Impact of New Therapies On the Survival of Elderly (≥75 Years of Age) Previously Untreated Patients with Multiple Myeloma in a Community Hospital

Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 4251-4251
Author(s):  
Romany Johnpulle ◽  
Simran Sindhu ◽  
Lynn Nichols ◽  
Lynda Dimitroff ◽  
Mehul Patel ◽  
...  

Abstract Abstract 4251 Multiple myeloma (MM) is an incurable clonal plasma cell malignancy. At least 50% of all MM patients are older than 70 years of age and 20% are older than 80 years of age (Siegel R, Naishadham D, Jemal A. CA Cancer J Clin. 2012 Jan-Feb;62(1):10–29). The approach to treatment of patients with MM depends on a multitude of factors including age, underlying comorbidities, and disease characteristics. Elderly patients are under-represented in clinical trials. The purpose of our study was to assess the overall outcomes and impact of novel agents in the treatment of newly diagnosed elderly (≥75 years of age) patients with MM in a community setting. We conducted a retrospective review of the records of MM patients seen at Rochester General Hospital, Rochester, NY, who were 75 years of age or older at the time of diagnosis of MM. The study period was from January 2001 to August 2012. Sixty-six patients met the study criteria. Patients with smoldering MM were excluded. Demographic information, comorbid conditions, disease characteristics, laboratory data, first line treatment given, response to treatment, and disease- and treatment-related complications were collected from medical records. Data were analyzed using SPSS software version 14. Univariate analysis was performed and the mean, median, and standard deviation were calculated. A statistically significant difference between variables was denoted by a p value < 0.05. Response to treatment was calculated using Bladé Criteria. Overall survival was estimated by using Kaplan-Meier curves. Grade III and IV toxicity was determined according to Common Terminology Criteria for Adverse Events (CTCAE) of the National Cancer Institute (NCI) version 4.0. Sixty-six patients (median age 81 years, range 75–95 years) with symptomatic MM were studied. Sixty-two percent were males. Twenty-seven percent had underlying diabetes mellitus, 29% had experienced a prior stroke or MI, and 68% had hypertension. Charlson Co-morbidity Index (CCI) was high (3–4) in 46% and very high (≥5) in 31%. Eastern Cooperative Oncology Group (ECOG) performance status (PS) was ≥3 in 27% of patients. Sixty-five percent of patients had IgG subtype, while 28% had IgA subtype. There was a predominance of kappa light chains over lambda (55% versus 42%). Twenty percent, 34%, and 40% of patients had International Staging System (ISS) stages 1, 2, and 3, respectively, while in 6% ISS could not be determined. The median hemoglobin level was 10.5 g/dL (range 6.1–14.8 g/dL), the median serum creatinine level was 1.3 mg/dL (range 0.1–8.0 mg/dL), the median serum albumin level was 3.2 g/dL (range 1.4–4.8 g/dL), and the median serum calcium level was 8.7 mg/dL (range 8.0–17.3 g/dL). As first line treatment 75% received standard therapy, while 25% received novel agents. The most commonly used standard therapies were cyclophosphamide + steroid (36%), melphalan + steroid (25%), and steroid alone (8%). First line therapy included bortezomib in 12%, thalidomide in 10%, and lenalidomide in 3% of patients. Median duration of first line treatment was 26 weeks (range 3–103 weeks). The median overall survival was 72 weeks (range 10–406 weeks). In those who received a novel agent as first line therapy the median overall survival was 127 weeks (range 38–318 weeks). Overall response rate (≥ partial response) was 55% in patients treated with a novel agent versus 23.6% in patients treated with standard therapy. There was no significant correlation between grade III/IV toxicity and the use of a novel agent (p=0.68). When including all non-transplant patients (> 65 years of age), there was a positive correlation between the use of a novel agent and overall survival at one year (Correlation coefficient, CC 0.281, p=0.01). The CC for elderly patients (≥ 75 years of age) was 0.175. The CC in 65–74 year-olds was 0.387. Percentage survival at one year was 59.6 % in patients ≥75 years of age versus 70.6% in those aged 65–74 years. In conclusion, our study shows that very elderly patients (≥75 years of age) with MM, who are considerably ill at baseline with a high or very high CCI and poor PS continue to experience shortened survival despite the use of new agents. However, notwithstanding this, the early use of novel agents has a positive impact on survival at one year, with improved response rates to new therapies, and without an increase in toxicity. Disclosures: Patel: Millennium Pharmaceuticals, Inc: Speakers Bureau; Eli Lilly and Company: Speakers Bureau.

