autologous blood and marrow transplantation - Blog Science ...

More documents

Recommendations

Info

384 Chapter 7: Solid Tumors months off therapy. For this platinum-resistant group, a variety of agents may produce remissions, including paclitaxel, 713 topotecan, 7,8 liposomal doxorubicin, 15 oral low-dose etoposide, 16 and hexamethymelamine. 17 Remissions occur in approximately 20% and last 3-4 months, and survival from the onset of first relapse is 5-12 months. In contrast, those whose remissions lasted more than 6 months can expect to respond to platinum in the range of 35^10%. Remissions for these patients usually last 6-9 months, and survival averages 20-24 months. No conventional single agent or combination chemotherapy is superior to the reintroduction of platinum for this patient group. 13 Our results indicate that for patients with recurrent platinum-sensitive, lowtumor-burden disease, transplant offers a superior overall survival to conventional options, with approximately 20% having long-term PFS. However, for those with platinum-resistant and, especially, bulky disease, transplant appears to offer similar PFS and OS to conventional therapies and, given its toxicity and costs, should not be generally recommended. Patients meeting the criteria of platinum-sensitive, low-tumor-burden disease then should be offered the option of transplant at the time of first relapse. Regarding the comparisons reported here, the only significant difference between the transplant patients and those treated with conventional-dose chemotherapy is that the median age for the transplant patients was approximately 10 years younger. While we found that age was an important prognostic factor for survival of the transplant patients, it was not so for PFS. In addition, Duska et al. 18 recently reported that controlling for stage and tumor grade, the median survival for women in the reproductive age group with advanced ovarian cancer was not different from that for older patients. None of the patients described here were treated for low malignant potential tumors. With the suggestion that platinum sensitivity and low tumor burden are important prognostic factors for patients undergoing transplants for this disease, it is possible that transplanting patients at an earlier point in their disease will yield superior results. The results with 10 patients described here treated with taxenebased therapy suggest that transplants are of value in this setting, with the best PFS reported for suboptimal III/IV disease with conventional platinum/taxene therapy at 18 months compared with the >26 months reported here. Several larger pilot studies have recently been reported that also describe transplants at the time of second-look surgery. The largest report to date is that by Legros et al. 19 Patients received chemotherapy with a platinum-based combination after debulking surgery, and after demonstrating platinum sensitivity, all were treated with high-dose chemotherapy with either melphalan at 140 mg/m 2 (23 patients) or carboplatin 1600 mg/m 2 and cyclophosphamide 6.4 g/m 2 (30 patients). At a median follow-up of >6.5 years, 23% are in continuous CR, and 45% are alive. Of 31 patients with no or only microscopic disease at second look, the disease-free survival at 5 years was 26.9%. For the 19
