Background Little is known regarding the efficacy of immune checkpoint inhibitors (ICI) in patients with advanced large-cell neuroendocrine lung carcinoma (aLCNEC).
Methods 125 consecutive patients with aLCNEC were identified in the electronic databases of 4 participating cancer centers. The patients were divided into group A (patients who received ICI, n=41) and group B (patients who did not receive ICI, n=84). Overall survival since advanced disease diagnosis (OS DX) and OS since ICI initiation (OS ICI) were captured.
Results With a median follow-up of 11.8 months (mo) (IQR 7.5–17.9) and 6.0mo (IQR 3.1–10.9), 66% and 76% of patients died in groups A and B, respectively. Median OS DX was 12.4mo (95% CI 10.7 to 23.4) and 6.0mo (95% CI 4.7 to 9.4) in groups A and B, respectively (log-rank test, p=0.02). For ICI administration, HR for OS DX was 0.59 (95% CI 0.38 to 0.93, p=0.02—unadjusted), and 0.58 (95% CI 0.34 to 0.98, p=0.04—adjusted for age, Eastern Cooperative Oncology Group (ECOG) performance status (PS), presence of liver metastases and chemotherapy administration). In a propensity score matching analysis (n=74; 37 patients in each group matched for age and ECOG PS), median OS DX was 12.5 mo (95% CI 10.6 to 25.2) and 8.4 mo (95% CI 5.4 to 16.9) in matched groups A and B, respectively (log-rank test, p=0.046). OS ICI for patients receiving ICI as monotherapy (n=36) was 11.0 mo (95% CI 6.1 to 19.4).
Conclusions With the limitations of retrospective design and small sample size, the results of this real-world cohort analysis suggest a positive impact of ICI on OS in aLCNEC.
- lung neoplasms
- programmed cell death 1 receptor
This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/.
Statistics from Altmetric.com
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Large-cell neuroendocrine carcinoma of lung (LCNEC) is a rare malignancy (<3% of all lung tumors) characterized by aggressive behavior and high recurrence rate.1–3 According to 2015 WHO criteria, LCNEC is composed of large cells with neuroendocrine differentiation (as demonstrated by typical morphology and immunoreactivity for chromogranin, synaptophysin or CD56), and, typically, a high mitotic rate.4 In up to 20% of cases, LCNEC demonstrates a mixed histology with an additional non-small cell lung cancer (NSCLC) component.4 From a molecular perspective, LCNEC can be further classified as SCLC-like subtype (characterized by tumor protein p53 (TP53) and Retinoblastoma gene-1 (RB1) comutations or loss) or NSCLC-like subtype (characterized by lack of TP53 +RB1 alterations and presence of mutations in the Kirsten rat sarcoma viral oncogene homolog, serine/threonine kinase 11, and Kelch-like ECH-associated protein 1 genes); LCNEC molecular subtype may affect response to systemic therapy.5–7
Systemic approach in advanced-stage LCNEC primarily includes platinum-based chemotherapy, with objective response rate (ORR) in the range of 12%–52%, median progression-free survival (mPFS) of 4.6–6.1 months and median overall survival (OS) of 10.2–11.1 months.2 8–10 The roles of somatostatin analogs and tyrosine-kinase inhibitors (TKIs) in the management of advanced LCNEC remain limited.2 8 9
Anti-programmed cell death-1 (anti-PD-1)/antiprogrammed cell death ligand-1 (anti-PD-L1) immune checkpoint inhibitors (ICI) are well incorporated into treatment algorithms for advanced NSCLC and SCLC—either with or without platinum-based chemotherapy. This is based on the results of numerous randomized clinical trials demonstrating a consistent OS benefit with early incorporation of immunotherapy across histological tumor types.11–20 The data regarding clinical activity of ICI in advanced LCNEC, while encouraging, is limited to case reports and small retrospective series.21–31 According to the results of several retrospective analyzes, ICI administration in advanced LCNEC is associated with ORR of 13%–60%, mPFS of 4.2–14.2 months and median OS of 11.8 months.29–31 For instance, the non-randomized DART trial assessed the clinical activity of combination nivolumab and ipilimumab in rare tumor types and reported an objective response in two out of three patients with advanced LCNEC.32 The impact of ICI on OS in advanced LCNEC, however, has not been fully determined. The largest report of ICI in patients with LCNEC from the American National Cancer Database, delivered in abstract form only, included only 37 patients. It did, however, suggest a positive impact of ICI on OS.33
Aiming to bridge this gap in the literature, we conducted a retrospective analysis of consecutive patients with advanced LCNEC treated at four tertiary cancer centers. We explored the impact of ICI on OS in this rare lung tumor type, with a keen emphasis on molecular subtype.