2021 ◽  
Vol 39 (15_suppl) ◽  
pp. 4043-4043
Author(s):  
Hiroo Katsuya ◽  
Koichi Suyama ◽  
Kazuma Kobayashi ◽  
Naoki Izawa ◽  
Yoshikazu Uenosono ◽  
...  

4043 Background: Elderly patients are often intolerable in the combination with cytotoxic agents. Therapy with S-1 alone is a key option for initial chemotherapy for Japanese elderly patients with unresectable gastric cancer in clinical practice. However, there are some cases in which the antitumor effects with S-1 alone are insufficient. We aimed to investigate the efficacy and safety of S-1 plus ramucirumab therapy to elderly patients with advanced/recurrent gastric cancer. Methods: Patients aged 70 years and older with previously untreated unresectable or recurrent gastric cancer patients were included in Japan. They received S-1 therapy (40-60 mg twice daily for 28 days, every 6 weeks) plus ramucirumab therapy (8 mg/kg, every 2 weeks) until disease progression. The primary endpoint was the one-year survival rate and null hypothesis of one-year survival was set as 40%, which is the lower bound of the 95% confidence interval in previously reported studies on S-1 therapy. The secondary endpoints included progression-free survival (PFS), overall survival (OS), response rate (RR), and safety. Results: Between September 2017 and November 2019, 48 patients were enrolled in this study. The characteristics of patients were male/female: 34/14, median age: 77.5 years (range: 71-87), and PS (0/1): 20/28. The one-year survival rate was 65.2% (95% confidence interval 49.8-78.6%), which means this trial met the primary endpoint. The median OS and PFS were 16.4 months (95%CI:12.0–20.7) and 5.8 months (95%CI:4.0–7.2), respectively. The best RR (CR+PR) was 60.9%. The frequent grade 3 or grade 4 adverse events were neutropenia (27.7%), anorexia (23.4%), anemia (19.1%), hypertension (14.9%), leucopenia (12.8%) and hypoalbuminemia (12.8%). Conclusions: Based on the observed efficacy and safety, S-1 plus ramucirumab is an appropriate first-line treatment for elderly patients with advanced/recurrent gastric cancer. Clinical trial information: UMIN000028309.


Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 5315-5315
Author(s):  
Sophia Farooki ◽  
Manjula Maganti ◽  
Donna E Reece ◽  
Esther Masih-Khan ◽  
Victor H Jimenez-Zepeda ◽  
...  