Stiff, Kerger, and Bayer 385 patients in this group with a negative second look, the 5-year disease-free survival (DFS) of 32.8% implies that the 12 patients with microscopic residual disease at second look have a similar DFS after the single transplant procedure. For those patients with bulky disease at the initiation of second-look surgery, the 5-year DFS was 19.2%, and the 5-year survival was 33.8%. These data appear superior for patients with a positive second look laparotomy to that described for those treated with only conventional therapy after second-look surgery. Considering recent reports of survival after second-look surgery for optimal or suboptimal disease, and the fact that 42% of this group had suboptimal disease at diagnosis, we would expect the median survival for this group to be ~45 months treated with conventional therapy rather than the 66 months reported. Given the improvements in the conventional therapy for this tumor and the patient selection biases inherent in these pilot studies of transplants as consolidation therapy, the true value of transplantation in the initial management of patients with advanced ovarian cancer will come only from randomized trials. Certainly, the preliminary results of our ongoing paclitaxel, mitoxantrone, and carboplatin trials would indicate that this therapy may be useful for this patient group, and in the absence of a comparative trial, should be considered. However, all eligible patients should be enrolled in any available comparative phase III trial. Under the auspices of the National Cancer Institute (NCI), the GOG as well as SWOG, CALGB, and ECOG recently began a randomized phase III trial. Patients with stage III or IV disease who respond to four to six cycles of a platinum-based regimen after debulking surgery and have a clinical CR (suboptimal III and IV) or a PR documented by a second-look laparotomy will be randomized between six cycles of paclitaxel (175 mg/m 3 over 3 hours) combined with carboplatin at an AUC of 7.5 and a single transplant using the carboplatin, mitoxantrone, cyclophosphamide regimen described by our program. The trial, which is expected to take 5 years, will include those initially debulked suboptimally including those with a pathologic CR in view of their high expected relapse rate. Accrual has been slow primarily because of the slow acceptance of this form of therapy by patients and their physicians. Also, some transplant physicians feel that no conventional therapy is acceptable for patients with a disease that has such a poor prognosis. Efforts to improve the understanding of this therapy by patients and physicians and a clear explanation of its rationale should help to increase accrual. Unlike the breast cancer trials, the goal was to initiate this trial before the publication of extensive pilot data indicating its effectiveness, which would result in patients demanding this therapy at all costs. Fortunately, the insurance industry has in large measure supported this trial, as it has the breast cancer transplant trials. Alternative approaches such as that reported by Fennelly et al. 20 that explore double-dose chemotherapy in rapid succession at the time of initial diagnosis with stem cell rescue (dose-dense), followed by a single cycle of high-dose melphalan,
Page 1:
AUTOLOGOUS BLOOD AND MARROW TRANSPL
Page 5 and 6:
AUTOLOGOUS BLOOD AND MARROW TRANSPL
Page 7:
ACKNOWLEDGMENTS We wish to thank Wi
Page 11:
THE VAN BEKKUM STEM CELL AWARD Prof
Page 14 and 15:
xii Table of Contents CHAPTER 2: AL
Page 16 and 17:
xiv Table of Contents Late Non-Rela
Page 18 and 19:
xvi Table of Contents Pretreatment
Page 20 and 21:
xviii Table of Contents CHAPTER 7:
Page 22 and 23:
XX Table of Contents Long-Term Obse
Page 24 and 25:
xxii Table of Contents CHAPTER 13:
Page 27 and 28:
