This report updates patient and primary graft survival statistics for the liver transplantation program at the University of Pittsburgh for 1984 through 1990. Minimum follow-up for all patients is one year and only patients who received a primary liver graft in Pittsburgh are included. Recipients of multiple organ or multivisceral transplants, patients who received a primary graft at another center and were sent to Pittsburgh for rescue with FK506 or for retransplantation, and patients who underwent an extended resection (“cluster operation”) for cancer were excluded

Bronsther, O

Fung, J

Gordon, RD

Martin, M

Starzl, TE

Stieber, A

Todo, S

Tzakis, AG

Van Thiel, DH

PubMed

Name not available

Liver transplantation at the University of Pittsburgh, 1984 to 1990

D-Scholarship@Pitt

CHAPTER Liver Transplantation at the University of Pittsburgh, 1984 to 1990 Robert D. Gordon, John Fung, Andreas G. Tzakis, Satoru Todo, Andrei Stieber, Oscar Bronsther, Maureen Martin, David H. Van Thiel, Thomas E. Starzl Division of Transplantation, Department of Surgery rnke~nyofmmsburgh pmsburgh, Pennsylvania This report updates patient and primary graft sur-vival statistics for the liver transplantation program at the University of Pittsburgh for 1984 through 1990. Minimum follow-up for all patients is one year and only patients who received a primary liver graft in Pittsburgh are included. Recipients of multiple organ ormultMsceral transplants, patients who received a primary graft at another center and were sent to Pittsburgh for rescue with FK506 or for retransplantation, and patients who underwent an extended resection ("cluster operation") for cancer were excluded. METHODS DEMOGRAPHICS Time Periods and Treatment Protocols. The liver transplant program at the University of Pittsburgh was established in 1981. Data are presented for three time periods (Table 1) which correspond to major changes in treatment protocols. In the first three years of the program, protocols for immunosuppres-sion with cyclosporine (CsA) and prednisone (Pred) were refined, the veno-venous bypass technique for management of the an hepatic phase of the recipient operation was developed, and the techniques of mUl-tiple organ procurement from cadaveric donors using Euro-Collins and ice slush preservation were standard-ized. In 1984, we began using OKT3 monoclonal anti-body (Orthoclone OKT38 , , Ortho Pharmaceuticals) for T 1/)/,-> 1 1/1/(" If J!I"pIUJ( dJ(Jr/ lJnll Df""Df~ (il f'/thIWfI;fI Period N % 1184-9187 CsA. vein bvDass. OKT·3 787 37.7% 10187·12188 UWsolution 481 23.0% 1/89·12190 FK506 822 39.3% Total 2090 100.0% treatment of steroid resistant acute allograft rejection, after Cosimi and his associates at the Massachusetts General Hospital demonstrated its effectiveness forthe treatment of acute renal allograft rejection. These pro-tocols remained the essentials of patient management in Pittsburgh for the period from 1984 through Septem-ber, 1987, during which time 787 patients received a primary liver transplant. Of these patients, 573 (72.8%) ultimately received only one graft, 163 (20.7%) re-ceived two grafts, and 51 (6.5%) required three or more grafts. As of December 31, 1991, there were 480 (61.0%) surviving patients including 396 (50.3%) with a functioning first graft. In October, 1987, we began the regular use of the University of Wisconsin solution instead of Euro-Collins for liver preservation. Between October, 1987 and December, 1988 there were 481 recipients of a primary liver graft in Pittsburgh under CsA-Pred therapy. Among these patients, 390 (81.1 %) received only one graft, 70 (14.6%) received two grafts, and 21 (4.4%) received three or more grafts. As of December 31, 1991, there were 331 (68.8%) surviving patients including 292 (60.7%) with functioning first grafts. Experimental trials with FK506 began in 1989. From January, 1989 through December, 1990,822 patients received liver transplants, including 684 (83.2%) who required only one graft to date, 120 (14.6%) who received a second graft, and 18 (2.2%) who have received three or more grafts. As of December 31, 1991, there were 650 (79.1 %) surviving patients includ-ing 