the North West Canceropole (Centre de Traitement des Données du Cancéropôle Nord-Ouest) in charge of data management. We would like to thank all patients who will consent to participate as well as theirs families. The investigators are also thanked.


This trial (NCT04736485) is granted in the context of the call for projects 2019 “Innovating molecules on HDM201, HDM2-P53 inhibitor, Spartalizumab (PDR001), anti-PD1, Capmatinib (INC280), c-met inhibitor, LSZ102, inhibitor and modulator of estrogen receptors”. The grant is jointly funded by the French Cancer Institute and the French Fondation ARC (Ref INCa-ARC_14842). Spartalizumab is provided free of charge to enrolled patients by Novartis. The French Cancer Institute, the Fondation ARC and Novartis are not involved in the design and conduct of the study, nor in the collection, management, analysis, and interpretation of the data. They are not involved in the writing of the manuscript.

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Authors and Affiliations



MDS, JL, AL and BC wrote the manuscript and devised the study concept and design. JL was responsible for overseeing the statistical section. All authors (MDS, JL, AL, SC, AP, JMG, SV, PEB, MD, DV, LBW, LP, CLG, MCT, MPG and BC) contributed to the study protocol, read and approved the final manuscript. Each author has been sufficiently involved in the work to take public responsibility for appropriate portions of the content.

Corresponding author

Correspondence to Mélanie Dos Santos.

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Ethics approval and consent to participate

This study has received ethical approval from the Comité de Protection des Personnes EST IV (N°EudraCT: 2020–004497-21) and from National Agency for Medical and Health products Safety (Reference: 2020–12-00012_2020-004497–21) in January 2021. All patients will be proposed to participate by the medical oncologists, gastroenterologists or digestive surgeons, who will give them an information file. All patients will give their written informed consent before any study-related assessment start.

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Not applicable.

Competing interests

Novartis provided Spartalizumab.

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Dos Santos, M., Lequesne, J., Leconte, A. et al. Perioperative treatment in resectable gastric cancer with spartalizumab in combination with fluorouracil, leucovorin, oxaliplatin and docetaxel (FLOT): a phase II study (GASPAR). BMC Cancer 22, 537 (2022).

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