Treatment completion and toxicity of trastuzumab or trastuzumab + lapatinib in older patients (pts): BIG 2-06; NCCTG N063D (Alliance).

Authors

null

Noam Falbel Ponde

AC Camargo Cancer Center, São Paulo, Brazil

Noam Falbel Ponde , Dominique Agbor-Tarh , Lissandra Dal Lago , Larissa A. Korde , Florentine Hilbers , Christian Jackisch , Olena Werner , Richard D. Gelber , Aminah Jatoi , Amylou C. Dueck , Alvaro Moreno-Aspitia , Christos Sotiriou , Evandro de Azambuja , Martine Piccart

Organizations

AC Camargo Cancer Center, São Paulo, Brazil, Frontier Science Scotland (FSS), Kincraig, United Kingdom, UFSM, Santa Maria, Brazil, Head, Breast Cancer Therapeutics, Clinical Investigations Branch, National Cancer Institute, Bethesda, MD, Breast International Group, Brussels, Belgium, Sana Klinikum, Offenbach, Germany, Novartis, Basel-City, Switzerland, Dana-Farber Cancer Institute, Harvard Medical School, Harvard TH Chan School of Public Health, and Frontier Science and Technology Research Foundation, Boston, MA, Mayo Clinic, Rochester, MN, Mayo Clinic, Scottsdale, AZ, Mayo Clinic, Jacksonville, FL, Institut Jules Bordet, Brussels, Belgium

Research Funding

Other Foundation

Background: Little is known about the toxicity of trastuzumab (T) or of trastuzumab + lapatinib (T + L), approved in the advanced setting, in older pts. We have performed a sub-analysis of the Adjuvant Lapatinib and/or Trastuzumab Treatment Optimisation (ALTTO) trial focused on treatment completion and toxicity of T and T+L in older pts (aged ≥65 years (yr)). Methods: The ALTTO trial (NCT00490139, NCCTG N063D) randomised 8381 pts with early HER2+ BC into 4 arms and we included the T and T+L arms in our analysis. Eligible pts for our study were those having received at least one dose of assigned treatment. Treatment completion was evaluated through the rate of temporary treatment interruptions (TTI), permanent treatment discontinuations (PTD) and lapatinib dose reductions (LDR). Toxicity was evaluated via a selected set of adverse events of interest (AEIs). Risk factors for TTI, PTD, LDR and AEIs were assessed, including comorbidities and polypharmacy at baseline (defined as use 5 or more co-medications) and AEIs during treatment. Results: A total of 430 pts≥65-year-old were identified for this sub-analysis, out of a total of 4190 pts with a median age of 68 yrs (range 65-80). Older pts were more likely to have comorbidities (70% vs 38%). Treatment completion was worse among older pts in the T+L arm but not in the T arm (Table). AEIs were more common in the T+L arm in all patients, with older patients having higher AEI rates (78.04% in older vs 63.38% in younger), particularly diarrhea (60.75% vs 38.0%). Identified risk factors (multivariate) for worse treatment completion in the T and T+ L arms included concomitant use of chemotherapy and the occurrence of grade 3 adverse events, among others. Conclusions: T + L has worse treatment completion and is more toxic in older patients, while T was well tolerated. Identifiable risk factors at baseline and during the course of treatment could be used to aid in regimen selection and management for both T and T + L in their respective indications. Support: UG1CA189823, Novartis;https://acknowledgments.alliancefound.org.

T
T + L
< 65 years
Events
(% of N)
>= 65 years
Events
(% of N)
Multivariate* OR (95%CI)< 65 years
Events
(% of N)
>= 65 years
Events
(% of N)
Multivariate* OR (95%CI)
PTD300 (15.95)44 (20.37)1.33
(0.93 to 1.91)
P= 0.122
625 (33.26)115 (53.74)2.08
(1.55 to 2.79)
P<0.001
TTI573 (30.46)75 (34.72)1.09
(0.80 to 1.48)
p= 0.602
1176 (62.59)162 (75.70)1.72
(1.23 to 2.42) p=0.002

*Multivariate analysis includes comorbidity, polypharmacy, type and timing of chemotherapy.

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Abstract Details

Meeting

2019 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Symptoms and Survivorship

Track

Symptom Science and Palliative Care

Sub Track

Geriatric Models of Care

Citation

J Clin Oncol 37, 2019 (suppl; abstr 11553)

DOI

10.1200/JCO.2019.37.15_suppl.11553

Abstract #

11553

Poster Bd #

245

Abstract Disclosures

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