CisPlatin plUs Gemcitabine and Nabpaclitaxel (GAP) as pReoperative Chemotherapy Versus Immediate Resection in patIents With resecTable BiliarY Tract Cancers (BTC) at High Risk for Recurrence

Cholangiocarcinoma Clinical Trial

— PURITY  

Official title:

A Phase II/III Randomized Clinical Trial of CisPlatin plUs Gemcitabine and Nabpaclitaxel (GAP) as pReoperative Chemotherapy Versus Immediate Resection in patIents With resecTable BiliarY Tract Cancers (BTC) at High Risk for Recurrence: PURITY Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06037980
• Other study ID #: PURITY
• Status: Recruiting
• Phase: Phase 2/Phase 3
• Start date: November 7, 2023
• Est. completion date: January 2029

Study information

• Verified date: October 2023
• Source: Gruppo Oncologico del Nord-Ovest
• Contact: Monica Niger, MD
• Phone: 02 2390 2919
• Email: monica.niger[@]istitutotumori.mi.it
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

PURITY is a multicentre, randomized adaptive phase II/III trial aimed at comparing the triplet combination of gemcitabine, cisplatin and nabpaclitaxel as neoadjuvant treatment (ARM A) versus standard upfront surgery (ARM B) in terms of 12-month PFS rate (phase II part) and PFS (phase III part) in patients with resectable BTC at high risk for recurrence.

Description:

PURITY is a multicentre, randomized adaptive phase II/III trial aimed at comparing the triplet combination of gemcitabine, cisplatin and nabpaclitaxel as neoadjuvant treatment (ARM A) versus standard upfront surgery (ARM B) in terms of 12-month PFS rate (phase II part) and PFS (phase III part) in patients with resectable BTC at high risk for recurrence. High risk for recurrence, for which patients will be eligible for study, is defined by the presence of at least one of the following risk features, as evaluated at baseline (pre-surgery): 1. For cholangiocarcinoma: - Suspected or definite locoregional lymph node involvement in the absence of jaundice (at least one of the following): - positive FNA cytology (obtained by EUS). - positive locoregional lymph nodes at PET-CT. - suspected positive locoregional lymph nodes at imaging (CT or MRI scan) according to local MTD discussion (eg. short axis > 1.5 cm, contrast enhancement uptake, round shape, restriction at DWI). - Macrovascular invasion at preoperative CT scan. - Expected R1 resection due to proximity to major intrahepatic vascular and biliary structures. - For iCCA, presence of satellitosis or multifocal disease or radiological suspicion of tumoral diaphragmatic adhesion. - For iCCA, size of the liver lesion >5 cm. - For eCCA, size of the primary lesion > 3cm. - Ca19.9 >100 U/mL. 2. For GBC: - Incidentally Detected Gallbladder Carcinoma (IGBC) After Simple Cholecystectomy with indication for radical second surgery (>pT2) or newly diagnosed GBC.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 300
• Est. completion date: January 2029
• Est. primary completion date: December 2028
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Patient able and willing to provide written informed consent and to comply with the study protocol and with the planned surgical procedures.

2. Female and male patients =18 years and <75 years.

3. Histologically or cytologically confirmed non metastatic resectable carcinoma of biliary tract (BTC), including gallbladder carcinoma (GBC), intrahepatic, periperihilar or distal Cholangiocarcinoma (CCA). Mixed tumor entities with hepatocellular carcinoma and ampullary cancers are excluded.

4. Availability of a tumoral sample

5. ECOG performance status of 0-1.

6. No prior tumor resection for BTC.

7. Exclusion of distant metastases by CT or MRI of abdomen, pelvis, and thorax and PET scan.

8. Technically resectable BTC as per local Multidisciplinary Team (MDT) assessment, including a core team with at least one medical oncologist, one surgeon, one radiologist, one endoscopist/gastroenterologist and one pathologist, all with expertise > 3 years on biliary tract cancer and hepatobiliary oncology.

