1 photofrin® pdt for high-grade dysplasia in barrett’s esophagus edvardas kaminskas, m.d. medical...

1

PHOTOFRIN® PDT for High-grade Dysplasia in Barrett’s

Esophagus Edvardas Kaminskas, M.D.

Medical Officer, CDER, ODE III, DGCDP

Milton Fan, Ph.D.

Statistical Reviewer, CDER, ODE III, DGCDP

CDER GI Drugs Advisory Committee

June 26, 2003

2

Overview

• Background

• Clinical trials

• Efficacy endpoints and results

• Patient disposition

• Other therapies

• Safety issues

3

Background

• HGD is treated to decrease the risk of progression to cancer.

• Incidence of adenocarcinoma of esophagus increasing; however,

– Most cancer cases (94% - 98%) do not have a prior diagnosis of BE

– Most BE patients do not develop cancer: annual incidence of 0.5% or less

– Cancer risk to an older patient with GERD is very low: 6500 cases per year among 10 million (0.00065 per year)

4

Proposed New Indication

• “the ablation of high-grade dysplasia (HGD) in Barrett’s esophagus (BE) among patients who are not considered to be candidates for esophagectomy.”

• “the ablation of HGD in BE among patients who refuse esophagectomy and who are in overall good health.”

5

Clinical Trials in Support of the New Indication

PHO BAR 01. Multicenter, randomized, 2-arm trial with minimum 24-month f/u. Patients randomized 2:1 ratio

• 138 patients to PHOTOFRIN PDT + omeprazole

• 70 patients to OM (omeprazole) only

TCSC 93-07 and TCSC 96-01. Single center, open-label trials, minimum 12-month follow-up. All patients treated with PHOTOFRIN PDT + omeprazole. In 93-07 patients randomized to 2 light doses; in 96-01, to +/- post-PDT steroids to test effect on stricture incidence.

• 186 patients, 86 with HGD

6

PHOTOFRIN Photodynamic Therapy in PHO BAR 01

Course 1 Course 2Course 3

Patients N = 130 N = 89 N = 42

First laser light session

Nodule pre-Rx N = 35 N = 27 N = 12

Balloon light N = 129 N = 89 N = 41

Second laser light session

Treatment of skip

areas N = 60 N = 49 N = 21

7

Efficacy Endpoints

Primary endpoint: Complete ablation of HGD and replacement with – normal squamous cell epithelium (CR1),– with some metaplasia remaining (CR2), or– with some low-grade dysplasia or indefinite

dysplasia (CR3)

at 24 months’ follow-up.

8

Efficacy Endpoints

Secondary endpoints:

• Complete Response (CR3 or better) at 6, 12, 18, and 24 months

• Quality of Complete Response (% of patients with CR1, CR2, and CR3)

• Duration of Response

• Time to Progression to Cancer

• Time to Treatment Failure (progression to cancer, or other intervening therapy than study treatment)

• Survival time

9

Efficacy Endpoints

Agency’s concerns at Initiation of PHO BAR 01 study:

• The primary response variable must reflect an improvement in the long-term clinical outcome.

• Histopathological effects might be a surrogate endpoint for measuring clinical benefit.

• A follow-up time of 5 years or more recommended, but follow-up of at least 2 to 3 years acceptable.

10

Efficacy Results

Study No. ofpatientswith CR

Total no. ofpatients

% ofpatientswith CR

PHO BAR 01PHOTOFRIN PDTOM Only

106

27

130

69

82%

39%

PHOTOFRIN PDTTCSC 93-07TCSC 96-01

41 40

44 42

93%95%

11

Efficacy Results

Quality ofresponse

PHOTOFRINPDT, N = 130

OM OnlyN = 69

CR1 55% 7%

CR2 7% 7%

CR3 19% 25%

No response 18% 61%

12

Study Numberprogressedto cancer

Totalnumber ofpatientstreated

%progressedto cancer

PHO BAR 01PHOTOFRINPDTOM Only(24-mo.)

18

20

130

69

14%

29%

TCSC 93-07 &TCSC 96-01(12-mo.)

11 86 13%

Efficacy Results

13

Efficacy Results

Response status No. of patientswhoprogressed tocancer

Total no.ofpatients

% of patientswhoprogressed tocancer

PHOTOFRIN PDTCR1+CR2+CR3No CR

612

10624

6%50%

OM OnlyCR1+CR2+CR3No CR

119

2742

4%45%

14

Efficacy Results

• PDT group: Patients who progressed to cancer were CR3 responders (6) and non-responders (12).

