Relationship of Baseline Tumor Angiogenesis with Kinetics of Inflammatory Markers in DLBCL

Blood ◽  
2015 ◽  
Vol 126 (23) ◽  
pp. 5056-5056
Author(s):  
Gaurav Prakash ◽  
Vaishali Aggarwal ◽  
Nidhi Jain ◽  
Amanjit Bal ◽  
Manupdesh Singh Sachdeva ◽  
...  

Abstract Introduction Angiogenesis is one of the central dogmas in growth and progression of a malignant tumor including malignant lymphoma. Lymphoma is a tumor originating from immune cells and lymphoid malignancies and it can alter normal immune function. However, nature of the immune dysfunction is not well defined. Inflammatory mediators acting through Th1/Th2 cytokines and growth factors secreted by the infiltrating inflammatory cells are known to have both direct and indirect angiogenic effects on endothelial cells.Whether tumor angiogenesis in lymphoma patients is associated with alteration in inflammatory cytokines is an unexplored area.Whether extent of angiogenesis at baseline and elevation of levels of biomarkers in the serum have any bearing on chemotherapy response in a patient of B-NHL remains an unanswered question. Methods Forty nine cases of de novo DLBCL with available formalin fixed paraffin embedded (FFPE) block, serum (stored at -80˚C)and IPI were reviewed using the diagnostic criteria defined in the Revised European-American Classification of Lymphoid Neoplasm's.BD Pharmigen™cytometric bead analysis (CBA) Human Th1/Th2 Cytokine Kit II (Catalog No. 560484) was used to quantitateInterleukin-2 (IL-2), Interleukin-4 (IL-4), Interleukin-6 (IL-6), Interleukin-10 (IL-10), Tumor Necrosis Factor (TNF-α), and Interferon-γ (IFN-γ) protein levels against internal standard controls. BD FCAP ArrayTM software was used to analyze all the cytokines levels respectively. Baseline angiogenesis in tumor was assessed by histopathologic examination for micro vessel density. Microvessel density was examined using CD34 antibody (clone QBEnd 10, Dako, Denmark), an endothelial cell marker. Vascular "Hot Spots" were identified at low power and the visual analog system was used for counting at 40X in at least five independent microscopic fields per tissue section. The mean of five fields was calculated and divided by the field area (1 HPF=0.19 mm2) to obtain the density count in mm2. Precautions were taken to count vessels at the center of the tumor and to avoid the periphery of the tumor to obtain true representation of tumor vasculature. Median value was calculated for the continuous data and CD34, IL-6, IL-10, IL-4, IL-2, IL-17, TNF-α, IFN-γ divided into categorical variables based on median value. Kaplan-Meier method was used to estimate event-free survival (EFS) distribution.Cytokine profile and microvessel density were correlated with EFS for identification of prognostic marker. Informed consent was taken from all the patients enrolled in the study in accordance with IEC, PGIMER guidelines. Results Forty nine DLBCL cases in the study included thirty (61%) males and nineteen (39%) females (male/female, 1.6:1). The median age of patients was 56 years (range, 17 - 80 years). Stage I/II were seen in 40% patients while stage III/IV were seen in 60% patients. Fifty-four patients had extranodal disease. Forty five, 15 and 40% patients had low, intermediate and high risk IPI respectively. All but 3 patients were treated with RCHOP based regimen. Remaining 3 patients 2 received bendamustine with rituximab while one recevied only CHOP. CR rate was 58.8% while ORR was 70%. At the time of analysis three patients had died. On univariate analysis, IL-10, a cytokine of TH2 response, was identified as a promising prognostic factor for EFS (p<0.05). However, association of levels of IL-6, IL-2, IL-4, TNF-α, IFN-γ, and IL-17 with EFS was not statistically significant. There was no statistically significant relation between any of the tested cytokine levels and chemotherapy response rates. Median EFS for patients with high IL10 level was 8.2 months. While median value of EFS for patients with low IL2 levels was not reached till the time of data analysis. Microvessel density was an independent predictor of EFS (p=0.024). Conclusion We conclude that high micro vessel density and high IL10 levels are associated with poorer event free survival in DLBCL patients. Figure 1. Concentration of TH1/TH2 response related cytokines Figure 1. Concentration of TH1/TH2 response related cytokines Figure 2. Box and whisker plot showing microvessel density in lymphnode tissue Figure 2. Box and whisker plot showing microvessel density in lymphnode tissue Figure 3. Kaplan Meier survival curve for Event Free Survival according to IL10 level elevation Figure 3. Kaplan Meier survival curve for Event Free Survival according to IL10 level elevation Disclosures No relevant conflicts of interest to declare.

