Literature DB >> 9667248

Quality-of-life-adjusted survival analysis of interferon alfa-2b treatment for advanced follicular lymphoma: an aid to clinical decision making.

B F Cole1, P Solal-Céligny, R D Gelber, E Lepage, C Gisselbrecht, F Reyes, C Sebban, D Sugano, C Tendler, A Goldhirsch.   

Abstract

PURPOSE: To evaluate the trade-off of toxicity versus improved clinical outcome with interferon alfa-2b (IFN) administered concomitantly with a doxorubicin-containing regimen for the treatment of advanced follicular lymphoma. PATIENTS AND METHODS: A quality-of-life-adjusted survival analysis (Quality-Adjusted Time Without Symptoms or Toxicity [Q-TWiST]) was applied to the Groupe d'Etude des Lymphomes Folliculaires (GELF) trial 86, which compared a regimen of cyclophosphamide, doxorubicin, teniposide, and prednisone (CHVP) versus CHVP plus IFN in 242 patients with confirmed follicular lymphoma. CHVP was administered monthly for 6 months then every other month for 12 months. The IFN dosage was 5 x 10(6) U three times weekly for 18 months.
RESULTS: After a median follow-up duration of 72 months, the IFN group gained a mean of 12.3 months of progression-free survival (PFS) and 7.4 months of overall survival (OS), but also experienced additional time with grade 3 or worse toxicity compared with the CHVP group. Sensitivity analysis demonstrated that CHVP plus IFN provided a greater amount of quality-adjusted survival regardless of the relative quality-of-life valuations placed on time with toxicity due to CVHP alone, time with toxicity due to CHVP plus IFN, and time following disease progression. This gain was significant (P < .05) in all cases except for patients who consider time with toxicity to have a low relative value and time following disease progression to have a high relative value.
CONCLUSION: In patients with advanced follicular lymphoma, the clinical benefits of concomitant IFN can significantly offset the associated grade 3 or worse toxic effects. The magnitude of this clinical benefit depends on an individual patient's relative quality-of-life valuations for time with toxicity and time following disease progression.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9667248     DOI: 10.1200/JCO.1998.16.7.2339

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  5 in total

1.  Quality-adjusted survival of nivolumab plus ipilimumab or nivolumab alone versus ipilimumab alone among treatment-naive patients with advanced melanoma: a quality-adjusted time without symptoms or toxicity (Q-TWiST) analysis.

Authors:  David F McDermott; Ruchit Shah; Komal Gupte-Singh; Javier Sabater; Linlin Luo; Marc Botteman; Sumati Rao; Meredith M Regan; Michael Atkins
Journal:  Qual Life Res       Date:  2018-09-06       Impact factor: 4.147

2.  Evaluating high dose therapy in Multiple Myeloma: use of quality-adjusted survival analysis.

Authors:  R Porcher; V Lévy; J P Fermand; S Katsahian; S Chevret; Ph Ravaud
Journal:  Qual Life Res       Date:  2002-03       Impact factor: 4.147

Review 3.  Analyzing oncology clinical trial data using the Q-TWiST method: clinical importance and sources for health state preference data.

Authors:  Dennis A Revicki; David Feeny; Timothy L Hunt; Bernard F Cole
Journal:  Qual Life Res       Date:  2006-04       Impact factor: 4.147

4.  A quality-adjusted survival analysis (Q-TWiST) of rituximab plus CVP vs CVP alone in first-line treatment of advanced follicular non-Hodgkin's lymphoma.

Authors:  R Marcus; R Aultman; F Jost
Journal:  Br J Cancer       Date:  2009-11-17       Impact factor: 7.640

5.  A quality-adjusted survival time without symptoms or toxicities analysis of glasdegib plus low-dose cytarabine versus low-dose cytarabine as initial therapy for acute myeloid leukemia in patients who are not considered candidates for intensive chemotherapy.

Authors:  Caitlyn T Solem; Timothy J Bell; Youngmin Kwon; Joseph C Cappelleri; Courtney Johnson; Helen Bhattacharyya; Caroline J Hoang; Jorge E Cortes
Journal:  Cancer       Date:  2020-07-22       Impact factor: 6.860

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.