0-9 LIST OF ABBREVIATIONS 2CDA 2-ch
Page 29 and 30:
List of Abbreviations xxvii EFS eve
Page 31 and 32:
List of Abbreviations MOPP mechlore
Page 33:
VOD veno-occlusive disease VPC viru
Page 37 and 38:
4HC-Purged Autologous Stem Cell Tra
Page 39 and 40:
1.0-1 + 0.2 Miller et al. 5 Event F
Page 41 and 42:
Miller et al. Adjusted probability
Page 43 and 44:
Who Benefits From Autograft in AML
Page 45 and 46:
Burnett 11 which to set the transpl
Page 47 and 48:
Table 1. Outcome after relapse in M
Page 49 and 50:
Immunotherapy in AML: No Positive E
Page 51 and 52:
Simonsson et al. inhibit IL-2 induc
Page 53 and 54:
Autologous Bone Marrow Transplantat
Page 55 and 56:
Ball et al. 21 CD15) and AML-2-23 (
Page 57 and 58:
Ball et al. 23 The ex vivo treatmen
Page 59 and 60:
Ball et al. 25 Table 2. Factors inv
Page 61 and 62:
Ball et al. Overall Survival for Pa
Page 63 and 64:
Ball et al. Overall Survival for Pa
Page 65 and 66:
Ball et al. 31 Overall Survival for
Page 67 and 68:
Ball et al. Table 4. Actuarial over
Page 69 and 70:
Ball et al. myeloid leukemia. The G
Page 71 and 72:
Ball et al. 1993. 38. Mehta J, Powl
Page 73 and 74:
Can Autologous Stem Cell Transplant
Page 75 and 76:
De Witte et al. 41 novo AML. Auer r
Page 77 and 78:
De Witte et al. hematopoietic engra
Page 79 and 80:
De Witte et al. 23. Fenaux P, Laï
Page 81 and 82:
Stein et al. and fever. No patient
Page 83 and 84:
Stein et al. after doses 1, 3, and
Page 85 and 86:
Stein et al. early after the transp
Page 87:
autologous stem-cell rescue. / Clin
Page 91 and 92:
Bone Marrow Transplantation for Acu
Page 93 and 94:
Table 2. Autologous BMT in ALL in f
Page 95 and 96:
Rowe 61 or adult patients with acut
Page 97 and 98:
Hoelzer and Gôkbuget minitransplan
Page 99 and 100:
Hoelzer and Gdkbuget 65 blood, earl
Page 101 and 102:
Table 3. Risk factors for the defin
Page 103 and 104:
Hoelzer and Gôkbuget treatment opt
Page 105 and 106:
Hoeker and Gökbuget tical sibling
Page 107 and 108:
Sierra et al. INTRODUCTION Two-thir
Page 109 and 110:
Sierra et al. Table 2. Adverse char
Page 111 and 112:
1,0 0,0 J Sierra et al. 0 20 40 60
Page 113 and 114:
Sierra et al. Months Figure 4 < 30,
Page 115 and 116:
Sierra et al. No adverse factors (n
Page 117 and 118:
1994. Sierra et al. 83 10. Canals C
Page 119 and 120:
Martin, Atta, and Hoelzer 85 adult
Page 121 and 122:
Martin, Atta, and Hoelzer 87 Single
Page 123 and 124:
100. Martin, Atta, and Hoelzer 89 P
Page 125 and 126:
Martin, Atta, and Hoelzer 91 chromo
Page 127 and 128:
Autologous vs. Unrelated Allogeneic
Page 129 and 130:
Boyer and Yeager 95 outcomes after
Page 131 and 132:
Boyer and Y eager 97 Table 2. Hypot
Page 133 and 134:
Boyer and Y eager SUMMARY Most of t
Page 135:
CHAPTER 3 CML
Page 138 and 139:
Autograft Followed by Allograft Wit
Page 140 and 141:
106 Chapter 3: CML (one low-grade a
Page 142 and 143:
108 Chapter 3: CML DISCUSSION Myelo
Page 144 and 145:
110 Chapter 3: CML Philadelphia-neg
Page 146 and 147:
The Case for Manipulation of CML Au
Page 148 and 149:
Toward a Cure by Drug Treatment? Th
Page 150 and 151:
116 Chapter 3 :CML Table 1. Prolong
Page 152 and 153:
118 Chapter 3: CML Table 3. German
Page 154 and 155:
120 Chapter 3: CML Table 5. Normal
Page 156 and 157:
122 Chapter 3: CML Table 8. Surviva
Page 158 and 159:
124 Chapter 3: CML 88:3118-3122, 19
Page 160 and 161:
126 Chapter 3: CML RK, Klingemann H
Page 162 and 163:
The Tyrphostin AG957 Inhibits the I
Page 164 and 165:
130 Chapter 3: CML mobilization. Al
Page 166 and 167:
132 Chapter 3: CML A B 100 n 0 1 5
Page 168 and 169:
134 Chapter 3: CML The in vitro sel
Page 170 and 171:
136 Chapter 3: CML detecting leukem
Page 173 and 174:
Progressive Hodglcin's Lymphoma Fol
Page 175 and 176:
Reece et al. survival is observed i
Page 177 and 178:
0.2 -I 0.0 0 Reece et al. 143 ii i
Page 179 and 180:
Reece et al. Table 3. Causes of non
Page 181 and 182:
Reece et al. carmustine, etoposide
Page 183 and 184:
CD34 + Selection of Hematopoietic B
Page 185 and 186:
Lazarus et al. 151 significantly de
Page 187 and 188:
Lazarus et al. 153 (Sigma, St Louis
Page 189 and 190:
Lazarus et al. 155 Table 2. Effect
Page 191 and 192:
Lazarus et al. 157 difference. Furt
Page 193 and 194:
Lazarus et al. 159 cells after myel
Page 195 and 196:
The European CUP/UP Trial: A Prelim
Page 197 and 198:
Table 1. Patient characteristics at
Page 199 and 200:
Schouten et al. licular non-Hodgkin
Page 201 and 202:
Sweetenham et al. vs. autologous pe
Page 203 and 204:
Table 1. Patient characteristics, g
Page 205 and 206:
Table 2. Patient characteristics, g
Page 207 and 208:
Table 3. Sites of relapse, group A
Page 209 and 210:
Table 4. Patterns of relapse, group
Page 211 and 212:
A 100 80 %OS 60 40 20 B 100 %OS | S
Page 213 and 214:
Sweetenham et al. new sites, and fi
Page 215 and 216:
Sweetenham et al. Treatment options
Page 217 and 218:
Molecular Remission: A Worthwhile A
Page 219 and 220:
Early or Late Autotransplant in Hig
Page 221 and 222:
Schenkein et al. 187 PATIENTS AND M
Page 223 and 224:
Schenkein et al. 189 Toxicity Toxic
Page 225 and 226:
Schenkein et al. 191 16. Glick JH,
Page 227 and 228:
Santini et al. 193 to evaluate the
Page 229 and 230:
Table 1. Continued Santini et al. 1
Page 231 and 232:
Santini et al. 197 cytosine arabino
Page 233 and 234:
1 0 0 1 90- 80- 70- (0 u. 60' o so-
Page 235 and 236:
Hodgkin's lymphoma. N EnglJ Med 333
Page 237:
CHAPTER 5 MYELOMA
Page 240 and 241:
206 Chapter 5: Myeloma independent
Page 242 and 243:
208 Chapter 5: Myeloma disease (MRD
Page 244 and 245:
210 Chapter 5: Myeloma Scandinavia,
Page 246 and 247:
212 Chapter 5: Myeloma (0 n o B co
Page 248 and 249:
214 Chapter 5: Myeloma B cq d ? o c
Page 250 and 251:
216 Chapter 5: Myeloma patients wit
Page 252 and 253:
218 Chapter 5: Myeloma PBSC transpl
Page 254 and 255:
220 Chapter 5: Myeloma 25. Seiden M
Page 256 and 257:
Autologous Transplantation in Multi
Page 258 and 259:
224 Chapter 5: Myeloma 0 52 44 U §
Page 260 and 261:
226 Chapter 5: Myeloma BM ^ (CD34±
Page 262 and 263:
228 Chapter 5: Myeloma IFM 94 : OS
Page 264 and 265:
230 Chapter 5: Myeloma two groups a
Page 266 and 267:
232 Chapter 5: Myeloma increase bot
Page 268 and 269:
234 Chapter 5: Myeloma REFERENCES 1
Page 270 and 271:
236 Chapter 5: Myeloma Intensified
Page 272 and 273:
238 Chapter 5: Myeloma of CD34 + ce
Page 274 and 275:
Chapter 5: Myeloma Table 2. Descrip
Page 276 and 277:
242 Chapter 5: Myeloma o 8H 0 2 4 6
Page 278 and 279:
244 Chapter 5: Myeloma ated with sh
Page 281 and 282:
The Presence of Micrometastases in
Page 283 and 284:
Kvalheim et al. 249 Table 1. Immuno
Page 285 and 286:
Kvalheim et al. 251 Figure 1. Sixty
Page 287 and 288:
Kvalheim et al. 253 DISCUSSION In t
Page 289 and 290:
Kvalheim et al. 255 Bastert G: Micr
Page 291 and 292:
Hood et al. 257 In an effort to inc
Page 293 and 294:
#CD34 + cells in blood = Hood et al
Page 295 and 296:
Hood et al. 261 Table 3. Frequency
Page 297 and 298:
Hood et al. 263 REFERENCES 1. Rill
Page 299 and 300:
The Clinical Significance of Breast
Page 301 and 302:
Moss et al. tests, and bilateral po
Page 303 and 304:
Moss et al. 269 0 15 70 143 200 400
Page 305 and 306:
Moss et al. 271 0 3 6 12 18 24 30 3
Page 307 and 308:
Moss et al. 273 8. Passos-Coelho J,
Page 309 and 310:
Autotransplantation for Men With Br
Page 311 and 312:
McCarthy et al. 277 radiation, two
Page 313 and 314:
High Dose Sequential Chemotherapy W
Page 315 and 316:
Viens et al. 281 3 g/m 2 and doxoru
Page 317 and 318:
Table 1. Tumor characteristics Exte
Page 319 and 320:
Table 4. Response Viens et al. 285
Page 321 and 322:
Viens et al. 287 Table 5. Pathologi
Page 323 and 324:
Viens et al. 289 apy for inoperable
Page 325 and 326:
Gliick et al. 291 INTRODUCTION The
Page 327 and 328:
Gluck et al. 293 RESULTS Patient de
Page 329 and 330:
Glück et al. 295 Table 3. Response
Page 331 and 332:
Gluck et al. 297 Overall Survival O
Page 333 and 334:
Gluck et al. 299 Sudbury patients w
Page 335 and 336:
Gluck et al. 301 anthracycline or t
Page 337 and 338:
Repetitive High-Dose Therapy With P
Page 339 and 340:
Prince et al. paramagnetic separati
Page 341 and 342:
Prince et al. Table 1. High-dose re
Page 343 and 344:
Table 2. Patient characteristics (n
Page 345 and 346:
Table 4. Hematopoietic recovery fol
Page 347 and 348:
1.0- M C .S 0.8- a c *fe o o> 0.6-
Page 349 and 350:
M 1.0 I 0.8H s? VI o.6H S 0.2 0.0 P
Page 351 and 352:
a Prince et al. days to platelets >
Page 353 and 354:
Table 5. Results of Isolex 300i CD3
Page 355 and 356:
Prince et al. 321 Figure 5, continu
Page 357 and 358:
Prince et al. 323 months after tran
Page 359 and 360:
Prince et al. 325 excessive to be u
Page 361 and 362:
Prince et al. 327 eight patients ha
Page 363 and 364:
Prince et al. 329 marrow transplant
Page 365 and 366:
Prince et al. intensive chemotherap
Page 367 and 368: -Q CO .Q O 1.0 0.9 0.8 0.7 0.6 0.5
Page 369 and 370: .Q CD .Q O 1.0 0.9 0.8 0.7 0.6 0.5
Page 371 and 372: oba Q. 1.0 0.9 Dicke et al. Stage I
Page 373 and 374: Vahdat with peripheral blood progen
Page 375 and 376: Evaluation of Prognostic Factors fo
Page 377 and 378: Fields et al. 343 PATIENTS AND METH
Page 379 and 380: Table 1. Chemotherapy regimens. Fie
Page 381 and 382: Fields et al. Stage II; 4-9 Pos LN
Page 383 and 384: U U Fields et al.
Page 385 and 386: Fields et al. 351 between 1 and 2 y
Page 387 and 388: European Trends and the EBMT Databa
Page 389 and 390: 25% % 22% / 17% \ Rosti et al. 355
Page 391 and 392: Rosti et al. 357 The new Italian St
Page 393 and 394:
Page 395 and 396: Rosti et al. 6. Haas R, Schmid H, H
Page 397 and 398: Bewick et al. 363 INTRODUCTION The
Page 399 and 400: Bewick et al. 365 Blood samples obt
Page 401 and 402: Bewick et al. 367 HDCT with ABSC su
Page 403 and 404: Bewick et al. Progression Free Surv
Page 405 and 406: Bewick et al. pression in MBC, i.e.
Page 407 and 408: Bewick et al. 14. Kandl HL, Seymour
Page 409: CHAPTER 7 OTHER SOLID TUMORS
Page 412 and 413: 378 Chapter 7: Solid Tumors INTRODU
Page 414 and 415: 380 Chapter 7: Solid Tumors Prepara
Page 416 and 417: 382 Chapter 7: Solid Tumors Surviva
Page 420 and 421: 386 Chapter 7: Solid Tumors have be
Page 422 and 423: High-Dose Chemotherapy in the Manag
Page 424 and 425: 390 Chapter 7: Solid Tumors followe
Page 426 and 427: 392 Chapter 7: Solid Tumors Table 1
Page 428 and 429: 394 Chapter 7: Solid Tumors (mucosi
Page 430 and 431: Three-Fold Intensification by Seque
Page 436 and 437: High-Dose Therapy for Small Cell Lu
Page 438 and 439: 404 Chapter 7: Solid Tumors chemoth
Page 440 and 441: 406 Chapter 7: Solid Tumors SCLC ha
Page 442 and 443: 408 Chapter 7: Solid Tumors relapse
Page 444 and 445: 410 Chapter 7: Solid Tumors 69:585-
Page 446 and 447: 412 Chapter 7: Solid Tumors ogous b
Page 448 and 449: 414 Chapter 7: Solid Tumors 64. Bru