Blood ◽  
2015 ◽  
Vol 126 (23) ◽  
pp. 180-180 ◽  
Author(s):  
Alison J Moskowitz ◽  
Sun Cho ◽  
Martin Fleisher ◽  
Kaitlin M Woo ◽  
Zhigang Zhang ◽  
...  

Abstract Background/methods: Hodgkin lymphoma (HL) is characterized by elevations in serum cytokines and chemokines, produced by HL Reed-Sternberg cells and surrounding inflammatory cells, several which have been found to be prognostic and/or predictive for response to therapy. We previously reported the results of our phase II study evaluating PET-adapted salvage therapy with single-agent brentuximab vedotin (BV) followed by augmented ICE for patients with relapsed or refractory (rel/ref) HL (Lancet Oncology 2015). In this study, patients who failed 1 line of therapy for HL were treated with 2 cycles of BV, 1.2mg/Kg, administered weekly, 3 weeks on and 1 week off. Those who acheived PET-normalization proceeded directly to consolidation with autologous stem cell transplantation (ASCT). Those with persistent abnormalities on PET received augmented ICE prior to consideration for ASCT. Patients with localized, nodal-based disease that had not previously been radiated received involved field radiation prior to ASCT. Interleukin-6 (IL-6), interleukin-10 (IL-10), tumor necrosis factor-α (TNF-α), interferon-γ (IFN-γ), and cysteine-cysteine thymus and activation related chemokine (TARC) were measured at baseline and after 2 cycles of BV by multiplex enzyme-linked immunosorbent assay (ELISA) array. We aimed to evaluate the prognostic and predictive significance of these cytokines and chemokines in this uniformly treated patient population. Results: Of the 45 patients enrolled onto this protocol 37 (82%) had serum samples available both at baseline and after 2 cycles of BV for analysis. Table 1 displays the median values and ranges at baseline and after treatment with BV. Baseline levels of IL-6, IL-10, TNF-α, IFN-γ, and TARC were abnormal in 32%, 8%, 78%, 97%, and 97%, respectively. Elevated baseline IFN-γ and IL-10 correlated with presence of extranodal sites of disease (p=0.003 and 0.049 respectively) whereas elevated IL-10 and TNF-α correlated with the presence of B-symptoms (p=0.019 and 0.019 respectively). With regard to response to treatment, percent change in TARC (TARC%) from baseline to post-BV predicted for PET-normalization following BV (OR 5.82, 95% C.I 1.18-43.74). Furthermore, lower post-BV TARC was significantly associated with improved event free survival (EFS) (2 year EFS 94% vs 67%, p=0.033) (Figure 1). No other factors correlated with response to therapy, event free survival, or overall survival. Conclusions: To date, this is the largest series evaluating the prognostic and predictive significance of TARC in rel/ref HL patients treated with BV. Our analysis confirms the role of TARC as a biomarker of response to BV and PET-normalization. In line with its correlation with PET-normalization, post-BV TARC level was also predictive of EFS. Continued incorporation of TARC evaluation in prospective clinical trials for HL is warranted to better define its role in predicting PET-normalization and prognosis. Table 1. Cytokine/chemokine Pre-brentuximab vedotin (pg/ml) Post-brentuximab vedotin (pg/ml) median range median range IL-6 2.27 0.10-154.44 1.41 0.09-34.00 IL-10 0.38 0.09-112.29 0.45 0.14-17.53 TNF-α 2.55 0.55-15.15 2.25 0.58-22.31 IFN-γ 8.66 1.45-1553.67 9.01 2.62-112.83 TARC 8250.00 236.10-220773.00 1026.70 241.70-34453.00 Figure 1. Figure 1. Disclosures No relevant conflicts of interest to declare.


Author(s):  
Sandeep Agarwala ◽  
Vishesh Jain ◽  
Anjan Dhua ◽  
Madur Srinivas ◽  
Prabudh Goel ◽  
...  

