Long Survival Confirmed in CML Patients Who Respond to Interferon

News
Article
Oncology NEWS InternationalOncology NEWS International Vol 11 No 2
Volume 11
Issue 2

ORLANDO-Patients with chronic myelogenous leukemia (CML) who have a complete cytogenetic response (CCgR) to interferon-alfa have a long survival, and low-risk patients have a projected 10-year survival of more than 80%, Francesca

ORLANDO—Patients with chronic myelogenous leukemia (CML) who have a complete cytogenetic response (CCgR) to interferon-alfa have a long survival, and low-risk patients have a projected 10-year survival of more than 80%, Francesca Bonifazi, MD, reported at the 43rd Annual Meeting of the American Society of Hematology (ASH abstract 1466).

Dr. Bonafazi, of Bologna University, Italy, presented data compiled in nine European countries by the European Study Group on Interferon-alfa in CML.

This study included 317 patients with Philadelphia chromosome-positive CML who had a CCgR after treatment with interferon-alfa alone. The median time to complete hematologic response was 2 to 7 months in the patients as a whole, and the median time to first CCgR was 19 months (range, 3 to 84 months).

At last contact, 212 patients (68%) were still in first continuous CCgR. The remaining 105 patients had lost CCgR, but 53% were still alive and in chronic phase. Ten-year survival from first CCgR was 72% for the group as a whole and was much higher for low-risk patients (89% for Sokal’s low risk and 81% for the IFN score low risk), Dr. Bonifazi said.

Interferon-alfa was discontinued in 23 patients for response loss, in 36 for chronic toxicity, and in 8 because they were in stable CCgR for more than 5 years. Dr. Bonifazi reported that 15 of the 36 cases discontinued for toxicity and 7 of the 8 discontinued after response of more than 5 years were still in unmaintained CCgR for 2 to 5 years after discontinuation of treatment.

Recent Videos
Experts at Yale Cancer Center highlight ongoing trials intended to improve outcomes across mantle cell lymphoma, T-cell lymphoma, and other populations.
Yale’s COPPER Center aims to address disparities and out-of-pocket costs for patients, thereby improving the delivery of complex cancer treatment.
Non-Hodgkin lymphoma and other indolent forms of disease may require sequencing new treatments for years or decades, said Scott Huntington, MD, MPH, MSc.
Fixed-duration therapy may be more suitable for younger patients, while continuous therapy may benefit those who are older with more comorbidities.
A new clinical trial aims to offer a novel allogenic CAR T-cell product for patients with lymphoma closer to home.
Determining the molecular characteristics of one’s disease may influence the therapy employed in the first line as well as subsequent settings.
Modification of REMS programs may help patients travel back to community practices sooner, according to Suman Kambhampati, MD.
Related Content