scholarly journals EVALUATION OF RESPONSE TO THE FIRST‐LINE THERAPY OF PATIENTS WITH CLASSICAL HODGKIN LYMPHOMA BASED ON INTERIM PET‐CT AT A PRIVATE BRAZILIAN INSTITUTION

2021 ◽  
Vol 39 (S2) ◽  
Author(s):  
J. M. De Almeida ◽  
A. Alves
2021 ◽  
Vol 19 (11.5) ◽  
pp. 1335-1338
Author(s):  
Ranjana H. Advani

Goals of first-line therapy in classic Hodgkin lymphoma (cHL) should focus on balancing risk versus benefit to the individual while increasing efficacy and decreasing toxicity. Overall, the ABVD regimen is well tolerated but slightly less effective, with a better safety profile compared with escalated BEACOPP. BV-AVD is somewhere in between ABVD and escalated BEACOPP on the cure/morbidity scale. Interim PET is predictive, but new prognostic biomarkers are emerging that may better identify patients at high risk for treatment failure. In patients with interim PET-negative cHL, de-escalating therapy does not impact overall survival along 1) with no proven role for radiotherapy. cHL is largely a disease of young people, and the choice of treatment should always take into account the potential for both short- and long-term toxicity with the goal of optimizing survivorship.


Oncology ◽  
2021 ◽  
pp. 1-6
Author(s):  
Ahmed Abdelhakeem ◽  
Madhavi Patnana ◽  
Xuemei Wang ◽  
Jane E. Rogers ◽  
Mariela Blum Murphy ◽  
...  

<b><i>Background:</i></b> The value of baseline fluorodeoxyglucose-positron emission tomography-computed tomography (PET-CT) remains uncertain once gastroesophageal cancer is metastatic. We hypothesized that assessment of detailed PET-CT parameters (maximum standardized uptake value [SUVmax] and/or total lesion glycolysis [TLG]), and the extent of metastatic burden could aid prediction of probability of response or prognosticate. <b><i>Methods:</i></b> We retrospectively analyzed treatment-naive patients with stage 4 gastroesophageal cancer (December 2002–August 2017) who had initial PET-CT for cancer staging at MD Anderson Cancer Center. SUVmax and TLG were compared with treatment outcomes for the full cohort and subgroups based on metastatic burden (≤2 or &#x3e;2 metastatic sites). <b><i>Results:</i></b> We identified 129 patients with metastatic gastroesophageal cancer who underwent PET-CT before first-line therapy. The median follow-up time was 61 months. The median overall survival (OS) was 18.5 months; the first progression-free survival (PFS) was 5.5 months. SUVmax or TLG of the primary tumor or of all metastases combined had no influence on OS or PFS, whether the number of metastases was ≤2 or &#x3e;2. Overall response rates (ORRs) to first-line therapy were 48% and 45% for patients with ≤2 and &#x3e;2 metastases, respectively (nonsignificant). ORR did not differ based on low or high values of SUVmax or TLG. <b><i>Conclusions:</i></b> This is the first assessment of a unique set of PET-CT data and its association with outcomes in metastatic gastroesophageal cancer. In our large cohort of patients, detailed analyses of PET-CT (by SUVmax and/or TLG) did not discriminate any parameters examined. Thus, baseline PET-CT in untreated metastatic gastroesophageal cancer patients has limited or no utility.


2019 ◽  
Vol 37 (S1) ◽  
pp. 82-86 ◽  
Author(s):  
Jemma Longley ◽  
Peter W.M. Johnson

Blood ◽  
2011 ◽  
Vol 118 (21) ◽  
pp. 3686-3686
Author(s):  
Herve Ghesquieres ◽  
Céline Ferlay ◽  
Emilie Lavergne ◽  
Emmanuelle Nicolas Virelizier ◽  
Izabela-Irina Domnisoru ◽  
...  