Background: Recent SIOPEL studies have shown cisplatin monotherapy to be equally effective in management of Standard risk Hepatoblastoma (SRHB) as compared to PLADO. Aim: To study the chemotherapy, response and outcomes in children with SRHB in a Resource Challenged Nation (RCN). Material and Methods: A retrospective study was conducted and all children with SRHB who were treated by us from June 2007 to December 2017 were included. All patients with standard risk hepatoblastoma who had received at least 2 courses of chemotherapy were included. Data regarding the demographics, PRETEXT stage, chemotherapy, response to chemotherapy and outcomes were recorded. Kaplan Meier survival analysis was performed to calculate 5-year overall survival (OS) and event free survival (EFS). Results: Thirty-two children were included in the study. Nineteen children (59.4%) received Cisplatin monotherapy and of these 6 patients (all PRETEXT III) had poor response and were upgraded to PLADO. The remaining 13 (40.6%) received upfront PLADO. The 5-year OS and EFS was 100% in the monotherapy group (n=13), 92% and 69% in the upfront PLADO group (n=13), and 62% and 22% in the upgraded to PLADO group (n=6). Patients in upgraded to PLADO group had significantly lower 5-year EFS (70% vs 22%; p= 0.036) compared to upfront PLADO group. Conclusion: Two thirds of SRHB patients with PRETEXT stage III who received cisplatin monotherapy showed poor response and were upgraded to PLADO chemotherapy. These patients had a significantly poorer outcome compared to the rest of the cohort. PRETEXT stage III standard-risk hepatoblastoma may benefit from PLADO chemotherapy instead of cisplatin monotherapy.


2021 ◽  
Vol 80 (Suppl 1) ◽  
pp. 180-181
Author(s):  
L. Chatzis ◽  
V. Pezoulas ◽  
A. Goules ◽  
I. Stergiou ◽  
C. Mavragani ◽  
...  

Background:Sjögren’s Syndrome (SS) is a chronic systemic autoimmune disease of unknown etiology, carrying the highest lymphoma risk among autoimmune diseases, with significant impact on mortality and morbidity of patients.Objectives:To describe: i) the clinical phenotype of SS, ii) the histologic type, stage, treatment options regarding lymphomas and iii) the prognosis of patients with SS related lymphoproliferative disorders.Methods:Eight hundred and fifteen consecutive SS patients’ records from a single center fulfilling the 2016 ACR/EULAR were reviewed retrospectively for the purpose of this study. One hundred twenty-one patients with a diagnosis of non-Hodgkin Lymphoma (NHL) were identified and enrolled in the study population. Cumulative clinical, laboratory and histologic data were recorded and overall survival as well as event free survival curves were constructed using the Kaplan-Meier method. An event was defined as a disease progression, lymphoma relapse, treatment failure, histologic transformation, development of a 2nd lymphoma or death from any cause.Results:From 121 pSS patients with lymphoma the most common histologic type encountered was MALT lymphoma (92/121, 76,0%) followed by DLBCL (11/121, 9.0%) and NMZL (8/119, 6.6%). The remaining 10 patients had various lymphomas of B (follicular, lymphoplasmacytic, chronic lymphocytic leukemia} and T cell origin (peripheral T cell lymphoma not otherwise specified, primary cutaneous T cell lymphoma, angioimmunoblastic t-cell lymphoma). Permanent salivary gland enlargement (66.1%, 80/121), palpable purpura (34,7% 42/121), peripheral nervous involvement (9,9%, 12/121), interstitial lung disease (8,2%, 10/121) presence of serum cryoglobulins (38,7%, 43/111) and C4 hypocomplementemia (69,8% 81/116) present at least 1 year before the development of lymphoma were the main pSS related features. The median age at lymphoma diagnosis was 58 years old (range 29-82) while MALT lymphomas developed earlier compared to DLBCL from pSS diagnosis (8 vs 3 OR= 3.84, 95%CI: 0.29 to 10.46; p=0.0266). The commonest biopsy proven extranodal sites included the labial minor salivary (43,8% patients) and parotid glands (30,5%) while 11% of patients had more than 1 extranodal sites affected. Bone marrow involvement was evident in 24,3% of patients (29/119) while nodal involvement in 35,5% (42/118). The majority of patients (65%) had limited disease (stage I or II). A watch and wait therapeutic policy was chosen in 40 patients while the rest received rituximab with or without chemotherapy. The 10-year survival and event free rates were 79% and 45,5% for MALT lymphomas, 40,9% and 24,2% for DLBCL and 46% and 31% for NMZL respectively (Figure 1). The Mantel-Cox log-rank comparison of the overall survival curves revealed a statistically significant difference (p=0.0016) among lymphoma subtypes.Figure 1.Overall and event free survival of SS-associated lymphoma patients. A. Kaplan-Meier overall survival analysis. B. A Kaplan-Meier event free survival analysis.Conclusion:This is the largest single center series of SS- associated lymphoma patients, providing a detailed description of SS and lymphoma related features, combined with a 10-year survival and event free curves for the first time in the literature.Disclosure of Interests:None declared.