Materials and methods
Patient selection and group assignment
Electronic databases of four participating cancer centers (Institute of Oncology, Sheba Medical Center, Tel HaShomer; Davidoff Cancer Center, Rabin Medical Center, Beilinson Campus; Rambam Healthcare Campus (Israel); Lombardi Comprehensive Cancer Center, MedStar Georgetown University Hospital (USA)) were systematically searched for patients diagnosed with LCNEC between 2009 and 2019. Mixed LCNEC and small-cell neuroendocrine tumors (NET) of lung origin as well as mixed LCNEC and non-small-cell lung carcinomas with a predominating LCNEC component were also included. Only advanced-stage tumors (stage IV or stage III disease not amenable to definitive treatment, or recurrent tumors not amenable to definitive treatment) were selected. Cases with Ki-67 <30% were excluded from the analysis given that, in small biopsies, this commonly accepted cut-off is frequently used to separate high-grade LCNEC and SCLC from low-grade NET (typical and atypical carcinoid) in the presence of crush artifact and poor tissue preservation.4 34–38
The patients were then divided into group A (patients who received ICI as any treatment line) and group B (patients who did not receive ICI whatsoever). Group A* subcategorized patients receiving ICI administered as monotherapy or in combination with different ICI agents, thereby excluding patients who received combination ICI and chemotherapy. Additionally, patients with an available molecular tumor profile were further classified into SCLC-like subtype (defined by the presence of TP53/RB1 co-mutations or loss) or NSCLC-like subtype (defined by the lack of TP53/RB1 alterations).
Study design and assessments
After obtaining institutional ethical review board approval, we retrospectively reviewed patients’ charts and hospital electronic medical records, and gathered baseline demographic, clinical, pathological and treatment characteristics. OS since advanced disease diagnosis (OS DX) was captured and compared between groups A and B among the whole cohort (primary endpoint) and between selected subgroups (according to age, Eastern Cooperative Oncology Group performance status (ECOG PS), presence of liver metastases and tumor molecular subtype). A propensity score matching analysis of OS DX was done, and patients in both groups were matched for age and ECOG PS. Univariate and multivariate analyzes were then performed to assess the impact of patient baseline characteristics, tumor subtype and treatment characteristics on OS DX. Additionally, OS after ICI initiation (OS ICI) was analyzed in group A* according to the tumor molecular subtype, with an additional univariate analysis exploring the impact of patient baseline characteristics, tumor subtype and treatment characteristics.
OS DX was defined as the time from advanced disease diagnosis until death or censored at last follow-up. OS ICI was calculated from the time of ICI initiation until death or censored at last follow-up. Duration of follow-up was calculated from the time of advanced disease diagnosis until last follow-up or censored at death. The cut-off date for data collection was January 13 2020.
The sample size was determined by the available patients meeting the inclusion criteria. We conducted the statistical analysis using R Core Team software (R Foundation for Statistical Computing, Vienna, Austria), version 2019.39 Categorical variables were presented by numbers and percentiles. Continuous variables were reported by medians and ranges. Categorical variables were compared using the χ2 method or Fisher’s exact test, while continuous variables were compared using either a t-test or Mann-Whitney-Wilcoxon test. OS was assessed by the Kaplan-Meier method, with the log-rank test for comparison between groups. The propensity score matching analysis matching patients in the two compared groups for age and ECOG PS was performed with a caliper of 0.5, a 1:1 matching (ICI administration vs no ICI administration), and an AUC (area under the curve) of 0.67. Cox proportional hazards univariable models including prespecified covariates were constructed. Covariates for the multivariate Cox regression model were selected from the statistically significant covariates found in the aforementioned univariate model. P values less than 0.05 were considered statistically significant. No correction for multiple comparisons was performed.
Patient and tumor characteristics
One hundred eighty-four consecutive patients with histologically confirmed LCNEC diagnosed between 2009 and 2019 were identified from the four participating cancer centers. Forty-nine patients with early-stage disease were excluded from the analysis, and an additional ten cases with Ki-67 <30% were excluded as well. The selected cohort thus comprised 125 patients (Thoracic Oncology Service, Institute of Oncology, Sheba Medical Center, Tel HaShomer, n=53; Davidoff Cancer Center, Rabin Medical Center, Beilinson Campus, n=47; Thoracic Cancer Service, Rambam Healthcare Campus, n=14; Lombardi Comprehensive Cancer Center, MedStar Georgetown University Hospital, n=11; online supplemental figure S1).
