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Cancer therapeutics targeting the immune system disrupted the landscape of oncology in recent years. To evade the immune system, cancer cells develop a series of immunosuppressive mechanisms, including up and downregulating functional pathways favoring tumor tolerance and T‐cell anergy. The Programmed Death (PD)‐1/PD Ligand‐1 (PD‐L1) pathway is one of such critical component of tumor‐mediated immunosuppression. In this setting, the administration of antibodies targeting PD‐1 and PD‐L1 demonstrated substantial clinical benefit in patients with advanced or metastatic cancer.
The novel mechanism of action of these antibodies is associated with specific adverse events (eg, immune‐related thyroiditis, pneumonitis, or colitis, etc) along with novel patterns of response such as profound and durable responses, pseudoprogression (PSPD) and hyperprogressive disease (HPD). Such findings have recently led to the development of immune Response Evaluation Criteria in Solid Tumors (iRECIST) that manage Pseudoprogression (PSPD) by introducing the notion of immune unconfirmed and confirmed progressive disease (iUPD and iCPD, respectively). PSPD is defined as an initial disease progression by RECIST followed by a subsequent response. Hypotheses suggest PSPD could be related to a transient infiltration of lymphocytes into the tumor and its stroma, preceding the tumor shrinkage. Several studies evaluating immune‐related responses in patients with advanced melanoma observed PSPD in 5%‐7% of patients receiving anti‐PD(L)1. Despite several case reports in the literature most of them including melanoma patients, the prevalence and the outcome of PSPD across solid tumors remains below 10%. Also, to predict this transient‐progression’ or PSPD remains a challenge at bedside. The establishment of predictors of PSPD seems an important task for health care providers, given the negative consequences of either promptly discontinuing a potentially effective or maintaining an ineffective drug beyond disease progression.
These issues appear more and more prominent given the advent of immunotherapies as the new standard therapy in many cancer types. This study aimed to: (a) first, evaluate the prevalence and the outcome of PSPD across tumor types; (b) second, describe potential clinical and pathological factors associated with PSPD.
All consecutive patients enrolled in phase 1 trials with advanced solid tumors and lymphomas treated in phase I clinical trials evaluating monotherapy by anti‐PD(L)‐1 at Gustave Roussy were analyzed. PD‐L1 positive tumors were assessed as per protocol.
Antitumor Response to anti‐PD(L)‐1 was assessed according to iRECIST criteria including immune complete response (iCR), partial response (iPR), stable disease (iSD), iUPD and iCPD. Briefly, PSPD is defined as an initial progressive disease defined by an increase in the size of lesions, or the visualization of new lesions, followed by a durable response. According to iRECIST criteria, an initial progressive disease is established by as unconfirmed progressive disease (iUPD), which requires a confirmation computerized tomography scanner (CT scan) 4 to 8 weeks later. The second assessment classifies the progression as confirmed progressive disease (iCPD) by a further increase in target or new target lesions (≥5 mm in sum of measures), further increase in nontarget or new nontarget lesions, or an increase in the number of new lesions. In our cohort of patients, PSPS was established in patients with iUPD and further response considered as iCR, iPR, and iSD.
As per the different protocols, first radiological evaluation was performed per protocol 6 to 8 weeks after treatment onset, and then every 6 to 8 weeks and/or 4 to 6 in the case of iUPD. All patients had at least two radiological evaluations: baseline and first radiological examination during ICI. Disease response was based on the assessment of target lesions, nontarget lesions, and new lesions. Treatment decisions were based on investigator assessment of response per RECIST 1.1 and iRECIST. Treatment beyond progression was continued conditional to a confirmatory CT scan 4‐6 weeks after the first evidence of disease progression, as defined per protocol. All the CT scans were independently reviewed by two senior radiologists.
Clinical and pathological factors potentially associated with PSPD were appraised. Fisher exact test was used to assess the association between categorical variables. Hazard Ratios were estimated from Cox proportional hazard models and were adjusted to the standard clinical and pathologic prognostic factors. All the tests were two‐sided and significance was assumed if P < .05. Survival estimates were calculated using the Kaplan‐Meier method. Median follow up was calculated with the inverse Kaplan‐Meier method. Overall survival (OS) was determined as the time between the landmark point considered as the baseline CT scan and the death from any cause or last contact when still alive. All the analyses were carried out using STATA statistical software (version 14; STATA).