Abstract Abstract 3686 Background: 18F-FDG Positron Emission Tomography (PET) had improved initial staging and response assessment after first line therapy of Diffuse Large B-cell Lymphoma (DLBCL). While the prognostic role of PET after induction therapy (interim PET) remains controversial, the outcome of patients with positive PET at the end of initial treatment is clearly worse as compared with negative ones. In clinical practice, many PET are performed before, during and after first line therapy for patients with DLBCL. A hypothetical effect of therapeutic decisions, guided by PET results, on DLBCL patients' outcome remained questionable. We evaluated our daily practice about PET prescription during first line therapy to explore how a complete PET could influence the DLBCL prognosis. Patients and Methods: From 1996 to 2008, 410 patients with DLBCL received first-line therapy in our institution. No selection was made on initial therapeutic intent (curative/palliative), medical history, patient's age or initial type of chemotherapy (CT) to be in accordance with daily practice setting. Study population was described and Overall Survival (OS) and Time To Progression (TTP) analysis was performed using the Kaplan Meier method. OS and TTP were compared between patients with or without PET, using the Log-Rank test. We first focused on interim PET considering patients who performed at least 3 months of the induction therapy (n=380). PET at the end of treatment were studied on patients who achieved a major part of their consolidation treatment (at least 6 months, n=354). As it was a practical study, the PET interpretation methods were not taken into account. Results: Median age at diagnosis was 65 years (range: 19–97). Most patients received CHOP-like CT (53%) or high-dose CHOP CT (31%). Rituximab was associated to CT for 269 patients (66%). PET was performed at initial staging, after induction therapy and at the end of initial treatment respectively on 77, 72 and 94 patients. We first observed that patients who had a pre-treatment PET presented a significantly higher rate of III-IV Ann Arbor stage than patients evaluated by conventional methods (71% vs. 57%, p =.021). Patients who had an interim PET were younger (median age: 55 vs. 67 years, p <.001), presented a higher age-adjusted IPI score (2–3, 66% vs. 47%, p =.004) and were more frequently treated by rituximab (96% vs. 61%, p <.001) than patients who did not have a PET, that is in accordance with the date of approval of rituximab for DLBCL in 2002. The same observation was done for patients who had a PET at the end of the treatment. No difference in TTP was observed between patients who had an interim PET and patients evaluated by conventional methods (p =.543), with 5-year TTP rates of 65.6% (CI95% [51.0–76.8]) and 70.3% (CI95% [64.5–75.3]) respectively. Similarly, no difference in OS was observed between these groups. Neither OS nor TTP were found to be statistically different between patients evaluated at the end of treatment with a 5-year TTP rates of 72.4% (CI95% [61.5–80.7]) for patients who performed a TEP at the end of the treatment and 73.8% (CI95% [67.6–78.9]) (p =.653) for the others. Preliminary results showed a worse prognosis for patients who had a positive PET at completion of first line therapy with a 5-year OS rate of 50.0% (CI95% [22.9–72.2]) compared with 84.4% (CI95% [70.4–92.1]) for patients with negative PET (p =. 001). However, no observe a prognostic value of positivity of interim PET performed at mid-treatment was observed. Conclusions: Results of this retrospective clinical practice study are consistent with the usefulness of PET for initial staging of DLBCL patients and a poor prognosis of positive PET at the end of first line therapy. Using PET for evaluation of treatment response after induction therapy or after treatment completion was not found to be significantly associated with patient's prognosis. Modification of therapeutic decision based on PET results need to be more accurately explored with a prospective clinical trial. Disclosures: No relevant conflicts of interest to declare.


Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 2742-2742
Author(s):  
Marcio M Andrade ◽  
Anel Montes ◽  
Ilda Murillo ◽  
Jose M Grasa ◽  
Teresa Baringo ◽  
...  