2021 ◽  
Vol 39 (15_suppl) ◽  
pp. e12548-e12548
Author(s):  
Xianghou Xia ◽  
Wenjuan Yin ◽  
Jiefei Mao ◽  
Jiejie Hu ◽  
Dehong Zou ◽  
...  

e12548 Background: Pyroptosis is a type of inflammatory cell death mediated by gasdermins. Pyroptosis is critical for macrophage against pathogen infection. Recently growing evidences show that pyroptosis may affect development and progression of many cancers. We aim to explore the expression and related function of pyroptosis executioner Gasdermin D (GSDMD) in breast cancer. Methods: We investigated the expression level of GSDMD using TNM plotter and Breast Cancer landscape proteome with TCGA, GTEx and TARGET databases, and the prognostic value of GSDMD in invasive breast cancer using Kaplan-Meier plotter with TCGA, GEO and EGA databases. The treatment response prediction values of GSDMD in invasive breast were calculated using ROC-plotter with GEO database. Further validation of the prognostic value and chemotherapy response prediction value of GSDMD were carried out with immunohistochemical staining on tissues from 165 cases of breast cancer patients receiving neoadjuvant chemotherapy in our cancer center. Results: TNM plotter and breast cancer landscape proteome portal analysis shows that overall expression level of GSDMD in invasive breast cancer tissue is 1.67 folds higher than it is in breast normal tissues ( p=1.05*e-06). Expression of GSDMD in LuminalB subtype (p=0.019) and Her2 subtype(p=0.04) is significantly higher than it is in TNBC subtype. Calculations with Kaplan-Meier plotter show expression of GSDMD is negatively correlated with overall survival(OS), HR=0.61(0.4−0.95) p=0.027 and relapse free survival (RFS), HR =0.65(0.58−0.63), p=8.7*e-14 and distant metastasis free survival (DMFS) HR =0.75(0.61−0.91), p=0.0038 in breast cancer patients. ROC-plotter calculations show high GSDMD expression is a powerful endocrine therapy (AUC=0.731 p=6*e-09 ) and chemotherapy response (AUC=0.64 p=8*e-05 ) predictor based on 5-year RFS in overall breast cancer patients. Our IHC staining analysis shows consistent prognostic and chemotherapy prediction value of GSDMD expression in TNBC patients. Conclusions: In conclusion, our findings suggest that high expression of GSDMD is positively correlated with prognosis and therapeutic response in breast cancer. GSDMD is a promising prognostic marker and therapeutic response predictor in invasive breast cancer.


Sari Pediatri ◽  
2016 ◽  
Vol 14 (1) ◽  
pp. 40
Author(s):  
Hikari Ambara Sjakti ◽  
Djajadiman Gatot ◽  
Endang Windiastuti