A total of 169 patients with solid tumors treated by anti‐PD(L)‐1 monotherapy were analyzed. All patients were enrolled in five different phase I trials at Gustave Roussy between December 2011 and July 2015. As illustrated in the flowchart of patients participating in the study (Figure ), baseline and first evaluation CT‐scans were available in all 169 patients. Patients’ characteristics are illustrated on Table . The most frequent tumor types included melanoma (n = 57) and NSCLC (n = 19). Median previous lines of chemotherapy were 2 (0‐9). Patients were treated by anti PD‐1 (96 [56.5%]) and anti PD‐L1 (73 [43.5%]) monotherapy.
Patient's characteristics
| Frequency (N = 169) | Proportion (%) | |
| Tumor type | ||
| Melanoma | 57 | 33.7% |
| NSCLC | 19 | 11.2% |
| Bladder and urothelial | 13 | 7.7% |
| Renal cell carcinoma | 12 | 7.1% |
| Colorectal | 10 | 5.9% |
| Lymphoma | 8 | 4.7% |
| HCC | 7 | 4.1% |
| Breast | 6 | 3.6% |
| HNSCC | 6 | 3.6% |
| GBM | 5 | 3% |
| Ovarian | 5 | 3% |
| Gastric | 4 | 2.4% |
| Cervix | 3 | 1.8% |
| Uveal melanoma | 3 | 1.8% |
| Cholangiocarcinoma | 2 | 1.2% |
| Endometrium | 2 | 1.2% |
| Thyroid | 2 | 1.2% |
| Mesothelioma | 1 | 0.6% |
| Pancreas | 1 | 0.6% |
| Sarcoma | 1 | 0.6% |
| Salivary gland | 1 | 0.6% |
| Prostate | 1 | 0.6% |
| Age (median, range) | 55 | 20‐82 |
| Gender | ||
| Male | 92 | 54.4% |
| Female | 77 | 45.6% |
| RMH score | ||
| 0 | 43 | 25.4% |
| 1 | 61 | 36.1% |
| 2 | 55 | 32.5% |
| 3 | 10 | 6% |
| Previous treatment lines (median, range) | 2 | 0‐9 |
| Type of previous treatment | ||
| Chemotherapy | 117 | 69.1% |
| Targeted therapy | 95 | 56.2% |
| Immunotherapy | 26 | 15.4% |
| Previous radiation | 92 | 54.8% |
| Type of drug | ||
| PD‐1 inhibitor | 95 | 56.5% |
| PD‐L1 inhibitor | 73 | 43.5% |
| PDL1 status | ||
| Positive | 7 | 4.1% |
| Negative | 40 | 23.7% |
| NA | 121 | 72.2% |
| Number of metastatic sites | ||
| <2 | 70 | 41.4% |
| ≥2 | 99 | 58.6% |
| Tumor burden estimated by RECIST 1.1 (mm, range) | 75 | 12‐364 |
All patients had baseline and first evaluation CT scan. The overall response rate at the first tumor evaluation and the best response rate, computed using the iRECIST criteria, are displayed in Table . Briefly, we observed at the first tumor evaluation: 77 patients (45.6%) with iUPD, 69 patients (40.8%) with iSD, 21 patients (12.4%) with iPR, and 2 patients (1.2%) with iCR.
Patterns of response, including PSPD| iRECIST | ||
| First radiological evaluation | Best overall response | |
| iCR | 2 (1.2%) | 10(5.9%) |
| iPR | 21 (12.4%) | 45 (26.6%) |
| iSD | 69 (40.8%) | 43 (24.2%) |
| iUPD | 77 (45.6%) | 59 (34.9%) |
| iCPD | — | 13 (7.7%) |
As defined above, we defined PSPD as a tumor progression (iUPD) that amended into iSD or iPR or iCR on further evaluations. Using this definition, we observed as much as 6 patients with PSPD (3.6%) out of the 169 patients. This consists in 7.8% of patients with iUPD at the first cycle (n = 76). Median time to the first CT scan showing tumor burden decrease compared with the prior CT scan was 2.2 months (range, 0.7‐3.7), and median time to the best overall response was 3.5 months (range, 0.7‐14.1). Overall, PSPD was observed in 6 patients (3.6%), with 4 (66.7%) and 2 (33.3%) patients exhibiting stable disease and partial responses respectively, after been classified as iUPD in the first evaluation. Distribution of the tumor responses across iRECIST criteria at the first tumor evaluation in patients with solid tumors treated by anti‐PD‐1/PD‐L1.) is described on Figure A.
