Can I clear the patient for chemotherapy given a left‑ventricular ejection fraction of 41% (up from 40%) but a global longitudinal strain of –16% (below normal)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: February 19, 2026View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Can You Clear This Patient for Chemotherapy?

You should NOT clear this patient for chemotherapy based on the abnormal GLS of -16% despite the minimal EF improvement from 40% to 41%. The patient requires cardiology consultation, initiation of cardioprotective therapy, and reassessment before proceeding with further chemotherapy.

Critical Decision Points

Why This Patient Cannot Be Cleared

The LVEF of 41% falls into a high-risk zone where chemotherapy continuation requires careful consideration. 1 Specifically:

  • For anthracycline-based regimens: chemotherapy should be withheld when LVEF falls below 45% 1
  • For trastuzumab (anti-HER2 therapy): treatment should be stopped when LVEF drops below 40% 1

The minimal improvement from 40% to 41% represents essentially no meaningful change and does not indicate cardiac recovery.

The GLS Finding is Particularly Concerning

A GLS of -16% is definitively abnormal and indicates subclinical myocardial dysfunction. 2 The normal range for GLS is -18% or lower (more negative), with -16% to -18% being borderline and -16% or higher (less negative) being abnormal. 2

The American College of Cardiology recommends starting beta-blockers or ACE inhibitors when GLS shows >15% drop from baseline or becomes abnormal. 1 This abnormal GLS value, combined with the borderline-low LVEF, represents significant cardiac dysfunction requiring intervention.

Required Actions Before Chemotherapy Continuation

Immediate Steps

  1. Repeat echocardiography in 3 weeks to confirm the LVEF and GLS findings 1

  2. Initiate cardioprotective therapy immediately:

    • Start ACE inhibitor (such as enalapril) 1
    • Consider adding beta-blocker 1
    • Early initiation within 2 months is critical for optimal cardiac recovery 1
  3. Refer to cardiology for co-management 1, 3

  4. Check cardiac biomarkers (troponin I or BNP) 1, 4

Reassessment Protocol

After 3 weeks of cardioprotective therapy, repeat echocardiography: 1

  • If LVEF improves to ≥45% (for anthracyclines) or ≥40% (for trastuzumab) AND GLS improves: Consider resuming chemotherapy with close monitoring 1

  • If LVEF remains <45% (anthracyclines) or <40% (trastuzumab): Discuss alternative non-cardiotoxic chemotherapy regimens with oncology 1

  • If LVEF deteriorates further or patient develops symptoms: Stop cardiotoxic chemotherapy permanently and treat as heart failure 1

Type of Chemotherapy Matters

For Anthracycline-Based Regimens

Withhold anthracyclines when LVEF <45%. 1 Your patient's LVEF of 41% is below this threshold. If anthracyclines are essential, consider:

  • Liposomal doxorubicin formulations (less cardiotoxic) 1
  • Dexrazoxane as cardioprotectant 1, 3
  • Dose reduction or continuous infusion rather than bolus 1

For Trastuzumab (HER2-Targeted Therapy)

Trastuzumab should be stopped when LVEF drops to <40%. 1 At 41%, this patient is just above the stopping threshold, but the abnormal GLS indicates ongoing myocardial injury.

If trastuzumab must continue, the patient can be observed with LVEF ≥40% if asymptomatic, but requires: 1

  • ACE inhibitor initiation 1
  • Repeat monitoring in 6-8 weeks 1
  • Immediate cessation if LVEF drops below 40% 1

Ongoing Monitoring Requirements

If chemotherapy is resumed after cardiac optimization:

  • Repeat echocardiography every 3 months during treatment 1, 4, 5
  • Monitor cardiac biomarkers every 3-6 weeks 4, 5
  • Increased vigilance for patients ≥60 years old 1, 4
  • Follow-up echocardiography at 3,6, and 12 months after completion of therapy 4, 3

Common Pitfalls to Avoid

Do not dismiss the abnormal GLS simply because LVEF is "borderline normal." GLS is more sensitive than LVEF for detecting early cardiotoxicity and predicts future cardiac events and LVEF deterioration. 2, 6, 7, 8, 9

Do not delay cardioprotective therapy. The likelihood of cardiac recovery is highest when ACE inhibitors and beta-blockers are started within 2 months of detecting dysfunction. 1

Do not continue cardiotoxic chemotherapy as the sole priority. Withholding chemotherapy should be considered only as a last resort, but in this case with LVEF 41% and abnormal GLS, the cardiac risk is substantial and requires intervention before proceeding. 1

Related Questions

Is a global longitudinal strain (GLS) of -18 considered normal in a patient with no symptoms or underlying medical conditions?
What is the management plan for a patient with mild concentric left ventricular hypertrophy, normal left ventricular systolic function, and mildly reduced Global Longitudinal Strain?
What is the management plan for a patient with abnormal left ventricular (LV) strain of -15%?
What does a global longitudinal strain (GLS) result of -16.2% indicate and how should it be managed?
What is global longitudinal strain (GLS) on an echocardiogram (echo)?
What are the differential diagnoses for a 74‑year‑old man with a two‑month history of bilateral pectoralis tendon pain that worsens with movement, is unresponsive to upper thoracic steroid injection, is on high‑dose opioids, and has a history of colon cancer in remission?
Is it safe to use Alenia (budesonide/formoterol) as maintenance therapy and salbutamol (albuterol) only as a rescue inhaler?
What are the causes of hypokalemia in a patient with an enterovesical fistula and a newly identified colonic lesion?
When is a thyroid storm considered refractory in a patient who remains clinically unstable after 24–48 hours of optimal therapy?
In anemic patients (hemoglobin <12 g/dL), what ferritin and transferrin saturation thresholds indicate the need for intravenous iron in cancer patients versus non‑cancer patients, and what are the recommended dosing regimens?
What is the complete management, with dosage details, for an adult patient with systemic inflammatory response syndrome (SIRS) in the medical intensive care unit (MICU)?

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.