577 (70.2%) surviving with their first graft. In the entire series of 2,090 patients, 1,633 (78.1 %) were transplanted using the CsA-Pred regimen (Table 2), but 272 were eventually switched to FK506, Clinical Transplants 1991, P. Terasaki, Ed. UCLA Tissue Typing Laboratory, Los Angeles, CA 2 GORDON, FUNG, STARZL, ET AL Table 2. Immunosuppressive protocol Period 1 Period 2 Primary FK 506 Rescue FK 506 99 29 12.6% 6.0% Randomized trial* Primary GsA 688 452 87.4% 94.0% Total 787 481 Period 3 399 103 12.5% 112 13.6% 208 25.3% 822 Total 399 19.1% 231 11.1% 112 5.4% 1348 64.5% 2090 Age Groups and Body Weight ·Includes 54 patients randomized to CsA and 58 patients randomized to FK 506. The distribution of pa-tients according to age is shown in Table 3. There has been an increase in the proportion of elderly pa-tients(over60yearsofage) accepted for transplanta-tion since 1984 from 5.7% ofthe patients in period 1 to 16.0% of the patients in period 3. The proportion of infants receiving trans-plants has remained fairly constant. Survival rates for 208 small patients (un-der 12 kg) and 21 obese patients(over115 kg) were compared with survival rates for 1 ,383 adults be-tween 50 and 115 kg .. Table 3. Age Groups Period 1 Period 2 Infants 63 45 (under 2 yrs) 8.0% 9.4% Children 171 40 (2 - 11 yrs) 21.7% 8.3% Adolescents 37 9 (12-17 yrs) 4.7% 1.9% Adults 471 333 (18-59 yrs) 59.8% 69.2% Seniors 45 54 (over 60 yrs) 5.7% 11.2% Total 787 481 Table 4. Medical urgency Period 2 Period 3 Total Elective 26 17 43 5.4% 2.1% 3.3% Out of hospital 94 89 183 19.6% 10.8% 14.1% In hospital 216 304 520 45.1% 37.0% 40.0% Critical 143 412 555 29.9% 50.1% 42.7% Total 479 822 1301 including 41 of 54 patients who were transplanted un-der CsA-Pred in 1990 as part of a randomized trial comparing CsA-Pred to FK506. Another 103 of the 311 patients in period 3 who were transplanted under CsA-Pred, but were not part of the randomized trial, were also converted to FK506. Approximately 5 to 1 0 percent of the patients per year who received a primary graft under CsA-Pred during periods 1 and 2 have been converted to FK 506. Period 3 59 7.2% 46 5.6% 23 2.8% 562 68.4% 132 16.0% 822 Total 167 8.0% 257 12.3% 69 3.3% 1366 65.4% 231 11.1% 2090 Medical Urgency Table 4 presents the dis-tribution of patients in peri-ods 2 and 3 according to patient condition at the time of transplantation. There has been a substantial increase in the percentage of patients at this center in critical condition at the time of transplantation. Primary liver disease Distribution of the most common primary indications for liver transplantation for each period is shown in Table 5. The most significant changes were the relative decrease in the percentage of adult patients with pri-mary biliary cirrhosis and the increase in the percentage of patients with alcoholic cirrhosis. STATISTICAL METHODS Actuarial survival Survival out to 5 years after transplantation is pre-sented in a series of actuarial survival plots. Most of the cohorts analyzed for this report are large (over 100 patients) and therefore suitable for analYSis by the life-table method in which survival is determined over predefined time intervals (1, 3, 6, and every 6 mos thereafter out to 60 mos). Life-table data are presented as a plot of the estimated survivor function (the probabil-3 Table 5 Most common pnmary liver diseases Period 1 Period 2 Period 3 Total % % % % Fulminant hepatic failure 36 4.6 33 6.9 54 2.9 93 4.5 Postnecrotic cirrhosis 222 28.2 140 29.1 280 34.1 642 30.7 Cryptogenic cirrhosis" 166 21.1 83 17.3 1n 21.5 426 20.4 HBsAg+ cirrhosis 27 3.4 34 7.1 53 6.4 114 5.5 Autoimmune CAH 17 2.2 16 3.3 25 3.0 58 2.8 Alcoholic cirrhosis 39 5.0 69 4.3 167 20.3 275 13.2 Biliary atresia 152 19.3 52 10.8 81 9.9 285 13.6 Primary biliary cirrhosis 123 15.6 59 12.3 66 8.0 248 11.9 Sclerosing cholangitis 55 7.0 36 7.5 55 6.8 146 7 Genetic disorders 72 9.1 27 5.6 33 4.0 132 6.3 Alpha-1-antitrypsin deficiency 40 5.1 13 2.7 18 2.2 71 3.4 Wilson's disease 13 1.7 7 1.5 5 0.6 25 1.2 Primary liver cancer 20 3.2 32 6.7 58 7.1 110 5.3 .. includes all non-A, non-B fonns of viral hepatitis and cryptogenic cirrhosis in HBsAg- patients