Enlarge this image.A, Distribution of the tumor responses across the iRECIST criteria at the first tumor evaluation in patients with solid tumors treated by anti‐PD‐1/PD‐L1. B, Distribution of PSPD according to best overall response in patients with solid tumors treated by anti PD‐1/PD‐L1. C, Frequency of PSPD across different tumors types (Red)
On the first evaluation iUPD (n = 77) was detected due to the appearance of new lesions and increase in the size of target lesions (TL) and both of them, in 9 patients, 29 patients and 38 patients, respectively (Figure B).
Frequency of PSPD across different tumors types is illustrated on Figure C. PSDP occurred in 2 (1.2%) melanoma patients and 4 (2.3%) nonmelanoma patients. Phenotype PSPD included: 3 patients with increase in TL, 2 patients with new lesions and 1 patient with both of them (Table S1). Overall, two patients presented a partial response: 1 patient with a melanoma and 1 patient with colorectal cancer MSI‐H. The remaining 4 patients with a renal cell carcinoma, a sarcoma, a melanoma and a hepatocellular carcinoma displayed a stabilization of the disease. A description of the tumor burden evolution in the 6 patients with PSPD is represented in Figure . Median time to best response in this subset of patients was 4.3 months (2.8‐5.9).
Enlarge this image.Description of the tumor burden evolution in the 6 patients with PSPD: 2 melanoma patients (orange) and 4 nonmelanoma patients (green)
Univariate analyses seeking for association between clinical and pathological variables and PSPD did not find any significant association (Table ).
Prognostic factors for PSPD disease are represented in Table . No association was found between PSPD and tumor burden at baseline (estimated by the RECIST sum; P = .3), number of metastatic sites (P = 1), or Royal Marsden Hospital (RMH) prognostic score (P = .85). Similarly tumor type did not show a significant association with a superior likelihood of achieving PSPD (P = 1).
Patient characteristics and association between PSPD and clinical variables (univariate analysis)| All patients (n = 169) | Non‐PSPD (n = 163) | PSPD (n = 6) | P (Fisher exact test) | |
| RMH score | ||||
| 0 | 43 (25%) | 38 (90.5%) | 2 (9.5%) | 0.85 |
| 1 | 61 (36.3%) | 55 (90.2%) | 2 (9.8%) | |
| 2 | 55 (32.7%) | 52 (94.5%) | 2 (5.5%) | |
| 3 | 10 (6%) | 10 (100%) | 0 | |
| Tumor type | ||||
| Melanoma | 57 (33.9%) | 55 (96.5%) | 2 (3.5%) | 1.00 |
| Non Melanoma | 112 (66.1%) | 108 (96.4%) | 4 (3.6%) | |
| Gender | ||||
| Male | 91 (54.2%) | 86 (96.6%) | 5 (3.4%) | 0.219 |
| Female | 78 (45.8%) | 77 (98.7%) | 1 (3.9%) | |
| Number of previous lines | ||||
| 0 | 21 (12.5%) | 20 (95.2%) | 1 (4.8%) | 0.5 |
| 1 | 33 (19%) | 31 (93.9%) | 2 (6.1%) | |
| 2 | 48 (28.6%) | 47 (97.9%) | 1 (2.1%) | |
| ≥3 | 67 (39.9%) | 65 (97%) | 2 (3%) | |
| Previous chemotherapy | ||||
| Yes | 117 (69.1%) | 93 (97.9%) | 2(2.1%) | 0.07 |
| No | 52 (30.9%) | 70 (94.6%) | 4(5.4%) | |
| Previous targeted therapy | ||||
| Yes | 95 (56.6%) | 92 (96.7%) | 3 (3.3%) | 1.00 |
| No | 74 (43.5%) | 71 (95.9%) | 3 (4.1%) | |
| Previous immunotherapy | ||||
| Yes | 26 (15.5%) | 24 (92.3%) | 2 (7.7%) | 0.23 |
| No | 143 (84.5%) | 139 (97.2%) | 4 (2.8%) | |
| Previous radiation therapy | ||||
| Yes | 93 (56.5%) | 91 (93.5%) | 2 (2.2%) | 0.69 |
| No | 76 (43.5%) | 72 (94.7%) | 4 (5.3%) | |
| Type of immunotherapy | ||||
| PD‐1 inhibitor | 95 (56.5%) | 93 (97.9%) | 2(2.1%) | 0.41 |
| PD‐L1 inhibitor | 74 (42.9%) | 68 (91.9%) | 6 (8.1%) | |
| Age (median, range) | 55 (20‐82) | 55 (20‐82) | 62 (22‐82) | 0.17 |
| Baseline LDH (UI/L) | 207 (9‐1998) | 207 (94‐1998) | 190 (9‐741) | 0.49 |
| Baseline Fibrinogen (g/L) | 4.8 (2.4‐9.6) | 4.8 (2.4‐2.6) | 4.3 (3‐7.9) | 0.99 |
| Baseline Albumin (g/L) | 36 (20‐61) | 36 (20‐61) | 38 (30‐41) | 0.35 |
| Tumor burden estimated by RECIST 1.1 (mm, range) | 75.5 (12‐ 364) | 73 (12‐364) | 62 (13‐140) | 0.30 |
| LIVER METS | ||||
| No | 105 (%) | 103 (98.1%) | 2 (1.9%) | 0.20 |
| Yes | 64 (%) | 60 (93.8%) | 4 (6.2%) | |
| Number of metastatic sites | ||||
| <2 | 70 (41.7%) | 65 (%) | 1 (%) | 1 |
