Table 2.
Flow chart study procedures
| Adjuvant Chemotherapy Phase | |||||||||||||
| Pre-study Phase | Pre-study Phase | Cycle 1 | Cycle 2 | Cycle 3 | Cycle 4 | 1st follow up (30 days after end of chemo-therapy) | Further Follow-Up | ||||||
| Treatment Arm | A | B | A | B | A | B | A | B | A | B | A &B | ||
| Timeframe (days) | -28 prior to Surgery | -14 prior to Chemotherapy start | 1–21 | 1–28 | 22–42 | 29–56 | 43–63 | 57–84 | 64–84 | 85–112 | 114 | 142 | until 3 years after CTX |
| day of visit | -28 prior to Surgery | -14 prior to Chemotherapy start | 1 | 1, 8, 15, 22 | 22 | 29, 36, 43, 50 | 43 | 57, 64, 71, 78 | 64 | 85, 92, 99, 106 | 114 | 142 | starting 3 month after 1st follow up in Years 1 & 2: 3-monthly, then 6-monthly |
| Informed Consent | X | ||||||||||||
| Demography | X | ||||||||||||
| Pregnancy test | X1 | ||||||||||||
| Medical history, Signs and symptoms | X | ||||||||||||
| Neurological Status | X | X | X | X | X | ||||||||
| Clinical Examination2 | X2 | X2 | X2 | X2 | X2 | X2 | X2 | ||||||
| Concomitant medication | X | X | X | X | X | X | X | ||||||
| Laboratory hematology | X | X3,4 | X3,4 | X3,4 | X3,4 | X | X | ||||||
| Laboratory hepatic | X | X4 | X4 | X4 | X4 | X | X | ||||||
| Laboratory renal | X | X4 | X4 | X4 | X4 | ||||||||
| Laboratory electrolytes | X | X4 | X4 | X4 | X4 | ||||||||
| Laboratory coagulation | X | ||||||||||||
| 12-lead ECG | X | ||||||||||||
| Assessment of LVEF9 | X | ||||||||||||
| Chest-X-ray | X | X5 | X5 | ||||||||||
| Abdomen ultrasound | X6 | X10 | X10 | ||||||||||
| MRT or CT skull | X | ||||||||||||
| CT6 lower liver marginliver | X | ||||||||||||
| Assessment of vital/total capacity | X | X | |||||||||||
| Assessment of FEV1 | X | X | |||||||||||
| Assessment of absolute DLCO or BGA under resting conditions | X | X | |||||||||||
| Bone Scintigraphy7 | X | ||||||||||||
| Audiometry8 | X | ||||||||||||
| Compliance | X | X | X | X | X | ||||||||
| Adverse events | X | X | X | X | X | X | |||||||
| Follow-Up tumor assessment5 | X | X | |||||||||||
1 in women with child-bearing potential
2 Clinical examination including physical examination, neurologic assessment, height (height only to be assessed at baseline), weight, vital signs, Karnofsky or ECOG Performance Status at the beginning of each chemotherapy cycle.
3 hematology parameters, including Hb, platelets, WBC, ANC at least once weekly during chemotherapy phase
4 Three days prior to or at least at day 1 of each chemotherapy-cycle
5 Relapse of disease should be confirmed by imaging techniques
6 CT scan of the thorax and abdomen including adrenal glands and the right lower liver margin (in case adrenal glands are not available further CT scan of the abdomen is mandatory; if only right lower liver margin is not available assessment by either CT scan of abdomen or abdominal ultrasound should be performed)
7 If a FDG-PET scan has been performed, bone scintigraphy can be omitted
8 Optional; patients with clinical suspicion of altered hearing capability or symptoms should undergo further evaluation by audiometry
9 Echocardiography optional, mandatory only in case of doubt whether cardiac function allows Cisplatin chemotherapy
10 optional, left to the discretion of the center prior to study initiation of the center