Spots Global Cancer Trial Database for 131I-IPA and Concurrent XRT in Recurrent GBM

Study Description

Brief Summary: A multi-centre, open-label, single-arm, dose-finding phase I/II study to evaluate safety, tolerability, dosing schedule, and preliminary efficacy of carrier-added 4-L-\[131I\]iodo-phenylalanine (131I-IPA), administered as single or repetitive injections in patients with recurrent glioblastoma multiforme (GBM), concomitantly to 2nd line external radiation therapy (XRT) - IPAX-1

Detailed Description: The IPAX-1 study is an open-label, single-arm, randomised, parallel-group, multi-centre dose-finding study to evaluate ascending radioactive dose levels of 131I-IPA, intravenously administered using different dose schedules (fractionations), concomitantly to 2nd line XRT (36 Gy, administered in 18 fractions of 2 Gy). Gross tumour volume will be determined using contrast-enhanced MRI and amino acid-based PET imaging (18F-FET or 11C-methionine). Patients will be included if they meet all of the following criteria: 1. Previously confirmed histological diagnosis of GBM, with current clinical or imaging evidence for first recurrence according to modified RANO criteria (2017). History of GBM standard therapy (debulking surgery, followed by radio-chemotherapy (50-60 Gy in 2 Gy fractions, temozolomide) 2. Interval since end of 1st line XRT ≥6 months 3. Amino acid-based molecular imaging (preferably 18F-FET- PETor 11C-methionine, as institutionally established) indicating pathologically increased amino acid uptake inside or in the vicinity of the tumour, clearly discernible from background activity. 4. Current indication for repeat radiation therapy as discussed at the multidisciplinary neuro-oncological tumour board meeting, planned as standard fractionated dose schedule (18\*2 Gy) 5. Gross tumour volume (GTV) of up to 4.8 cm diameter, clinical target volume (CTV) 0.5 cm margin and planning target volume (PTV) less than or equal to 0.5 cm margin 6. Male or female ≥18 years of age. 7. Karnofsky performance status (KPS) ≥70. Life expectancy of at least 16 weeks. 8. Haematological, liver and renal function test results as follows: * WBC: \>3\*109/L * Haemoglobin \>80 g/L * PLT \>100\*109/L * ALT, ALP, AST: ≤5 times upper international limit of normal (UILN) * Bilirubin ≤3 times UILN * Serum creatinine: within normal limits or \<120 μmol/L for patients aged 60 years or older * Urine protein dipstick: no protein 9. Female patients surgically sterile or postmenopausal for at least 2 years. Participants of generative potential agreeing to use effective contraception during the period of therapy and 6 months after the end of study. 10. Written informed consent A patient will be excluded from participation in the trial if one or more of the following criteria are met: 1. Primary XRT dose greater than 60 Gy 2. Doses to organs at risk defined by Yasar and Tugrul (2005) exceeded or reached by prior radiation therapy; e.g. cumulative total dose on the optical chiasm greater than 54 Gy for 2 Gy/fraction 3. Multifocal distant recurrence, defined as tumour lesion outside the primary XRT field, as evidenced by amino acid-based PET imaging 4. Prior treatment with brachytherapy 5. Prior treatment with bevacizumab 6. History or evidence of delayed-type hypersensitivity (DTH)-dependent chronic infection (e.g. tuberculosis, systemic fungal or parasitic infection), potentially exacerbating under systemic corticoid therapy 7. Localisation of tumour related to brain stem or axis, unless sufficient reserve capacity (e.g. remnant resection cavity, marked atrophy) to accommodate possible post- procedural tissue reactions, or pre-therapeutic consent for emergency trepanation 8. Haemostaseologic conditions, precluding catheterisation or invasive procedures 9. Clinically significant illness or clinically relevant trauma within 2 weeks before the administration of the investigational product 10. Known impairment of liver or kidney function or known liver or kidney disease, such as hepatitis, cirrhosis, renal failure 11. Known human immunodeficiency virus (HIV) positive serology or chronically active hepatitis B or C 12. Ongoing toxicity \> grade 2 NCI-CTC (version 4.03) from previous standard or investigational therapies 13. Administration of another investigational medicinal product within 90 days prior to screening 14. Expected non-compliance with longer-term admission at isolated nuclear medicine ward 15. In pre-menopausal women: Pregnant as evidenced by a positive pregnancy test, or breast-feeding 16. Patients with known phenylketonuria Study Design: At the first dose level of 2 GBq, 131I-IPA will be administered in one of three different dosing regimens: * Single dose regimen (1f group): Full 131I-IPA activity (2.0 GBq at the 2 GBq dose level) will be administered 1- 3 days prior to 1st XRT as a single injection. * Fractionated dose regimen (3f - parallel group): 131I-IPA activity will be administered in 3 fractions corresponding to ⅓ full dose activity (0.67 GBq for the 2.0 GBq dose level). The 1st fraction of 131I-IPA will be administered as above, 1- 3 days prior to 1st XRT. The 2nd and 3rd 131I-IPA fractions will be administered after 5-9 XRT fractions (subject to investigator's discretion and day of IMP administration) following the previous 