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PAXUS PM Refreshing Quiz

Total questions: 10

Worksheet time: 10mins

Name
Class
Date
1.

PAXUS PM is well known as novel nanotechnology non cremophor paclitaxel formulation, and PM stands for

a)

Product Material from biological component of human albumin

b)

Polimeric Micelle from non biologic and biodegradable stuff

c)

Proof material from high temperature and humidity

d)

Protective matter from high acidity and unstable temperature

2.

Choose the correct technology to produce paclitaxel of PAXUS PM

a)

Semi synthesis

b)

Extraction

c)

Fully synthesis

d)

Plant Cell Culture

3.

Below is the right statement about the feature of PAXUS PM, except ....

a)

Non cremophor formulation of paclitaxel

b)

Has similar results like conventional paclitaxel

c)

Has phase III clinical study in Metastatic Breast Cancer with Asian population

d)

Studied in locally advanced pancreatic cancer both as single and combination regimen

4.

Please choose the group of indications for PAXUS PM below

a)

MBC. NPC, APC

b)

NSCLC, Cervical Ca, MBC

c)

MBC, NSCLC, Ovary Ca

d)

MBC only as single drug

5.

Below are the correct statements about bioequivalent study between Paxus PM and nab-paclitaxel, except

a)

Done in multi centers & multi countries with more than 100 cases

b)

Has more higher Maximum Tolerated Dose (MTD) vs Nab-paclitaxel

c)

MBC with 260 mg/m2 dosing given in 30 minutes of infusion rate

d)

NSCLC with 260 mg/m2 given in 30 minutes of infusion rate

6.

The recommended dose of PAXUS PM as single agent in metastatic breast cancer according to phase III study is ...

a)

175 mg/m2

b)

200 mg/m2

c)

260 mg/m2

d)

300 mg/m2

7.

Below are solid tumors that can be treated with PAXUS PM beside the on-label indication named before ....

a)

Head & Neck Ca, Prostate Ca

b)

Gastric Ca, Cervical Ca

c)

Thymic Ca, Biliary Ca

d)

Sarcoma, Glioma

8.

Below are the common adverse events of PAXUS PM

a)

Headache, Rashes, Anemia

b)

Alopecia, Diarrhea, Neutropenia

c)

Allergic reactions, thrombocytopenia, rashes

d)

Alopecia, neutropenia, neuropathy

9.

Below are the results of published phase III clinical studies in MBC, except ....

a)

Manageable both non-hematology and hematological toxicities

b)

Improved CR and PFS vs cremophor-based and Nab-Paclitaxel

c)

Prolonged median OS more than 5 months vs cremophor - based formulation & Nab-Paclitaxel (28.6 months vs 12.7 month vs 15.2 months)

d)

Higher dose than nab-paclitaxel with similar infusion rate of administration

10.

Which statement is correct about PAXUS PM?

a)

PAXUS PM has no pre-clinical trials, only clinical stages

b)

PAXUS PM only conducted phase I clinical studies and limited pre-clinical evidences in solid tumors

c)

No phase II and III clinical studies were published last 10 year ago

d)

Has complete owned pre-clinical, phase I, II, III, IV and BE vs nab-paclitaxel