| ≥2 | 9 (58.3%) | 90 (%) | 5 (%) | |
| Appearance of new lesions at E1 (iUPD = 76) | ||||
| Yes | 48 (63.2%) | 45 (95.7%) | 3 (6.9%) | 0.76 |
| No | 28 (36.8%) | 25 (89.3%) | 3 (10.7%) | |
| Increase target lesions (iUPD = 76) | ||||
| Yes | 64 (54.4%) | 60 (93.8%) | 4 (6.2%) | 0.04 |
| No | 12 (45.6%) | 10 (83.3%) | 2 (16.7%) | |
| Increase nontarget lesions (iUPD = 76) | ||||
| Yes | 43 (%) | 42 (97.7%) | 1 (2.4%) | 0.97 |
| No | 33 (%) | 28 (84.8%) | 5 (15.2%) |
2Abbreviations: CRP, C‐reactive protein; LDH, lactate dehydrogenase.
*For continuous variables P value was calculated from Wilcoxon Rank Sum Test.
We examined the potential influence of previous therapies, including chemotherapy, radiation therapy, targeted therapies, and earlier immunotherapy. Results did not display association between PSPD and the number of previous lines (P = .49), nor previous treatment type including targeted therapy (P = 1), radiotherapy (P = .7) and immunotherapy (P = .41). The absence of previous conventional chemotherapy was associated with a trend for PSPD (P = .07).
Results did not show statistically significant differences in the rate of PSPD between patients treated with anti‐PD(L)‐1 agents (P = .41).
There was no difference within the baseline blood characteristics between PSPD and non‐PSPD patients at baseline such as LDH (P = .49), fibrinogen (P = 1), and albumin (P = .35).
The association between PSPD and changes in target and nontarget lesions was also evaluated. Patients with an increase in target lesions were more likely to present PSPD (P = .04). We did not observe a significant difference between PSPD status and either an increase of nontarget lesions or the appearance of new lesions.
The median follow‐up time was 46 months (95% CI, 39.7‐49.3). Median PFS and OS were 17.4 months (95% CI, 6.2‐33.9) and 20.6 months (95% CI, 15.5‐34.7), respectively.
Time to best overall response in PSPD patients was 4.3 months (range, 2.8‐5.9).
To investigate the association between PSPD and prognosis, we performed Kaplan‐Meier OS estimates (landmark survival analysis) according to the following classes: iCR, iPR, iSD, PSPD, and progressive patients (iUPD and iCPD). Patients with a PSPD had a similar OS (median OS, 10.7 months; 95% CI, 6.5‐NA) when compared to patients with patients progressing in the first CT scan (median OS, 8.7 months; 95% CI, 7.1‐11.6 [HR 0.39, 95% CI, 0.14‐1.07; P = .07). Median OS was not reached in patients with CR and PR, and was 23.8 months (95% CI, 12.9‐41.3) in patients with SD. The overall log‐rank test was significant (P < 1e‐5) as well between all groups.
After being classified as progressive disease within the first radiological assessment, there is a small subset of patients treated with anti‐PD(L)‐1 monotherapy that appears to experience tumor responses as our results demonstrate. PSPD has been recently defined as an initial disease progression either by an increase in the size of lesions, or the appearance of new lesions within the first weeks after treatment onset. Conventional criteria for tumor response assessment is also known as Response Evaluation Criteria in Solid Tumors (RECIST) have been the standardized method to evaluate tumor responses to cytotoxic agents. The development of immunotherapy has implied the development of new criteria to appraise immune‐related responses. Within the first evaluation, 45% of patients displayed progressive disease classified as iUPD. Among these patients classified as iUPD, 8% of patients actually presented PSPD beyond the first evaluation. Nevertheless, this patient subgroup represents a substantial challenge given the absence of standardized criteria regarding clinical management of these patients. In this regard, a prompt therapy discontinuation in these patients presenting an early progressive disease within the first evaluation could imply a risk of dismissing a potentially effective drug. Interruption of treatment should be decided depending on whether patients are experiencing a clinical benefit and in the absence of severe toxicities.