Of the selected 125 patients, 41 were treated with ICI (group A), and 84 did not receive ICI (group B). Baseline demographic, clinical and pathological characteristics for these 125 included are displayed in table 1. This cohort mainly comprised smokers (84%); the majority were males (62%). Patients with ECOG PS 2–4 at the time of advanced disease diagnosis constituted 26% of the cohort; brain metastases were present in 32%, and liver metastasis in 34% of the patients. Patients in group A demonstrated a younger median age of 63 years (IQR 58–68) compared with group B median age of 67.5 years (IQR 62–75) (p=0.003). Group A included more patients with ECOG PS 0 or 1 (75%) compared with group B (44%) (p=0.02).
Given these differences in baseline characteristics, we performed a propensity score matching analysis to account for age and ECOG PS. The matched cohort (n=74) included 37 patients in each group with a median age of 64 years for both groups (IQR 59–68 and 59–69 in matched groups A and B, respectively) (p=0.79); the proportion of matched patients with ECOG PS 0 or 1 yielded 84% and 78% in matched groups A and B, respectively (p=0.77), while the percentage of matched patients with ECOG PS 2–4 was 16% and 22% in matched groups A and B, respectively (p=0.77). No other significant differences in baseline patient and tumor characteristics between the matched groups were observed (online supplemental table S1).
Use of molecular tumor testing was generally limited. Comprehensive genomic profiling was complete for only 16 patients (39%) and 6 patients (7%) in groups A and B, respectively. PD-L1 expression was assessed in 21 patients (51%) and 14 patients (17%) in groups A and B, respectively. Tumor mutation burden was available in seven patients (17%) and one patient (1%) in groups A and B, respectively. Finally, microsatellite instability was calculated in eight patients (19%) in group A only (table 1).
Group A* comprised 36 patients. This group’s baseline characteristics according to tumor molecular subtype are presented in online supplemental table S2. Since the molecular testing was likewise limited (39% of patients in group A*, n=14), tumors with NSCLC-like molecular subtype (n=9) were compared with all others (n=27, including tumors with SCLC-like subtype (n=5) and tumors with unknown molecular subtype (n=22)). In group A*, NSCLC-like tumors were more likely to have a mixed histology (p=0.03).
ICI regimens used in group A included nivolumab (n=19, 46% of patients in group A), pembrolizumab (n=4, 10%), atezolizumab (n=6, 15%), durvalumab (n=3, 7%), nivolumab/ipilimumab (n=4, 10%), platinum/pemetrexed/pembrolizumab (n=3, 7%) and platinum/etoposide/atezolizumab (n=2, 5%).
Significantly more patients in group A (95%) compared with group B (74%) received chemotherapy (p=0.01) (table 1). The proportion of patients receiving SCLC-based chemotherapy regimens (eg, cisplatin/etoposide and carboplatin/etoposide) was numerically similar (73% and 61% in groups A and B, respectively) (p=0.40). Thirty-six percent of patients in group A and 20% of patients in group B received NSCLC-based chemotherapy regimens (p=0.11); such NSCLC-based regimens included platinum/pemetrexed (n=9), platinum/paclitaxel (n=6), platinum/pemetrexed/bevacizumab (n=4), platinum/vinorelbine (n=4), pemetrexed (n=3), paclitaxel (n=2), docetaxel (n=2), vinorelbine (n=2), platinum/docetaxel (n=1), gemcitabine (n=1), gemcitabine/paclitaxel (n=1), and capecitabine/temozolomide (n=1). Three patients in group B received somatostatin analogs. Two patients in group B and one patient in group A received epidermal growth factor receptor (EGFR) TKIs on diagnosis of an activating mutation in the EGFR gene (exon 19 del); two additional patients in group A received anaplastic lymphoma kinaseTKIs, though confirmatory comprehensive tumor molecular testing did not confirm the presence of a targetable abnormality, later halting such treatment. Overall, patients in group A received more lines of systemic treatment (p<0.001).
In the matched cohort (n=74), no significant differences between groups were observed in terms of chemotherapy administration or chemotherapy regimens (online supplemental table S1).
Treatment characteristics of patients in group A* are presented in the online supplemental table S2. Systemic treatments were similar between patients with NSCLC-like molecular tumor subtype and the rest of the group. Most patients received nivolumab, pembrolizumab or atezolizumab as second-line treatment.
