| CTRI Number |
CTRI/2024/08/072504 [Registered on: 14/08/2024] Trial Registered Prospectively |
| Last Modified On: |
12/08/2024 |
| Post Graduate Thesis |
No |
| Type of Trial |
Observational |
|
Type of Study
|
Cohort Study |
| Study Design |
Other |
|
Public Title of Study
|
Scientific data review of prostate cancer patients to study treatment patterns and understand need gaps. |
|
Scientific Title of Study
|
Real-World Treatment Patterns and Clinical Outcomes Among Patients with Metastatic Castration-resistant Prostate Cancer (mCRPC): An Emerging Market Medical Record Review Study |
| Trial Acronym |
NIL |
|
Secondary IDs if Any
|
| Secondary ID |
Identifier |
| Protocol C3441067 version 1 dated 15 December 2023 |
Protocol Number |
|
|
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
|
| Name |
Antara Chaudhri |
| Designation |
Medical Advisor |
| Affiliation |
Pfizer Limited |
| Address |
The Capital
Plot No. C, The Capital, 1802, 18th Floor, 70, G Block Rd, Bandra Kurla Complex, Bandra East
Mumbai MAHARASHTRA 400051 India |
| Phone |
9971012224 |
| Fax |
|
| Email |
Antara.Chaudhri@pfizer.com |
|
Details of Contact Person Scientific Query
|
| Name |
Antara Chaudhri |
| Designation |
Medical Advisor |
| Affiliation |
Pfizer Limited |
| Address |
The Capital
Plot No. C, The Capital, 1802, 18th Floor, 70, G Block Rd, Bandra Kurla Complex, Bandra East
Mumbai MAHARASHTRA 400051 India |
| Phone |
9971012224 |
| Fax |
|
| Email |
Antara.Chaudhri@pfizer.com |
|
Details of Contact Person Public Query
|
| Name |
Antara Chaudhri |
| Designation |
Medical Advisor |
| Affiliation |
Pfizer Limited |
| Address |
The Capital
Plot No. C, The Capital, 1802, 18th Floor, 70, G Block Rd, Bandra Kurla Complex, Bandra East
MAHARASHTRA 400051 India |
| Phone |
9971012224 |
| Fax |
|
| Email |
Antara.Chaudhri@pfizer.com |
|
|
Source of Monetary or Material Support
|
| Pfizer Limited,
The Capital
Plot No. C, The Capital, 1802, 18th Floor, 70, G Block Rd, Bandra Kurla Complex, Bandra East, Mumbai, Maharashtra 400051 |
|
|
Primary Sponsor
|
| Name |
Pfizer Limited |
| Address |
The Capital Plot No. C, The Capital, 1802, 18th Floor, 70, G Block Rd, Bandra Kurla Complex, Bandra East, Mumbai, Maharashtra 400051 |
| Type of Sponsor |
Pharmaceutical industry-Indian |
|
|
Details of Secondary Sponsor
|
|
|
Countries of Recruitment
|
India Argentina Brazil Saudi Arabia Taiwan Turkey United Arab Emirates |
|
Sites of Study
|
| No of Sites = 4 |
| Name of Principal
Investigator |
Name of Site |
Site Address |
Phone/Fax/Email |
| Dr J B Sharma |
Action Cancer Hospital |
Room No FC-34, A - 4, Department of Medical Oncology, Paschim Vihar, New Delhi - 110063, India New Delhi DELHI |
9811167505
dr_sharmajb@rediffmail.com |
| Dr Srikant Tiwari |
Jawaharlal Nehru Cancer Hospital & Research center |
Room No- 10, Department of Medical Oncology RP.O. Box No. 32, Jawaharlal Nehru Cancer Hospital & Research center, Cancer Hospital Road, Idgah Hills, Bhopal, Madhya Pradesh - 462001, India Bhopal MADHYA PRADESH |
0755-2665720
srikantabhinov@gmail.com |
| Dr Sandeep Batra |
Max Super Speciality Hospital |
Service Floor, 2, Department of Medical Oncology, Press Enclave Road, Saket Institutional Area, Saket, New Delhi, Delhi – 110017, India New Delhi DELHI |
9811035061
sandeepriya2000@yahoo.com |
| Dr Amit Joshi |
Tata Memorial Hospital |
Room No - 1105, 11th floor, Tata Memorial Centre, Homi bhabha block, Dr. Ernest Borges Road, Parel, Mumbai - 400012, India Mumbai MAHARASHTRA |
9769331525
dramitjoshi74@gmail.com |
|
|
Details of Ethics Committee
|
| No of Ethics Committees= 4 |
| Name of Committee |
Approval Status |
| Action Cancer Hospital Ethics Committee |
Submittted/Under Review |
| Instituational Ethics Committee Jawaharlal Nehru Cancer Hospital & Research center |
Approved |
| Max Healthcare Ethics Committee |
Submittted/Under Review |
| TMH, Institutional Ethics Committee-I |
Submittted/Under Review |
|
|
Regulatory Clearance Status from DCGI
|
|
|
Health Condition / Problems Studied
|
| Health Type |
Condition |
| Patients |
(1) ICD-10 Condition: N428||Other specified disorders of prostate, |
|
|
Intervention / Comparator Agent
|
| Type |
Name |
Details |
| Intervention |
NIL |
NIL |
| Comparator Agent |
NIL |
NIL |
|
|
Inclusion Criteria
|
| Age From |
18.00 Year(s) |
| Age To |
99.00 Year(s) |
| Gender |
Male |
| Details |
1. New diagnosis of mCRPC during the case selection window (between 15 April 2019 to 14 January 2022, inclusive). mCRPC is defined as the current and/or historical presence of metastases on any imaging modality with evidence of disease progression (a rising PSA or radiographic progression (as defined by the investigator) despite ongoing castration therapy [LHRH agonist / antagonist or prior surgical
orchiectomy]).
