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Response of chemotherapy with cisplatin and etoposide versus cisplatin and paclitaxel in advanced non-small cell lung cancer patient

Response of chemotherapy with cisplatin and etoposide versus cisplatin and paclitaxel in advanced non-small cell lung cancer patient

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20181011005
Enrollment
Unknown
Registered
2018-10-11
Start date
2017-01-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced non small cell lung cancer NSCLC Cisplatin Etoposide Paclitaxel

Interventions

Inj. Cisplatin 75 mg/m2 IV Day 1 and Inj. Etoposide 120 mg/m2 IV Day 1 to Day 3
three week regimen,Inj. Paclitaxel 135 mg/m2 IV Day 1 and Inj. Cisplatin 75 mg/m2 IV Day 2
three week regimen
Experimental Drug,Experimental Drug
Arm A&#45
Cisplatin and Etoposide,Arm B&#45

Sponsors

Dr. Munshi Md. Arif Hosen
Lead Sponsor
BSMMU&#44
Collaborator
Shahbag&#44
Collaborator
Dhaka&#44
Collaborator
Bangladesh
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients with histology confirmed advanced NSCLC - stage IIIB and stage IV includes liver metastasis, metastasis to opposite lung and pleural effusion

Exclusion criteria

Exclusion criteria: •Patients with other than non-small cell lung cancer. •Poor performance status: ECOG score >2. •Those who were not willing. •Age below 18 years and above 70 years. •Patients with history of prior chemotherapy or radiotherapy to the chest. •Initial surgery (excluding diagnostic biopsy) of the primary site. •Patients with double primaries. •Pregnant or lactating woman. •Patient dropped out or lost to follow up before completion of study. •Serious concomitant medical illness including severe cardiac disease, uncontrolled diabetes mellitus, hypertension or renal diseases. •Prisoners.

Design outcomes

Primary

MeasureTime frame
Response 1 year clinical and radiological

Secondary

MeasureTime frame
Toxicity 1 year Clinical and Biochemical

Countries

Bangladesh

Contacts

Public ContactMunshi Md. Hosen

BSMMU, Shahbag, Dhaka

dr.arif43@gmail.com+8801717783198

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026