Latar belakang. Leukemia mieloblastik akut (LMA) merupakan penyakit keganasan yang sering ditemukan pada anak. Hasil pengobatan LMA di Departemen Ilmu Kesehatan Anak RSCM dalam satu dekade terakhir belum pernah dievaluasi. Tujuan. Mengetahui karakteristik pasien LMA dan evaluasi hasil pengobatan serta protokol pengobatan.Metode. Penelitian deskritif dilakukan secara retrospektif terhadap rekam medis pasien LMA yang didiagnosis antara Januari 2007-Desember 2010 di Departemen Ilmu Kesehatan Anak RSCM. Karakteristik pasien secara klinis dan laboratoris dicatat, dan hasil pengobatan dianalisis. Estimasi kesintasan dihitung menggunakan metode Kaplan-Meier dengan bantuan program statistik.Hasil. Selama rentang waktu penelitian didapatkan 93 pasien baru LMA. Overall survival (OS) adalah 46,2% (95% IK: 21,1%;31,2%) dan event-free survival(EFS) 6,5% (95% IK: 3,1%;6,2%). Angka loss to follow-upmencapai sepertiga jumlah pasien yang mempengaruhi hasil estimasi kesintasan (overall survival). Rendahnya EFS disebabkan oleh angka kematian yang tinggi mencapai 50 dari 93 pasien dan 62% di antaranya disebabkan oleh sepsis.Kesimpulan. Keberhasilan pengobatan LMA masih sangat rendah dibandingkan laporan penelitian dari negara lain. Faktor yang paling berperan terhadap hal ini adalah kematian yang tinggi akibat infeksi berat atau sepsis. Komplikasi infeksi mungkin terjadi akibat toksisitas obat dan fasilitas perawatan untuk pasien LMA kurang memadai. Stratifikasi risiko pasien LMA dan evaluasi protokol kemoterapi yang diberikan serta penyediaan fasilitas perawatan yang baik akan memperbaiki hasil pengobatan LMA


2021 ◽  
Vol 42 (Supplement_1) ◽  
Author(s):  
Z Meiszterics ◽  
T Simor ◽  
R J Van Der Geest ◽  
N Farkas ◽  
B Gaszner

Abstract Introduction Increased aortic pulse wave velocity (PWV) as a strong predictor of major advanced cardiovascular events (MACE) has a prognostic relevance in patients after myocardial infarction (MI). Several non-invasive methods have been proposed for the assessment of arterial stiffness, but the PWV values show significant differences according to the applied techniques. Cardiac magnetic resonance imaging (CMR) provides an accurate method to measure PWV and infarct size in patients after MI. Purpose Calculated PWV values of CMR based phase-contrast (PC) and invasively validated oscillometric methods were compared in this prospective observational study. We aimed to evaluate the cut-off PWV values for each method, while MACE predicted and validated the prognostic value of high PWV in post-infarcted patients in a 6-year follow-up. Methods 3D aortic angiography and PC velocity imaging was performed using a Siemens Avanto 1,5 T CMR device. Oscillometric based Arteriograph (AG) was used to assess PWV using direct body surface distance measurements. The comparison between the two techniques was tested. Patients received follow-up for MACE comprising all-cause death, non-fatal MI, ischemic stroke, hospitalization for heart failure and coronary revascularization. Event-free survival was analysed using Kaplan-Meier plots and log-rank tests. Univariable and multivariable Cox regression analysis was performed to identify outcome predictors. Results 75 patients (56 male, 19 female, average age: 56±13 years) referred for CMR were investigated, of whom 50 had coronary artery disease (CAD) including 35 patients with previous MI developing ischaemic late gadolinium enhancement (LGE) pattern. AG and CMR derived PWV values were significantly correlated (rho: 0,343, p&lt;0,05), however absolute PWV values were significantly higher for AG (median (IQR): 10,4 (9,2–11,9) vs. 6,44 (5,64–7,5); p&lt;0,001). Bland Altman analysis showed an acceptable agreement with a mean difference of 3,7 m/s between the two measures. In patients with CAD significantly (p&lt;0,01) higher PWV values were measured by AG and CMR, respectively. During the median follow-up of 6 years, totally 69 MACE events occurred. Optimized PWV cut-off values for MACE prediction were calculated (CMR: 6,47 m/s; AG: 9,625 m/s) by receiver operating characteristic analysis. Kaplan-Meier analysis in both methods showed a significantly lower event-free survival in case of high PWV (p&lt;0,01, respectively). Cox regression analysis revealed PWV for both methods as a predictor of MACE (PWV CMR hazard ratio (HR): 2,6 (confidence interval (CI) 1,3–5,1), PWV AG HR: 3,1 (CI: 1,3–7,1), p&lt;0,005, respectively). Conclusions Our study showed good agreement between the AG and CMR methods for PWV calculation. Both techniques are feasible for MACE prediction in postinfarcted patients. However, different AG and CMR PWV cut-off values were calculated to improve risk stratification. FUNDunding Acknowledgement Type of funding sources: None. Agreement between the two methods Kaplan-Meier event curves for MACE