9. High risk for recurrence defined as the presence of at least one of the following risk

features, as evaluated at baseline (pre-surgery):

1. For cholangiocarcinoma:

• Suspected or definite locoregional lymph node involvement (at least one of

the following):

• positive FNA cytology (obtained by EUS).
• positive locoregional lymph nodes at PET-CT.
• suspected positive locoregional lymph nodes at imaging (CT or MRI scan) according to local MDT discussion (eg. short axis > 1.5 cm, contrast enhancement uptake, round shape, restriction at DWI).
• Macrovascular invasion at preoperative CT scan.
• Expected R1 resection due to proximity to major intrahepatic vascular and biliary structures.
• For iCCA, presence of satellitosis or multifocal disease or radiological suspicion of tumoral diaphragmatic adhesion.
• For iCCA, size of the liver lesion >5 cm.
• For eCCA, size of the primary lesion > 3cm.
• Ca19.9 >100 U/mL.

2. For GBC:

• Incidentally Detected Gallbladder Carcinoma (IGBC) after simple cholecystectomy with indication for radical second surgery (>pT2) or newly diagnosed GBC.

10. Estimated life expectancy > 3 months.

11. Adequate baseline hematologic function characterized by the following at screening:

1. ANC = 1.5 × 109/L

2. platelets = 100 × 109/L

3. hemoglobin = 9 g/dl. Note: prior transfusions for patients with low hemoglobin are allowed.

12. Adequate liver function characterized by the following at screening:

1. Serum total bilirubin = 1.5 × ULN and < 2 mg/dL. Note: Subjects with Serum total bilirubin = 1.5 × ULN and conjugated bilirubin = ULN or < 40% of total bilirubin are allowed.

2. Serum transaminases (AST and/or ALT) < 3 x ULN.

13. Adequate renal function, i.e. serum creatinine = 1.5 x institutional ULN and calculated by Cockroft-Gault formula or directly measured creatinine clearance = 50 mL/min

14. Adequate coagulation functions as defined by International Normalized Ratio (INR) = 1.5, and a partial thromboplastin time (PTT) = 5 seconds above the ULN (unless receiving anticoagulation therapy).

15. No presence of complete dihydropyrimidine dehydrogenase (DPD) enzyme deficiency with DPYD gene testing mandatory at screening as per national guidelines

16. Females of childbearing potential must agree to remain abstinent (refrain from sexual intercourse) or use highly effective contraceptive methods, as defined in APPENDIX V of the full protocol, during the treatment period and for at least 7 months after the last administration of study treatments.

17. Males must agree to remain abstinent (refrain from sexual intercourse) or use highly effective contraceptive methods, as defined in APPENDIX V of the full protocol.

18. Negative serum pregnancy test within 7 days of starting study treatment in pre-menopausal women and women <1 year after the onset of menopause.

19. A participant must agree not to donate eggs/sperm for future use for the purposes of assisted reproduction during the study and for a period of 7 months after receiving the last dose of study treatment. Female and male participants should consider preservation of eggs/sperm prior to study treatment as anti-cancer treatments may impair fertility.

Exclusion Criteria:

1. Known allergy or hypersensitivity to any of the study drugs.

2. Any known additional malignancy that is progressing or requires active treatment, or history of other malignancy within 2 years of study entry except for curatively treated basal cell carcinoma of the skin, in situ carcinoma of the cervix, and prostate cancer.

3. Locally unresectable tumor according to local MDT (including radiological evidence suggesting inability to resect with curative intent whilst maintaining adequate vascular inflow and outflow, and sufficient future liver remnant).

4. Evidence of distant metastases at any site.

5. Tumors requiring multi-step surgical procedures such as two-stage hepatectomy or Associating Liver Partition and Portal vein Ligation for Staged hepatectomy (ALPPS) due to liver volumetry-based assessment of anticipated inadequate future liver remnant.

6. Cirrhosis at a level of Child-Pugh B (or worse) or cirrhosis (any degree) and a history of hepatic decompensation in the year before enrolment.

7. Know active uncontrolled hepatitis B or hepatitis C. Patients with a past or resolved HBV infection are eligible. Patients with chronic disease controlled by antiviral therapy or requiring prophylactic treatment are eligible.

8. Chronic or current active infectious disease requiring systemic antibiotics or antifungal treatment within 2 weeks prior to enrollment.

9. Known uncontrolled HIV infection. HIV-positive patients are eligible if their CD4+ cell count amounts to 300 cells per µL or more; HIV viral load must be undetectable per standard of care assay, and they must be compliant with antiretroviral treatment.

10. Pregnant or breast-feeding patient, or patient is planning to become pregnant within 7 months after the end of treatment.