ity that a subject will survive to at least a specified time or longer) and as a plot of the cumulative hazard function (negative natural logarithm of the estimated survivor function). In the few series in which the number of cases was small, we used the product-limit (Kaplan-Meier) method of computation for the survivor function. Observed (actual) Survival This year the National Organ Sharing Network (UNOS) will release center-specific survival data (ob-served 3- and 12-month patient and primary graft survival rates) for transplantations performed between October 1, 1987 and December 31, 1989. The ob-served survival rate is simply the proportion of patients who survive to a specified cut point. Since follow-up for our series was complete and all patients were followed for at least 1 year, the 3- and 12-month estimated survivor functions determined by life-table calculation and by observed survival rate calculation should be identical. Figure 1 compares observed and actuarial patient and primary graft survival rates for each of the 3 periods at 3 and 12 months. Statistical significance Statistical significance between observed survival rates was determined using the chi-square statistic. For comparison of life-table survival curves, Breslow, Mantel-Cox, Peto, and Tarone-Ware statistics were calculated. Differences were considered statistically significant if p was less than 0.05. RESULTS Time Periods There has been a significant improvement in patient survival over the periods analyzed. Figures 2 and 3 present the life-table analysis plots for patient and primary graft survival by period. Table 6 shows the observed 3- and 12-month patient and primary graft survival rates. The life-table plots demonstrate that most of the mortality after liver transplantation (12-21 %) occurs within the first 3-months posttransplantation. The 3-month observed patient survival rate improved from 78.9% in period 1 to 88.7% in period 3. The 12-month patient survival rate improved from 72.3% in period 1 to 83.1 % in period 3. Immunosuppressive Protocol Table 7 presents the observed survival rates for 399 patients who received a transplant under an FK506 protocol, 391 historical control patients from period 2 who received transplants under a CsA protocol, and 161 patients converted from CsA to FK506. Survival rates under the FK506 protocol improved over those obtained for the historical CsA protocol controls. The differences in patient survival at 3 months and at 12 months between the FK506 treated patients and the CsA treated historical controls are highly significant (p < 0.01). The differences between the 2 groups for first graft survival at 3 and 12 months were significant (p< 0.02). The rescue series included aU patients who re-tained their first grafts and were converted to FK506 prior to January 1, 1991. The observed survival rates 4 GORDON, FUNG, STARZL, ET AL were calculated from the time of crossover to FK506. There is a high rate of successful patient and graft rescue out to 12 months after crossover. Results of the randomized trial comparing FK506 and GsA were presented recently by Fung et al1 and are not included here. _1184-9187 _10187·12188 -6-1/89-12190 --1184-9187 _10187-12188 .....A.-1189-1219O Table 6. Observed patient and graft survival rates by period Period 1 Period 2 Surviving Lost Surviving Lost 3 -month patient* 621 166 400 81 78.9% 21.1% 83.2% 16.8% 12-month patient* 569 218 366 115 72.3% 27.7% 76.1% 23.9% 3-month first graft* 548 239 363 118 69.6% 30.4% 75.5% 24.5% 12-month first graft* 491 296 331 150 62.4% 37.6% 68.8% 31.2% *p < 0.001 5 Period 3 Surviving Lost 729 93 88.7% 11.3% 683 139 83.1% 16.9% 654 168 79.6% 20.4% 604 218 73.5% 26.5% Table 7. Observed patient and graft survival rates - immunosuppression Primary FK 506 Historical CsA* After FK 506 rescue** Surviving Lost Surviving Lost Surviving Lost 3 -month patient 358 41 318 73 151 10 89.7% 10.3% 81.3% 18.7% 93.8% 6.2% 12-month patient 333 66 291 100 138 23 83.5% 16.5% 74.4% 25.6% 85.7% 14.3% 3-month first graft 327 72 294 97 144 17 82.0% 18.0% 75.2% 24.8% 89.4% 10.6% 12-month first graft 304 95 266 125 132 29 76.2% 23.8% 68.0% 32.0% 82.0% 