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
Developing odronextamab combinations following CAR T-cell therapy failure may help elicit responses in patients with diffuse large B-cell lymphoma.
Cytokine release syndrome was primarily low or intermediate in severity, with no grade 5 instances reported among those with diffuse large B-cell lymphoma.
Safety results from a phase 2 trial show that most toxicities with durvalumab treatment were manageable and low or intermediate in severity.
Investigators are currently evaluating mosunetuzumab in relapsed disease or comparing it with rituximab in treatment-naïve follicular lymphoma.
Compared with second-generation tyrosine kinase inhibitors, asciminib was better tolerated in patients with chronic myeloid leukemia.
Bulkiness of disease did not appear to impact PFS outcomes with ibrutinib plus venetoclax in the phase 2 CAPTIVATE study.
Greater direct access to academic oncologists may help address challenges associated with a lack of CAR T education in the community setting.
Certain bridging therapies and abundant steroid use may complicate the T-cell collection process during CAR T therapy.
Educating community practices on CAR T referral and sequencing treatment strategies may help increase CAR T utilization.
Harmonizing protocols across the health care system may bolster the feasibility of giving bispecifics to those with lymphoma in a community setting.
Related Content