2019 ◽  
Vol 37 (15_suppl) ◽  
pp. e14043-e14043
Author(s):  
Lynn G. Feun ◽  
Ying-Ying Li ◽  
Chunjing Wu ◽  
Medhi Wangpaichitr ◽  
Patricia Denise Jones ◽  
...  

e14043 Background: Pembrolizumab (PEM) has been approved as second line therapy for the treatment of hepatocellular carcinoma (HCC). We conducted a single institution investigator-initiated clinical/biomarkers trial to assess potential biomarkers to predict response in unresectable HCC patients (pts) receiving PEM. Methods: PEM was administered at 200mg iv. every 3 weeks for advanced HCC pts who progressed on, were intolerant of, or refused sorafenib. The circulating levels of cytokines/chemokines included IL-1β, IL-6, IL-8, IL-12, IL-18, IFN-γ, TGF-β, IL-10, CXCL9, CCL4, CCL5, as well as PD-1, PD-L1, PD-L2 were measured by ELISA at baselines and at day 60-90. PD-L1 expression in tumor was also assessed by histopathological staining. Results: 29 pts have been treated and 28 were evaluated for response. One pt had complete response, 8 had partial response and 4 had stable disease. Among all the biomarkers tested, only TGF-β at baseline predict response. The mean of plasma TGF-β in responders were 141.9pg/ml vs. 1071.8pg/ml in nonresponders. The cut-off values was determined based on the near medians. The plasma concentration of TGF-β of ≥200pg/ml was an index for nonresponder (P = 0.003). Kaplan-Meier analysis showed that the median overall survival (OS) and progression-free survival (PFS) in pts with TGF-β ≥200pg/ml were 7 months and 2 months, respectively, while in pts with TGF-β < 200 pg/ml, the OS and PFS were over 25 months(P = 0.005 and P = 0.008, respectively). Plasma IFN-γ or IL-10 levels positively correlated with plasma PD-1/PD-L-1 (P < 0.05). Since tumor PD-L1 expression is upregulated by IFN-γ, and IL-10, and interacts with PD-1 to suppress T cell, to confirm these relationships, the linear regression was used to analyze the data. Plasma IFN-γ or IL-10 levels positively correlated with plasma PD-1 and PD-L1 levels ( P < 0.05). Nine of these 24 patients had tumor available for PD-L1 scoring (PD-L1-positive:3 pts and PD-L1-negative:6pts). Similar to plasma PD-L1 concentration, pts with positive tumor PD-L1 had high levels of plasma IFN-γ or IL-10 ( P < 0.05). Conclusions: Our study confirmed that PEM is active in HCC and TGF-β is a predictive markers for tumor response, PFS, and OS. Support by grant from Merck


BMC Cancer ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Hui-Hui Chen ◽  
Wei-Yu Meng ◽  
Run-Ze Li ◽  
Qing-Yi Wang ◽  
Yu-Wei Wang ◽  
...  

Abstract Background Cervical cancer continues to be one of the leading causes of cancer deaths among females in low and middle-income countries. In this study, we aimed to assess the independent prognostic value of clinical and potential prognostic factors in progression-free survival (PFS) in cervical cancer. Methods We conducted a retrospective study on 92 cervical cancer patients treated from 2017 to 2019 at the Zhuhai Hospital of Traditional Chinese and Western Medicine. Tumor characteristics, treatment options, progression-free survival and follow-up information were collected. Kaplan–Meier method was used to assess the PFS. Results Results showed that the number of retrieved lymph nodes had a statistically significant effect on PFS of cervical cancer patients (P = 0.002). Kaplan-Meier survival curve analysis showed that cervical cancer patients with initial symptoms age 25–39 had worse survival prognoses (P = 0.020). And the using of uterine manipulator in laparoscopic treatment showed a better prognosis (P < 0.001). A novel discovery of our study was to verify the prognostic values of retrieved lymph nodes count combining with FIGO staging system, which had never been investigated in cervical cancer before. According to the Kaplan-Meier survival curve analysis and receiver operating characteristic (ROC) curve analysis, significant improvements were found after the combination of retrieved lymph nodes count and FIGO stage in predicting PFS for cervical cancer patients (P < 0.001, AUC = 0.826, 95% CI: 0.689–0.962). Conclusion Number of retrieved lymph nodes, initial symptoms age, uterine manipulator, and retrieved lymph nodes count combining with FIGO staging system could be potential prognostic factors for cervical cancer patients.


