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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1161217 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type/ r* i& Z) Z. d; N. i: a  Q* E! Y
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
- _/ E1 ^" D0 P3 {: `: `, U9 t) H+ Author Affiliations
' f) _0 U- M' I  }
& C) J6 s2 j# o; I- @1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
6 }* h  _+ S  i9 a' n, T! D2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan " Q4 w+ I( l2 ~& `" a& F$ d
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
! c. \( y8 b7 b$ q4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
+ [9 L! U& X7 p& |/ t7 A5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
  i2 m7 `' x" d, M/ v6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 8 [$ Q; G$ A( ]6 {7 ~  X
7Kinki University School of Medicine, Osaka 589-8511, Japan
; o" C9 m9 ~% z0 |; n8Izumi Municipal Hospital, Osaka 594-0071, Japan
5 W( [  ]3 P1 ~9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
" V$ V$ ?0 u/ mCorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
1 W2 ]9 C1 l$ PAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. / x, P5 v8 I7 d

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato   |7 C+ F; z, |9 _1 [2 z9 b! ]

* s& A/ E: I1 h" mAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  7 Y" K, X0 d, \

0 U3 K8 `. I& z7 W  ]0 [% k+ t) CPublished online on: Thursday, December 1, 2011 % ~( ], D8 N1 u; \

/ E  W- G3 E* r" bDoi: 10.3892/ol.2011.507
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$ @5 W- d1 S. L9 F5 APages: 405-410
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Abstract:
1 h( ^# V3 \8 i) H9 _- U/ R  R$ IS-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.$ i8 {+ s# e' u, I! b0 v0 l
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population0 j. y0 z; Y$ s+ L
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 & J& J' m% r, M! b
+ Author Affiliations
8 x1 |* V2 {# K* C1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu - ]! V, ^7 `/ @' i$ s* J
2Department of Thoracic Surgery, Kyoto University, Kyoto : x2 h; \8 z# a. t4 x& N
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan ( E8 b# e" [9 U# b0 Z) P
&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp ! D4 C: U0 H' a3 t& E
Received September 3, 2010. & C: m1 x% p" G3 o
Revision received November 11, 2010.
# {5 F; t, q5 _& D6 y9 g2 MAccepted November 17, 2010. + o" f- R! m" @1 {
Abstract
- Y, a" z7 A7 m, a2 U, F+ J1 a% E- rBackground: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. ! j8 S6 o: s+ x! O5 n
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. 4 `, f0 w( y5 L0 k
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
! l" o& L+ A# m, h; Z) a* ]. DConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. % r; c0 p: R: q# D
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。% P0 s" I3 \9 ?( m5 K8 O9 M# }7 j
今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?9 \* s% I8 u" Y
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy6 X, B! I1 a. z3 L& N
http://clinicaltrials.gov/ct2/show/NCT01523587, _( h: N# W& \: v* Y/ q3 x* D! s
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
' K" d8 o. [4 Q/ k/ O1 }# Lhttp://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑
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/ B# E/ t+ d+ x' h% _7 K+ b从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
$ ]0 J3 B" `. S" _! ]7 _至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53 # w' D1 h( Q# P, Z2 P6 C' X  L
从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。" x& s5 C/ [/ t! V- O% K9 U( Z1 T
至今为止,未出 ...

" Q0 X; V' {) R没有副作用是第一追求,效果显著是第二追求。7 ?" N7 z9 f7 O: Y: @4 A, e: S
不错。

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