Abstract Abstract 2742 Introduction: 90Y Ibritumomab tiuxetan (90Y-IT) has become an efficient alternative to therapy in non-Hodgkin Lymphoma, mainly in elderly patients. The aim of this study is to analyse our updated information of patients treated with 90YIbritumomab/tiuxetan in a prospective study according clinical practice setting and to analyse treatment outcome. Subjects and Methods: 39 non Hodgkin lymphoma patients were included in a clinical protocol conducted by a multidisciplinary team and treated in the same centre. According the inclusion criteria: patients over 65 years old diagnosed as CD20+ NHL with neutrophils ≥ 1,5 × 109/L, platelets ≥ 100 × 109/L, bone marrow lymphocytes CD20+ ≤ 25%. All patients received 0,3 or 0,4 mCi /kg IV (88%) of 90YIbritumomab/tiuxetan and response evaluation was performed 12 weeks after. Period of study: September 2005/July 2012. The 90Y-IT was administered as consolidation of first line therapy (Rituximab alone, R-COP, R-CHOP21) or in relapsed/refractory status. Endpoints: Objective response rate (ORR), time to relapse (PFS) overall survival (OS) and safety. Other clinical prognostic factors were observed to assess their possible influence upon treatment value. Results: Until May 2012, 39 patients had received treatment with 90YIbritumomab/tiuxetan and completed the evaluation protocol and were considered to analysis; M/F 18/21 mean age 72.8 years (65–87); ECOG 0–1 92.3%. According OMS classification: NHL-follicular 27 (69.2%), mantle cell Lymphoma 7 (17.9%), DLBCL 4 (10.3%) and 1MALT (2.6%). Score distribution: low risk 19 (48.7%), intermediate 12 (30.8.2%) and advanced 8 (20.5%). Previous therapy schedules ≤2 (66.7%), >2 (33.3%). The median follow-up time: 42.0 months (95% CI: 4.0; 62.0), mean PFS: 38.1 months (95% CI: 30.8; 45.4) median NR. 13 patients received 90Y-IT as consolidation of first line therapy (33.3%) and 26 relapsed/refractory (66.6%). ORR was 84.6 % CR: 29 (74.3%); PR 4 (10.2%) and 6 failures (15.4%) in relapsed/refractory disease. Mean estimated OS since 90Y-IT: 54.4 months (95% CI: 49.4; 59.3) and mean estimated OS since diagnosis 159 months. Median PFS was NR. The mean PFS for patients in consolidation therapy was 54.2 months (95% CI: 47.4; 61.1). Safety: thrombocytopenia being the most frequent, G3–4 (35.9%), median time to developed haematological toxicity: fourth week, and neutropenia G3–4 (41.0%), the median time to recover normal values was 4.2 and 2.6 weeks respectively. In 5 (12.9%) of patients red blood cell transfusion was required, and 10 platelet transfusions (25.6%). The most frequent non haematological toxicity was asthenia. One patient developed a severe mucositis. Four patients have concomitant associated tumours (colon, breast, lung and prostate) and two patients over 77 years developed a rectum carcinoma after 18 months of 90Y-IT and another prostate and renal tumour after 8 years. Comments: In our experience 90Y Ibritumomab tiuxetan is a safety and effective therapy in patients with NHL over 65 years. According to obtained PFS results, it seems like the use of this kind of therapy as used in early part of therapy offers good and maintained response rate with lower toxicity in this fragile population. The OS in this population was not inferior to observed in younger NHL patients. Disclosures: No relevant conflicts of interest to declare.


2018 ◽  
Vol 36 (15_suppl) ◽  
pp. 7542-7542 ◽  
Author(s):  
Jonathan W. Friedberg ◽  
Andres Forero-Torres ◽  
Beata Holkova ◽  
Jerome H. Goldschmidt ◽  
Ralph V. Boccia ◽  
...  

Hematology ◽  
2012 ◽  
Vol 2012 (1) ◽  
pp. 322-327 ◽  
Author(s):  
Martin Hutchings

Abstract Positron emission tomography/computed tomography (PET/CT) has emerged as the most accurate tool for staging, treatment monitoring, and response evaluation in Hodgkin lymphoma (HL). Accurate staging and restaging are very important for the optimal management of HL, but we are only beginning to understand how to use PET/CT to improve treatment outcome. More precise determination of disease extent may result in more precise pretreatment risk stratification, and is also essential for the minimal and highly individualized radiotherapy volumes of the present era. Several trials are currently investigating the use of PET/CT for early response-adapted therapy, with therapeutic stratification based on interim PET/CT results. Posttreatment PET/CT is a cornerstone of the revised response criteria and enables the selection of advanced-stage patients without the need for consolidation radiotherapy. Once remission is achieved after first-line therapy, PET/CT seems to have little or no role in the routine surveillance of HL patients. PET/CT looks promising for the selection of therapy in relapsed and refractory disease, but its role in this setting is still unclear.


Sign in / Sign up

Export Citation Format

Share Document