OS since advanced disease diagnosis
After a median follow-up period of 11.8 months (IQR 7.5–17.9) for group A and 6.0 months (IQR 3.1–10.9) for group B, (p<0.001 for the comparison), 27 (66%) patients died in group A while 64 (76%) patients died in group B. Median OS DX was 12.4 months (95% CI 10.7 to 23.4) in group A and 6.0 months (95% CI 4.7 to 9.4) in group B (p=0.02) (figure 1A). In group A, projected 1-year and 2-year survival rates since advanced disease diagnosis were 55% and 25%, respectively (figure 1A). In group B, projected 1-year and 2-year survival rates since advanced disease diagnosis were 32% and 18%, respectively (figure 1A).
In the matched cohort (n=74), median follow-up comprised 12.0 months (IQR 6.5–19.9) for matched group A and 6.1 months (IQR 4.4–10.1) for matched group B, (p=0.004). Twenty-four (65%) patients in matched group A and 26 (70%) patients in matched group B died during the study period. Median OS DX was 12.5 months (95% CI 10.6 to 25.2) in matched group A and 8.4 months (95% CI 5.4 to 16.9) in matched group B (p=0.046) (figure 1B). In matched group A, projected 1-year and 2-year survival rates since advanced disease diagnosis were 57% and 27%, respectively (figure 1B). For matched group B, projected 1-year and 2-year survival rates since advanced disease diagnosis were 33% and 19%, respectively (figure 1B).
Univariate and multivariate analysis of OS DX
In the univariate analysis, age (p=0.02), ECOG PS on diagnosis of advanced disease (p<0.001), presence of liver metastases (p=0.005), chemotherapy administration (p<0.001) and ICI administration (p=0.02) all demonstrated a significant correlation with OS DX, whereas sex, smoking status, molecular subtype, stage at diagnosis and presence of brain metastases did not (p>0.05) (table 2).
ICI administration (p=0.04), chemotherapy administration (p=0.002), ECOG-PS on diagnosis of advanced disease (p=0.002) and presence of liver metastasis (p=0.03) remained statistically associated with OS DX in a multivariate Cox regression analysis model that incorporated all factors found to significantly correlate with OS DX in univariate analysis (table 2).
OS DX in selected subgroups
We analyzed the effect of ICI exposure on OS DX in several patient subgroups (figure 2). ICI administration positively affected OS DX in elderly (≥65 years old) patients (p=0.03) and patients without liver metastases (p=0.05). A trend toward longer OS DX with ICI exposure was seen in patients with ECOG PS 0 or 1 (p=0.052). In smaller subgroups of patients younger than 65 years (p=0.45), patients with liver metastases (p=0.09), and patients with ECOG PS 2–4 (p=0.2), there was no statistically significant OS benefit seen with ICI administration. Additionally, the smaller subgroup of patients with NSCLC-like tumors did not seem to derive OS benefit from ICI administration (p=0.63) as opposed to the remainder of the cohort comprizing patients with SCLC-like or unknown molecular subtype tumors (p=0.02) (figure 2).
OS with ICI
After a median follow-up after ICI initiation in group A* of 6.2 months (IQR 2.7–14.0), 24 (67%) patients died. In group A*, median OS ICI was 11.0 months (95% CI 6.1 to 19.4) (figure 3). The projected 1-year and 2-year survival rates after ICI initiation were 44% and 22%, respectively (figure 3).
Median follow-up after ICI initiation was 6.9 months (IQR 6.1–12.9) in patients with NSCLC-like tumors and 5.7 months (IQR 2.0–14.3) in the remainder of patients in group A* (p=0.25). Six patients (67% of patients with NSCLC-like tumor subtype) and 18 patients (67% of the rest of group A*) died. Median OS ICI was 9.3 months (95% CI 6.1 to not reached (NR)) in patients with NSCLC-like tumors, and 11.0 months (95% CI 3.7 to NR) in the rest of group A* (p=0.65) (online supplemental figure S2).
In the univariate analysis, only ECOG PS at ICI initiation (p=0.02) and presence of liver metastases (p=0.01) demonstrated a significant correlation with OS ICI. Sex, age, smoking status, stage at diagnosis, PD-L1 TPS (≥1% vs <1%), molecular subtype (NSCLC-like vs all others), presence of brain metastases, ICI type (monotherapy with an anti-PD-1/PD-L1 agent vs combination of an anti-PD-1 agent with an anticytotoxic T-lymphocyte-associated protein 4 (anti-CTLA4) agent), administration of chemotherapy, and number of systemic treatment lines prior to ICI administration did not correlate with OS ICI (online supplemental table S3). Multivariate analysis of OS ICI was not performed because of small sample size.