18.0% * 391 patients treated with CsA-Pred in period 2 (10/87-12/88) **Observed sUlVival rates after rescue with FK 506 6 dloal~crkdIpqAowiIbqAi Age Group and Body Weight There were significant differences in survival rates among patients in different age groups and significant improvements in survival rates for most age groups across the 3 time periods. Figures 4 and 5 present the life-table plots for patient and primary graft survival by age groups. Table 8 shows the observed 3- and 12-month patient and primary graft survival rates. Survival rates for infants have been generally lower than for older children and adults, but in period 3, infant survival rates attained parity. Early survival rates for patients over 60 compared favorably with those for younger adult patients, but, as would be expected, for older patients there was a modest increase in the rate of patient loss over the longer term. In Figure 6 the estimated survivor and cumulative hazard functions (Kaplan-Meier method) were stratified into 3 weight groups, under 12 kg (small), 50-115 kg (normal adults), and over 115 kg (obese). Survival rates for small and obese patients were significantly lower than those for normal weight adult patients. 7 Medical Urgency Table 9 presents the observed patient and graft survival rates and Figure 7 presents the estimated patient survivor and cumulative hazard functions after liver transplantation according to patient condition the time of transplantation. A significant penalty is demon-strated for patients in high urgency status at the time of transplantation. Primary Liver Disease Tables 10 through 12 show the observed 3- and 12-month patient and primary graft survival rates for each time period according to primary liver disease. _-NormoI (&0-115 kg) _0bMe(>1151cg) """"_«12 kg) 8 GORDOMFUNG,STARZL,ETAL Table 9. Observed patient and graft survival rates by medical urgency Elective Out of hospital In hospital Critical Survivine Lost Surviving 3 -month patient 56 1 171 98.2% 1.8% 88.6% 12-month patient 54 3 167 94.7% 5.3% 86.5% 3-month first graft 54 3 154 94.7% 5.3% 79.8% 12-month first graft 49 8 148 86.0% 14.0% 76.7% Based on 1.345 patients from periods 2 and 3. Figures 8 and 9 illustrate the estimated survivor and cumulative hazard functions for patient and primary graft survival for patients with postnecrotic cirrhosis (excluding HBsAg+ patients), adult cholestatic liver disease (primary biliary cirrhosis and primary scleros-ing cholangitis), biliary atresias, and alcoholic cirrhosis. Figures 10 and 11 present the life-table functions for patient and primary graft survival for patients with fulminant failure, chronic active hepatitis B (HBsAg+ patients), and primary liver cancer (mostly hepatomas). As mentioned earlier, overall results for the most recent period have improved significantly over earlier results. The most dramatic improvements in survival rates were seen in patients receiving liver transplants for fulminant hepatic failure, chronic active hepatitis B, biliary atresia, and primary sclerosing cholangitis. I n the case of fulminant hepatiC failure, new protocols for monitoring of intracerebral blood flow and prevention of excess intracranial pressure were probably responsible ..... -E_tNoo57) __ Out alh_tN='.') --.. hoopilal 1"00532) Lost Survivine Lost Surviving Lost 22 482 50 481 102 11.4% 90.6% 9.4% 81.9% 18.1% 26 451 81 415 148 13.5% 84.8% 15.2% 73.7% 26.3% 39 440 92 403 160 20.2% 82.7% 17.3% 71.6% 28.4% 45 398 134 366 197 23.3% 74.8% 25.2% 65.0% 35.0% for the improved results. In biliary atresia, technical improvements in arterial reconstruction, increased use of reduced grafts to find organs for smaller children, and improved immunosuppression with FK506 protocols may have all contributed to the improvements. For chronic active hepatitis B, immunoprophylaxis, includ-ing both active and passive immunization, and a re-duced requirement for steroids in patients receiving FK506 may have a beneficial effect. Earlier referral of patients, decreasing technical difficulties in performing liver transplantation in patients with prior surgery (in-cluding biliary diversion or prior bowel resection), and improvements in immunosuppression have probably contributed to the improved results for patients with sclerosing cholangitis. We continue to offer liver transplantation to patients with alcoholic cirrhosis and to obtain results which compare favorably to those obtained in patients with other forms of postnecrotic cirrhosis. ---__ Out aI hoopilal --.. hoopiIaI __ Critical.,.,. cln1losis Cryptogenic cirrhosis· HBsA(JI- cirrhosis Autoimmune CAH cln1losls Cryptogenic cirrhosis· HBsA(JI- cirrhosis Autoimmune CAH 9 10 GORDON, FUNG, STARZL, ETAL __ Pootrwa* _ ChdM _  ........ _--r--.y __ 11 12 GORDON, FUNG, STARZL, ET AL New protocols for liver transplantation for primary cancer which have been instituted in our program have not yet been analyzed and are not presented here. Iwatsuki et al2 recently summarized our experience for 1980-1989 with hepatocellular carcinoma in a report which favorably compared results for liver transplanta-tion with hepatic resection. The reader is advised to consult this paper for additional information. CONCLUSION Survival after liver transplantation continues to im-prove, reflecting continuing advances in surgical meth-ods, organ preservation, and immunosuppressive pro-tocols. At the present time, the Health Care Financing Administration (Medicare) has approved liver trans-plantation for biliary atresia in children and for postnecrotic cirrhosis (except for HBsAg+ patients), alcoholic cirrhosis, primary sclerosing cholangitis, pri-mary biliary cirrhosis, alpha-1-antitrypsin deficiency, Wilson's disease, and hemochromatosis in adults. Liver transplantation for fulminant hepatic failure and for chronic active hepatitis B has not yet been approved. Given the improved results now being obtained, expan-sion of the approved indications for liver transplantation to include fulminant hepatiC failure and chronic active hepatitis B seems warranted. References 1. Fung J, Abu-Elmagd K, Jain A, et al. A randomized trial of primary liver transplantation under immuno-suppression with FK 506 vs cyclosporine. Trans-plant Proc 1991; 23:2977. 2. Iwatsuki S, Starzl TE, Sheahan DG, et al. Hepatic resection versus transplantation for hepatocellular carcinoma. Ann Surg 1991; 214:221. SUMMARY Patient and primary graft survival for 2,090 pa-tients who received primary liver transplants at the University of Pittsburgh from 1984 through 1990 are presented. Observed (actual) 3- and 12-month pa-tient and first graft survival rates were compared for three time periods: 1) January, 1984 -September, 1987 (cyclosporine, OKT3, and Euro-Collins pres-ervation period); 2) October, 1987 - December, 1988 (University of Wisconsin solution preservation period); and 3) January, 1989 - December, 1990 (FKS06 period). Data for results according to age group, medical urgency, and primary diagnosis are provided. In addition, estimated survivor and cumu-lative hazard functions (Iife-tanle method) for pa-tient and first graft survival out to 60 months after transplantation are presented. Overall results have improved significantly in recent experience. Most notable are the improved results seen in liver transplantation for patients with biliary atresia (especially in infants), primary scle-rosing cholangitis, fulminant hepatic failure, and chronic active hepatitis B. For all but a few condi-tions, most of the mortality after liver transplantation occurs in the first three months after surgery. Less than 2% of patients are lost in each 6-month interval beyond the first 6 months after transplantation. Outcome is related to patient condition at the time of transplantation. Observed patient survival rates at 3 and at 12 months for patients called in to the hospital to receive a graft were 88.6% and 86.S%, respectively, compared to 81.9% and 73.7% for patients in critical condition. The continuing shortage of organs for transplantation, which often forces patients to wait longer for an organ than they can afford to, continues to impose a significant penalty. 

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Liver transplantation at the University of Pittsburgh, 1984 to 1990

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