Page 450 and 451: 416 Chapter 7: Solid Tumors Prignot
Page 452 and 453: 418 Chapter 7: Solid Tumors CO > CO
Page 454 and 455: 420 Chapter 7: Solid Tumors TANDEM
Page 456 and 457: Multiple Courses of Cyclophosphamid
Page 458 and 459: 424 Chapter 7: Solid Tumors and the
Page 460 and 461: 426 Chapter 7: Solid Tumors Thiotep
Page 464 and 465: 430 Chapter 7: Solid Tumors E 100 0
Page 466 and 467: 432 Chapter 7: Solid Tumors course
Page 468 and 469:
434 Chapter 7: Solid Tumors boplati
Page 470 and 471:
436 Chapter 7: Solid Tumors INTRODU
Page 472 and 473:
438 - Chapter 7: Solid Tumors Table
Page 474 and 475:
440 Chapter 7: Solid Tumors seeded
Page 476 and 477:
442 Chapter 7: Solid Tumors DISCUSS
Page 478 and 479:
444 Chapter 7: Solid Tumors 10. Di
Page 480 and 481:
446 Chapter 7: Solid Tumors plasma
Page 483 and 484:
Autologous Stem Cell Transplantatio
Page 485 and 486:
Keystone 451 hypertension, anemia,
Page 487 and 488:
Fassas et al. 453 INTRODUCTION Mult
Page 489 and 490:
Fassas et al. Table 2. Stem cell mo
Page 491 and 492:
Table 3. Toxicity after stem cell i
Page 493 and 494:
Fassas et al. Table 5. Trial 1: cha
Page 495 and 496:
Fassas et al. MS PROGRESSION FREE S
Page 497 and 498:
Fassas et al. ic or autologous bone
Page 499 and 500:
1 2 1 6 EAE. Burt et al. 465 Becaus
Page 501 and 502:
Burt et al. Since cyclophosphamide
Page 503 and 504:
Burt et al. 469 toxicity study, we
Page 505 and 506:
Burt et dl. All 23. Mor F, Cohen IR
Page 507 and 508:
Hasler, Gratwohl, and Tyndall an ev
Page 509 and 510:
Hasler, Gratwohl, and Tyndall 475 B
Page 511 and 512:
Kuis, Wulffraat, and Sanders 477 st
Page 513 and 514:
Kuis, Wulffraat, and Sanders neousl
Page 515:
CHAPTER 9 LONG-TERM EFFECTS
Page 518 and 519:
484 Chapter 9: Long-Term Effects po
Page 520 and 521:
486 Chapter 9: Long-Term Effects Ta
Page 522 and 523:
488 Chapter 9: Long-Term Effects ml
Page 524 and 525:
490 Chapter 9: Long-Term Effects 4.
Page 526 and 527:
492 Chapter 9: Long-Term Effects us
Page 528 and 529:
494 Chapter 9: Long-Term Effects AB
Page 530 and 531:
Page 532 and 533:
498 Chapter 9: Long-Term Effects En
Page 534 and 535:
500 Chapter 9: Long-Term Effects Rl
Page 536 and 537:
502 Chapter 9: Long-Term Effects RE
Page 538 and 539:
504 Chapter 9: Long-Term Effects A,
Page 540 and 541:
Long-Term Follow-Up of Autologous T
Page 542 and 543:
Page 545:
CHAPTER 10 GRAFT MANIPULATION
Page 548 and 549:
514 Chapter 10: Graft Manipulation
Page 550 and 551:
Page 552 and 553:
Page 554 and 555:
Page 556 and 557:
Page 558 and 559:
Page 560 and 561:
Page 562 and 563:
Page 564 and 565:
Page 566 and 567:
Page 568 and 569:
Page 570 and 571:
Page 572 and 573:
Page 574 and 575:
Page 576 and 577:
Page 578 and 579:
Page 580 and 581:
Page 582 and 583:
Page 584 and 585:
Page 586 and 587:
Page 588 and 589:
Page 590 and 591:
Page 592 and 593:
Page 594 and 595:
Page 596 and 597:
Page 598 and 599:
Page 600 and 601:
Page 602 and 603:
Page 604 and 605:
Page 606 and 607:
Stem Cell Reinfusion Over Two Conse
Page 608 and 609:
Page 610 and 611:
Page 612 and 613:
Page 614 and 615:
Final Report of the First Prospecti
Page 616 and 617:
Page 618 and 619:
Page 620 and 621:
Page 622 and 623:
Page 624 and 625:
Page 626 and 627:
Page 628 and 629:
Page 630 and 631:
Page 632 and 633:
Page 635 and 636:
Canine Hematopoietic Stem Allograft
Page 637 and 638:
Sandmaier et al. 603 The resultant
Page 639 and 640:
Sandmaier et al. 605 synthesis path
Page 641 and 642:
Sandmaier et al. 607 interactions o
Page 643 and 644:
Sandmaier et al. 1991. 2. Burchenal
Page 645 and 646:
87:3508-3513,1996. Sandmaier et al.
