Study

Comprehensive Genomic and Transcriptomic Analysis of Rare Cancers for Guiding of Therapy (H021)

Study ID Alternative Stable ID Type
EGAS00001004813 Other

Study Description

Here we analyzed the molecular profiles and clinical outcomes of 1,310 patients (proportion of rare cancers, 75%) enrolled in a prospective observational study by the German Cancer Consortium that applies whole-genome/exome and RNA sequencing to inform the care of adults with incurable cancers. Based on 472 single and six composite biomarkers, a cross-institutional molecular tumor board provided evidence-based management recommendations, including diagnostic reevaluation, genetic counseling, and experimental treatment, in 88% of cases. Recommended therapies were administered in 362 of 1,138 patients (31.8%) and resulted in significantly improved response and disease control rates (23.9% and 55.3%, respectively) compared to previous therapies, translating into a progression-free survival ratio >1.3 in 35.7% of patients.

Study Datasets 67 datasets.

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID Description Technology Samples
EGAD00001008844
Rare cancer sequencing data of 23 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2500,Illumina HiSeq 4000 16
EGAD00001008845
Rare cancer sequencing data of 28 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2500,Illumina HiSeq 4000 22
EGAD00001008846
Rare cancer sequencing data of 45 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2500,Illumina HiSeq 4000 26
EGAD00001008847
Rare cancer sequencing data of 95 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2500,Illumina HiSeq 4000 64
EGAD00001008848
Rare cancer sequencing data of 55 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2500,Illumina HiSeq 4000 44
EGAD00001008849
Rare cancer sequencing data of 87 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2500,Illumina HiSeq 4000 58
EGAD00001008850
Rare cancer sequencing data of 59 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 38
EGAD00001008851
Rare cancer sequencing data of 75 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2500,Illumina HiSeq 4000 49
EGAD00001008852
Rare cancer sequencing data of 50 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 34
EGAD00001008853
Rare cancer sequencing data of 44 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 30
EGAD00001008854
Rare cancer sequencing data of 40 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 26
EGAD00001008855
Rare cancer sequencing data of 97 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 61
EGAD00001008856
Rare cancer sequencing data of 48 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 33
EGAD00001008857
Rare cancer sequencing data of 58 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 40
EGAD00001008858
Rare cancer sequencing data of 49 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 35
EGAD00001008859
Rare cancer sequencing data of 243 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 164
EGAD00001008860
Rare cancer sequencing data of 47 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 41
EGAD00001008861
Rare cancer sequencing data of 92 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2500,Illumina HiSeq 4000 62
EGAD00001008862
Rare cancer sequencing data of 145 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2500,Illumina HiSeq 4000 104
EGAD00001008863
Rare cancer sequencing data of 119 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 2500,Illumina HiSeq 4000 76
EGAD00001008865
Rare cancer sequencing data of 87 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2500,Illumina HiSeq 4000 87
EGAD00001008866
Rare cancer sequencing data of 48 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 48
EGAD00001008867
Rare cancer sequencing data of 12 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 12
EGAD00001008868
Rare cancer sequencing data of 94 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 91
EGAD00001008869
Rare cancer sequencing data of 46 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 46
EGAD00001008870
Rare cancer sequencing data of 62 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 59
EGAD00001008871
Rare cancer sequencing data of 119 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 117
EGAD00001008872
Rare cancer sequencing data of 54 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 52
EGAD00001008873
Rare cancer sequencing data of 30 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2500,Illumina HiSeq 4000 30
EGAD00001008874
Rare cancer sequencing data of 18 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 18
EGAD00001008875
Rare cancer sequencing data of 64 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2500,Illumina HiSeq 4000 61
EGAD00001008876
Rare cancer sequencing data of 18 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 12
EGAD00001008877
Rare cancer sequencing data of 55 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 55
EGAD00001008878
Rare cancer sequencing data of 38 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 31
EGAD00001008879
Rare cancer sequencing data of 56 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 54
EGAD00001008880
Rare cancer sequencing data of 86 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2500,Illumina HiSeq 4000 83
EGAD00001008881
Rare cancer sequencing data of 49 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 44
EGAD00001008882
Rare cancer sequencing data of 91 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 78
EGAD00001008883
Rare cancer sequencing data of 162 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2500,Illumina HiSeq 4000 149
EGAD00001008884
Rare cancer sequencing data of 83 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 71
EGAD00001008885
Rare cancer sequencing data of 96 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 89
EGAD00001008886
Rare cancer sequencing data of 29 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 28
EGAD00001008887
Rare cancer sequencing data of 66 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 58
EGAD00001008888
Rare cancer sequencing data of 48 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 41
EGAD00001008889
Rare cancer sequencing data of 22 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 17
EGAD00001008890
Rare cancer sequencing data of 76 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 72
EGAD00001008891
Rare cancer sequencing data of 164 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 159
EGAD00001008892
Rare cancer sequencing data of 42 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 42
EGAD00001008893
Rare cancer sequencing data of 112 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 100
EGAD00001008894
Rare cancer sequencing data of 34 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 28
EGAD00001008895
Rare cancer sequencing data of 49 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 43
EGAD00001008896
Rare cancer sequencing data of 137 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 138
EGAD00001008897
Rare cancer sequencing data of 246 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 250
EGAD00001008898
Rare cancer sequencing data of 34 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2500,Illumina HiSeq 4000 34
EGAD00001008899
Rare cancer sequencing data of 6 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 6
EGAD00001008900
Rare cancer sequencing data of 142 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 134
EGAD00001008901
Rare cancer sequencing data of 28 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 4000 24
EGAD00001008902
Rare cancer sequencing data of 85 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 77
EGAD00001008903
Rare cancer sequencing data of 36 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 34
EGAD00001008904
Rare cancer sequencing data of 112 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 106
EGAD00001008905
RNA-Seq, WES and WGS data of 5 rare tumor/control pairs which were submitted to other HIPO projects, not MASTER. The sequencing was always paired.
HiSeq X Ten,Illumina HiSeq 2000 11
EGAD00001008906
Part of the published data from EGAS00001004662 resulted in the publication of this study EGAS00001004813
HiSeq X Ten 5
EGAD00001009273
WES/WGS sequencing data of 86 chromothriptic tumor and control runs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2000,Illumina HiSeq 2500,Illumina HiSeq 4000 86
EGAD00001009274
WES/WGS sequencing data of 337 chromothriptic tumor and control runs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten,Illumina HiSeq 4000 319
EGAD00001009277
WES/WGS sequencing data of 44 chromothriptic tumor and control runs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 40
EGAD00001009278
WES/WGS sequencing data of 242 chromothriptic tumor and control runs, which were uploaded to umbrella studies. The sequencing was always paired
Illumina HiSeq 2500,Illumina HiSeq 4000 242
EGAD00001009279
WES/WGS sequencing data of 239 chromothriptic tumor and control runs, which were uploaded to umbrella studies. The sequencing was always paired
HiSeq X Ten 218

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