• OM Only group: The one (1) responder who progressed to cancer had CR3. The rest (19) were non-responders.

15

Selection of Appropriate Patients

Patients without HGD may be referred for PHOTOFRIN PDT. In PHO BAR 01:

• Patients with HGD referred 485

• Diagnosis not confirmed 237 (49%)

• Diagnosis of HGD should be confirmed by a Reference Laboratory

16

Patient Disposition

Patientpopulation

PHOTOFRINPDT, No. (%)

OM OnlyNo. patients(%)

Intent-to-Treat 138 70

Completedstudy(min. 24 mos.)

81 (61%) 11 (16%)

17

Other Therapies

Study No.patientswith OtherTherapies

Totalno. ofpatients

% patientswith OtherTherapies

PHO BAR 01PHOTOFRINPDTOM Only(24-mo.)

18

22

130

69

14%

32%

TCSC 93-06& TCSC 96-01(12-mo.)

17 86 20%

18

Safety Issues

• Acute events related to light treatment (chest pain, abdominal pain, fever, nausea, vomiting, dysphagia, odynophagia)

• Skin photosensitivity

• Sub-acute events related to healing– Esophageal strictures, defined as

• Esophageal narrowing (on endoscopy) that required dilation

19

Safety IssuesStrictures

TCSC 93-07

N = 99

TCSC 96-01

N = 86

PHO BAR 01

N = 133

TOTAL

N = 318

42 (42.4%) 31 (36.0%) 48 (36.1%) 121 (38.1%)

20

Safety IssuesNumber of Dilations

Number ofdilations

Number of patientswith dilations

N=121

Percent of patientswith dilations

1 - 2 42 35%

3 - 5 35 29%

6 - 10 26 21%

> 10 18 15%

21

Summary

• Aggressive surveillance: – Not a good option for most patients in PHO BAR 01

study; 84% chose active treatment.

– Information on risk of cancer in HGD is essential for evaluation of treatment options, but may be difficult to obtain.

• Esophagectomy: – Follow-up information not available.

22

Summary

• PHOTOFRIN PDT: – Relatively well tolerated. Few withdrew

because of adverse events.– No deaths due to treatment or esophageal

cancer.– Most SAEs were GI and dehydration.– Strictures were troublesome but

manageable.

23

Summary

2-year follow-up suggests PHOTOFRIN PDT is effective. PDT patients had: – 50% lower cancer rate– CR rates twice as high. CR associated with

lower risk of cancer– Mainly in high quality CR1. Only patients

with CR3 progress to cancer

24

Summary

• But a 2-year follow-up is too short to demonstrate effectiveness in reducing the long-term risk of cancer.

• Rate of recurrence of HGD not known

• Rate of HGD progression to cancer not known

• PHO BAR 02 in process

26

Questions for the Committee - 1

Is the proposed INDICATION for PHOTOFRIN PDT appropriate?

• “the ablation of HGD in BE among patients who refuse esophagectomy and who are in overall good health”

If not, what would be an appropriate INDICATION?

27


• Is a 2-year follow-up period adequate for the claim of cancer risk reduction in High-grade Dysplasia patients treated with PHOTOFRIN PDT?

28


• In view of failure to confirm the diagnosis of High-grade Dysplasia in about 50% of patients, what safeguards would the Committee recommend to insure that only HGD patients are treated with PHOTOFRIN PDT?

29


• Should treatment with proton pump inhibitors be recommended, and for what length of time, before treatment of High-grade Dysplasia patients with PHOTOFRIN PDT?

• Should the diagnosis of High-grade Dysplasia be confirmed by a reference laboratory of acknowledged expertise before PHOTOFRIN PDT is undertaken?

30


• Are there ethical concerns about continuing patients in the Omeprazole Only arm of the study?

31


• Are there patients with High-grade Dysplasia who should not undergo PHOTOFRIN PDT, because of – safety concerns– uncertainties in the natural history of HGD– other considerations?

32


• How would the availability of PHOTOFRIN PDT on the market impact the current approach to the treatment of HGD?

1 photofrin® pdt for high-grade dysplasia in barrett’s esophagus edvardas kaminskas, m.d. medical...

Documents