Skip to content

Improving Performance status of Advanced lung cancer patients with Chemotherapy

The feasibility of weekly paclitaxel in improving performance status of advanced NSCLC patients with poor performance status: A single arm phase two trial - ImPACt

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/01/022617
Enrollment
125
Registered
2020-01-06
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: C349- Malignant neoplasm of unspecifiedpart of bronchus or lung

Interventions

Intervention1: Part 1: weekly paclitaxel,best suportive care Part 2 ( for eligible patients): paclitaxel and carboplatin,best supportive care: Part 1: weekly Paclitaxel (60mg/m2 per dose) in 250ml NS

Sponsors

All India Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Cytologically/pathologically confirmed NSCLC either stage 4 disease or those stage IIIC not amenable to definitive chemoradiation. (AJCC 8th) 2.ECOG Performance status more than or equal to 2 ECOG with: i. Charlson comorbidity index of less than 9 ii. Comorbidities, if any, should be controlled. iii. Serum albumin more than or equal to 3.5g/dl iv. Acceptable renal and liver function, v. eGFR of more than or equal to 30ml/min, vi. LFT with Bilirubin less than 2 times ULN and transaminases less than 3 times ULN vii. Adequate bone marrow function:Hb of more than or equal to 8g/dl,Platelet count of more than or equal to 1,00,000/mm3,ANC of more than or equal to 1500/mm3 3.Able to understand the PIS (patient information sheet) and give informed consent

Exclusion criteria

Exclusion criteria: 1.Active malignancy other than NSCLC 2.Lactating and pregnant woman 3.HIV positive patients 4.Driver mutation positive: EGFR/ALK/ROS1 (Patients who have unknown or awaited status of these driver mutations will be eligible, however, if during the study, they are found to harbour these mutations, they will be out of the study.) 5.Symptomatic untreated brain metastasis. (Asymptomatic incidentally detected brain metastasis and treated brain metastasis will not be excluded.)

Design outcomes

Primary

MeasureTime frame
Proportion of patients with improvement in ECOG performance status score by at least one point.Timepoint: At four weeks from start of treatment.

Secondary

MeasureTime frame
For part 2 of study: Overall Response rate (ORR) at 12 weeks Progression free survival (PFS) rate at 6 monthsTimepoint: ORR at 12 weeks PFS rate at 6 months;Quality of life with LC13 and EORTC QLQ C30Timepoint: 0 weeks,4 weeks, and for selected patients, at 12 weeks.

Countries

India

Contacts

Public ContactDr Neha Pathak

DR. B.R.A.I.R.C.H, A.I.I.M.S

drneha1pathak@gmail.com9560229392

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 12, 2026