Patient Maintenance Plan
The recommended maintenance plan depends entirely on the underlying disease being treated—maintenance therapy is disease-specific and cannot be generalized across conditions.
Disease-Specific Maintenance Strategies
For Non-Small Cell Lung Cancer (NSCLC)
Maintenance therapy should be offered only to patients with performance status (PS) 0-1 after first-line chemotherapy. 1
Non-Squamous Histology
- Pemetrexed switch maintenance is recommended following four cycles of platinum-based chemotherapy, demonstrating improvements in both progression-free survival (PFS) and overall survival (OS) 1
- Continuing pemetrexed following cisplatin plus pemetrexed first-line therapy is the preferred approach 1
- Bevacizumab continuation maintenance may be continued beyond 4-6 cycles until disease progression or unacceptable toxicity in eligible patients 1
- Erlotinib switch maintenance demonstrates PFS and OS benefit across all histologies, with greatest benefit in patients with stable disease after first-line treatment 1
Squamous Histology
- Cetuximab continuation maintenance may be continued beyond 4-6 cycles following cisplatin, vinorelbine, and cetuximab therapy 1
- Erlotinib switch maintenance is an option for patients with unknown EGFR status or EGFR wild-type 1
Key Decision Factors
- Histology type (squamous vs. non-squamous) 1
- Response to platinum-doublet chemotherapy 1
- Remaining toxicity after first-line chemotherapy 1
- Performance status 1
- Patient preference 1
Common Pitfall: Four cycles of chemotherapy are recommended for most patients, with a maximum of six cycles—continuation beyond this requires specific maintenance agents, not continuation of cytotoxic doublet chemotherapy 1
For Acute Lymphoblastic Leukemia (ALL)
Maintenance therapy is strongly recommended in all patients—attempts to omit maintenance have resulted in inferior outcomes. 1
Standard Maintenance Regimen
- Mercaptopurine (MP) and methotrexate (MTX) are the main drugs in maintenance therapy 1
- Total treatment duration of 2 to 2.5 years including maintenance is recommended 1
- Intermittent intrathecal (IT) prophylaxis is part of most regimens 1
What NOT to Include
- Maintenance without vincristine or steroid pulses is preferred by most groups—the benefit of these additions is debated and dexamethasone may increase infection-related deaths 1
Monitoring During Maintenance
- MRD testing intervals of approximately 3 months are suggested during maintenance 1
- Long-term drug exposure is necessary to eradicate minimal residual disease (MRD) 1
For Ovarian Cancer
Maintenance therapy selection depends on BRCA/HRD status, prior treatments, and response to platinum-based chemotherapy. 1
BRCA Wild-Type or Unknown, No Prior PARPi or Bevacizumab
- PARPi maintenance (after CR/PR/NED) or bevacizumab are both recommended options 1
- Bevacizumab added to chemotherapy followed by maintenance should be prioritized for patients needing rapid symptom control 1
Prior Bevacizumab, No Prior PARPi
- Platinum-based chemotherapy followed by PARPi maintenance is preferred as long as CR/PR/NED is achieved, regardless of BRCA/HRD status 1
Prior PARPi, No Prior Bevacizumab
- Platinum-based combination with bevacizumab followed by maintenance is recommended 1
- Carboplatin-pegylated liposomal doxorubicin (PLD) is the preferred chemotherapy partner for bevacizumab in recurrent setting 1
Duration
- PARPi maintenance should continue until progressive disease or unacceptable toxicity 1
For Autoimmune Hepatitis (AIH)
Long-term azathioprine 2 mg/kg/day is recommended as maintenance therapy after achieving remission. 1
After First Remission
- Continuing azathioprine long-term is recommended in younger patients, those with predictors of relapse (LKM- and SLA-positive), those with cirrhosis or decompensation, and those with observed or anticipated prednisolone-related side effects 1
- After treatment of one relapse, continuation of azathioprine 2 mg/kg/day as long-term maintenance therapy is recommended 1
Alternative Approach
- Treatment withdrawal with monitoring may be considered in select patients: those without cirrhosis, without features associated with relapse, with good tolerance of initial prednisolone, with potential precipitant of initial episode, or with history of malignancy 1
Monitoring
- Monitoring should be lifelong regardless of strategy pursued 1
For Tuberculosis
Directly observed therapy (DOT) is the preferred core management strategy for all patients with tuberculosis. 1
DOT Implementation
- DOT involves providing antituberculosis drugs directly to the patient and watching as they swallow the medications 1
- A patient-centered approach with tailored treatment plans is essential, with the patient as an active participant 1
- A specific case manager should be assigned individual responsibility for assuring treatment completion 1
Promoting Adherence
- Identify and address barriers including cultural/linguistic barriers, homelessness, substance abuse, and competing priorities 1
- Use the least restrictive measures likely to achieve success, ranging from monthly outpatient monitoring to legally mandated hospitalization if needed 1
General Principles for Medication Adherence
Successful long-term maintenance requires combinations of interventions—no single approach is sufficient. 2, 3
Evidence-Based Adherence Strategies
- Clinical pharmacist consultation for chronic disease co-management (maximum observed absolute improvement in adherence: 15%) 3
- Medication-taking reminders such as telephone calls to prompt refills (maximum observed absolute improvement: 33%) 3
- Using combination pills to reduce daily pill burden (maximum observed absolute improvement: 10%) 3
- Recurrent and personalized telephone counseling sessions with health educators 3
Key Components
- Clear information about the regimen 2
- Counseling about importance of adherence and how to organize medication taking 2
- Reminders about appointments and adherence 2
- Rewards and recognition for patient efforts 2
- Enlisting social support from family and friends 2
Common Pitfall: Typical adherence rates are only about 50% for medications—simply prescribing maintenance therapy without implementing adherence strategies will result in treatment failure 2