131I-IPA fraction. The remainder of XRT fractions will be given following the 3rd 131I-IPA fraction. * Fractionated dose regimen (3f - sequential group): 131I-IPA activity will be administered in 3 fractions corresponding to ⅓ full dose activity (0.67 GBq for the 2.0 GBq dose level). The 1st fraction of 131I-IPA will be administered as above 1- 3 days prior to 1st XRT. The 2nd 131I-IPA fraction will be administered after all 18 XRT fractions have been completed, and the 3rd 131I-IPA fraction will be administered 1 week after the 2nd 131I-IPA fraction. The 2nd and 3rd 131I-IPA injections should be given on the same day of the week, and some hours after administration of the respective XRT dose of that day. The day of IMP administration is subject to change at investigator's discretion. The three different treatment groups at the first (2.0 GBq) dose level (131I-IPA single dose 1f and 131I-IPA fractionated dose either 3f parallel or 3f sequential) will be recruited in parallel, as appropriate. Patients will be allocated to one of the three IPA dosing regimens. N=3 patients will be enrolled for each of the three treatment schedules. A 10th patient can be added to any of the three groups, in order to corroborate evidence for possible differences in safety and efficacy. Patients at the entry dose level of 2 GBq will undergo 131I-IPA brain SPECT for tumour dosimetry (performed in all patients), whole body planar imaging for determination of biodistribution and whole body safety dosimetry. In addition, these patients will be comparatively assessed for possible differences in safety and/or efficacy among the different dosing regimens. Dose escalation beyond 2 GBq will be made using the fractionated dosing regimen only, unless the outcome of the 2 GBq dose level suggests otherwise. The best treatment schedule (3f parallel or 3f sequential, see above) for higher doses shall be selected after completion of the 2 GBq dose level. Dose escalation will be made in steps of 2.0 GBq, i.e. 4.0 (3\*1.33 GBq), 6.0 GBq (3\*2.0 GBq), up to 8.0 GBq (3\*2.67 GBq) until the maximum tolerated dose (MTD) is reached, using cohorts of N=3 patients. If MTD has not been reached at 8.0 GBq, dose escalation may further proceed, increasing the dose fractions to a total dose 131I- IPA greater than 8 GBq using cohorts of N=3 as follows: 10 GBq, 3f (i.e. 3\*3.33 GBq); 12 GBq, 3f (i.e. 3\*4 GBq), etc., until MTD is reached or until a satisfactory anti-neoplastic efficacy is observed. For assessment of possible anti-neoplastic effects during dose escalation, only amino acid-based molecular imaging (preferably 18F-FET-PET) will be used, which allows assessment of treatment-induced changes based on a single post-therapeutic imaging study. MTD is defined as the dose level, inducing dose limiting toxicity (DLT), in not more than 1/6 of the subjects receiving such dose. MTD will be determined on day 45 from the first IPA injection. DLT is defined as grade 4 neurotoxicity or any other grade 4 toxicity according to NCI-CTC (version 4.03). If DLT is observed in 1 subject of a cohort, 3 additional patients will be treated at the same dose level, under which such toxicity occurred. If one or more of these patients (i.e. 2/4, 2/5 or 2/6) experience grade 4 toxicity, MTD will have been exceeded for the respective dose level. In such a case, 3 additional patients will be treated at the preceding dose level. Therapy-induced early necrosis, (also termed pseudo-progression, which has been associated with improved survival will not be classified as DLT if asymptomatic, or if symptomatic and at least partially reversible within three months with or without therapy. Disease progression/PsPD will be diagnosed according to the current RANO criteria (2017). The highest dose under which no more than 1/6 of the patients experience DLT will be declared the MTD level. Safety, tolerability and evidence of anti-tumour effects will be compared between all dose levels, in order to identify a most suitable dose level (MSDL) for the phase II part. The MSDL will not necessarily be identical to the MTD, but might be selected by jointly considering efficacy, safety and radiation protection aspects. The identification of the MSDL will be made by a Drug Data Safety Monitoring Board (DSMB), based on an integrated review of efficacy and safety from the first part. Based on a comprehensive analysis of the first part results, the DSMB will make a conclusion regarding safety and efficacy, and recommend to the sponsor a dosing strategy and dose level (MSDL) for the phase II part, if merited. Prior to initiating phase II, the sponsor commits to submit a substantial amendment, containing a summary of the phase I results to the Austrian BASG, other competent authorities, and the responsible Ethics Committee, as appropriate. Upon establishment of the MSDL, 12-22 further patients will be treated at the MSDL (Phase II). If unequivocal evidence of efficacy is observed, another 10 patients shall be included in the phase II part. It is planned to include approximately 34 (22+12) patients with recurrent GBM with the option to extend phase II study by another 10 patients if the results are encouraging (22+22 patients).

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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