2. Aged at least 18 years upon diagnosis of mCRPC.
Of note, patients may be alive or deceased at the date of data abstraction. |
|
| ExclusionCriteria |
| Details |
Previously enrolled in an interventional trial related to CRPC (patients may have been
enrolled in trials of primary treatment and/or hormone-sensitive prostate cancer). |
|
|
Method of Generating Random Sequence
|
Computer generated randomization |
|
Method of Concealment
|
On-site computer system |
|
Blinding/Masking
|
Not Applicable |
|
Primary Outcome
|
| Outcome |
TimePoints |
Describe demographic and clinical characteristics at first diagnosis of mCRPC.
Document treatment patterns from original prostate cancer diagnosis leading up to,
upon and following diagnosis of mCRPC.
Assess clinical outcomes among patients diagnosed with mCRPC, including
prostate-specific antigen (PSA) response, real-world progression-free survival (PFS),
real-world objective response rate (ORR), OS, and death by treatment lines.
Report mCRPC-specific HCRU where applicable
Document time on treatment for each line of treatment for mCRPC
Document time to next treatment from initiation of a systemic therapy line to the
commencement of the subsequent systemic therapy line for mCRPC
Document time to subsequent chemotherapy from initiation of first-line systemic
treatment for mCRPC |
24 Months |
|
|
Secondary Outcome
|
|
|
Target Sample Size
|
Total Sample Size="950" Sample Size from India="150"
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" |
|
Phase of Trial
|
N/A |
|
Date of First Enrollment (India)
|
30/08/2024 |
| Date of Study Completion (India) |
Applicable only for Completed/Terminated trials |
| Date of First Enrollment (Global) |
11/07/2024 |
| Date of Study Completion (Global) |
Applicable only for Completed/Terminated trials |
|
Estimated Duration of Trial
|
Years="2" Months="0" Days="0" |
|
Recruitment Status of Trial (Global)
|
Open to Recruitment |
| Recruitment Status of Trial (India) |
Not Yet Recruiting |
|
Publication Details
|
N/A |
|
Individual Participant Data (IPD) Sharing Statement
|
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
Response - NO
|
|
Brief Summary
|
Prostate cancer is the second most common cancer worldwide and the
fifth leading cause of cancer-related mortality among men. In 2020, there were
1.4 million new cases of prostate cancer worldwide, accounting for 7.3% of all
cancer cases; and 0.4 million deaths, accounting for 3.8% of all cancer-related
deaths. Incidence rates (per 100,000 people) vary globally, with the highest
rates being reported in Northern Europe (83.4) and Western Europe (77.6),
whilst the lowest rates are reported in South Central Asia (6.3), South-East
Asia (13.5), and Northern Africa (16.6). Specifically, the incidence rates (per
100,000 people) in Emerging Market (EM) (eg: India: 5.0-9.1,
Taiwan: 17.2-52.9, Turkey: 42.5, Saudi Arabia: 7.0, United Arab Emirates
[UAE]:13.4, Egypt: 13.9, Argentina: 42.0) were lower than developed countries.
Mortality rates due to prostate cancer, since mid-1990s, have
decreased in most high-income countries, including those in North America,
Oceania, and Northern and Western Europe. However, during the same period,
increased mortality rates have been observed in Central and Eastern Europe,
Asia, and Africa. Around 4%-15% of prostate cancer cases are already metastatic
at diagnosis; and approximately 10%-50% of prostate cancer cases progress into
mCRPC within 3 years of diagnosis. The long-term prognosis for mCRPC is poor,
with an OS since development of castration resistance ranging from 13 to 33
months, which varies depending on individual and disease characteristics, as
well as treatment.
Data on mCRPC epidemiology, disease burden, and treatment
landscape is scarce across EM compared with the US and other developed markets.
The lack of this data is an important barrier to formulating treatment
strategies and guidelines. To bridge this gap, it is planned to capture
real-world data to yield an enhanced picture of patient characteristics and
treatment patterns; these data can uncover areas where current clinical needs
are not being met and offer insights into how innovative therapies can enhance
patient outcomes. This study therefore seeks to describe demographic and
clinical characteristics, treatment patterns, clinical outcomes, and healthcare
resource use (HCRU) where applicable among patients with mCRPC in EM.
By means of study we would hereby like to
notify your Directorate about conduct of non-interventional study- ‘Real-World
Treatment Patterns and Clinical Outcomes Among Patients with Metastatic
Castration-resistant Prostate Cancer (mCRPC): An Emerging Market Medical Record
Review Study’.
Protocol Number C3441067, Version 1.0 Dated 15 December 2023.’ |