Globally, approximately 4% of our patients treated with an anti‐PD(L)‐1 agents displayed a PSPD at first evaluation. Together with previously published results, our study confirms that PSPD represents a relatively uncommon event as well a real challenge in the daily oncological practice. Our results showed that PSPD appears to be more frequent in patients experiencing an initial increase in target lesions, suggesting that PSPD should be investigated only in these patients. Biologic explanation of the increase in lesions including enlarging nodal, pulmonary or other visceral lesions has been reported as immune‐mediated sarcoid reactions with pathological reports of nonmalignant granulomas. Nevertheless, an initial increment of tumor burden along with the appearance of new lesions usually corresponds to a real disease progression and is accompanied by a clinical deterioration. To acknowledge the real impact of PSPD requires further studies in larger and prospective cohorts.
Immune checkpoint inhibitors are now approved in a wide range of tumor types, including melanoma, NSCLC, RCC, HNSCC, urothelial, and microsatellite instability‐high (MSI) cancer, although response rates are different. Similarly, different rates of PSPD have been described depending on the tumor type. Partial responses following an initial progression have been reported in 5%‐8% of melanoma and renal cell carcinoma patients treated with anti‐PD(L)‐1. Lower rates of radiological responses or stabilizations have been outlined in other tumor types such as NSCLC, HNSCC and urothelial carcinomas, ranging from 1% to 7% in patients also treated with anti‐PD(L)‐1 agents. Pseudoprogression has also been pointed out in patients with MSI tumors treated with anti‐PD(L)‐1 agents. Overall, this event does not exceed 10% independent of tumor type. Interestingly, the two patients presenting a PSPD in our series had a melanoma and an MSI‐high CRC. These two tumor types are well‐known as hypermutated tumors and most likely to have immune responses, although translational studies exploring PSPD underlying mechanisms and how to predict this event are lacking. Circulating Tumor DNA (ctDNA) profiles have been evaluated as an early accurate biomarker able to identify pseudoprogressors and differentiate them from true progressors. Performing sequential ctDNA tests to patients receiving anti‐PD(L)‐1 agents could represent an alternative to dynamically monitor these patients, although further validation is needed in larger cohorts of patients.
In our series, patients who had not received a prior conventional chemotherapy tend to have more frequently a PSPD when compared to patients already treated with chemotherapy. Usually, heavily pretreated patients tend to have limited responses and these are short‐lasting. When analyzed by subgroups median survival of patients with PSPD was numerically superior to patients truly progressing (10.7 vs 8.7 months; P = .07). A recently published study demonstrated responder patients displayed a higher 12‐month OS rate than those with an initial increase in tumor burden (82% vs. 53%). Time to best overall response in PSPD patients ranged up to 5.9 months, with a median of 4 months. Interestingly, a similar study assessing only NSCLC patients reported tumor regression at 3 and 4 months after PSPD. Limitations of our study include its retrospective nature, heterogeneity of the patients including melanoma and nonmelanoma patients and the fact that it was developed in a single institution. Patients from our series had been previously heavily pretreated with a median of 2 previous therapy lines, including nearly 70% who had received chemotherapy and 57% targeted therapy. On the other hand, all patients from our study were treated on the basis of a phase I trial from 2011 to 2015, when most immunotherapy trials assessed anti‐PD(L)‐1 agents in the monotherapy setting. This fact implies that most patients were treated out of the scope of iRECIST criteria, that a percentage of these patients might have discontinued treatment without a confirmation of disease progression and, moreover, without the evolution of a potentially beneficial therapy. In addition and given the small number of patients included in our study, it seems clear that larger cohorts are needed to further assess the importance of immune‐related response and its impact on long‐term results.
In conclusion, PSPD is a rare phenomenon observed in less than 5% of patients receiving anti‐PD(L)‐1 therapy. These patients present a longer overall survival than patients presenting a progressive disease, although not as encouraging as patients with real responses. We have not identified any clinical or analytical factor that may predict this type of response. Further investigation is warranted in order to identify PSPD patients and avoid therapy discontinuation, since a benefit in terms of OS may be observed after.