Page 647 and 648:
Giralt, Khouri, and Champlin Table
Page 649 and 650:
Giralt, Khouri, and Champlin seven
Page 651 and 652:
1.0 3 0.2 Giralt, Khouri, and Champ
Page 653:
CHAPTER 12 GENE THERAPY
Page 656 and 657:
622 Chapter 12: Gene Therapy INTROD
Page 658 and 659:
624 Chapter 12: Gene Therapy RESULT
Page 660 and 661:
626 Chapter 12: Gene Therapy envisi
Page 662 and 663:
628 Chapter 12: Gene Therapy cer in
Page 664 and 665:
A Vaccine of Melanoma Peptide Loade
Page 667 and 668:
B43(anti-CD 19)-Gen i stein Immunot
Page 669 and 670:
Targeting Immunotherapy for the Tre
Page 671 and 672:
McGuinness andArceci 637 modified m
Page 673 and 674:
McGuinness andArceci 639 leukemic c
Page 675 and 676:
McGuinness and Arced 641 in G418. T
Page 677 and 678:
McGuinness andArceci 643 Figure 2
Page 679 and 680:
mRNA for hB7-1 (1491 bp) mRNA for C
Page 681 and 682:
McGuinness and Arced CD80PE C080PE
Page 683 and 684:
McGuinness andArceci 649 8. Robert
Page 685 and 686:
McGuinness andArceci immune respons
Page 687 and 688:
McGuinness andArceci 75. Jubinsky F
Page 689 and 690:
Slavin et al. 655 up suggests, as p
Page 691 and 692:
Slavin et al. 657 was a phase lib c
Page 693 and 694:
Slavin et al. presented, appears to
Page 695 and 696:
Antitumor Immunotherapy in Autologo
Page 697 and 698:
Klingemann et al. 663 Table 3. Meth
Page 699:
CHAPTER 14 RADIOIMMUNOTHERAPY
Page 702 and 703:
668 Chapter 14: Radioimmunotherapy
Page 704 and 705:
Page 706 and 707:
Page 708 and 709:
Page 710 and 711:
Page 712 and 713:
Page 714 and 715:
Selection of Radioisotopes, Chelate
Page 716 and 717:
Page 718 and 719:
Page 720 and 721:
Page 722 and 723:
Page 724 and 725:
Page 726 and 727:
Radioimmunotherapy of Common Epithe
Page 729:
CHAPTER 15 NEW AVENUES
Page 732 and 733:
698 Chapter 15: New Avenues Table 1
Page 734 and 735:
700 Chapter 15: New Avenues An alte
Page 736 and 737:
702 Chapter 15: New Avenues who can
Page 738 and 739:
704 Chapter 15: New Avenues myeloid
Page 740 and 741:
706 Chapter 15: New Avenues 48. Gir
Page 742 and 743:
Emerging Viral Infections in Blood
Page 744 and 745:
710 Chapter 15: New Avenues influen
Page 746 and 747:
712 Chapter 15: New Avenues Among a
Page 748 and 749:
714 Chapter 15: New Avenues physica
Page 750 and 751:
716 Chapter 15: New Avenues respira
Page 752 and 753:
Minimal Therapy Models of Transplan
Page 755:
CHAPTER 16 SUMMARIES
Page 758 and 759:
724 Chapter 16: Summaries although
Page 760 and 761:
726 Chapter 16: Summaries use of po
Page 762 and 763:
728 Chapter 16: Summaries Table 1.
Page 764 and 765:
Page 766 and 767:
Page 768 and 769:
Page 770 and 771:
736 Chapter 16: Summaries IL-15. Th
Page 772 and 773:
738 Chapter 16: Summaries Patterns
Page 774 and 775:
740 List of Participants Thomas L.
Page 776 and 777:
742 List of Participants Sergio A.
Page 778 and 779:
744 List of Participants Hans Marti
Page 780 and 781:
746 List of Participants David P. S
Page 782 and 783:
748 List of Participants AUTHOR IND
Page 784 and 785:
750 Author Index Hurd, D.D. 483 Kui
Page 786 and 787:
752 Author Index Stiff, Patrick J.
Page 788 and 789:
754 Key Word Index Hematologic mali
Page 792:
ISBN 1-891524-04-6
show all

autologous blood and marrow transplantation - Blog Science ...

You also want an ePaper? Increase the reach of your titles

Delete template?

Save as template?