11. Any other concurrent antineoplastic treatment including radiotherapy.

12. Previous or concurrent systemic (eg cytotoxic or targeted or other experimental drugs) therapy for BTC.

13. Prior surgery or locoregional therapy for BTC.

14. Severe or uncontrolled cardiovascular disease (congestive heart failure NYHA III or IV, unstable angina pectoris, history of myocardial infarction in the last three months, significant arrhythmia).

15. Presence of psychiatric disorder precluding understanding of information of trial related topics and giving informed consent.

16. Any serious underlying medical conditions (judged by the investigator), that could impair the ability of the patient to participate in the trial.

17. Presence of complete dihydropyrimidine dehydrogenase (DPD) enzyme deficiency with DPYD gene testing mandatory at screening as per national guidelines.

18. Lack of physical integrity of the upper gastrointestinal tract, malabsorption syndrome, or inability to take oral medication.

Related Conditions & MeSH terms

• Biliary Tract Cancer
• Biliary Tract Neoplasms
• Cholangiocarcinoma
• Recurrence

Intervention

Drug:
• Gemcitabine
? Gemcitabine 800 mg/mq iv, day 1 and 8 of 21-day cycles, for 3 cycles
• Nab paclitaxel
? Nab-paclitaxel 100 mg/mq, day 1 and 8 of 21-day cycles, for 3 cycles
• Cisplatin
? Cisplatin 25 mg/mq iv, day 1 and 8 of 21-day cycles, for 3 cycles

Procedure:
• Curative Surgery
Curative surgery on primary tumor

Drug:
• Capecitabine
1250 mg/m2 given orally twice daily on days 1 to 14 of a 3 weekly cycle for a total of 8 cycles

Locations

Country	Name	City	State
Italy	Ospedali Riuniti di Ancona	Ancona
Italy	ASST Papa Giovanni XXIII	Bergamo
Italy	Oncologia Medica Policlinico Sant'Orsola - Malpighi	Bologna
Italy	ASST Spedali Civili	Brescia
Italy	Azienda Ospedaliera S. Croce e Carle	Cuneo
Italy	IRST Dino Amadori	Meldola
Italy	Fondazione IRCCS Istituto Nazionale dei Tumori	Milan
Italy	Humanitas Cancer Center	Milan
Italy	Ospedale Niguarda Cancer Center	Milan
Italy	Ospedale San Raffaele	Milano
Italy	Università di Modena	Modena
Italy	Ospedale S. Gerardo	Monza
Italy	IOV	Padova
Italy	Policlinico San Matteo	Pavia
Italy	Azienda Ospedaliera Universitaria Pisa	Pisa
Italy	IRST (Cesena-Forlì-Meldola)	Ravenna
Italy	Policlinico Gemelli	Rome
Italy	Azienda Ospedaliera Ordine Mauriziano	Turin
Italy	AOUI Verona - Policlinico "G.B. Rossi"	Verona

Sponsors (1)

Lead Sponsor	Collaborator
Gruppo Oncologico del Nord-Ovest

Country where clinical trial is conducted

Italy, 

References & Publications (3)

Maithel SK, Keilson JM, Cao HST, Rupji M, Mahipal A, Lin BS, Javle MM, Cleary SP, Akce M, Switchenko JM, Rocha FG. NEO-GAP: A Single-Arm, Phase II Feasibility Trial of Neoadjuvant Gemcitabine, Cisplatin, and Nab-Paclitaxel for Resectable, High-Risk Intrah — View Citation

Shroff RT, Javle MM, Xiao L, Kaseb AO, Varadhachary GR, Wolff RA, Raghav KPS, Iwasaki M, Masci P, Ramanathan RK, Ahn DH, Bekaii-Saab TS, Borad MJ. Gemcitabine, Cisplatin, and nab-Paclitaxel for the Treatment of Advanced Biliary Tract Cancers: A Phase 2 Cl — View Citation