Blood ◽  
2020 ◽  
Vol 136 (Supplement 1) ◽  
pp. 18-19
Author(s):  
Sara Ghorashian ◽  
Caroline Furness ◽  
Michelle Cummins ◽  
John A Snowden ◽  
Maeve A O'Reilly ◽  
...  

Background: Tisagenlecleucel was approved in Europe for relapsed/refractory acute lymphoblastic leukemia (ALL) in young patients in 2018. In England, a national CAR T cell panel (NCCP ALL) ensures equity of access and assesses eligibility using inclusion and exclusion criteria based on the ELIANA study. All UK cases are discussed. Eligible cases are allocated to one of 9 JACIE-FACT IEC-approved centres based on age-appropriate service, capacity, distance and patient preference. We systematically reviewed all cases from panel inception providing an opportunity to analyse complete real-world ALL outcomes from this national access programme for tisagenlecleucel on an intention-to-treat (ITT) basis. Methods: We included all patients discussed in the NCCP ALL from Nov 2018 up to July 16th 2020. Clinical data were retrospectively reported in a standardised dataset to allow central analysis of disease and toxicity-related outcomes. Survival outcomes were assessed as for other CAR studies, using Kaplan-Meier estimates of survival from infusion. These included overall survival (interval to death from any cause) and event-free survival as defined in the ELIANA study (interval to death, disease relapse, or treatment failure defined in turn as failure to respond by day 30, with patients receiving further therapy being censored). In order to report outcomes on an ITT basis, survival outcomes were also assessed from time of treatment allocation for all patients considered eligible for tisagenlecleucel. Further, a more comprehensive event-free survival measure encompassing interval to molecular or frank relapse, further therapy, B cell recovery, death or treatment failure was analysed. Median follow up was calculated using a reverse Kaplan-Meier method. Results: Figure 1 demonstrates all patients: 66 patients were screened, 60 patients were deemed eligible for therapy (the ITT cohort), 57 patients were harvested and 49 infused. A total of 3 patients were not harvested and 2 not infused because of progressive disease (n=4) and 1 manufacturing failure. Patient and disease characteristics are summarised in Table 1. The cohort comprised patients with advanced ALL, having been treated with a median of 2.5 therapy lines not including HSCT (range 1-6), and with 47.5% of the cohort having had a prior HSCT. The median follow-up from infusion was 9.9 months and from treatment allocation for the ITT cohort was 11.9 months. The median lead time from allocation to infusion was 2 months. The CR/CRi rate was 95% in the first 90 days, 78.9% were MRD-. On an ITT basis, CR/CRi rate was 84.8%. Median OS and EFS as defined in the ELIANA study were not reached. Overall survival at 6 and 12 months for infused patients was 97.6% and 86.1%, and for the ITT cohort was 90.4% and 78.3%. EFS for infused patients at 6 and 12 months were 74.8% and 68.2%, and for the ITT cohort were 78.5% and 60.9%. Of 49 patients infused, 14 (28.5%) received further therapy including 6 (8.2%) who received allogeneic SCT for relapse or B cell recovery. For patients relapsing following CR (n=10 infused) there were 4/10 CD19- relapses. A composite EFS including molecular or frank relapse, further therapy, B cell recovery, death or treatment failure was analysed. Using this more stringent definition from infusion, the 6, 12 month EFS were 47.6%, and 33.6% and from treatment allocation for the ITT cohort were 63% and 34.3% Toxicity outcomes are summarised in Table 2. Severe (grade ≥3) CRS, neurotoxicity, infection or cytopenia after day 30 post infusion occurred in 20.4%, 10.2% 27.1% and 54.2% respectively. 71.4% of the cohort developed hypogammaglobulinaemia, (Figure 3A). The 6 and 12 month probabilities of B cell depletion were 67.1% and 51.3% respectively. Conclusions: Whilst registry data provide outcomes of large cohorts receiving Tisagenlecleucel, standardised data collection on complete populations are lacking. The framework of a national access scheme provides a unique opportunity to study outcomes on an ITT basis. The CR and MRD negative CR rates, as well as conventional EFS and OS and severe toxicities noted in our cohort compare favourably to published registry reports (Grupp et al., 2019). We found a greater proportion of CD19+ compared to CD19- relapses than noted in the ELIANA study. Consideration of OS and EFS on an ITT basis are informative for clinicians when screening patients for eligibility. If selected for presentation at ASH 2020, updated data will be presented Disclosures Ghorashian: Amgen: Honoraria; Novartis: Honoraria; UCLB: Patents & Royalties. O'Reilly:Gilead: Honoraria; Novartis: Honoraria, Other: Travel support. Roddie:Celgene: Honoraria; Gilead: Honoraria; Novartis: Honoraria. Neill:Novartis: Other: Funded attendance at academic conferences; Celgene: Other: Funded attendance at academic conferences. Pagliuca:Jazz Pharmaceuticals: Membership on an entity's Board of Directors or advisory committees. Patel:Novartis: Honoraria, Other: travel support. Hough:Novartis: Other: Travel support.


Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 5456-5456
Author(s):  
Nalini K. Pati ◽  
Yiu-Lam Kwan ◽  
Arumugam Manoharan ◽  
Michael Teh

Abstract INTRODUCTION: In many centers an initial period of induction treatment followed by peripheral blood stem cell (PBSC) harvest and autologous stem cell transplantation (ASCT) has become standard of care for multiple myeloma (MM) in patients =< 65 years of age. Commonly induction regimens contain intravenous cytotoxic agents and oral corticosteroids. There are interests in oral regimens, including thalidomide-containing combinations (1). Recently Spencer et al from Australia reported a small multicenter study in which the induction treatment prior to ASCT comprised an outpatient-based oral chemotherapeutic regimen CID-- cyclophosphamide, idarubicin, dexamethasone, in previously untreated MM patients (2). AIM: To evaluate the efficacy of oral CID in MM in our own institution. METHODS: thirteen patients with MM (relapsed n=2, previously untreated n=11) were treated with CID. Courses were repeated every four weeks, with the aim of harvesting PBSC after 3 to 6 courses, depending on response. Efficacy of treatment was assessed on the following parameters: paraprotein level, b2 microglubulin and bone marrow plasma cell content. Wilcoxon Signed Ranks Test was used to analyze treatment outcomes and Kaplan-Meier curves were used for analysis of overall survival and event free survival. RESULTS: All 13 patients (median age 61 yrs, range-41–72 yrs; male-7, female-6) were evaluable for response, with a median follow up of 40 (12–84) weeks. In total, eleven patients (10 previously untreated, and one relapsed) were planned to have an elective ASCT. All had successful stem cell mobilization after 3–6 cycles of chemotherapy, and subsequently received an ASCT. One patient died 42 days post transplantation due to infection and ARDS. The median time between completion of CID and ABMT was 6 weeks (range 4–16). One previously untreated patient and one relapsed patient, both aged >65, received CID only without an ASCT. Comparison of pre and post chemotherapy levels of paraprotein, b2 microglubulin and bone marrow plasma cell content showed statistically significant results with p values of 0.002, 0.001 and 0.002 respectively. According to International standard criteria, 3/13 achieved complete response (CR), 7/13 had very good partial response (VGPR) or partial response (PR), 1/13 stable disease (SD) and 2/13 had relapse or progressive disease (PD), resulting in an overall response rate (>/=SD) of 84%. The median time to maximum response was 4 months. The Kaplan-Meier estimates of event-free survival and overall survival at 1 year were 64% and 84%, respectively. There were no major toxicities except weight gain (National Cancer Institute Common Toxicity Criteria Grade III) was seen in 23% of the patients, possibly due to the dexamethasone component in CID. CONCLUSIONS: Our results confirm the efficacy and safety of this outpatient based all oral induction regimen for patients with MM. The favorable side effect profile, the convenience of drug delivery with oral dosing, and the ease of PBSC mobilisation are the main advantages.


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