To the best of our knowledge, our data set represents the largest series to date reporting on mature outcomes of ICI in advanced-stage LCNEC. It is also one of the first analyzes to assess the impact of ICI administration on OS in advanced LCNEC. We found ICI administration in LCNEC to be associated with longer OS DX in the entire cohort, as well as in the cohort matched for age and ECOG PS. The positive impact of ICI administration on OS of patients with advanced LCNEC was further supported by the results of univariate and multivariate analyzes. Since prospective randomized clinical trials focusing on patients with this rare tumor subtype are challenging to complete, these data provide valuable insight regarding possible therapeutic options for advanced LCNEC.
According to our observations, the median OS was twice as long in patients who received ICI (12.4 months, 95% CI −10.7 to 23.4) compared with those who did not (6.0 months, 95% CI −4.7 to 9.4) (p=0.02). Similar results were detected when matching patients for age and ECOG PS: the median OS was longer in patients who received ICI (12.5 months, 95% CI −10.6 to 25.2) compared with those who did not (8.4 months, 95% CI −5.4 to 16.9) (p=0.046). Projected landmark OS rates were also higher in patients who were exposed to ICI: 1-year survival rates of 55% vs 32%–33%, and 2-year survival rates of 25%–27% vs 18%–19% in patients who did and did not receive ICI, respectively. Our observations correspond to the results of the retrospective analysis of advanced LCNEC patients presented by Komiya and Powell as an ASCO 2020 virtual meeting abstract. Analysis of Komiya and Powell demonstrated that the use of ICI was associated with improved OS (p=0.0168); a landmark OS analysis in the ICI group showed 12-month and 18-month survival rates of 34% and 29%, respectively, compared with 24% and 15% in the non-ICI group.33
Importantly, the OS rates in patients not exposed to ICI in our cohort were consistent with historical data retrieved from the majority of large retrospective series and some prospective clinical studies assessing platinum-based chemotherapy in advanced LCNEC.1 33 40 41 Other prospective studies which evaluated platinum-based chemotherapy in patients with advanced LCNEC reported higher OS rates compared with those we observed, probably reflecting the differences in baseline and treatment characteristics between patients in real-world cohorts and those enrolled in clinical trials.42 Our cohort notably included patients with poor prognosis, 25% of whom did not receive any systemic treatment.
We acknowledge some differences in baseline and treatment characteristics in favor of patients treated with ICI in our presented cohort. Specifically, these patients were younger, had a better ECOG PS at the time of diagnosis of advanced disease, and were more likely to be treated with systemic therapy. However, the results of propensity score matching analysis along with multivariate analysis accounting for these imbalances confirmed a positive correlation between ICI administration and OS beyond traits including younger age, better ECOG PS, lack of liver metastases and administration of chemotherapy. Our conclusions are further supported by the analysis presented by Komiya and Powell which also demonstrated a significant correlation between ICI administration and OS in advanced LCNEC patients, along with chemotherapy administration, surgery, female sex and absence of liver metastases.33
We also confirmed our previous observation regarding outcomes related to IO exposure in advanced LCNEC.31 In this expanded cohort comprised 36 patients treated with ICI administered as either anti-PD-1/PD-L1 monotherapy or in combination with anti-CTLA 4 therapy, we again observed a median OS of 11.0 months (95% CI 6.1 to 19.4)—similar to the median OS of 11.8 months (95% CI 3.7 to NR) we previously had demonstrated in the cohort of 21 patients. Our data set is the only known report to date detailing mature OS outcomes related to ICI exposure in patients with advanced LCNEC.