Yadav S, Xie H, Bin-Riaz I, Sharma P, Durani U, Goyal G, Borah B, Borad MJ, Smoot RL, Roberts LR, Go RS, McWilliams RR, Mahipal A. Neoadjuvant vs. adjuvant chemotherapy for cholangiocarcinoma: A propensity score matched analysis. Eur J Surg Oncol. 2019 Au — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	12-month progression-free survival (PFS) rate	the proportion of patients alive and free from progression/post-resection recurrence by 12-months timepoint from randomization (to be considered as primary endpoint in the phase II part of the study and as secondary endpoint in the phase III part of the study).	12 months
Primary	median PFS	i.e. the time from randomization to disease progression, post-resection recurrence or death from any cause (to be considered as secondary endpoint in the phase II part of the study and as primary endpoint in the phase III part of the study).	From date of randomization until the date of first documented progression (as assessed by radiological evaluation and clinical examination) or date of death from any cause, whichever came first, assessed up to 120 months
Secondary	Median event free survival	i.e. the time from randomization to disease progression that precludes definitive surgery, treatment discontinuation for any reason, post-resection recurrence, a second primary cancer, or death from any cause.	from date of randomization to disease progression that precludes definitive surgery, treatment discontinuation for any reason, post-resection recurrence, diagnosis of second cancer, or death from any cause, assessed up to 120 months
Secondary	Median relapse free survival	i.e. the time from surgery to disease recurrence or death in patients who undergo to surgery with curative intent.	from date of surgery to date of disease recurrence or date of death, whichever came first, in patients who undergo surgery with curative intent, assessed up to 120 months.
Secondary	Median Overall survival	i.e. the time from randomization to death or last follow-up for alive patients.	from date of randomization to date of death (or last follow up for alive patients), assessed up to 120 months.
Secondary	R0 resection rate	i.e. the percentage of patients, relative to the total of randomized patients, for whom a R0 resection is achieved.	At surgery
Secondary	R0+R1 resection rate	i.e. the percentage of patients, relative to the total of randomized patients, for whom the tumor was macroscopically removed and the intent of surgery is considered curative.	At surgery
Secondary	Quality of life EORTC QLQ-C30 scores	QoL will be estimated with EORTC QLQ-C30; mean score changes from baseline, proportion of patients with improved, stable, or deteriorated scores from baseline and time to deterioration in the EORTC QLQ-C30 scores will be compared between the two arms. Time to deterioration will be defined as the time from baseline to the first onset of a 10-point or greater decrease (for functional scales)/increase (for symptoms scale) from baseline, with confirmation under the right-censoring rule. All available observations will be used to calculate time to deterioration.	Quality of life questionnaires will be compiled during screening (28 days before randomisation) and at restaging before (week 8 to 10 after randomisation) and after surgery (week 6 to 16 after surgery)
Secondary	Quality of life BIL21 scores	QoL will be estimated with the module BIL21; mean score changes from baseline, proportion of patients with improved, stable, or deteriorated scores from baseline and time to deterioration in the BIL21 physical functioning, social functioning, and fatigue scores will be compared between the two arms. Time to deterioration was defined as the time from baseline to the first onset of a 10-point or greater decrease from baseline for functional scales or a 10-point or greater increase for symptom scales, with confirmation under the right-censoring rule. All available observations will be used to calculate time to deterioration.	Quality of life questionnaires will be compiled during screening (28 days before randomisation) and at restaging before (week 8 to 10 after randomisation) and after surgery (week 6 to 16 after surgery)
Secondary	Overall response rate	of neoadjuvant therapy as per investigator assessment and central review, i.e. the percentage of patients, relative to the total of enrolled subjects receiving neoadjuvant treatment, achieving a complete (CR) or partial (PR) response, according to RECIST 1.1 criteria.	At radiological evaluation as performed at restaging before surgery (week 8 to 10 after randomisation)
Secondary	Resectability rate of primary tumor	i.e. the retrospective evaluation of patients with unresectable disease, as assessed by the central review committee, in the two arms, and of the rate of conversion to resectability in the neoadjuvant arm.	Resectability rate will be assessed before surgery (after the 3 cycles of neoadjuvant chemotherapy for the experimental treatment arm)
Secondary	Toxicity rates	.e. the percentage of patients, relative to the total of subjects randomized to neoadjuvant treatment, experiencing a specific adverse event, according to National Cancer Institute Common Toxicity Criteria (version 5.0).	Through study completion, an average of 1 year for each patient
Secondary	Perioperative morbidity and mortality	i.e. the percentage of patients, relative to the total of enrolled subjects undergoing surgery, with any serious perioperative morbidity or mortality according to Clavien-Dindo classification.	At surgery