We thank the patients and their families who participated in this study.
The authors declare the following COI: Principal/sub‐Investigator of Clinical Trials for Abbvie, Agios Pharmaceuticals, Amgen, Argen‐X Bvba, Arno Therapeutics, Astex Pharmaceuticals, Astra Zeneca, Aveo, Bayer Healthcare Ag, Bbb Technologies Bv, Blueprint Medicines, Boehringer Ingelheim, Bristol Myers Squibb, Celgene Corporation, Chugai Pharmaceutical Co., Clovis Oncology, Daiichi Sankyo, Debiopharm SA, Eisai, Eli Lilly, Exelixis, Forma, Gamamabs, Genentech, Inc, Glaxosmithkline, H3 Biomedicine, Inc, Hoffmann La Roche Ag, Innate Pharma, Iris Servier, Janssen Cilag, Kyowa Kirin Pharm. Dev., Inc, Loxo Oncology, Lytix Biopharma As, Medimmune, Menarini Ricerche, Merck Sharp & Dohme Chibret, Merrimack Pharmaceuticals, Merus, Millennium Pharmaceuticals, Nanobiotix, Nektar Therapeutics, Novartis Pharma, Octimet Oncology Nv, Oncoethix, Onyx Therapeutics, Orion Pharma, Oryzon Genomics, Pfizer, Pharma Mar, Pierre Fabre, Roche, Sanofi Aventis, Taiho Pharma, Tesaro, Inc, Xencor. Research Grants from Astrazeneca, BMS, Boehringer Ingelheim, Janssen Cilag, Merck, Novartis, Pfizer, Roche, Sanofi. Non‐financial support (drug supplied) from Astrazeneca, Bayer, BMS, Boringher Ingelheim, Johnson & Johnson, Lilly, Medimmune, Merck, NH TherAGuiX, Pfizer, Roche. CM has received honoraria from Astellas, Astra Zeneca, Bayer, BeiGene, BMS, Celgene, Debiopharm, Genentech, Ipsen, Janssen, Lilly, MedImmune, MSD, Novartis, Pfizer, Roche, Sanofi, Orion; SC has received honoraria from AstraZeneca, BMS, Janssen, MSD, Novartis and Roche. A. H. has received honoraria from Amgen, Spectrum Pharmaceuticals, Lilly. Over the last 5 years, Dr Soria has received consultancy fees from AstraZeneca, Astex, Clovis, GSK, GamaMabs, Lilly, MSD, Mission Therapeutics, Merus, Pfizer, PharmaMar, Pierre Fabre, Roche/Genentech, Sanofi, Servier, Symphogen, and Takeda. Dr Soria has been a full‐time employee of AstraZeneca since September 2017. He is a shareholder of AstraZeneca and Gritstone. CF became a full‐time employee of Medimmune/AstraZeneca after this article was commissioned. AM has received honoraria from GSK, AstraZeneca, Oncovir, Merck Serono, eTheRNA, Lytix pharma, Kyowa Kirin Pharma, Bayer, Novartis, BMS, Symphogen, Genmab, Amgen, Biothera, Nektar, Pfizer, Seattle Genetics, Flexus Bio, Roche/Genentech, OSE immunotherapeutics, Transgene, Gritstone, Merck (MSD), Cerenis, Innate pharma, Protagen, Partner Therapeutics, Servier. SPV has received honoraria from Merck KGaA, AstraZeneca. EC has received honoraria from BMS, Roche, MSD and Medimmune.
Conception and design: PMR, SA, ECA, CF, CM. Provision of study materials or patients: All authors. Collection and assembly of data: PMR, SA, ECA, CF, CM. Data analysis and interpretation: All authors. Manuscript writing: All authors. Final approval of manuscript: All authors. Accountable for all aspects of the work: All authors.
All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1964 and later versions. Informed consent was obtained from all patients for being included in the study.
Not applicable.
The data used and/or analyzed for this study is available from the corresponding author at reasonable request.
© 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Details
; Perrine Vuagnat 1 ; Marabelle, Aurélien 4 ; Jean‐Charles Soria 4 ; Ferté, Charles 4 ; Massard, Christophe 4
1 Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France
2 Oncology Department, Clínica Universidad de Navarra, Madrid, Spain
3 Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France; Department of Radiology, Gustave Roussy Cancer Campus, Villejuif, France
4 Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France; INSERM, VILLEJUIF, France