Malignant Pleural Mesothelioma
Conditions
Keywords
MPM
Brief summary
The prognosis of mesothelioma is generally poor. The median survival of patients with unresectable malignant mesothelioma ranges approximately between 6-12 months. Survival is poor because there is no curative treatment. Treatment options include surgery, chemotherapy and radiotherapy. Recently multimodality treatment regimens have been reported to prolong survival. Other new therapeutic approaches include immunotherapy, gene therapy, hyperthermic chemoperfusion of the pleura and photodynamic therapy, but the results have not yet been completely validated. Even with the introduction of this new therapeutic protocol, the response does not exceed 41%, with a mean survival of 12 months. The current standard of care for unresectable malignant pleural mesothelioma is pemetrexed/cisplatin. This regimen was compared to cisplatin alone in a study including 448 patients from 19 countries which was the largest trial to date among patients suffering from malignant mesothelioma. Results showed statistically significant increase in overall survival by about 30 % (12.1 months for pemetrexed /cisplatin versus 9.3 months for cisplatin alone. In addition, there was an improvement in lung function (forced vital capacity) in the pemetrexed /cisplatin arm in comparison to the cisplatin arm. Until now, however, there is no consensus on the number of cycles of pemetrexed/cisplatin in malignant mesothelioma and there are no approved predictive markers for response. Pemetrexed/cisplatin regimen is an expensive regimen and associated with considerable toxicity and so we need to rationalize its use in our Egyptian patients. Therefore, the investigators aim in this work to compare 4 cycles versus 6 cycles of pemetrexed/cisplatin in malignant mesothelioma and to identify a predictive marker for response.
Interventions
DRUGpemetrexed/platinum chemotherapy
Four cycles of pemetrexed/platinum chemotherapy
DRUGPemetrexed/platinum chemotherapy
Six cycles of pemetrexed/platinum chemotherapy
Sponsors
Ain Shams University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Histologic or cytologic diagnosis of malignant pleural Mesothelioma 2. No prior chemotherapy. 3. ECOG less than or equal to 2 . 4. Measurable disease according to the requirements of SWOG criteria. 5. Age ≥ 18 years . 6. Estimated life expectancy of at least 12 weeks . 7. Adequate bone marrow reserve (white blood cells \[WBC\] ≥ 3.5 × 109 /L, neutrophils ≥ 1.5 × 109 /L, platelets ≥ 100 × 109 /L, and hemoglobin ≥ 9.0 gm/dL).
Exclusion criteria
1. Presence of central nervous system metastases. 2. Inadequate liver function (bilirubin \> 1.5 times upper normal limit \[UNL\] and alanine transaminase \[ALT\] or aspartate transaminase \[AST\] \> 3.0 UNL or up to 5.0 UNL in the presence of hepatic metastases). 3. Inadequate renal function (creatinine \> 1.25 times UNL, creatinine clearance \< 50mL/min). 4. Serious concomitant systemic disorder incompatible with the study. 5. Second primary malignancy (except in situ carcinoma of the cervix, adequately treated basal cell carcinoma of the skin, T1 vocal cord cancer in remission, or prior malignancy treated more than 5 years prior to enrollment without recurrence). 6. Pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Progression free survival | one year |
Secondary
| Measure | Time frame |
|---|---|
| Overall survival | 3 years |
Countries
Egypt
Contacts
Primary ContactOmar Abdel-Rahman, MD
Outcome results
None listed