Of note, no significant correlation was seen between the level of PD-L1 expression and OS with ICI exposure, although the small number of cases with PD-L1 TPS available for analysis limited the value of this observation. Positive PD-L1 expression in LCNEC represents a rare event, and its prognostic value is controversial.43–46 It is unknown if PD-L1 TPS may serve as a predictive factor in the context of ICI therapy in advanced LCNEC, and it remains to be seen whether such a relationship exists with either of the two LCNEC molecular subtypes. We hypothesize such an association might be limited to NSCLC-like LCNEC if one extrapolates known data from NSCLC and SCLC.19 47 48
One of the major limitations of our study is lack of comprehensive molecular tumor profiling data available for most patients, thereby weakening conclusions regarding the correlation between the established molecular LCNEC subtypes and outcomes related to ICI exposure. Based on data available from our series and another series from Sabari et al,29 the NSCLC-like LCNEC subtype appears to derive less benefit from ICI compared with the SCLC-like molecular subtype. For example, the Sabari et al series demonstrated ORR with ICI of 43% (3/7) in SCLC-like LCNEC vs 13% (1/8) in NSCLC-like LCNEC.29 In our series, patients with the NSCLC-like molecular subtype trended towards a numerically lower median OS with ICI (9.3 months) compared with the remainder of the patients treated with ICI (11.0 months) (p=0.65). Additionally, a numerically lower median OS DX was witnessed in NSCLC-like LCNEC patients exposed to ICI (11.6 months) compared with NSCLC-like LCNEC patients not exposed to ICI (18.6 months) (p=0.63), while the opposite held true in the rest of the cohort (ie, 12.5 months and 6.0 months for patients who received and did not receive ICI, respectively) (p=0.02). Given the overall low molecular testing rate in our cohort, these observations are only hypothesis generating.
Our analysis has additional important limitations, including retrospective nature, lack of central pathological assessment and relatively small sample size of patients treated with ICI.
Prospective phase II clinical trials are underway to assess the efficacy of anti-PD-1/PD-L1 ICI and the combination of anti-PD-1 ICI with anti-CTLA ICI in high-grade neuroendocrine tumors.49 Some of these allow enrollment of patients with LCNEC (g, NCT03352934, NCT03190213, NCT03136055, NCT03290079 and NCT02834013). Additional questions remaining to be addressed include the correlation between ICI treatment efficacy and the LCNEC molecular subtype, as well as the value of a combined approach implementing concurrent platinum-based chemotherapy with ICI administration.
In conclusion, the results of this real-world data analysis suggest that the use of ICI to be associated with superior OS in advanced LCNEC. The impact of molecular tumor subtype on ICI outcomes requires further evaluation.
Twitter @chulkimMD, @StephenVLiu
ED and SK contributed equally.
Contributors ED, SK and JB have made substantial contribution to the conception and design of the work, acquisition and analysis of the data; all the listed authors contributed substantially to the data collection and manuscript drafting; and all the listed authors revised the submitted manuscript and approved its final version before submission.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests ED reported consulting fees from MSD, BMS, Astra Zeneca, Roche, Boehringer Ingelheim, Pfizer, Novartis, Takeda. MM reported consulting fees from Boehringer Ingelheim, Roche, Astra Zeneca, MSD, BMS, Abbvie, Takeda, Pomicell. CK reported research funding (to institution) from AstraZeneca, BMS, Novartis, Regeneron, Tesaro, Karyopharm, Debiopharm, Jassen, and Mirati and consulting fees from Novartis. SVL reported consulting fees from AstraZeneca, Beigene, Blueprint, Boehringer Ingelheim, Bristol-Myers Squibb, Catalyst, Celgene, Clovis, Corvus, G1 Therapeutics, Genentech, Guardant Health, Inivata, Janssen, Jazz, Lilly, LOXO, MSD, PharmaMar, Pfizer, Regeneron, and Takeda and research grants (to institution) from Alkermes, AstraZeneca, Bayer, Blueprint, Bristol-Myers Squibb, Genentech, Lilly, Lycera, Merck, Molecular Partners, Pfizer, Rain Therapeutics, RAPT, Spectrum, and Turning Point Therapeutics. DU reported consulting fees and non-financial support from BMS, Astra Zeneca, Takeda, consulting fees MSD, Roche and Boehringer Ingelheim. AZ reported grants from BMS, personal fees from Roche, MSD, BMS, Astra Zeneca, Takeda. AO reported advisory fees from MSD, BMS, Roche, Astra Zeneca, Novartis, Boehringer Ingelheim. MW reported speaker fees and funding (to institution) from Roche, MSD. JB reported grants and personal fees from MSD, Roche, BMS, Abbvie, Pfizer, Novartis, Astra Zeneca, Boehringer Ingelheim, Takeda.
Patient consent for publication Not required.
Ethics approval The study was conducted in accordance with the principles of good clinical practice, and institutional review board approval was obtained at each participating oncological center before the study initiation. No patient identifying data were included in the central data collection.
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement Data are available on reasonable request. Data are not publicly available according to the Rabin Medical Center’s strict institutional policy with regards to public availability of unidentified patient data. However, those data which are minimally required to replicate the outcomes of the study will be made available on reasonable request.
Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.