Effect of Age on Treatment Decision-Making in Elderly Patients With Acute Myeloid Leukemia

NCT02844218 | Completed

• 1 other identifier: 69HCL16_0463
• Study Type: observational
• Target: 183
• Locations: 1 country
• Sites: 1

Brief Summary

Patients aged ≥70 years with acute myeloid leukemia (AML) have a poorer prognosis than those aged 60 to 69 years. The poor outcome is the result of treatment-related toxicity in elderly patients, owing to comorbidities, the greater possibility of other hematopoietic disorders, and a biologically poor risk prognosis. Anthracycline- and cytarabine-based therapy, administered for 3 and 7 days respectively (3 +7), remains the standard induction therapy for this patient population. This approach improved survival compared with supportive care (median, 5 vs. 3 months) for adults aged ≥ 65 years. However, the overall view has been that the results of intensive chemotherapy in elderly patients remain poor. Although complete remission (CR) rates of 40% to 80% can be achieved in highly selected populations, long-term survival has been poor. Furthermore, most clinical trials have only enrolled patients with an adequate performance status (PS). Prognostic models have been developed from clinical trial data to predict the outcomes for older patients. However; each model relies on chronologic age. Age is a surrogate measure for both changes in tumor biology and patient characteristics. Understanding which patients are likely to benefit from intensive therapies versus low-intensity therapies or supportive care is critical. The definition of "fit" to undergo intensive induction therapy has not been established, and the therapeutic choice is mainly determined by physician and patient decision. In older patients, low-dose cytarabine (LD-AraC) has been demonstrated to be more beneficial than best supportive care and hydroxyurea. The recent availability of new drugs that could have an improved side effect profile and, in some cases, bioavailability might offer future improvement for this patient population. In this setting, the investigators have tended to consider, since 2007, patients aged ≥70 years as potential candidates for alternative lower intensity therapy (LD-AraC, hypomethylating agents) even when they presented in good physical condition. The investigators goal was to determine whether age ≥ 70 years could represent a useful and simple cut off for treatment decision-making in clinical practice and whether low-intensity therapy could be an alternative therapeutic approach to intensive chemotherapy even for patients aged ≥ 70 years who were theoretically "fit" (WHO /ECOG/ PS of ≤ 2).

Conditions

Acute Myeloid Leukemia

Keywords

Acute myeloid leukemia; Chemotherapy; Low-intensity therapy; Older patients; Prognosis; Supportive care

Outcome Measures

Primary Outcomes (1)

• Overall survival (OS)

  OS was the main endpoint for this analysis. The event for OS was death, and patients were censored at the date of last contact, if alive.

  Date of last contact if alive (up to 11 months)

Secondary Outcomes (2)

• Complete remission rate (CR)

  Date of last contact if alive or death (up to 11 months)

• First Relapse

  Duration of the study (11 months)

Study Arms (3)

Intensive chemotherapy group

Group 1: Patients' age ≥ 70 years treated from 1985 to 1999 with intensive induction chemotherapy.

Other: Age of patient

Lower intensity treatment group

Group 2: patients treated from 2000 to 2006 with intensive chemotherapy plus improved supportive care and a follow-up protocol systematically performed at the university hospital.

Other: Age of patient

personalized treatment group

Group 3: patients who had received, starting in 2007, more "personalized" treatment with either intensive chemotherapy or lower-intensity therapy determined by the clinical judgment of the treating physician.

Other: Age of patient

Interventions

Age of patient OTHER

* Historical Comparison Between Patients Aged 60 to 69 and Patients Aged ≥ 70 Years Treated With Intensive Chemotherapy. * Comparison between Intensive Chemotherapy and Low-Intensity Treatments in Patients Aged ≥70 Years. * Improvement of Treatments Over Time * Overall Survival (OS) of patients aged ≥ 70 Years during3 study periods. Period 1, from 1985 to 1999, during which all patients with acute Myeloid Leukemia received an intensive chemotherapy regimen at the University Hospital. Period 2, from 2000 to 2006, during which all patients received an Intensive Chemotherapy regimen, Improved Supportive Care and follow-Up protocol at the University Hospital. Period 3, From 2007 to 2014, during Which patients received Improved Supportive Care and follow-up protocol at the University Hospital and "Personalized" Therapy (Intensive Chemotherapy or Low-Dose Intensity Treatment)

Intensive chemotherapy group; Lower intensity treatment group; personalized treatment group

Eligibility Criteria

• Age: 70 Years - 79 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Acute myeloid leukemia (AML)

You may qualify if:

• Are at least 70 years of age
• Have a diagnosis of AML according to World Health Organization (WHO) classification
• Provide signed, written informed consent

You may not qualify if:

• Patients with acute promyelocytic leukemia
• Have an ECOG score ≥2

Sponsors & Collaborators

• Hospices Civils de Lyon: lead

Study Sites (1)

Hospices Civils de Lyon - Centre Hospitalier Lyon Sud, 165 Chemin du Grand Revoyet

Pierre-Bénite, 69310, France

Location

MeSH Terms

Conditions

Leukemia, Myeloid, Acute

Condition Hierarchy (Ancestors)

Leukemia, Myeloid; Leukemia; Neoplasms by Histologic Type; Neoplasms; Hematologic Diseases; Hemic and Lymphatic Diseases

Study Officials

• Xavier THOMAS, MD-PhD

  Hospices Civils de Lyon - Centre Hospitalier Lyon Sud

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: RETROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: July 20, 2016
• First Posted: July 26, 2016
• Study Start: January 1, 2014
• Primary Completion: December 1, 2014
• Study Completion: February 1, 2015
• Last Updated: July 26, 2016

Record last verified: 2016-07

Locations

FR (1)