Abstract Translocation (4;14) is identified by FISH cytogenetics in approximately 15% of myeloma patients (pts). Pts with this translocation have a poor outcome characterized by initial response to induction chemotherapy but followed by rapid relapse and resistance to alkylating agents. Recent studies have suggested that novel agents such as bortezomib may improve both event-free survival and overall survival (OS). We reviewed the outcome of 74 consecutive myeloma pts with t(4;14) managed at Princess Margaret Cancer Centre between October 2002 and July 2012. Our goal was to evaluate the impact of specific pts' characteristics on OS and to assess outcome according to treatments received. Clinical characteristics at time of diagnosis for the 74 myeloma pts with t(4;14) are presented in table 1. The average age was 57 years (range 31-82 years) and 58% were male. Pts received a median of 2 lines of therapy (range 1-6). Of the 69 pts requiring treatment, 46% of pts received one year of bortezomib as part of the Canadian t(4;14) clinical trial, 32% of pts were treated with novel agents including bortezomib (given for an average of 4 months) and lenalidomide, 22% of pts received conventional treatment such as dexamethasone alone, thalidomide and/or melphalan. 20 pts underwent autologous stem cell transplantation (ASCT) as part of their first line treatment; 16 were single ASCT, 4 were tandem ASCT. The overall response rate to induction chemotherapy was 70%, with 60% complete response/very good partial response and 10% partial response. The median OS was 5 years and 3 year OS was 66%. Presence of p53 significantly decreased the 3 year OS (71% vs 29% for absence and presence of p53, respectively, log-rank p value=0.0017). Median follow-up was 2.43 years (range: 0.24-11.81 years). There was no significant difference in OS based on the type of first line treatment received. The 3 year OS was 69% for pts enrolled in the t(4;14) clinical trial, 65% for pts who received novel agents and 53% for pts who received conventional treatment (log-rank p value=0.33). In a multivariable analysis looking at pts' initial characteristics, p53 deletion, LDH, bone lesions and age at diagnosis were found to be significant predictors of overall survival while ISS staging and immunoglobulin isotype were not found to be significant for overall survival. In conclusion, in our retrospective single institution study, the median OS for pts with t(4;14) was 5 years. Older age, addition of p53 deletion, high LDH and presence of bone disease predicted a worse OS. Although the lack of significant difference in OS based on the type of first line treatment received may be due to the limited number of pts in our study, there was a trend towards improvement in OS for pts that received a bortezomib containing regimen versus those who received conventional agents. While the median OS for pts with t(4;14) in our study has increased compared to historical controls, new therapeutic options are still needed to further improve the outcome in this subset of pts3. 3 Keats JJ et al. In multiple myeloma, t(4;14)(p16;q32) is an adverse prognostic factor irrespective of FGFR3 expression. Blood. 2003 Feb 15;101(4):1520-9.Table 1Clinical characteristics for the 74 myeloma pts with t(4;14)Clinical characteristicsAverageRange%Hemoglobin (g/L)10051-157Creatinine (μmol/L)13933-796Calcium (mmol/L)2.41.89-3.84B2-microglobulin (mg/L)4.51.58-20.25Albumin (g/L)3518-46ISS stage 145%ISS stage 236%ISS stage 319%Presence of bone lesions68%Mean % of nuclei positive for t(4;14)3%-71.5%25%Presence of del 13q/monosomy 13 by FISH77%Presence of del 17p by FISH10% Disclosures: Reece: Celgene: Honoraria, Research Funding; Jansen: Honoraria, Research Funding; Onyx: Honoraria; Novartis: Honoraria; BMS: Research Funding; Merk: Honoraria, Research Funding; Millennium: Research Funding.


BMC Cancer ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Rafaela Pirolli ◽  
Viviane Teixeira Loiola de Alencar ◽  
Felipe Leonardo Estati ◽  
Adriana Regina Gonçalves Ribeiro ◽  
Daniella Yumi Tsuji Honda ◽  
...  

Abstract Background Benefit of carboplatin and dose-dense weekly paclitaxel (ddCT) in first line treatment of ovarian cancer patients has been different in Western and Asian studies. In the present study we compare progression-free survival (PFS) of ddCT to three-weekly carboplatin and paclitaxel (CT) in first-line treatment of ovarian carcinoma in a single institution in a Western population. Materials and methods We conducted a retrospective review of medical records from patients with ovarian carcinoma treated in a tertiary cancer center from 2007 to 2018. All patients treated with ddCT or CT in the first-line setting were included. Patients who received first-line bevacizumab were not included. PFS and overall survival (OS) were compared in a propensity score-matched cohort to address selection bias. Patients were matched according to age, ECOG performance status, CA 125, FIGO stage, residual disease, and histological subtype, in a 1:2 ratio. Results Five hundred eighty-eight patients were eligible for propensity score matching, the final cohort consisted of 69 patients treated with ddCT and 138 CT group. Baseline characteristics were well-balanced. After a median follow-up of 65.1 months, median PFS was 29.3 vs 20.0 months, favouring ddCT treatment (p = 0.035). In the multivariate cox regression ddCT showed a 18% lower risk of progression (HR 0.82, 95% CI 0.68–0.99, p = 0.04). Overall survival data is immature, but suggested better outcomes for ddCT (not reached versus 78.8 months; p = 0.07). Conclusion Our retrospective study has shown superior PFS of ddCT over CT regimen in first-line treatment of ovarian carcinoma in a Western population not treated with bevacizumab.


2010 ◽  
Vol 102 (10) ◽  
pp. 1468-1473 ◽  
Author(s):  
J Feliu ◽  
M J Safont ◽  
A Salud ◽  
F Losa ◽  
C García-Girón ◽  
...  

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